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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 stars
reviewed by expert panel
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no 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
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)
Observations:
20

Condition(s)

Name:
Breast-ovarian cancer, familial, susceptibility to, 1 (BROVCA1)
Synonyms:
OVARIAN CANCER, SUSCEPTIBILITY TO; Breast cancer, familial 1
Identifiers:
MONDO: MONDO:0011450; MedGen: C2676676; Orphanet: 145; OMIM: 604370

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000144344Breast Cancer Information Core (BIC) (BRCA1)
no assertion criteria provided
Benign
(Jul 19, 2006)
germline, unknownclinical testing

SCV000154026Counsyl
criteria provided, single submitter

(Counsyl Autosomal Dominant Disease Classification criteria (2015))
Benign
(Mar 13, 2014)
unknownliterature only

PubMed (6)
[See all records that cite these PMIDs]

Counsyl Autosomal Dominant Disease Classification criteria (2015),

Citation Link,

SCV000189325Sharing Clinical Reports Project (SCRP)
no assertion criteria provided
Benign
(Mar 3, 2011)
germlineclinical testing

SCV000244845Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA)
reviewed by expert panel

(ENIGMA BRCA1/2 Classification Criteria (2015))
Benign
(Jan 12, 2015)
germlinecuration

ENIGMA BRCA1/2 Classification Criteria (2015),

Citation Link,

SCV000403076Illumina Laboratory Services, Illumina
criteria provided, single submitter

(ICSL Variant Classification Criteria 13 December 2019)
Benign
(Mar 6, 2018)
germlineclinical testing

Citation Link,

SCV000733682Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen - VKGL Data-share Consensus
no assertion criteria provided
Benigngermlineclinical testing

SCV001241896Brotman Baty Institute, University of Washington
no classification provided
not providednot applicablein vitro

PubMed (1)
[See all records that cite this PMID]

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providednot applicablenot applicablenot providednot providednot providednot providednot providedin vitro
not providedgermlinenot provided3not providednot provided3not providedclinical testing
not providednot providedyes1not providednot providednot providednot providedclinical testing
unknownunknownnot providednot providednot providednot providednot providedliterature only
not providedgermlineyes10not providednot providednot providednot providedclinical testing
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing, curation
Caucasiangermlineyes6not providednot providednot providednot providedclinical 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.

PubMed [citation]
PMID:
15726418

Novel germline BRCA1 mutations detected in women in singapore who developed breast carcinoma before the age of 36 years.

Ho GH, Phang BH, Ng IS, Law HY, Soo KC, Ng EH.

Cancer. 2000 Aug 15;89(4):811-6.

PubMed [citation]
PMID:
10951344
See all PubMed Citations (7)

Details of each submission

From Breast Cancer Information Core (BIC) (BRCA1), SCV000144344.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided4not providednot providedclinical testingnot provided
2not provided6not providednot providedclinical testingnot provided
3not provided1not providednot providedclinical testingnot provided
4Caucasian6not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided4not providednot providednot provided
2germlineyesnot providednot providednot provided6not providednot providednot provided
3unknownyesnot providednot providednot provided1not providednot providednot provided
4germlineyesnot providednot providednot provided6not providednot providednot provided

From Counsyl, SCV000154026.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providedliterature only PubMed (6)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

From Sharing Clinical Reports Project (SCRP), SCV000189325.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenot provided3not providednot providednot providednot providednot providednot provided

From Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA), SCV000244845.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedcurationnot 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).

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

From Illumina Laboratory Services, Illumina, SCV000403076.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot 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.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

From Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen - VKGL Data-share Consensus, SCV000733682.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

From Brotman Baty Institute, University of Washington, SCV001241896.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedin vitro PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1not applicablenot applicablenot providednot providednot providednot providednot providednot providednot provided

Last Updated: Nov 10, 2024