NM_007294.4(BRCA1):c.114G>A (p.Lys38=) AND Breast-ovarian cancer, familial, susceptibility to, 1
- Germline classification:
- Benign (7 submissions)
- Last evaluated:
- Jan 12, 2015
- Review status:
- 3 stars out of maximum of 4 starsreviewed by expert panel
- Somatic classification
of clinical impact: - None
- Review status:
- (0/4) 0 stars out of maximum of 4 starsno assertion criteria provided
- Somatic classification
of oncogenicity: - None
- Review status:
- (0/4) 0 stars out of maximum of 4 starsno assertion criteria provided
- Record status:
- current
- Accession:
- RCV000111799.22
Allele description [Variation Report for NM_007294.4(BRCA1):c.114G>A (p.Lys38=)]
NM_007294.4(BRCA1):c.114G>A (p.Lys38=)
- Gene:
- BRCA1:BRCA1 DNA repair associated [Gene - OMIM - HGNC]
- Variant type:
- single nucleotide variant
- Cytogenetic location:
- 17q21.31
- Genomic location:
- Preferred name:
- NM_007294.4(BRCA1):c.114G>A (p.Lys38=)
- Other names:
- 233G/A; K38K; 233 G>A; NP_009225.1:p.Lys38=
- HGVS:
- NC_000017.11:g.43115746C>T
- NG_005905.2:g.102238G>A
- NM_001407571.1:c.-75G>A
- NM_001407581.1:c.114G>A
- NM_001407582.1:c.114G>A
- NM_001407583.1:c.114G>A
- NM_001407585.1:c.114G>A
- NM_001407587.1:c.114G>A
- NM_001407590.1:c.114G>A
- NM_001407591.1:c.114G>A
- NM_001407593.1:c.114G>A
- NM_001407594.1:c.114G>A
- NM_001407596.1:c.114G>A
- NM_001407597.1:c.114G>A
- NM_001407598.1:c.114G>A
- NM_001407602.1:c.114G>A
- NM_001407603.1:c.114G>A
- NM_001407605.1:c.114G>A
- NM_001407610.1:c.114G>A
- NM_001407611.1:c.114G>A
- NM_001407612.1:c.114G>A
- NM_001407613.1:c.114G>A
- NM_001407614.1:c.114G>A
- NM_001407615.1:c.114G>A
- NM_001407616.1:c.114G>A
- NM_001407617.1:c.114G>A
- NM_001407618.1:c.114G>A
- NM_001407619.1:c.114G>A
- NM_001407620.1:c.114G>A
- NM_001407621.1:c.114G>A
- NM_001407622.1:c.114G>A
- NM_001407623.1:c.114G>A
- NM_001407624.1:c.114G>A
- NM_001407625.1:c.114G>A
- NM_001407626.1:c.114G>A
- NM_001407627.1:c.114G>A
- NM_001407628.1:c.114G>A
- NM_001407629.1:c.114G>A
- NM_001407630.1:c.114G>A
- NM_001407631.1:c.114G>A
- NM_001407632.1:c.114G>A
- NM_001407633.1:c.114G>A
- NM_001407634.1:c.114G>A
- NM_001407635.1:c.114G>A
- NM_001407636.1:c.114G>A
- NM_001407637.1:c.114G>A
- NM_001407638.1:c.114G>A
- NM_001407639.1:c.114G>A
- NM_001407640.1:c.114G>A
- NM_001407641.1:c.114G>A
- NM_001407642.1:c.114G>A
- NM_001407644.1:c.114G>A
- NM_001407645.1:c.114G>A
- NM_001407646.1:c.114G>A
- NM_001407647.1:c.114G>A
- NM_001407648.1:c.114G>A
- NM_001407649.1:c.114G>A
- NM_001407652.1:c.114G>A
- NM_001407653.1:c.114G>A
- NM_001407654.1:c.114G>A
- NM_001407655.1:c.114G>A
- NM_001407656.1:c.114G>A
- NM_001407657.1:c.114G>A
- NM_001407658.1:c.114G>A
- NM_001407659.1:c.114G>A
- NM_001407660.1:c.114G>A
- NM_001407661.1:c.114G>A
- NM_001407662.1:c.114G>A
- NM_001407663.1:c.114G>A
- NM_001407664.1:c.114G>A
- NM_001407665.1:c.114G>A
- NM_001407666.1:c.114G>A
- NM_001407667.1:c.114G>A
- NM_001407668.1:c.114G>A
- NM_001407669.1:c.114G>A
- NM_001407670.1:c.114G>A
- NM_001407671.1:c.114G>A
- NM_001407672.1:c.114G>A
- NM_001407673.1:c.114G>A
- NM_001407674.1:c.114G>A
- NM_001407675.1:c.114G>A
- NM_001407676.1:c.114G>A
- NM_001407677.1:c.114G>A
- NM_001407678.1:c.114G>A
- NM_001407679.1:c.114G>A
- NM_001407680.1:c.114G>A
- NM_001407681.1:c.114G>A
- NM_001407682.1:c.114G>A
- NM_001407683.1:c.114G>A
- NM_001407684.1:c.114G>A
- NM_001407685.1:c.114G>A
- NM_001407686.1:c.114G>A
- NM_001407687.1:c.114G>A
- NM_001407688.1:c.114G>A
- NM_001407689.1:c.114G>A
- NM_001407690.1:c.114G>A
- NM_001407691.1:c.114G>A
- NM_001407692.1:c.-7-9213G>A
- NM_001407694.1:c.-144G>A
- NM_001407695.1:c.-148G>A
- NM_001407696.1:c.-144G>A
- NM_001407697.1:c.-28G>A
- NM_001407698.1:c.-8+8271G>A
- NM_001407724.1:c.-144G>A
- NM_001407725.1:c.-28G>A
- NM_001407726.1:c.-8+5812G>A
- NM_001407727.1:c.-144G>A
- NM_001407728.1:c.-28G>A
- NM_001407729.1:c.-28G>A
- NM_001407730.1:c.-28G>A
- NM_001407731.1:c.-144G>A
- NM_001407732.1:c.-8+8271G>A
- NM_001407733.1:c.-144G>A
- NM_001407734.1:c.-28G>A
- NM_001407735.1:c.-28G>A
- NM_001407736.1:c.-8+8271G>A
- NM_001407737.1:c.-28G>A
- NM_001407738.1:c.-8+8271G>A
- NM_001407739.1:c.-28G>A
- NM_001407740.1:c.-28G>A
- NM_001407741.1:c.-28G>A
- NM_001407742.1:c.-8+8271G>A
- NM_001407743.1:c.-28G>A
- NM_001407744.1:c.-8+8271G>A
- NM_001407745.1:c.-28G>A
- NM_001407746.1:c.-144G>A
- NM_001407747.1:c.-7-9213G>A
- NM_001407748.1:c.-28G>A
- NM_001407749.1:c.-144G>A
- NM_001407750.1:c.-8+8271G>A
- NM_001407751.1:c.-8+5812G>A
- NM_001407752.1:c.-28G>A
- NM_001407838.1:c.-28G>A
- NM_001407839.1:c.-28G>A
- NM_001407841.1:c.-24G>A
- NM_001407842.1:c.-144G>A
- NM_001407843.1:c.-144G>A
- NM_001407844.1:c.-28G>A
- NM_001407845.1:c.-8+8271G>A
- NM_001407846.1:c.-28G>A
- NM_001407847.1:c.-28G>A
- NM_001407848.1:c.-28G>A
- NM_001407849.1:c.-8+8271G>A
- NM_001407850.1:c.-28G>A
- NM_001407851.1:c.-28G>A
- NM_001407852.1:c.-8+8271G>A
- NM_001407853.1:c.-75G>A
- NM_001407854.1:c.114G>A
- NM_001407858.1:c.114G>A
- NM_001407859.1:c.114G>A
- NM_001407860.1:c.114G>A
- NM_001407861.1:c.114G>A
- NM_001407862.1:c.114G>A
- NM_001407863.1:c.114G>A
- NM_001407874.1:c.114G>A
- NM_001407875.1:c.114G>A
- NM_001407879.1:c.-75G>A
- NM_001407881.1:c.-55+8271G>A
- NM_001407882.1:c.-75G>A
- NM_001407884.1:c.-75G>A
- NM_001407885.1:c.-75G>A
- NM_001407886.1:c.-75G>A
- NM_001407887.1:c.-75G>A
- NM_001407889.1:c.-191G>A
- NM_001407894.1:c.-75G>A
- NM_001407895.1:c.-75G>A
- NM_001407896.1:c.-75G>A
- NM_001407897.1:c.-75G>A
- NM_001407898.1:c.-55+8271G>A
- NM_001407899.1:c.-75G>A
- NM_001407900.1:c.-191G>A
- NM_001407902.1:c.-55+8271G>A
- NM_001407904.1:c.-75G>A
- NM_001407906.1:c.-75G>A
- NM_001407907.1:c.-75G>A
- NM_001407908.1:c.-75G>A
- NM_001407909.1:c.-75G>A
- NM_001407910.1:c.-75G>A
- NM_001407915.1:c.-75G>A
- NM_001407916.1:c.-75G>A
- NM_001407917.1:c.-75G>A
- NM_001407918.1:c.-75G>A
- NM_001407919.1:c.114G>A
- NM_001407920.1:c.-28G>A
- NM_001407921.1:c.-28G>A
- NM_001407922.1:c.-28G>A
- NM_001407923.1:c.-28G>A
- NM_001407924.1:c.-8+8271G>A
- NM_001407925.1:c.-8+8271G>A
- NM_001407926.1:c.-28G>A
- NM_001407927.1:c.-28G>A
- NM_001407928.1:c.-8+8271G>A
- NM_001407929.1:c.-8+8271G>A
- NM_001407930.1:c.-144G>A
- NM_001407931.1:c.-7-9213G>A
- NM_001407932.1:c.-8+8271G>A
- NM_001407933.1:c.-28G>A
- NM_001407934.1:c.-28G>A
- NM_001407935.1:c.-28G>A
- NM_001407936.1:c.-8+8271G>A
- NM_001407937.1:c.114G>A
- NM_001407938.1:c.114G>A
- NM_001407939.1:c.114G>A
- NM_001407940.1:c.114G>A
- NM_001407941.1:c.114G>A
- NM_001407942.1:c.-144G>A
- NM_001407943.1:c.-28G>A
- NM_001407944.1:c.-28G>A
- NM_001407945.1:c.-8+8271G>A
- NM_001407946.1:c.-75G>A
- NM_001407947.1:c.-75G>A
- NM_001407948.1:c.-75G>A
- NM_001407949.1:c.-75G>A
- NM_001407950.1:c.-75G>A
- NM_001407951.1:c.-75G>A
- NM_001407952.1:c.-75G>A
- NM_001407953.1:c.-75G>A
- NM_001407954.1:c.-75G>A
- NM_001407955.1:c.-75G>A
- NM_001407956.1:c.-75G>A
- NM_001407957.1:c.-75G>A
- NM_001407958.1:c.-75G>A
- NM_001407959.1:c.-170+9531G>A
- NM_001407960.1:c.-190G>A
- NM_001407962.1:c.-190G>A
- NM_001407963.1:c.-170+9525G>A
- NM_001407964.1:c.-28G>A
- NM_001407965.1:c.-306G>A
- NM_001407966.1:c.-219+9525G>A
- NM_001407967.1:c.-219+9531G>A
- NM_001407968.1:c.114G>A
- NM_001407969.1:c.114G>A
- NM_001407970.1:c.114G>A
- NM_001407971.1:c.114G>A
- NM_001407972.1:c.114G>A
- NM_001407973.1:c.114G>A
- NM_001407974.1:c.114G>A
- NM_001407975.1:c.114G>A
- NM_001407976.1:c.114G>A
- NM_001407977.1:c.114G>A
- NM_001407978.1:c.114G>A
- NM_001407979.1:c.114G>A
- NM_001407980.1:c.114G>A
- NM_001407981.1:c.114G>A
- NM_001407982.1:c.114G>A
- NM_001407983.1:c.114G>A
- NM_001407984.1:c.114G>A
- NM_001407985.1:c.114G>A
- NM_001407986.1:c.114G>A
- NM_001407990.1:c.114G>A
- NM_001407991.1:c.114G>A
- NM_001407992.1:c.114G>A
- NM_001407993.1:c.114G>A
- NM_001408392.1:c.114G>A
- NM_001408396.1:c.114G>A
- NM_001408397.1:c.114G>A
- NM_001408398.1:c.114G>A
- NM_001408399.1:c.114G>A
- NM_001408400.1:c.114G>A
- NM_001408401.1:c.114G>A
- NM_001408402.1:c.114G>A
- NM_001408403.1:c.114G>A
- NM_001408404.1:c.114G>A
- NM_001408406.1:c.114G>A
- NM_001408407.1:c.114G>A
- NM_001408408.1:c.114G>A
- NM_001408409.1:c.114G>A
- NM_001408410.1:c.-28G>A
- NM_001408411.1:c.114G>A
- NM_001408412.1:c.114G>A
- NM_001408413.1:c.114G>A
- NM_001408414.1:c.114G>A
- NM_001408415.1:c.114G>A
- NM_001408416.1:c.114G>A
- NM_001408418.1:c.114G>A
- NM_001408419.1:c.114G>A
- NM_001408420.1:c.114G>A
- NM_001408421.1:c.114G>A
- NM_001408422.1:c.114G>A
- NM_001408423.1:c.114G>A
- NM_001408424.1:c.114G>A
- NM_001408425.1:c.114G>A
- NM_001408426.1:c.114G>A
- NM_001408427.1:c.114G>A
- NM_001408428.1:c.114G>A
- NM_001408429.1:c.114G>A
- NM_001408430.1:c.114G>A
- NM_001408431.1:c.114G>A
- NM_001408432.1:c.114G>A
- NM_001408433.1:c.114G>A
- NM_001408434.1:c.114G>A
- NM_001408435.1:c.114G>A
- NM_001408436.1:c.114G>A
- NM_001408437.1:c.114G>A
- NM_001408438.1:c.114G>A
- NM_001408439.1:c.114G>A
- NM_001408440.1:c.114G>A
- NM_001408441.1:c.114G>A
- NM_001408442.1:c.114G>A
- NM_001408443.1:c.114G>A
- NM_001408444.1:c.114G>A
- NM_001408445.1:c.114G>A
- NM_001408446.1:c.114G>A
- NM_001408447.1:c.114G>A
- NM_001408448.1:c.114G>A
- NM_001408450.1:c.114G>A
- NM_001408451.1:c.80+8271G>A
- NM_001408452.1:c.-28G>A
- NM_001408453.1:c.-28G>A
- NM_001408454.1:c.-8+8271G>A
- NM_001408455.1:c.-144G>A
- NM_001408456.1:c.-144G>A
- NM_001408457.1:c.-7-9213G>A
- NM_001408458.1:c.-28G>A
- NM_001408459.1:c.-8+8271G>A
- NM_001408460.1:c.-8+8271G>A
- NM_001408461.1:c.-8+8271G>A
- NM_001408462.1:c.-28G>A
- NM_001408463.1:c.-28G>A
- NM_001408464.1:c.-8+8271G>A
- NM_001408465.1:c.-148G>A
- NM_001408466.1:c.-28G>A
- NM_001408467.1:c.-8+8271G>A
- NM_001408468.1:c.-144G>A
- NM_001408469.1:c.-28G>A
- NM_001408470.1:c.-28G>A
- NM_001408472.1:c.114G>A
- NM_001408473.1:c.114G>A
- NM_001408474.1:c.114G>A
- NM_001408475.1:c.114G>A
- NM_001408476.1:c.114G>A
- NM_001408478.1:c.-75G>A
- NM_001408479.1:c.-75G>A
- NM_001408480.1:c.-75G>A
- NM_001408481.1:c.-75G>A
- NM_001408482.1:c.-75G>A
- NM_001408483.1:c.-75G>A
- NM_001408484.1:c.-75G>A
- NM_001408485.1:c.-75G>A
- NM_001408489.1:c.-75G>A
- NM_001408490.1:c.-75G>A
- NM_001408491.1:c.-75G>A
- NM_001408492.1:c.-191G>A
- NM_001408493.1:c.-75G>A
- NM_001408494.1:c.114G>A
- NM_001408495.1:c.114G>A
- NM_001408496.1:c.-8+8271G>A
- NM_001408497.1:c.-28G>A
- NM_001408498.1:c.-8+8271G>A
- NM_001408499.1:c.-28G>A
- NM_001408500.1:c.-28G>A
- NM_001408501.1:c.-144G>A
- NM_001408502.1:c.-75G>A
- NM_001408503.1:c.-28G>A
- NM_001408504.1:c.-28G>A
- NM_001408505.1:c.-28G>A
- NM_001408506.1:c.-75G>A
- NM_001408507.1:c.-75G>A
- NM_001408508.1:c.-75G>A
- NM_001408509.1:c.-75G>A
- NM_001408510.1:c.-190G>A
- NM_001408511.1:c.-7-9213G>A
- NM_001408512.1:c.-190G>A
- NM_001408513.1:c.-75G>A
- NM_001408514.1:c.-75G>A
- NM_007294.4:c.114G>AMANE SELECT
- NM_007297.4:c.-8+8271G>A
- NM_007298.4:c.114G>A
- NM_007299.4:c.114G>A
- NM_007300.4:c.114G>A
- NM_007304.2:c.114G>A
- NP_001394510.1:p.Lys38=
- NP_001394511.1:p.Lys38=
- NP_001394512.1:p.Lys38=
- NP_001394514.1:p.Lys38=
- NP_001394516.1:p.Lys38=
- NP_001394519.1:p.Lys38=
- NP_001394520.1:p.Lys38=
- NP_001394522.1:p.Lys38=
- NP_001394523.1:p.Lys38=
- NP_001394525.1:p.Lys38=
- NP_001394526.1:p.Lys38=
- NP_001394527.1:p.Lys38=
- NP_001394531.1:p.Lys38=
- NP_001394532.1:p.Lys38=
- NP_001394534.1:p.Lys38=
- NP_001394539.1:p.Lys38=
- NP_001394540.1:p.Lys38=
- NP_001394541.1:p.Lys38=
- NP_001394542.1:p.Lys38=
- NP_001394543.1:p.Lys38=
- NP_001394544.1:p.Lys38=
- NP_001394545.1:p.Lys38=
- NP_001394546.1:p.Lys38=
- NP_001394547.1:p.Lys38=
- NP_001394548.1:p.Lys38=
- NP_001394549.1:p.Lys38=
- NP_001394550.1:p.Lys38=
- NP_001394551.1:p.Lys38=
- NP_001394552.1:p.Lys38=
- NP_001394553.1:p.Lys38=
- NP_001394554.1:p.Lys38=
- NP_001394555.1:p.Lys38=
- NP_001394556.1:p.Lys38=
- NP_001394557.1:p.Lys38=
- NP_001394558.1:p.Lys38=
- NP_001394559.1:p.Lys38=
- NP_001394560.1:p.Lys38=
- NP_001394561.1:p.Lys38=
- NP_001394562.1:p.Lys38=
- NP_001394563.1:p.Lys38=
- NP_001394564.1:p.Lys38=
- NP_001394565.1:p.Lys38=
- NP_001394566.1:p.Lys38=
- NP_001394567.1:p.Lys38=
- NP_001394568.1:p.Lys38=
- NP_001394569.1:p.Lys38=
- NP_001394570.1:p.Lys38=
- NP_001394571.1:p.Lys38=
- NP_001394573.1:p.Lys38=
- NP_001394574.1:p.Lys38=
- NP_001394575.1:p.Lys38=
- NP_001394576.1:p.Lys38=
- NP_001394577.1:p.Lys38=
- NP_001394578.1:p.Lys38=
- NP_001394581.1:p.Lys38=
- NP_001394582.1:p.Lys38=
- NP_001394583.1:p.Lys38=
- NP_001394584.1:p.Lys38=
- NP_001394585.1:p.Lys38=
- NP_001394586.1:p.Lys38=
- NP_001394587.1:p.Lys38=
- NP_001394588.1:p.Lys38=
- NP_001394589.1:p.Lys38=
- NP_001394590.1:p.Lys38=
- NP_001394591.1:p.Lys38=
- NP_001394592.1:p.Lys38=
- NP_001394593.1:p.Lys38=
- NP_001394594.1:p.Lys38=
- NP_001394595.1:p.Lys38=
- NP_001394596.1:p.Lys38=
- NP_001394597.1:p.Lys38=
- NP_001394598.1:p.Lys38=
- NP_001394599.1:p.Lys38=
- NP_001394600.1:p.Lys38=
- NP_001394601.1:p.Lys38=
- NP_001394602.1:p.Lys38=
- NP_001394603.1:p.Lys38=
- NP_001394604.1:p.Lys38=
- NP_001394605.1:p.Lys38=
- NP_001394606.1:p.Lys38=
- NP_001394607.1:p.Lys38=
- NP_001394608.1:p.Lys38=
- NP_001394609.1:p.Lys38=
- NP_001394610.1:p.Lys38=
- NP_001394611.1:p.Lys38=
- NP_001394612.1:p.Lys38=
- NP_001394613.1:p.Lys38=
- NP_001394614.1:p.Lys38=
- NP_001394615.1:p.Lys38=
- NP_001394616.1:p.Lys38=
- NP_001394617.1:p.Lys38=
- NP_001394618.1:p.Lys38=
- NP_001394619.1:p.Lys38=
- NP_001394620.1:p.Lys38=
- NP_001394783.1:p.Lys38=
- NP_001394787.1:p.Lys38=
- NP_001394788.1:p.Lys38=
- NP_001394789.1:p.Lys38=
- NP_001394790.1:p.Lys38=
- NP_001394791.1:p.Lys38=
- NP_001394792.1:p.Lys38=
- NP_001394803.1:p.Lys38=
- NP_001394804.1:p.Lys38=
- NP_001394848.1:p.Lys38=
- NP_001394866.1:p.Lys38=
- NP_001394867.1:p.Lys38=
- NP_001394868.1:p.Lys38=
- NP_001394869.1:p.Lys38=
- NP_001394870.1:p.Lys38=
- NP_001394897.1:p.Lys38=
- NP_001394898.1:p.Lys38=
- NP_001394899.1:p.Lys38=
- NP_001394900.1:p.Lys38=
- NP_001394901.1:p.Lys38=
- NP_001394902.1:p.Lys38=
- NP_001394903.1:p.Lys38=
- NP_001394904.1:p.Lys38=
- NP_001394905.1:p.Lys38=
- NP_001394906.1:p.Lys38=
- NP_001394907.1:p.Lys38=
- NP_001394908.1:p.Lys38=
- NP_001394909.1:p.Lys38=
- NP_001394910.1:p.Lys38=
- NP_001394911.1:p.Lys38=
- NP_001394912.1:p.Lys38=
- NP_001394913.1:p.Lys38=
- NP_001394914.1:p.Lys38=
- NP_001394915.1:p.Lys38=
- NP_001394919.1:p.Lys38=
- NP_001394920.1:p.Lys38=
- NP_001394921.1:p.Lys38=
- NP_001394922.1:p.Lys38=
- NP_001395321.1:p.Lys38=
- NP_001395325.1:p.Lys38=
- NP_001395326.1:p.Lys38=
- NP_001395327.1:p.Lys38=
- NP_001395328.1:p.Lys38=
- NP_001395329.1:p.Lys38=
- NP_001395330.1:p.Lys38=
- NP_001395331.1:p.Lys38=
- NP_001395332.1:p.Lys38=
- NP_001395333.1:p.Lys38=
- NP_001395335.1:p.Lys38=
- NP_001395336.1:p.Lys38=
- NP_001395337.1:p.Lys38=
- NP_001395338.1:p.Lys38=
- NP_001395340.1:p.Lys38=
- NP_001395341.1:p.Lys38=
- NP_001395342.1:p.Lys38=
- NP_001395343.1:p.Lys38=
- NP_001395344.1:p.Lys38=
- NP_001395345.1:p.Lys38=
- NP_001395347.1:p.Lys38=
- NP_001395348.1:p.Lys38=
- NP_001395349.1:p.Lys38=
- NP_001395350.1:p.Lys38=
- NP_001395351.1:p.Lys38=
- NP_001395352.1:p.Lys38=
- NP_001395353.1:p.Lys38=
- NP_001395354.1:p.Lys38=
- NP_001395355.1:p.Lys38=
- NP_001395356.1:p.Lys38=
- NP_001395357.1:p.Lys38=
- NP_001395358.1:p.Lys38=
- NP_001395359.1:p.Lys38=
- NP_001395360.1:p.Lys38=
- NP_001395361.1:p.Lys38=
- NP_001395362.1:p.Lys38=
- NP_001395363.1:p.Lys38=
- NP_001395364.1:p.Lys38=
- NP_001395365.1:p.Lys38=
- NP_001395366.1:p.Lys38=
- NP_001395367.1:p.Lys38=
- NP_001395368.1:p.Lys38=
- NP_001395369.1:p.Lys38=
- NP_001395370.1:p.Lys38=
- NP_001395371.1:p.Lys38=
- NP_001395372.1:p.Lys38=
- NP_001395373.1:p.Lys38=
- NP_001395374.1:p.Lys38=
- NP_001395375.1:p.Lys38=
- NP_001395376.1:p.Lys38=
- NP_001395377.1:p.Lys38=
- NP_001395379.1:p.Lys38=
- NP_001395401.1:p.Lys38=
- NP_001395402.1:p.Lys38=
- NP_001395403.1:p.Lys38=
- NP_001395404.1:p.Lys38=
- NP_001395405.1:p.Lys38=
- NP_001395423.1:p.Lys38=
- NP_001395424.1:p.Lys38=
- NP_009225.1:p.Lys38=
- NP_009225.1:p.Lys38=
- NP_009229.2:p.Lys38=
- NP_009230.2:p.Lys38=
- NP_009231.2:p.Lys38=
- NP_009235.2:p.Lys38=
- LRG_292t1:c.114G>A
- LRG_292:g.102238G>A
- LRG_292p1:p.Lys38=
- NC_000017.10:g.41267763C>T
- NM_007294.2:c.114G>A
- NM_007294.3:c.114G>A
- NM_007294.4:c.114G>A
- NM_007299.3:c.114G>A
- NM_007300.3:c.114G>A
- NR_027676.2:n.316G>A
- U14680.1:n.233G>A
- p.K38K
- p.Lys38Lys
This HGVS expression did not pass validation- Nucleotide change:
- 233G>A
- Links:
- Breast Cancer Information Core (BIC) (BRCA1): 233&base_change=G to A; dbSNP: rs1800062
- NCBI 1000 Genomes Browser:
- rs1800062
- Molecular consequence:
- NM_001407571.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407694.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407695.1:c.-148G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407696.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407697.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407724.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407725.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407727.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407728.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407729.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407730.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407731.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407733.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407734.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407735.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407737.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407739.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407740.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407741.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407743.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407745.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407746.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407748.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407749.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407752.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407838.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407839.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407841.1:c.-24G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407842.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407843.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407844.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407846.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407847.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407848.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407850.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407851.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407853.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407879.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407882.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407884.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407885.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407886.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407887.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407889.1:c.-191G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407894.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407895.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407896.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407897.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407899.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407900.1:c.-191G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407904.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407906.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407907.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407908.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407909.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407910.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407915.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407916.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407917.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407918.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407920.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407921.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407922.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407923.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407926.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407927.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407930.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407933.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407934.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407935.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407942.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407943.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407944.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407946.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407947.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407948.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407949.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407950.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407951.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407952.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407953.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407954.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407955.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407956.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407957.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407958.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407960.1:c.-190G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407962.1:c.-190G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407964.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407965.1:c.-306G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408410.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408452.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408453.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408455.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408456.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408458.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408462.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408463.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408465.1:c.-148G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408466.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408468.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408469.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408470.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408478.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408479.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408480.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408481.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408482.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408483.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408484.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408485.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408489.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408490.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408491.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408492.1:c.-191G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408493.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408497.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408499.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408500.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408501.1:c.-144G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408502.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408503.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408504.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408505.1:c.-28G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408506.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408507.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408508.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408509.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408510.1:c.-190G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408512.1:c.-190G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408513.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001408514.1:c.-75G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
- NM_001407692.1:c.-7-9213G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407698.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407726.1:c.-8+5812G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407732.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407736.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407738.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407742.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407744.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407747.1:c.-7-9213G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407750.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407751.1:c.-8+5812G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407845.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407849.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407852.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407881.1:c.-55+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407898.1:c.-55+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407902.1:c.-55+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407924.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407925.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407928.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407929.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407931.1:c.-7-9213G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407932.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407936.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407945.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407959.1:c.-170+9531G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407963.1:c.-170+9525G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407966.1:c.-219+9525G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407967.1:c.-219+9531G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408451.1:c.80+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408454.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408457.1:c.-7-9213G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408459.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408460.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408461.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408464.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408467.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408496.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408498.1:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408511.1:c.-7-9213G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_007297.4:c.-8+8271G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407581.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407582.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407583.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407585.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407587.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407590.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407591.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407593.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407594.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407596.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407597.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407598.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407602.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407603.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407605.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407610.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407611.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407612.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407613.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407614.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407615.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407616.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407617.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407618.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407619.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407620.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407621.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407622.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407623.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407624.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407625.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407626.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407627.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407628.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407629.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407630.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407631.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407632.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407633.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407634.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407635.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407636.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407637.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407638.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407639.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407640.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407641.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407642.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407644.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407645.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407646.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407647.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407648.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407649.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407652.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407653.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407654.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407655.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407656.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407657.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407658.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407659.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407660.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407661.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407662.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407663.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407664.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407665.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407666.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407667.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407668.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407669.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407670.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407671.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407672.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407673.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407674.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407675.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407676.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407677.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407678.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407679.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407680.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407681.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407682.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407683.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407684.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407685.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407686.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407687.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407688.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407689.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407690.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407691.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407854.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407858.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407859.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407860.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407861.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407862.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407863.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407874.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407875.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407919.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407937.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407938.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407939.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407940.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407941.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407968.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407969.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407970.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407971.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407972.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407973.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407974.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407975.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407976.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407977.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407978.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407979.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407980.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407981.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407982.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407983.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407984.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407985.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407986.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407990.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407991.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407992.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001407993.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408392.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408396.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408397.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408398.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408399.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408400.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408401.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408402.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408403.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408404.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408406.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408407.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408408.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408409.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408411.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408412.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408413.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408414.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408415.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408416.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408418.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408419.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408420.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408421.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408422.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408423.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408424.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408425.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408426.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408427.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408428.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408429.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408430.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408431.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408432.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408433.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408434.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408435.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408436.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408437.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408438.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408439.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408440.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408441.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408442.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408443.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408444.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408445.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408446.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408447.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408448.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408450.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408472.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408473.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408474.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408475.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408476.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408494.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_001408495.1:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_007294.4:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_007298.4:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_007299.4:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_007300.4:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- NM_007304.2:c.114G>A - synonymous variant - [Sequence Ontology: SO:0001819]
- Functional consequence:
- functionally_normal [Sequence Ontology: SO:0002219] - Comment(s)
- The saturation genome editing (SGE) assay for BRCA1 NM_007294.3:c.114G>A, a SYNONYMOUS variant, produced a function score of -0.29, corresponding to a functional classification of FUNCTIONAL. SGE function score ranges for classification are as follows: ‘functional’, score > -0.748; ‘intermediate’, -0.748 > score > -1.328; ‘non-functional’, score < -1.328. The median synonymous SNV scored 0.0 and the median nonsense SNV scored -2.12.
- Observations:
- 20
Condition(s)
-
Neisseria gonorrhoeae strain FA19 tbpB gene upstream region genomic sequence
Neisseria gonorrhoeae strain FA19 tbpB gene upstream region genomic sequencegi|643358107|gb|KJ579425.1|Nucleotide
-
Dental Restoration, Permanent
Dental Restoration, PermanentA restoration designed to remain in service for not less than 20 to 30 years, usually made of gold casting, cohesive gold, or amalgam. (Jablonski, Dictionary of Dentistry, 199...<br/>Year introduced: 1965MeSH
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See more...Assertion and evidence details
Submission Accession | Submitter | Review Status (Assertion method) | Clinical Significance (Last evaluated) | Origin | Method | Citations |
---|---|---|---|---|---|---|
SCV000144344 | Breast Cancer Information Core (BIC) (BRCA1) | no assertion criteria provided | Benign (Jul 19, 2006) | germline, unknown | clinical testing | |
SCV000154026 | Counsyl | criteria provided, single submitter (Counsyl Autosomal Dominant Disease Classification criteria (2015)) | Benign (Mar 13, 2014) | unknown | literature only | PubMed (6) Counsyl Autosomal Dominant Disease Classification criteria (2015), |
SCV000189325 | Sharing Clinical Reports Project (SCRP) | no assertion criteria provided | Benign (Mar 3, 2011) | germline | clinical testing | |
SCV000244845 | Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) | reviewed by expert panel (ENIGMA BRCA1/2 Classification Criteria (2015)) | Benign (Jan 12, 2015) | germline | curation | ENIGMA BRCA1/2 Classification Criteria (2015), |
SCV000403076 | Illumina Laboratory Services, Illumina | criteria provided, single submitter (ICSL Variant Classification Criteria 13 December 2019) | Benign (Mar 6, 2018) | germline | clinical testing | |
SCV000733682 | Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen - VKGL Data-share Consensus | no assertion criteria provided | Benign | germline | clinical testing | |
SCV001241896 | Brotman Baty Institute, University of Washington | no classification provided | not provided | not applicable | in vitro |
Summary from all submissions
Ethnicity | Origin | Affected | Individuals | Families | Chromosomes tested | Number Tested | Family history | Method |
---|---|---|---|---|---|---|---|---|
not provided | not applicable | not applicable | not provided | not provided | not provided | not provided | not provided | in vitro |
not provided | germline | not provided | 3 | not provided | not provided | 3 | not provided | clinical testing |
not provided | not provided | yes | 1 | not provided | not provided | not provided | not provided | clinical testing |
unknown | unknown | not provided | not provided | not provided | not provided | not provided | literature only | |
not provided | germline | yes | 10 | not provided | not provided | not provided | not provided | clinical testing |
not provided | germline | unknown | not provided | not provided | not provided | not provided | not provided | clinical testing, curation |
Caucasian | germline | yes | 6 | not provided | not provided | not provided | not provided | clinical testing |
Citations
PubMed
BRCA1 variants in a family study of African-American and Latina women.
McKean-Cowdin R, Spencer Feigelson H, Xia LY, Pearce CL, Thomas DC, Stram DO, Henderson BE.
Hum Genet. 2005 May;116(6):497-506. Epub 2005 Feb 23.
- PMID:
- 15726418
Ho GH, Phang BH, Ng IS, Law HY, Soo KC, Ng EH.
Cancer. 2000 Aug 15;89(4):811-6.
- PMID:
- 10951344
Details of each submission
From Breast Cancer Information Core (BIC) (BRCA1), SCV000144344.2
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | 4 | not provided | not provided | clinical testing | not provided |
2 | not provided | 6 | not provided | not provided | clinical testing | not provided |
3 | not provided | 1 | not provided | not provided | clinical testing | not provided |
4 | Caucasian | 6 | not provided | not provided | clinical testing | not provided |
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | yes | not provided | not provided | not provided | 4 | not provided | not provided | not provided | |
2 | germline | yes | not provided | not provided | not provided | 6 | not provided | not provided | not provided | |
3 | unknown | yes | not provided | not provided | not provided | 1 | not provided | not provided | not provided | |
4 | germline | yes | not provided | not provided | not provided | 6 | not provided | not provided | not provided |
From Counsyl, SCV000154026.2
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | literature only | PubMed (6) |
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | unknown | unknown | not provided | not provided | not provided | not provided | not provided | not provided | not provided |
From Sharing Clinical Reports Project (SCRP), SCV000189325.1
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | clinical testing | not provided |
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | not provided | 3 | not provided | not provided | not provided | not provided | not provided | not provided |
From Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA), SCV000244845.1
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | curation | not provided |
Description
Class 1 not pathogenic based on frequency >1% in an outbred sampleset. Frequency 0.05769 (Asian), derived from 1000 genomes (2012-04-30).
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | unknown | not provided | not provided | not provided | not provided | not provided | not provided | not provided |
From Illumina Laboratory Services, Illumina, SCV000403076.3
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | clinical testing | not provided |
Description
This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | unknown | not provided | not provided | not provided | not provided | not provided | not provided | not provided |
From Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen - VKGL Data-share Consensus, SCV000733682.1
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | clinical testing | not provided |
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | yes | not provided | not provided | not provided | not provided | not provided | not provided | not provided |
From Brotman Baty Institute, University of Washington, SCV001241896.1
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | in vitro | PubMed (1) |
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | not applicable | not applicable | not provided | not provided | not provided | not provided | not provided | not provided | not provided |
Last Updated: Nov 10, 2024