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NM_007294.4(BRCA1):c.130T>A (p.Cys44Ser) AND not provided

Germline classification:
Pathogenic (3 submissions)
Last evaluated:
Aug 15, 2023
Review status:
2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts
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:
RCV000444956.16

Allele description [Variation Report for NM_007294.4(BRCA1):c.130T>A (p.Cys44Ser)]

NM_007294.4(BRCA1):c.130T>A (p.Cys44Ser)

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.130T>A (p.Cys44Ser)
Other names:
249T>A
HGVS:
  • NC_000017.11:g.43115730A>T
  • NG_005905.2:g.102254T>A
  • NM_001407571.1:c.-59T>A
  • NM_001407581.1:c.130T>A
  • NM_001407582.1:c.130T>A
  • NM_001407583.1:c.130T>A
  • NM_001407585.1:c.130T>A
  • NM_001407587.1:c.130T>A
  • NM_001407590.1:c.130T>A
  • NM_001407591.1:c.130T>A
  • NM_001407593.1:c.130T>A
  • NM_001407594.1:c.130T>A
  • NM_001407596.1:c.130T>A
  • NM_001407597.1:c.130T>A
  • NM_001407598.1:c.130T>A
  • NM_001407602.1:c.130T>A
  • NM_001407603.1:c.130T>A
  • NM_001407605.1:c.130T>A
  • NM_001407610.1:c.130T>A
  • NM_001407611.1:c.130T>A
  • NM_001407612.1:c.130T>A
  • NM_001407613.1:c.130T>A
  • NM_001407614.1:c.130T>A
  • NM_001407615.1:c.130T>A
  • NM_001407616.1:c.130T>A
  • NM_001407617.1:c.130T>A
  • NM_001407618.1:c.130T>A
  • NM_001407619.1:c.130T>A
  • NM_001407620.1:c.130T>A
  • NM_001407621.1:c.130T>A
  • NM_001407622.1:c.130T>A
  • NM_001407623.1:c.130T>A
  • NM_001407624.1:c.130T>A
  • NM_001407625.1:c.130T>A
  • NM_001407626.1:c.130T>A
  • NM_001407627.1:c.130T>A
  • NM_001407628.1:c.130T>A
  • NM_001407629.1:c.130T>A
  • NM_001407630.1:c.130T>A
  • NM_001407631.1:c.130T>A
  • NM_001407632.1:c.130T>A
  • NM_001407633.1:c.130T>A
  • NM_001407634.1:c.130T>A
  • NM_001407635.1:c.130T>A
  • NM_001407636.1:c.130T>A
  • NM_001407637.1:c.130T>A
  • NM_001407638.1:c.130T>A
  • NM_001407639.1:c.130T>A
  • NM_001407640.1:c.130T>A
  • NM_001407641.1:c.130T>A
  • NM_001407642.1:c.130T>A
  • NM_001407644.1:c.130T>A
  • NM_001407645.1:c.130T>A
  • NM_001407646.1:c.130T>A
  • NM_001407647.1:c.130T>A
  • NM_001407648.1:c.130T>A
  • NM_001407649.1:c.130T>A
  • NM_001407652.1:c.130T>A
  • NM_001407653.1:c.130T>A
  • NM_001407654.1:c.130T>A
  • NM_001407655.1:c.130T>A
  • NM_001407656.1:c.130T>A
  • NM_001407657.1:c.130T>A
  • NM_001407658.1:c.130T>A
  • NM_001407659.1:c.130T>A
  • NM_001407660.1:c.130T>A
  • NM_001407661.1:c.130T>A
  • NM_001407662.1:c.130T>A
  • NM_001407663.1:c.130T>A
  • NM_001407664.1:c.130T>A
  • NM_001407665.1:c.130T>A
  • NM_001407666.1:c.130T>A
  • NM_001407667.1:c.130T>A
  • NM_001407668.1:c.130T>A
  • NM_001407669.1:c.130T>A
  • NM_001407670.1:c.130T>A
  • NM_001407671.1:c.130T>A
  • NM_001407672.1:c.130T>A
  • NM_001407673.1:c.130T>A
  • NM_001407674.1:c.130T>A
  • NM_001407675.1:c.130T>A
  • NM_001407676.1:c.130T>A
  • NM_001407677.1:c.130T>A
  • NM_001407678.1:c.130T>A
  • NM_001407679.1:c.130T>A
  • NM_001407680.1:c.130T>A
  • NM_001407681.1:c.130T>A
  • NM_001407682.1:c.130T>A
  • NM_001407683.1:c.130T>A
  • NM_001407684.1:c.130T>A
  • NM_001407685.1:c.130T>A
  • NM_001407686.1:c.130T>A
  • NM_001407687.1:c.130T>A
  • NM_001407688.1:c.130T>A
  • NM_001407689.1:c.130T>A
  • NM_001407690.1:c.130T>A
  • NM_001407691.1:c.130T>A
  • NM_001407694.1:c.-128T>A
  • NM_001407695.1:c.-132T>A
  • NM_001407696.1:c.-128T>A
  • NM_001407697.1:c.-12T>A
  • NM_001407724.1:c.-128T>A
  • NM_001407725.1:c.-12T>A
  • NM_001407727.1:c.-128T>A
  • NM_001407728.1:c.-12T>A
  • NM_001407729.1:c.-12T>A
  • NM_001407730.1:c.-12T>A
  • NM_001407731.1:c.-128T>A
  • NM_001407733.1:c.-128T>A
  • NM_001407734.1:c.-12T>A
  • NM_001407735.1:c.-12T>A
  • NM_001407737.1:c.-12T>A
  • NM_001407739.1:c.-12T>A
  • NM_001407740.1:c.-12T>A
  • NM_001407741.1:c.-12T>A
  • NM_001407743.1:c.-12T>A
  • NM_001407745.1:c.-12T>A
  • NM_001407746.1:c.-128T>A
  • NM_001407748.1:c.-12T>A
  • NM_001407749.1:c.-128T>A
  • NM_001407752.1:c.-12T>A
  • NM_001407838.1:c.-12T>A
  • NM_001407839.1:c.-12T>A
  • NM_001407841.1:c.-8T>A
  • NM_001407842.1:c.-128T>A
  • NM_001407843.1:c.-128T>A
  • NM_001407844.1:c.-12T>A
  • NM_001407846.1:c.-12T>A
  • NM_001407847.1:c.-12T>A
  • NM_001407848.1:c.-12T>A
  • NM_001407850.1:c.-12T>A
  • NM_001407851.1:c.-12T>A
  • NM_001407853.1:c.-59T>A
  • NM_001407854.1:c.130T>A
  • NM_001407858.1:c.130T>A
  • NM_001407859.1:c.130T>A
  • NM_001407860.1:c.130T>A
  • NM_001407861.1:c.130T>A
  • NM_001407862.1:c.130T>A
  • NM_001407863.1:c.130T>A
  • NM_001407874.1:c.130T>A
  • NM_001407875.1:c.130T>A
  • NM_001407879.1:c.-59T>A
  • NM_001407882.1:c.-59T>A
  • NM_001407884.1:c.-59T>A
  • NM_001407885.1:c.-59T>A
  • NM_001407886.1:c.-59T>A
  • NM_001407887.1:c.-59T>A
  • NM_001407889.1:c.-175T>A
  • NM_001407894.1:c.-59T>A
  • NM_001407895.1:c.-59T>A
  • NM_001407896.1:c.-59T>A
  • NM_001407897.1:c.-59T>A
  • NM_001407899.1:c.-59T>A
  • NM_001407900.1:c.-175T>A
  • NM_001407904.1:c.-59T>A
  • NM_001407906.1:c.-59T>A
  • NM_001407907.1:c.-59T>A
  • NM_001407908.1:c.-59T>A
  • NM_001407909.1:c.-59T>A
  • NM_001407910.1:c.-59T>A
  • NM_001407915.1:c.-59T>A
  • NM_001407916.1:c.-59T>A
  • NM_001407917.1:c.-59T>A
  • NM_001407918.1:c.-59T>A
  • NM_001407919.1:c.130T>A
  • NM_001407920.1:c.-12T>A
  • NM_001407921.1:c.-12T>A
  • NM_001407922.1:c.-12T>A
  • NM_001407923.1:c.-12T>A
  • NM_001407926.1:c.-12T>A
  • NM_001407927.1:c.-12T>A
  • NM_001407930.1:c.-128T>A
  • NM_001407933.1:c.-12T>A
  • NM_001407934.1:c.-12T>A
  • NM_001407935.1:c.-12T>A
  • NM_001407937.1:c.130T>A
  • NM_001407938.1:c.130T>A
  • NM_001407939.1:c.130T>A
  • NM_001407940.1:c.130T>A
  • NM_001407941.1:c.130T>A
  • NM_001407942.1:c.-128T>A
  • NM_001407943.1:c.-12T>A
  • NM_001407944.1:c.-12T>A
  • NM_001407946.1:c.-59T>A
  • NM_001407947.1:c.-59T>A
  • NM_001407948.1:c.-59T>A
  • NM_001407949.1:c.-59T>A
  • NM_001407950.1:c.-59T>A
  • NM_001407951.1:c.-59T>A
  • NM_001407952.1:c.-59T>A
  • NM_001407953.1:c.-59T>A
  • NM_001407954.1:c.-59T>A
  • NM_001407955.1:c.-59T>A
  • NM_001407956.1:c.-59T>A
  • NM_001407957.1:c.-59T>A
  • NM_001407958.1:c.-59T>A
  • NM_001407960.1:c.-174T>A
  • NM_001407962.1:c.-174T>A
  • NM_001407964.1:c.-12T>A
  • NM_001407965.1:c.-290T>A
  • NM_001407968.1:c.130T>A
  • NM_001407969.1:c.130T>A
  • NM_001407970.1:c.130T>A
  • NM_001407971.1:c.130T>A
  • NM_001407972.1:c.130T>A
  • NM_001407973.1:c.130T>A
  • NM_001407974.1:c.130T>A
  • NM_001407975.1:c.130T>A
  • NM_001407976.1:c.130T>A
  • NM_001407977.1:c.130T>A
  • NM_001407978.1:c.130T>A
  • NM_001407979.1:c.130T>A
  • NM_001407980.1:c.130T>A
  • NM_001407981.1:c.130T>A
  • NM_001407982.1:c.130T>A
  • NM_001407983.1:c.130T>A
  • NM_001407984.1:c.130T>A
  • NM_001407985.1:c.130T>A
  • NM_001407986.1:c.130T>A
  • NM_001407990.1:c.130T>A
  • NM_001407991.1:c.130T>A
  • NM_001407992.1:c.130T>A
  • NM_001407993.1:c.130T>A
  • NM_001408392.1:c.130T>A
  • NM_001408396.1:c.130T>A
  • NM_001408397.1:c.130T>A
  • NM_001408398.1:c.130T>A
  • NM_001408399.1:c.130T>A
  • NM_001408400.1:c.130T>A
  • NM_001408401.1:c.130T>A
  • NM_001408402.1:c.130T>A
  • NM_001408403.1:c.130T>A
  • NM_001408404.1:c.130T>A
  • NM_001408406.1:c.130T>A
  • NM_001408407.1:c.130T>A
  • NM_001408408.1:c.130T>A
  • NM_001408409.1:c.130T>A
  • NM_001408410.1:c.-12T>A
  • NM_001408411.1:c.130T>A
  • NM_001408412.1:c.130T>A
  • NM_001408413.1:c.130T>A
  • NM_001408414.1:c.130T>A
  • NM_001408415.1:c.130T>A
  • NM_001408416.1:c.130T>A
  • NM_001408418.1:c.130T>A
  • NM_001408419.1:c.130T>A
  • NM_001408420.1:c.130T>A
  • NM_001408421.1:c.130T>A
  • NM_001408422.1:c.130T>A
  • NM_001408423.1:c.130T>A
  • NM_001408424.1:c.130T>A
  • NM_001408425.1:c.130T>A
  • NM_001408426.1:c.130T>A
  • NM_001408427.1:c.130T>A
  • NM_001408428.1:c.130T>A
  • NM_001408429.1:c.130T>A
  • NM_001408430.1:c.130T>A
  • NM_001408431.1:c.130T>A
  • NM_001408432.1:c.130T>A
  • NM_001408433.1:c.130T>A
  • NM_001408434.1:c.130T>A
  • NM_001408435.1:c.130T>A
  • NM_001408436.1:c.130T>A
  • NM_001408437.1:c.130T>A
  • NM_001408438.1:c.130T>A
  • NM_001408439.1:c.130T>A
  • NM_001408440.1:c.130T>A
  • NM_001408441.1:c.130T>A
  • NM_001408442.1:c.130T>A
  • NM_001408443.1:c.130T>A
  • NM_001408444.1:c.130T>A
  • NM_001408445.1:c.130T>A
  • NM_001408446.1:c.130T>A
  • NM_001408447.1:c.130T>A
  • NM_001408448.1:c.130T>A
  • NM_001408450.1:c.130T>A
  • NM_001408452.1:c.-12T>A
  • NM_001408453.1:c.-12T>A
  • NM_001408455.1:c.-128T>A
  • NM_001408456.1:c.-128T>A
  • NM_001408458.1:c.-12T>A
  • NM_001408462.1:c.-12T>A
  • NM_001408463.1:c.-12T>A
  • NM_001408465.1:c.-132T>A
  • NM_001408466.1:c.-12T>A
  • NM_001408468.1:c.-128T>A
  • NM_001408469.1:c.-12T>A
  • NM_001408470.1:c.-12T>A
  • NM_001408472.1:c.130T>A
  • NM_001408473.1:c.130T>A
  • NM_001408474.1:c.130T>A
  • NM_001408475.1:c.130T>A
  • NM_001408476.1:c.130T>A
  • NM_001408478.1:c.-59T>A
  • NM_001408479.1:c.-59T>A
  • NM_001408480.1:c.-59T>A
  • NM_001408481.1:c.-59T>A
  • NM_001408482.1:c.-59T>A
  • NM_001408483.1:c.-59T>A
  • NM_001408484.1:c.-59T>A
  • NM_001408485.1:c.-59T>A
  • NM_001408489.1:c.-59T>A
  • NM_001408490.1:c.-59T>A
  • NM_001408491.1:c.-59T>A
  • NM_001408492.1:c.-175T>A
  • NM_001408493.1:c.-59T>A
  • NM_001408494.1:c.130T>A
  • NM_001408495.1:c.130T>A
  • NM_001408497.1:c.-12T>A
  • NM_001408499.1:c.-12T>A
  • NM_001408500.1:c.-12T>A
  • NM_001408501.1:c.-128T>A
  • NM_001408502.1:c.-59T>A
  • NM_001408503.1:c.-12T>A
  • NM_001408504.1:c.-12T>A
  • NM_001408505.1:c.-12T>A
  • NM_001408506.1:c.-59T>A
  • NM_001408507.1:c.-59T>A
  • NM_001408508.1:c.-59T>A
  • NM_001408509.1:c.-59T>A
  • NM_001408510.1:c.-174T>A
  • NM_001408512.1:c.-174T>A
  • NM_001408513.1:c.-59T>A
  • NM_001408514.1:c.-59T>A
  • NM_007294.4:c.130T>AMANE SELECT
  • NM_007297.4:c.-8+8287T>A
  • NM_007298.4:c.130T>A
  • NM_007299.4:c.130T>A
  • NM_007300.4:c.130T>A
  • NM_007304.2:c.130T>A
  • NP_001394510.1:p.Cys44Ser
  • NP_001394511.1:p.Cys44Ser
  • NP_001394512.1:p.Cys44Ser
  • NP_001394514.1:p.Cys44Ser
  • NP_001394516.1:p.Cys44Ser
  • NP_001394519.1:p.Cys44Ser
  • NP_001394520.1:p.Cys44Ser
  • NP_001394522.1:p.Cys44Ser
  • NP_001394523.1:p.Cys44Ser
  • NP_001394525.1:p.Cys44Ser
  • NP_001394526.1:p.Cys44Ser
  • NP_001394527.1:p.Cys44Ser
  • NP_001394531.1:p.Cys44Ser
  • NP_001394532.1:p.Cys44Ser
  • NP_001394534.1:p.Cys44Ser
  • NP_001394539.1:p.Cys44Ser
  • NP_001394540.1:p.Cys44Ser
  • NP_001394541.1:p.Cys44Ser
  • NP_001394542.1:p.Cys44Ser
  • NP_001394543.1:p.Cys44Ser
  • NP_001394544.1:p.Cys44Ser
  • NP_001394545.1:p.Cys44Ser
  • NP_001394546.1:p.Cys44Ser
  • NP_001394547.1:p.Cys44Ser
  • NP_001394548.1:p.Cys44Ser
  • NP_001394549.1:p.Cys44Ser
  • NP_001394550.1:p.Cys44Ser
  • NP_001394551.1:p.Cys44Ser
  • NP_001394552.1:p.Cys44Ser
  • NP_001394553.1:p.Cys44Ser
  • NP_001394554.1:p.Cys44Ser
  • NP_001394555.1:p.Cys44Ser
  • NP_001394556.1:p.Cys44Ser
  • NP_001394557.1:p.Cys44Ser
  • NP_001394558.1:p.Cys44Ser
  • NP_001394559.1:p.Cys44Ser
  • NP_001394560.1:p.Cys44Ser
  • NP_001394561.1:p.Cys44Ser
  • NP_001394562.1:p.Cys44Ser
  • NP_001394563.1:p.Cys44Ser
  • NP_001394564.1:p.Cys44Ser
  • NP_001394565.1:p.Cys44Ser
  • NP_001394566.1:p.Cys44Ser
  • NP_001394567.1:p.Cys44Ser
  • NP_001394568.1:p.Cys44Ser
  • NP_001394569.1:p.Cys44Ser
  • NP_001394570.1:p.Cys44Ser
  • NP_001394571.1:p.Cys44Ser
  • NP_001394573.1:p.Cys44Ser
  • NP_001394574.1:p.Cys44Ser
  • NP_001394575.1:p.Cys44Ser
  • NP_001394576.1:p.Cys44Ser
  • NP_001394577.1:p.Cys44Ser
  • NP_001394578.1:p.Cys44Ser
  • NP_001394581.1:p.Cys44Ser
  • NP_001394582.1:p.Cys44Ser
  • NP_001394583.1:p.Cys44Ser
  • NP_001394584.1:p.Cys44Ser
  • NP_001394585.1:p.Cys44Ser
  • NP_001394586.1:p.Cys44Ser
  • NP_001394587.1:p.Cys44Ser
  • NP_001394588.1:p.Cys44Ser
  • NP_001394589.1:p.Cys44Ser
  • NP_001394590.1:p.Cys44Ser
  • NP_001394591.1:p.Cys44Ser
  • NP_001394592.1:p.Cys44Ser
  • NP_001394593.1:p.Cys44Ser
  • NP_001394594.1:p.Cys44Ser
  • NP_001394595.1:p.Cys44Ser
  • NP_001394596.1:p.Cys44Ser
  • NP_001394597.1:p.Cys44Ser
  • NP_001394598.1:p.Cys44Ser
  • NP_001394599.1:p.Cys44Ser
  • NP_001394600.1:p.Cys44Ser
  • NP_001394601.1:p.Cys44Ser
  • NP_001394602.1:p.Cys44Ser
  • NP_001394603.1:p.Cys44Ser
  • NP_001394604.1:p.Cys44Ser
  • NP_001394605.1:p.Cys44Ser
  • NP_001394606.1:p.Cys44Ser
  • NP_001394607.1:p.Cys44Ser
  • NP_001394608.1:p.Cys44Ser
  • NP_001394609.1:p.Cys44Ser
  • NP_001394610.1:p.Cys44Ser
  • NP_001394611.1:p.Cys44Ser
  • NP_001394612.1:p.Cys44Ser
  • NP_001394613.1:p.Cys44Ser
  • NP_001394614.1:p.Cys44Ser
  • NP_001394615.1:p.Cys44Ser
  • NP_001394616.1:p.Cys44Ser
  • NP_001394617.1:p.Cys44Ser
  • NP_001394618.1:p.Cys44Ser
  • NP_001394619.1:p.Cys44Ser
  • NP_001394620.1:p.Cys44Ser
  • NP_001394783.1:p.Cys44Ser
  • NP_001394787.1:p.Cys44Ser
  • NP_001394788.1:p.Cys44Ser
  • NP_001394789.1:p.Cys44Ser
  • NP_001394790.1:p.Cys44Ser
  • NP_001394791.1:p.Cys44Ser
  • NP_001394792.1:p.Cys44Ser
  • NP_001394803.1:p.Cys44Ser
  • NP_001394804.1:p.Cys44Ser
  • NP_001394848.1:p.Cys44Ser
  • NP_001394866.1:p.Cys44Ser
  • NP_001394867.1:p.Cys44Ser
  • NP_001394868.1:p.Cys44Ser
  • NP_001394869.1:p.Cys44Ser
  • NP_001394870.1:p.Cys44Ser
  • NP_001394897.1:p.Cys44Ser
  • NP_001394898.1:p.Cys44Ser
  • NP_001394899.1:p.Cys44Ser
  • NP_001394900.1:p.Cys44Ser
  • NP_001394901.1:p.Cys44Ser
  • NP_001394902.1:p.Cys44Ser
  • NP_001394903.1:p.Cys44Ser
  • NP_001394904.1:p.Cys44Ser
  • NP_001394905.1:p.Cys44Ser
  • NP_001394906.1:p.Cys44Ser
  • NP_001394907.1:p.Cys44Ser
  • NP_001394908.1:p.Cys44Ser
  • NP_001394909.1:p.Cys44Ser
  • NP_001394910.1:p.Cys44Ser
  • NP_001394911.1:p.Cys44Ser
  • NP_001394912.1:p.Cys44Ser
  • NP_001394913.1:p.Cys44Ser
  • NP_001394914.1:p.Cys44Ser
  • NP_001394915.1:p.Cys44Ser
  • NP_001394919.1:p.Cys44Ser
  • NP_001394920.1:p.Cys44Ser
  • NP_001394921.1:p.Cys44Ser
  • NP_001394922.1:p.Cys44Ser
  • NP_001395321.1:p.Cys44Ser
  • NP_001395325.1:p.Cys44Ser
  • NP_001395326.1:p.Cys44Ser
  • NP_001395327.1:p.Cys44Ser
  • NP_001395328.1:p.Cys44Ser
  • NP_001395329.1:p.Cys44Ser
  • NP_001395330.1:p.Cys44Ser
  • NP_001395331.1:p.Cys44Ser
  • NP_001395332.1:p.Cys44Ser
  • NP_001395333.1:p.Cys44Ser
  • NP_001395335.1:p.Cys44Ser
  • NP_001395336.1:p.Cys44Ser
  • NP_001395337.1:p.Cys44Ser
  • NP_001395338.1:p.Cys44Ser
  • NP_001395340.1:p.Cys44Ser
  • NP_001395341.1:p.Cys44Ser
  • NP_001395342.1:p.Cys44Ser
  • NP_001395343.1:p.Cys44Ser
  • NP_001395344.1:p.Cys44Ser
  • NP_001395345.1:p.Cys44Ser
  • NP_001395347.1:p.Cys44Ser
  • NP_001395348.1:p.Cys44Ser
  • NP_001395349.1:p.Cys44Ser
  • NP_001395350.1:p.Cys44Ser
  • NP_001395351.1:p.Cys44Ser
  • NP_001395352.1:p.Cys44Ser
  • NP_001395353.1:p.Cys44Ser
  • NP_001395354.1:p.Cys44Ser
  • NP_001395355.1:p.Cys44Ser
  • NP_001395356.1:p.Cys44Ser
  • NP_001395357.1:p.Cys44Ser
  • NP_001395358.1:p.Cys44Ser
  • NP_001395359.1:p.Cys44Ser
  • NP_001395360.1:p.Cys44Ser
  • NP_001395361.1:p.Cys44Ser
  • NP_001395362.1:p.Cys44Ser
  • NP_001395363.1:p.Cys44Ser
  • NP_001395364.1:p.Cys44Ser
  • NP_001395365.1:p.Cys44Ser
  • NP_001395366.1:p.Cys44Ser
  • NP_001395367.1:p.Cys44Ser
  • NP_001395368.1:p.Cys44Ser
  • NP_001395369.1:p.Cys44Ser
  • NP_001395370.1:p.Cys44Ser
  • NP_001395371.1:p.Cys44Ser
  • NP_001395372.1:p.Cys44Ser
  • NP_001395373.1:p.Cys44Ser
  • NP_001395374.1:p.Cys44Ser
  • NP_001395375.1:p.Cys44Ser
  • NP_001395376.1:p.Cys44Ser
  • NP_001395377.1:p.Cys44Ser
  • NP_001395379.1:p.Cys44Ser
  • NP_001395401.1:p.Cys44Ser
  • NP_001395402.1:p.Cys44Ser
  • NP_001395403.1:p.Cys44Ser
  • NP_001395404.1:p.Cys44Ser
  • NP_001395405.1:p.Cys44Ser
  • NP_001395423.1:p.Cys44Ser
  • NP_001395424.1:p.Cys44Ser
  • NP_009225.1:p.Cys44Ser
  • NP_009225.1:p.Cys44Ser
  • NP_009229.2:p.Cys44Ser
  • NP_009229.2:p.Cys44Ser
  • NP_009230.2:p.Cys44Ser
  • NP_009231.2:p.Cys44Ser
  • NP_009235.2:p.Cys44Ser
  • LRG_292t1:c.130T>A
  • LRG_292:g.102254T>A
  • LRG_292p1:p.Cys44Ser
  • NC_000017.10:g.41267747A>T
  • NM_007294.3:c.130T>A
  • NM_007298.3:c.130T>A
  • NR_027676.2:n.332T>A
  • U14680.1:n.249T>A
Protein change:
C44S
Links:
BRCA1-HCI: BRCA1_00115; dbSNP: rs80357327
NCBI 1000 Genomes Browser:
rs80357327
Molecular consequence:
  • NM_007297.4:c.-8+8287T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407581.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407968.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407969.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407970.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407971.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407972.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407973.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407974.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407975.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407976.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407977.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407978.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407979.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407980.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407981.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407982.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407983.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407984.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407985.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407986.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407990.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407991.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407992.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407993.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408392.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408396.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408397.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408398.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408399.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408400.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408401.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408402.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408403.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408404.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408406.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408407.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408408.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408409.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408411.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408412.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408413.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408414.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408415.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408416.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408418.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408419.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408420.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408421.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408422.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408423.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408424.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408425.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408426.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408427.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408428.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408429.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408430.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408431.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408432.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408433.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408434.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408435.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408436.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408437.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408438.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408439.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408440.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408441.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408442.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408443.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408444.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408445.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408446.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408447.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408448.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408450.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408472.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408473.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408474.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408475.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408476.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408494.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408495.1:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007298.4:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007299.4:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007304.2:c.130T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_027676.2:n.332T>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Functional consequence:
functionally_abnormal [Sequence Ontology: SO:0002218] - Comment(s)

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000516958GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Pathogenic
(Oct 10, 2019)
germlineclinical testing

Citation Link,

SCV002551072Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital
criteria provided, single submitter

(ACMG Guidelines, 2015)
Pathogenic
(Aug 15, 2023)
germlineclinical testing

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

SCV005199760Clinical Genetics Laboratory, Skane University Hospital Lund
criteria provided, single submitter

(ACMG Guidelines, 2015)
Pathogenic
(May 27, 2022)
germlineclinical testing

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From GeneDx, SCV000516958.4

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

Description

Published functional studies demonstrate a damaging effect: classified as non-functional based on a saturation genome editing assay assessing ability to support growth, and demonstrated defective homology-directed repair activity and BARD1 binding (Starita 2015, Findlay 2018, Caleca 2019); Multi-factorial studies suggest this variant is associated with breast and ovarian cancer (Lindor 2012); In silico analysis, which includes protein predictors and evolutionary conservation, supports a deleterious effect; No data available from control populations to assess the frequency of this variant; Observed in women with a history of breast and/or ovarian cancer and has been suggested to be a recurrent variant in the Greenlandic population (Borg 2010, Hansen 2010, Sweet 2010, Karami 2013); This variant is associated with the following publications: (PMID: 26295337, 21990134, 18182601, 19543972, 24489791, 20104584, 21520273, 20437199, 24312913, 25525159, 25823446, 30209399, 26833046, 21990165, 29339979, 29446198, 18465347, 30678073, 25348012, 30696104, 33087888)

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

From Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital, SCV002551072.4

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

From Clinical Genetics Laboratory, Skane University Hospital Lund, SCV005199760.1

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

Last Updated: Nov 10, 2024