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NM_007294.4(BRCA1):c.133A>C (p.Lys45Gln) AND Breast-ovarian cancer, familial, susceptibility to, 1

Germline classification:
Benign (5 submissions)
Last evaluated:
Aug 10, 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:
RCV000191155.15

Allele description [Variation Report for NM_007294.4(BRCA1):c.133A>C (p.Lys45Gln)]

NM_007294.4(BRCA1):c.133A>C (p.Lys45Gln)

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.133A>C (p.Lys45Gln)
HGVS:
  • NC_000017.11:g.43115727T>G
  • NG_005905.2:g.102257A>C
  • NM_001407571.1:c.-56A>C
  • NM_001407581.1:c.133A>C
  • NM_001407582.1:c.133A>C
  • NM_001407583.1:c.133A>C
  • NM_001407585.1:c.133A>C
  • NM_001407587.1:c.133A>C
  • NM_001407590.1:c.133A>C
  • NM_001407591.1:c.133A>C
  • NM_001407593.1:c.133A>C
  • NM_001407594.1:c.133A>C
  • NM_001407596.1:c.133A>C
  • NM_001407597.1:c.133A>C
  • NM_001407598.1:c.133A>C
  • NM_001407602.1:c.133A>C
  • NM_001407603.1:c.133A>C
  • NM_001407605.1:c.133A>C
  • NM_001407610.1:c.133A>C
  • NM_001407611.1:c.133A>C
  • NM_001407612.1:c.133A>C
  • NM_001407613.1:c.133A>C
  • NM_001407614.1:c.133A>C
  • NM_001407615.1:c.133A>C
  • NM_001407616.1:c.133A>C
  • NM_001407617.1:c.133A>C
  • NM_001407618.1:c.133A>C
  • NM_001407619.1:c.133A>C
  • NM_001407620.1:c.133A>C
  • NM_001407621.1:c.133A>C
  • NM_001407622.1:c.133A>C
  • NM_001407623.1:c.133A>C
  • NM_001407624.1:c.133A>C
  • NM_001407625.1:c.133A>C
  • NM_001407626.1:c.133A>C
  • NM_001407627.1:c.133A>C
  • NM_001407628.1:c.133A>C
  • NM_001407629.1:c.133A>C
  • NM_001407630.1:c.133A>C
  • NM_001407631.1:c.133A>C
  • NM_001407632.1:c.133A>C
  • NM_001407633.1:c.133A>C
  • NM_001407634.1:c.133A>C
  • NM_001407635.1:c.133A>C
  • NM_001407636.1:c.133A>C
  • NM_001407637.1:c.133A>C
  • NM_001407638.1:c.133A>C
  • NM_001407639.1:c.133A>C
  • NM_001407640.1:c.133A>C
  • NM_001407641.1:c.133A>C
  • NM_001407642.1:c.133A>C
  • NM_001407644.1:c.133A>C
  • NM_001407645.1:c.133A>C
  • NM_001407646.1:c.133A>C
  • NM_001407647.1:c.133A>C
  • NM_001407648.1:c.133A>C
  • NM_001407649.1:c.133A>C
  • NM_001407652.1:c.133A>C
  • NM_001407653.1:c.133A>C
  • NM_001407654.1:c.133A>C
  • NM_001407655.1:c.133A>C
  • NM_001407656.1:c.133A>C
  • NM_001407657.1:c.133A>C
  • NM_001407658.1:c.133A>C
  • NM_001407659.1:c.133A>C
  • NM_001407660.1:c.133A>C
  • NM_001407661.1:c.133A>C
  • NM_001407662.1:c.133A>C
  • NM_001407663.1:c.133A>C
  • NM_001407664.1:c.133A>C
  • NM_001407665.1:c.133A>C
  • NM_001407666.1:c.133A>C
  • NM_001407667.1:c.133A>C
  • NM_001407668.1:c.133A>C
  • NM_001407669.1:c.133A>C
  • NM_001407670.1:c.133A>C
  • NM_001407671.1:c.133A>C
  • NM_001407672.1:c.133A>C
  • NM_001407673.1:c.133A>C
  • NM_001407674.1:c.133A>C
  • NM_001407675.1:c.133A>C
  • NM_001407676.1:c.133A>C
  • NM_001407677.1:c.133A>C
  • NM_001407678.1:c.133A>C
  • NM_001407679.1:c.133A>C
  • NM_001407680.1:c.133A>C
  • NM_001407681.1:c.133A>C
  • NM_001407682.1:c.133A>C
  • NM_001407683.1:c.133A>C
  • NM_001407684.1:c.133A>C
  • NM_001407685.1:c.133A>C
  • NM_001407686.1:c.133A>C
  • NM_001407687.1:c.133A>C
  • NM_001407688.1:c.133A>C
  • NM_001407689.1:c.133A>C
  • NM_001407690.1:c.133A>C
  • NM_001407691.1:c.133A>C
  • NM_001407694.1:c.-125A>C
  • NM_001407695.1:c.-129A>C
  • NM_001407696.1:c.-125A>C
  • NM_001407697.1:c.-9A>C
  • NM_001407724.1:c.-125A>C
  • NM_001407725.1:c.-9A>C
  • NM_001407727.1:c.-125A>C
  • NM_001407728.1:c.-9A>C
  • NM_001407729.1:c.-9A>C
  • NM_001407730.1:c.-9A>C
  • NM_001407731.1:c.-125A>C
  • NM_001407733.1:c.-125A>C
  • NM_001407734.1:c.-9A>C
  • NM_001407735.1:c.-9A>C
  • NM_001407737.1:c.-9A>C
  • NM_001407739.1:c.-9A>C
  • NM_001407740.1:c.-9A>C
  • NM_001407741.1:c.-9A>C
  • NM_001407743.1:c.-9A>C
  • NM_001407745.1:c.-9A>C
  • NM_001407746.1:c.-125A>C
  • NM_001407748.1:c.-9A>C
  • NM_001407749.1:c.-125A>C
  • NM_001407752.1:c.-9A>C
  • NM_001407838.1:c.-9A>C
  • NM_001407839.1:c.-9A>C
  • NM_001407842.1:c.-125A>C
  • NM_001407843.1:c.-125A>C
  • NM_001407844.1:c.-9A>C
  • NM_001407846.1:c.-9A>C
  • NM_001407847.1:c.-9A>C
  • NM_001407848.1:c.-9A>C
  • NM_001407850.1:c.-9A>C
  • NM_001407851.1:c.-9A>C
  • NM_001407853.1:c.-56A>C
  • NM_001407854.1:c.133A>C
  • NM_001407858.1:c.133A>C
  • NM_001407859.1:c.133A>C
  • NM_001407860.1:c.133A>C
  • NM_001407861.1:c.133A>C
  • NM_001407862.1:c.133A>C
  • NM_001407863.1:c.133A>C
  • NM_001407874.1:c.133A>C
  • NM_001407875.1:c.133A>C
  • NM_001407879.1:c.-56A>C
  • NM_001407882.1:c.-56A>C
  • NM_001407884.1:c.-56A>C
  • NM_001407885.1:c.-56A>C
  • NM_001407886.1:c.-56A>C
  • NM_001407887.1:c.-56A>C
  • NM_001407889.1:c.-172A>C
  • NM_001407894.1:c.-56A>C
  • NM_001407895.1:c.-56A>C
  • NM_001407896.1:c.-56A>C
  • NM_001407897.1:c.-56A>C
  • NM_001407899.1:c.-56A>C
  • NM_001407900.1:c.-172A>C
  • NM_001407904.1:c.-56A>C
  • NM_001407906.1:c.-56A>C
  • NM_001407907.1:c.-56A>C
  • NM_001407908.1:c.-56A>C
  • NM_001407909.1:c.-56A>C
  • NM_001407910.1:c.-56A>C
  • NM_001407915.1:c.-56A>C
  • NM_001407916.1:c.-56A>C
  • NM_001407917.1:c.-56A>C
  • NM_001407918.1:c.-56A>C
  • NM_001407919.1:c.133A>C
  • NM_001407920.1:c.-9A>C
  • NM_001407921.1:c.-9A>C
  • NM_001407922.1:c.-9A>C
  • NM_001407923.1:c.-9A>C
  • NM_001407926.1:c.-9A>C
  • NM_001407927.1:c.-9A>C
  • NM_001407930.1:c.-125A>C
  • NM_001407933.1:c.-9A>C
  • NM_001407934.1:c.-9A>C
  • NM_001407935.1:c.-9A>C
  • NM_001407937.1:c.133A>C
  • NM_001407938.1:c.133A>C
  • NM_001407939.1:c.133A>C
  • NM_001407940.1:c.133A>C
  • NM_001407941.1:c.133A>C
  • NM_001407942.1:c.-125A>C
  • NM_001407943.1:c.-9A>C
  • NM_001407944.1:c.-9A>C
  • NM_001407946.1:c.-56A>C
  • NM_001407947.1:c.-56A>C
  • NM_001407948.1:c.-56A>C
  • NM_001407949.1:c.-56A>C
  • NM_001407950.1:c.-56A>C
  • NM_001407951.1:c.-56A>C
  • NM_001407952.1:c.-56A>C
  • NM_001407953.1:c.-56A>C
  • NM_001407954.1:c.-56A>C
  • NM_001407955.1:c.-56A>C
  • NM_001407956.1:c.-56A>C
  • NM_001407957.1:c.-56A>C
  • NM_001407958.1:c.-56A>C
  • NM_001407960.1:c.-171A>C
  • NM_001407962.1:c.-171A>C
  • NM_001407964.1:c.-9A>C
  • NM_001407965.1:c.-287A>C
  • NM_001407968.1:c.133A>C
  • NM_001407969.1:c.133A>C
  • NM_001407970.1:c.133A>C
  • NM_001407971.1:c.133A>C
  • NM_001407972.1:c.133A>C
  • NM_001407973.1:c.133A>C
  • NM_001407974.1:c.133A>C
  • NM_001407975.1:c.133A>C
  • NM_001407976.1:c.133A>C
  • NM_001407977.1:c.133A>C
  • NM_001407978.1:c.133A>C
  • NM_001407979.1:c.133A>C
  • NM_001407980.1:c.133A>C
  • NM_001407981.1:c.133A>C
  • NM_001407982.1:c.133A>C
  • NM_001407983.1:c.133A>C
  • NM_001407984.1:c.133A>C
  • NM_001407985.1:c.133A>C
  • NM_001407986.1:c.133A>C
  • NM_001407990.1:c.133A>C
  • NM_001407991.1:c.133A>C
  • NM_001407992.1:c.133A>C
  • NM_001407993.1:c.133A>C
  • NM_001408392.1:c.133A>C
  • NM_001408396.1:c.133A>C
  • NM_001408397.1:c.133A>C
  • NM_001408398.1:c.133A>C
  • NM_001408399.1:c.133A>C
  • NM_001408400.1:c.133A>C
  • NM_001408401.1:c.133A>C
  • NM_001408402.1:c.133A>C
  • NM_001408403.1:c.133A>C
  • NM_001408404.1:c.133A>C
  • NM_001408406.1:c.133A>C
  • NM_001408407.1:c.133A>C
  • NM_001408408.1:c.133A>C
  • NM_001408409.1:c.133A>C
  • NM_001408410.1:c.-9A>C
  • NM_001408411.1:c.133A>C
  • NM_001408412.1:c.133A>C
  • NM_001408413.1:c.133A>C
  • NM_001408414.1:c.133A>C
  • NM_001408415.1:c.133A>C
  • NM_001408416.1:c.133A>C
  • NM_001408418.1:c.133A>C
  • NM_001408419.1:c.133A>C
  • NM_001408420.1:c.133A>C
  • NM_001408421.1:c.133A>C
  • NM_001408422.1:c.133A>C
  • NM_001408423.1:c.133A>C
  • NM_001408424.1:c.133A>C
  • NM_001408425.1:c.133A>C
  • NM_001408426.1:c.133A>C
  • NM_001408427.1:c.133A>C
  • NM_001408428.1:c.133A>C
  • NM_001408429.1:c.133A>C
  • NM_001408430.1:c.133A>C
  • NM_001408431.1:c.133A>C
  • NM_001408432.1:c.133A>C
  • NM_001408433.1:c.133A>C
  • NM_001408434.1:c.133A>C
  • NM_001408435.1:c.133A>C
  • NM_001408436.1:c.133A>C
  • NM_001408437.1:c.133A>C
  • NM_001408438.1:c.133A>C
  • NM_001408439.1:c.133A>C
  • NM_001408440.1:c.133A>C
  • NM_001408441.1:c.133A>C
  • NM_001408442.1:c.133A>C
  • NM_001408443.1:c.133A>C
  • NM_001408444.1:c.133A>C
  • NM_001408445.1:c.133A>C
  • NM_001408446.1:c.133A>C
  • NM_001408447.1:c.133A>C
  • NM_001408448.1:c.133A>C
  • NM_001408450.1:c.133A>C
  • NM_001408452.1:c.-9A>C
  • NM_001408453.1:c.-9A>C
  • NM_001408455.1:c.-125A>C
  • NM_001408456.1:c.-125A>C
  • NM_001408458.1:c.-9A>C
  • NM_001408462.1:c.-9A>C
  • NM_001408463.1:c.-9A>C
  • NM_001408465.1:c.-129A>C
  • NM_001408466.1:c.-9A>C
  • NM_001408468.1:c.-125A>C
  • NM_001408469.1:c.-9A>C
  • NM_001408470.1:c.-9A>C
  • NM_001408472.1:c.133A>C
  • NM_001408473.1:c.133A>C
  • NM_001408474.1:c.133A>C
  • NM_001408475.1:c.133A>C
  • NM_001408476.1:c.133A>C
  • NM_001408478.1:c.-56A>C
  • NM_001408479.1:c.-56A>C
  • NM_001408480.1:c.-56A>C
  • NM_001408481.1:c.-56A>C
  • NM_001408482.1:c.-56A>C
  • NM_001408483.1:c.-56A>C
  • NM_001408484.1:c.-56A>C
  • NM_001408485.1:c.-56A>C
  • NM_001408489.1:c.-56A>C
  • NM_001408490.1:c.-56A>C
  • NM_001408491.1:c.-56A>C
  • NM_001408492.1:c.-172A>C
  • NM_001408493.1:c.-56A>C
  • NM_001408494.1:c.133A>C
  • NM_001408495.1:c.133A>C
  • NM_001408497.1:c.-9A>C
  • NM_001408499.1:c.-9A>C
  • NM_001408500.1:c.-9A>C
  • NM_001408501.1:c.-125A>C
  • NM_001408502.1:c.-56A>C
  • NM_001408503.1:c.-9A>C
  • NM_001408504.1:c.-9A>C
  • NM_001408505.1:c.-9A>C
  • NM_001408506.1:c.-56A>C
  • NM_001408507.1:c.-56A>C
  • NM_001408508.1:c.-56A>C
  • NM_001408509.1:c.-56A>C
  • NM_001408510.1:c.-171A>C
  • NM_001408512.1:c.-171A>C
  • NM_001408513.1:c.-56A>C
  • NM_001408514.1:c.-56A>C
  • NM_007294.4:c.133A>CMANE SELECT
  • NM_007297.4:c.-8+8290A>C
  • NM_007298.4:c.133A>C
  • NM_007299.4:c.133A>C
  • NM_007300.4:c.133A>C
  • NM_007304.2:c.133A>C
  • NP_001394510.1:p.Lys45Gln
  • NP_001394511.1:p.Lys45Gln
  • NP_001394512.1:p.Lys45Gln
  • NP_001394514.1:p.Lys45Gln
  • NP_001394516.1:p.Lys45Gln
  • NP_001394519.1:p.Lys45Gln
  • NP_001394520.1:p.Lys45Gln
  • NP_001394522.1:p.Lys45Gln
  • NP_001394523.1:p.Lys45Gln
  • NP_001394525.1:p.Lys45Gln
  • NP_001394526.1:p.Lys45Gln
  • NP_001394527.1:p.Lys45Gln
  • NP_001394531.1:p.Lys45Gln
  • NP_001394532.1:p.Lys45Gln
  • NP_001394534.1:p.Lys45Gln
  • NP_001394539.1:p.Lys45Gln
  • NP_001394540.1:p.Lys45Gln
  • NP_001394541.1:p.Lys45Gln
  • NP_001394542.1:p.Lys45Gln
  • NP_001394543.1:p.Lys45Gln
  • NP_001394544.1:p.Lys45Gln
  • NP_001394545.1:p.Lys45Gln
  • NP_001394546.1:p.Lys45Gln
  • NP_001394547.1:p.Lys45Gln
  • NP_001394548.1:p.Lys45Gln
  • NP_001394549.1:p.Lys45Gln
  • NP_001394550.1:p.Lys45Gln
  • NP_001394551.1:p.Lys45Gln
  • NP_001394552.1:p.Lys45Gln
  • NP_001394553.1:p.Lys45Gln
  • NP_001394554.1:p.Lys45Gln
  • NP_001394555.1:p.Lys45Gln
  • NP_001394556.1:p.Lys45Gln
  • NP_001394557.1:p.Lys45Gln
  • NP_001394558.1:p.Lys45Gln
  • NP_001394559.1:p.Lys45Gln
  • NP_001394560.1:p.Lys45Gln
  • NP_001394561.1:p.Lys45Gln
  • NP_001394562.1:p.Lys45Gln
  • NP_001394563.1:p.Lys45Gln
  • NP_001394564.1:p.Lys45Gln
  • NP_001394565.1:p.Lys45Gln
  • NP_001394566.1:p.Lys45Gln
  • NP_001394567.1:p.Lys45Gln
  • NP_001394568.1:p.Lys45Gln
  • NP_001394569.1:p.Lys45Gln
  • NP_001394570.1:p.Lys45Gln
  • NP_001394571.1:p.Lys45Gln
  • NP_001394573.1:p.Lys45Gln
  • NP_001394574.1:p.Lys45Gln
  • NP_001394575.1:p.Lys45Gln
  • NP_001394576.1:p.Lys45Gln
  • NP_001394577.1:p.Lys45Gln
  • NP_001394578.1:p.Lys45Gln
  • NP_001394581.1:p.Lys45Gln
  • NP_001394582.1:p.Lys45Gln
  • NP_001394583.1:p.Lys45Gln
  • NP_001394584.1:p.Lys45Gln
  • NP_001394585.1:p.Lys45Gln
  • NP_001394586.1:p.Lys45Gln
  • NP_001394587.1:p.Lys45Gln
  • NP_001394588.1:p.Lys45Gln
  • NP_001394589.1:p.Lys45Gln
  • NP_001394590.1:p.Lys45Gln
  • NP_001394591.1:p.Lys45Gln
  • NP_001394592.1:p.Lys45Gln
  • NP_001394593.1:p.Lys45Gln
  • NP_001394594.1:p.Lys45Gln
  • NP_001394595.1:p.Lys45Gln
  • NP_001394596.1:p.Lys45Gln
  • NP_001394597.1:p.Lys45Gln
  • NP_001394598.1:p.Lys45Gln
  • NP_001394599.1:p.Lys45Gln
  • NP_001394600.1:p.Lys45Gln
  • NP_001394601.1:p.Lys45Gln
  • NP_001394602.1:p.Lys45Gln
  • NP_001394603.1:p.Lys45Gln
  • NP_001394604.1:p.Lys45Gln
  • NP_001394605.1:p.Lys45Gln
  • NP_001394606.1:p.Lys45Gln
  • NP_001394607.1:p.Lys45Gln
  • NP_001394608.1:p.Lys45Gln
  • NP_001394609.1:p.Lys45Gln
  • NP_001394610.1:p.Lys45Gln
  • NP_001394611.1:p.Lys45Gln
  • NP_001394612.1:p.Lys45Gln
  • NP_001394613.1:p.Lys45Gln
  • NP_001394614.1:p.Lys45Gln
  • NP_001394615.1:p.Lys45Gln
  • NP_001394616.1:p.Lys45Gln
  • NP_001394617.1:p.Lys45Gln
  • NP_001394618.1:p.Lys45Gln
  • NP_001394619.1:p.Lys45Gln
  • NP_001394620.1:p.Lys45Gln
  • NP_001394783.1:p.Lys45Gln
  • NP_001394787.1:p.Lys45Gln
  • NP_001394788.1:p.Lys45Gln
  • NP_001394789.1:p.Lys45Gln
  • NP_001394790.1:p.Lys45Gln
  • NP_001394791.1:p.Lys45Gln
  • NP_001394792.1:p.Lys45Gln
  • NP_001394803.1:p.Lys45Gln
  • NP_001394804.1:p.Lys45Gln
  • NP_001394848.1:p.Lys45Gln
  • NP_001394866.1:p.Lys45Gln
  • NP_001394867.1:p.Lys45Gln
  • NP_001394868.1:p.Lys45Gln
  • NP_001394869.1:p.Lys45Gln
  • NP_001394870.1:p.Lys45Gln
  • NP_001394897.1:p.Lys45Gln
  • NP_001394898.1:p.Lys45Gln
  • NP_001394899.1:p.Lys45Gln
  • NP_001394900.1:p.Lys45Gln
  • NP_001394901.1:p.Lys45Gln
  • NP_001394902.1:p.Lys45Gln
  • NP_001394903.1:p.Lys45Gln
  • NP_001394904.1:p.Lys45Gln
  • NP_001394905.1:p.Lys45Gln
  • NP_001394906.1:p.Lys45Gln
  • NP_001394907.1:p.Lys45Gln
  • NP_001394908.1:p.Lys45Gln
  • NP_001394909.1:p.Lys45Gln
  • NP_001394910.1:p.Lys45Gln
  • NP_001394911.1:p.Lys45Gln
  • NP_001394912.1:p.Lys45Gln
  • NP_001394913.1:p.Lys45Gln
  • NP_001394914.1:p.Lys45Gln
  • NP_001394915.1:p.Lys45Gln
  • NP_001394919.1:p.Lys45Gln
  • NP_001394920.1:p.Lys45Gln
  • NP_001394921.1:p.Lys45Gln
  • NP_001394922.1:p.Lys45Gln
  • NP_001395321.1:p.Lys45Gln
  • NP_001395325.1:p.Lys45Gln
  • NP_001395326.1:p.Lys45Gln
  • NP_001395327.1:p.Lys45Gln
  • NP_001395328.1:p.Lys45Gln
  • NP_001395329.1:p.Lys45Gln
  • NP_001395330.1:p.Lys45Gln
  • NP_001395331.1:p.Lys45Gln
  • NP_001395332.1:p.Lys45Gln
  • NP_001395333.1:p.Lys45Gln
  • NP_001395335.1:p.Lys45Gln
  • NP_001395336.1:p.Lys45Gln
  • NP_001395337.1:p.Lys45Gln
  • NP_001395338.1:p.Lys45Gln
  • NP_001395340.1:p.Lys45Gln
  • NP_001395341.1:p.Lys45Gln
  • NP_001395342.1:p.Lys45Gln
  • NP_001395343.1:p.Lys45Gln
  • NP_001395344.1:p.Lys45Gln
  • NP_001395345.1:p.Lys45Gln
  • NP_001395347.1:p.Lys45Gln
  • NP_001395348.1:p.Lys45Gln
  • NP_001395349.1:p.Lys45Gln
  • NP_001395350.1:p.Lys45Gln
  • NP_001395351.1:p.Lys45Gln
  • NP_001395352.1:p.Lys45Gln
  • NP_001395353.1:p.Lys45Gln
  • NP_001395354.1:p.Lys45Gln
  • NP_001395355.1:p.Lys45Gln
  • NP_001395356.1:p.Lys45Gln
  • NP_001395357.1:p.Lys45Gln
  • NP_001395358.1:p.Lys45Gln
  • NP_001395359.1:p.Lys45Gln
  • NP_001395360.1:p.Lys45Gln
  • NP_001395361.1:p.Lys45Gln
  • NP_001395362.1:p.Lys45Gln
  • NP_001395363.1:p.Lys45Gln
  • NP_001395364.1:p.Lys45Gln
  • NP_001395365.1:p.Lys45Gln
  • NP_001395366.1:p.Lys45Gln
  • NP_001395367.1:p.Lys45Gln
  • NP_001395368.1:p.Lys45Gln
  • NP_001395369.1:p.Lys45Gln
  • NP_001395370.1:p.Lys45Gln
  • NP_001395371.1:p.Lys45Gln
  • NP_001395372.1:p.Lys45Gln
  • NP_001395373.1:p.Lys45Gln
  • NP_001395374.1:p.Lys45Gln
  • NP_001395375.1:p.Lys45Gln
  • NP_001395376.1:p.Lys45Gln
  • NP_001395377.1:p.Lys45Gln
  • NP_001395379.1:p.Lys45Gln
  • NP_001395401.1:p.Lys45Gln
  • NP_001395402.1:p.Lys45Gln
  • NP_001395403.1:p.Lys45Gln
  • NP_001395404.1:p.Lys45Gln
  • NP_001395405.1:p.Lys45Gln
  • NP_001395423.1:p.Lys45Gln
  • NP_001395424.1:p.Lys45Gln
  • NP_009225.1:p.Lys45Gln
  • NP_009225.1:p.Lys45Gln
  • NP_009229.2:p.Lys45Gln
  • NP_009229.2:p.Lys45Gln
  • NP_009230.2:p.Lys45Gln
  • NP_009231.2:p.Lys45Gln
  • NP_009235.2:p.Lys45Gln
  • LRG_292t1:c.133A>C
  • LRG_292:g.102257A>C
  • LRG_292p1:p.Lys45Gln
  • NC_000017.10:g.41267744T>G
  • NM_007294.3:c.133A>C
  • NM_007298.3:c.133A>C
  • NR_027676.2:n.335A>C
  • P38398:p.Lys45Gln
  • p.K45Q
Nucleotide change:
252A>C
Protein change:
K45Q
Links:
BRCA1-HCI: BRCA1_00116; UniProtKB: P38398#VAR_070459; dbSNP: rs769650474
NCBI 1000 Genomes Browser:
rs769650474
Molecular consequence:
  • NM_007297.4:c.-8+8290A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407581.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407968.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407969.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407970.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407971.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407972.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407973.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407974.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407975.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407976.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407977.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407978.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407979.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407980.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407981.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407982.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407983.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407984.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407985.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407986.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407990.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407991.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407992.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407993.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408392.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408396.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408397.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408398.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408399.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408400.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408401.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408402.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408403.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408404.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408406.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408407.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408408.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408409.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408411.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408412.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408413.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408414.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408415.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408416.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408418.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408419.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408420.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408421.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408422.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408423.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408424.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408425.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408426.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408427.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408428.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408429.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408430.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408431.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408432.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408433.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408434.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408435.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408436.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408437.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408438.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408439.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408440.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408441.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408442.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408443.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408444.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408445.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408446.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408447.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408448.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408450.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408472.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408473.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408474.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408475.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408476.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408494.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408495.1:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007298.4:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007299.4:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007304.2:c.133A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NR_027676.2:n.335A>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Functional consequence:
functionally_normal [Sequence Ontology: SO:0002219] - Comment(s)
Observations:
6

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
SCV000244300Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA)
reviewed by expert panel

(ENIGMA BRCA1/2 Classification Criteria (2015))
Benign
(Aug 10, 2015)
germlinecuration

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

ENIGMA BRCA1/2 Classification Criteria (2015),

Citation Link,

SCV000297585Sharing Clinical Reports Project (SCRP)
no assertion criteria provided
Benign
(Jan 31, 2011)
germlineclinical testing

SCV000489579Counsyl
criteria provided, single submitter

(Counsyl Autosomal Dominant Disease Classification criteria (2015))
Benign
(Oct 26, 2016)
unknownclinical testing

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

Counsyl Autosomal Dominant Disease Classification criteria (2015),

Citation Link,

SCV001237902Brotman Baty Institute, University of Washington
no classification provided
not providednot applicablein vitro

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

Citation Link,

SCV004823697All of Us Research Program, National Institutes of Health
criteria provided, single submitter

(ACMG Guidelines, 2015)
Likely Benign
(Nov 2, 2023)
germlineclinical testing

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenot provided2not providednot provided2not providedclinical testing
not providednot applicablenot applicablenot providednot providednot providednot providednot providedin vitro
not providedgermlineunknown4not providednot provided108544not providedclinical testing, curation
not providedunknownunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS).

Lindor NM, Guidugli L, Wang X, Vallée MP, Monteiro AN, Tavtigian S, Goldgar DE, Couch FJ.

Hum Mutat. 2012 Jan;33(1):8-21. doi: 10.1002/humu.21627. Epub 2011 Nov 3. Review.

PubMed [citation]
PMID:
21990134
PMCID:
PMC3242438

Characterization of BRCA1 ring finger variants of uncertain significance.

Sweet K, Senter L, Pilarski R, Wei L, Toland AE.

Breast Cancer Res Treat. 2010 Feb;119(3):737-43. doi: 10.1007/s10549-009-0438-6. Epub 2009 Jun 20.

PubMed [citation]
PMID:
19543972
PMCID:
PMC4283813
See all PubMed Citations (8)

Details of each submission

From Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA), SCV000244300.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedcuration PubMed (1)

Description

IARC class based on posterior probability from multifactorial likelihood analysis, thresholds for class as per Plon et al. 2008 (PMID: 18951446). Class 1 based on posterior probability = 0.0008

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

From Sharing Clinical Reports Project (SCRP), SCV000297585.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenot provided2not providednot providednot providednot providednot provided See 1

Co-occurrences

#ZygosityAllelesNumber of Observations
1SingleHeterozygoteBRCA2:6400T>A (F2058I)1

From Counsyl, SCV000489579.2

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

From Brotman Baty Institute, University of Washington, SCV001237902.1

#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

From All of Us Research Program, National Institutes of Health, SCV004823697.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided4not providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknown108544not providednot provided4not providednot providednot provided

Last Updated: Nov 10, 2024