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NM_007294.4(BRCA1):c.4535G>T (p.Ser1512Ile) AND Hereditary breast ovarian cancer syndrome

Germline classification:
Benign/Likely benign (5 submissions)
Last evaluated:
Feb 1, 2024
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:
RCV000048591.30

Allele description [Variation Report for NM_007294.4(BRCA1):c.4535G>T (p.Ser1512Ile)]

NM_007294.4(BRCA1):c.4535G>T (p.Ser1512Ile)

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.4535G>T (p.Ser1512Ile)
Other names:
NP_009225.1:p.Ser1512Ile
HGVS:
  • NC_000017.11:g.43074471C>A
  • NG_005905.2:g.143513G>T
  • NM_001407571.1:c.4322G>T
  • NM_001407581.1:c.4601G>T
  • NM_001407582.1:c.4601G>T
  • NM_001407583.1:c.4598G>T
  • NM_001407585.1:c.4598G>T
  • NM_001407587.1:c.4598G>T
  • NM_001407590.1:c.4595G>T
  • NM_001407591.1:c.4595G>T
  • NM_001407593.1:c.4535G>T
  • NM_001407594.1:c.4535G>T
  • NM_001407596.1:c.4535G>T
  • NM_001407597.1:c.4535G>T
  • NM_001407598.1:c.4535G>T
  • NM_001407602.1:c.4535G>T
  • NM_001407603.1:c.4535G>T
  • NM_001407605.1:c.4535G>T
  • NM_001407610.1:c.4532G>T
  • NM_001407611.1:c.4532G>T
  • NM_001407612.1:c.4532G>T
  • NM_001407613.1:c.4532G>T
  • NM_001407614.1:c.4532G>T
  • NM_001407615.1:c.4532G>T
  • NM_001407616.1:c.4532G>T
  • NM_001407617.1:c.4532G>T
  • NM_001407618.1:c.4532G>T
  • NM_001407619.1:c.4532G>T
  • NM_001407620.1:c.4532G>T
  • NM_001407621.1:c.4532G>T
  • NM_001407622.1:c.4532G>T
  • NM_001407623.1:c.4532G>T
  • NM_001407624.1:c.4532G>T
  • NM_001407625.1:c.4532G>T
  • NM_001407626.1:c.4532G>T
  • NM_001407627.1:c.4529G>T
  • NM_001407628.1:c.4529G>T
  • NM_001407629.1:c.4529G>T
  • NM_001407630.1:c.4529G>T
  • NM_001407631.1:c.4529G>T
  • NM_001407632.1:c.4529G>T
  • NM_001407633.1:c.4529G>T
  • NM_001407634.1:c.4529G>T
  • NM_001407635.1:c.4529G>T
  • NM_001407636.1:c.4529G>T
  • NM_001407637.1:c.4529G>T
  • NM_001407638.1:c.4529G>T
  • NM_001407639.1:c.4529G>T
  • NM_001407640.1:c.4529G>T
  • NM_001407641.1:c.4529G>T
  • NM_001407642.1:c.4529G>T
  • NM_001407644.1:c.4526G>T
  • NM_001407645.1:c.4526G>T
  • NM_001407646.1:c.4523G>T
  • NM_001407647.1:c.4520G>T
  • NM_001407648.1:c.4478G>T
  • NM_001407649.1:c.4475G>T
  • NM_001407652.1:c.4535G>T
  • NM_001407653.1:c.4457G>T
  • NM_001407654.1:c.4457G>T
  • NM_001407655.1:c.4457G>T
  • NM_001407656.1:c.4454G>T
  • NM_001407657.1:c.4454G>T
  • NM_001407658.1:c.4454G>T
  • NM_001407659.1:c.4451G>T
  • NM_001407660.1:c.4451G>T
  • NM_001407661.1:c.4451G>T
  • NM_001407662.1:c.4451G>T
  • NM_001407663.1:c.4451G>T
  • NM_001407664.1:c.4412G>T
  • NM_001407665.1:c.4412G>T
  • NM_001407666.1:c.4412G>T
  • NM_001407667.1:c.4412G>T
  • NM_001407668.1:c.4412G>T
  • NM_001407669.1:c.4412G>T
  • NM_001407670.1:c.4409G>T
  • NM_001407671.1:c.4409G>T
  • NM_001407672.1:c.4409G>T
  • NM_001407673.1:c.4409G>T
  • NM_001407674.1:c.4409G>T
  • NM_001407675.1:c.4409G>T
  • NM_001407676.1:c.4409G>T
  • NM_001407677.1:c.4409G>T
  • NM_001407678.1:c.4409G>T
  • NM_001407679.1:c.4409G>T
  • NM_001407680.1:c.4409G>T
  • NM_001407681.1:c.4406G>T
  • NM_001407682.1:c.4406G>T
  • NM_001407683.1:c.4406G>T
  • NM_001407684.1:c.4535G>T
  • NM_001407685.1:c.4406G>T
  • NM_001407686.1:c.4406G>T
  • NM_001407687.1:c.4406G>T
  • NM_001407688.1:c.4406G>T
  • NM_001407689.1:c.4406G>T
  • NM_001407690.1:c.4403G>T
  • NM_001407691.1:c.4403G>T
  • NM_001407692.1:c.4394G>T
  • NM_001407694.1:c.4394G>T
  • NM_001407695.1:c.4394G>T
  • NM_001407696.1:c.4394G>T
  • NM_001407697.1:c.4394G>T
  • NM_001407698.1:c.4394G>T
  • NM_001407724.1:c.4394G>T
  • NM_001407725.1:c.4394G>T
  • NM_001407726.1:c.4394G>T
  • NM_001407727.1:c.4394G>T
  • NM_001407728.1:c.4394G>T
  • NM_001407729.1:c.4394G>T
  • NM_001407730.1:c.4394G>T
  • NM_001407731.1:c.4394G>T
  • NM_001407732.1:c.4391G>T
  • NM_001407733.1:c.4391G>T
  • NM_001407734.1:c.4391G>T
  • NM_001407735.1:c.4391G>T
  • NM_001407736.1:c.4391G>T
  • NM_001407737.1:c.4391G>T
  • NM_001407738.1:c.4391G>T
  • NM_001407739.1:c.4391G>T
  • NM_001407740.1:c.4391G>T
  • NM_001407741.1:c.4391G>T
  • NM_001407742.1:c.4391G>T
  • NM_001407743.1:c.4391G>T
  • NM_001407744.1:c.4391G>T
  • NM_001407745.1:c.4391G>T
  • NM_001407746.1:c.4391G>T
  • NM_001407747.1:c.4391G>T
  • NM_001407748.1:c.4391G>T
  • NM_001407749.1:c.4391G>T
  • NM_001407750.1:c.4391G>T
  • NM_001407751.1:c.4391G>T
  • NM_001407752.1:c.4391G>T
  • NM_001407838.1:c.4388G>T
  • NM_001407839.1:c.4388G>T
  • NM_001407841.1:c.4388G>T
  • NM_001407842.1:c.4388G>T
  • NM_001407843.1:c.4388G>T
  • NM_001407844.1:c.4388G>T
  • NM_001407845.1:c.4388G>T
  • NM_001407846.1:c.4388G>T
  • NM_001407847.1:c.4388G>T
  • NM_001407848.1:c.4388G>T
  • NM_001407849.1:c.4388G>T
  • NM_001407850.1:c.4388G>T
  • NM_001407851.1:c.4388G>T
  • NM_001407852.1:c.4388G>T
  • NM_001407853.1:c.4388G>T
  • NM_001407854.1:c.4535G>T
  • NM_001407858.1:c.4532G>T
  • NM_001407859.1:c.4532G>T
  • NM_001407860.1:c.4532G>T
  • NM_001407861.1:c.4529G>T
  • NM_001407862.1:c.4334G>T
  • NM_001407863.1:c.4409G>T
  • NM_001407874.1:c.4328G>T
  • NM_001407875.1:c.4328G>T
  • NM_001407879.1:c.4325G>T
  • NM_001407881.1:c.4325G>T
  • NM_001407882.1:c.4325G>T
  • NM_001407884.1:c.4325G>T
  • NM_001407885.1:c.4325G>T
  • NM_001407886.1:c.4325G>T
  • NM_001407887.1:c.4325G>T
  • NM_001407889.1:c.4325G>T
  • NM_001407894.1:c.4322G>T
  • NM_001407895.1:c.4322G>T
  • NM_001407896.1:c.4322G>T
  • NM_001407897.1:c.4322G>T
  • NM_001407898.1:c.4322G>T
  • NM_001407899.1:c.4322G>T
  • NM_001407900.1:c.4322G>T
  • NM_001407902.1:c.4322G>T
  • NM_001407904.1:c.4322G>T
  • NM_001407906.1:c.4322G>T
  • NM_001407907.1:c.4322G>T
  • NM_001407908.1:c.4322G>T
  • NM_001407909.1:c.4322G>T
  • NM_001407910.1:c.4322G>T
  • NM_001407915.1:c.4319G>T
  • NM_001407916.1:c.4319G>T
  • NM_001407917.1:c.4319G>T
  • NM_001407918.1:c.4319G>T
  • NM_001407919.1:c.4412G>T
  • NM_001407920.1:c.4271G>T
  • NM_001407921.1:c.4271G>T
  • NM_001407922.1:c.4271G>T
  • NM_001407923.1:c.4271G>T
  • NM_001407924.1:c.4271G>T
  • NM_001407925.1:c.4271G>T
  • NM_001407926.1:c.4271G>T
  • NM_001407927.1:c.4268G>T
  • NM_001407928.1:c.4268G>T
  • NM_001407929.1:c.4268G>T
  • NM_001407930.1:c.4268G>T
  • NM_001407931.1:c.4268G>T
  • NM_001407932.1:c.4268G>T
  • NM_001407933.1:c.4268G>T
  • NM_001407934.1:c.4265G>T
  • NM_001407935.1:c.4265G>T
  • NM_001407936.1:c.4265G>T
  • NM_001407937.1:c.4412G>T
  • NM_001407938.1:c.4412G>T
  • NM_001407939.1:c.4409G>T
  • NM_001407940.1:c.4409G>T
  • NM_001407941.1:c.4406G>T
  • NM_001407942.1:c.4394G>T
  • NM_001407943.1:c.4391G>T
  • NM_001407944.1:c.4391G>T
  • NM_001407945.1:c.4391G>T
  • NM_001407946.1:c.4202G>T
  • NM_001407947.1:c.4202G>T
  • NM_001407948.1:c.4202G>T
  • NM_001407949.1:c.4202G>T
  • NM_001407950.1:c.4199G>T
  • NM_001407951.1:c.4199G>T
  • NM_001407952.1:c.4199G>T
  • NM_001407953.1:c.4199G>T
  • NM_001407954.1:c.4199G>T
  • NM_001407955.1:c.4199G>T
  • NM_001407956.1:c.4196G>T
  • NM_001407957.1:c.4196G>T
  • NM_001407958.1:c.4196G>T
  • NM_001407959.1:c.4154G>T
  • NM_001407960.1:c.4151G>T
  • NM_001407962.1:c.4151G>T
  • NM_001407963.1:c.4148G>T
  • NM_001407965.1:c.4028G>T
  • NM_001407966.1:c.3647G>T
  • NM_001407967.1:c.3644G>T
  • NM_001407968.1:c.1931G>T
  • NM_001407969.1:c.1928G>T
  • NM_001407970.1:c.1292G>T
  • NM_001407971.1:c.1292G>T
  • NM_001407972.1:c.1289G>T
  • NM_001407973.1:c.1226G>T
  • NM_001407974.1:c.1226G>T
  • NM_001407975.1:c.1226G>T
  • NM_001407976.1:c.1226G>T
  • NM_001407977.1:c.1226G>T
  • NM_001407978.1:c.1226G>T
  • NM_001407979.1:c.1223G>T
  • NM_001407980.1:c.1223G>T
  • NM_001407981.1:c.1223G>T
  • NM_001407982.1:c.1223G>T
  • NM_001407983.1:c.1223G>T
  • NM_001407984.1:c.1223G>T
  • NM_001407985.1:c.1223G>T
  • NM_001407986.1:c.1223G>T
  • NM_001407990.1:c.1223G>T
  • NM_001407991.1:c.1223G>T
  • NM_001407992.1:c.1223G>T
  • NM_001407993.1:c.1223G>T
  • NM_001408392.1:c.1220G>T
  • NM_001408396.1:c.1220G>T
  • NM_001408397.1:c.1220G>T
  • NM_001408398.1:c.1220G>T
  • NM_001408399.1:c.1220G>T
  • NM_001408400.1:c.1220G>T
  • NM_001408401.1:c.1220G>T
  • NM_001408402.1:c.1220G>T
  • NM_001408403.1:c.1220G>T
  • NM_001408404.1:c.1220G>T
  • NM_001408406.1:c.1217G>T
  • NM_001408407.1:c.1217G>T
  • NM_001408408.1:c.1217G>T
  • NM_001408409.1:c.1214G>T
  • NM_001408410.1:c.1151G>T
  • NM_001408411.1:c.1148G>T
  • NM_001408412.1:c.1145G>T
  • NM_001408413.1:c.1145G>T
  • NM_001408414.1:c.1145G>T
  • NM_001408415.1:c.1145G>T
  • NM_001408416.1:c.1145G>T
  • NM_001408418.1:c.1109G>T
  • NM_001408419.1:c.1109G>T
  • NM_001408420.1:c.1109G>T
  • NM_001408421.1:c.1106G>T
  • NM_001408422.1:c.1106G>T
  • NM_001408423.1:c.1106G>T
  • NM_001408424.1:c.1106G>T
  • NM_001408425.1:c.1103G>T
  • NM_001408426.1:c.1103G>T
  • NM_001408427.1:c.1103G>T
  • NM_001408428.1:c.1103G>T
  • NM_001408429.1:c.1103G>T
  • NM_001408430.1:c.1103G>T
  • NM_001408431.1:c.1103G>T
  • NM_001408432.1:c.1100G>T
  • NM_001408433.1:c.1100G>T
  • NM_001408434.1:c.1100G>T
  • NM_001408435.1:c.1100G>T
  • NM_001408436.1:c.1100G>T
  • NM_001408437.1:c.1100G>T
  • NM_001408438.1:c.1100G>T
  • NM_001408439.1:c.1100G>T
  • NM_001408440.1:c.1100G>T
  • NM_001408441.1:c.1100G>T
  • NM_001408442.1:c.1100G>T
  • NM_001408443.1:c.1100G>T
  • NM_001408444.1:c.1100G>T
  • NM_001408445.1:c.1097G>T
  • NM_001408446.1:c.1097G>T
  • NM_001408447.1:c.1097G>T
  • NM_001408448.1:c.1097G>T
  • NM_001408450.1:c.1097G>T
  • NM_001408451.1:c.1091G>T
  • NM_001408452.1:c.1085G>T
  • NM_001408453.1:c.1085G>T
  • NM_001408454.1:c.1085G>T
  • NM_001408455.1:c.1085G>T
  • NM_001408456.1:c.1085G>T
  • NM_001408457.1:c.1085G>T
  • NM_001408458.1:c.1082G>T
  • NM_001408459.1:c.1082G>T
  • NM_001408460.1:c.1082G>T
  • NM_001408461.1:c.1082G>T
  • NM_001408462.1:c.1082G>T
  • NM_001408463.1:c.1082G>T
  • NM_001408464.1:c.1082G>T
  • NM_001408465.1:c.1082G>T
  • NM_001408466.1:c.1082G>T
  • NM_001408467.1:c.1082G>T
  • NM_001408468.1:c.1079G>T
  • NM_001408469.1:c.1079G>T
  • NM_001408470.1:c.1079G>T
  • NM_001408472.1:c.1223G>T
  • NM_001408473.1:c.1220G>T
  • NM_001408474.1:c.1025G>T
  • NM_001408475.1:c.1022G>T
  • NM_001408476.1:c.1022G>T
  • NM_001408478.1:c.1016G>T
  • NM_001408479.1:c.1016G>T
  • NM_001408480.1:c.1016G>T
  • NM_001408481.1:c.1013G>T
  • NM_001408482.1:c.1013G>T
  • NM_001408483.1:c.1013G>T
  • NM_001408484.1:c.1013G>T
  • NM_001408485.1:c.1013G>T
  • NM_001408489.1:c.1013G>T
  • NM_001408490.1:c.1013G>T
  • NM_001408491.1:c.1013G>T
  • NM_001408492.1:c.1010G>T
  • NM_001408493.1:c.1010G>T
  • NM_001408494.1:c.986G>T
  • NM_001408495.1:c.980G>T
  • NM_001408496.1:c.962G>T
  • NM_001408497.1:c.962G>T
  • NM_001408498.1:c.962G>T
  • NM_001408499.1:c.962G>T
  • NM_001408500.1:c.962G>T
  • NM_001408501.1:c.962G>T
  • NM_001408502.1:c.959G>T
  • NM_001408503.1:c.959G>T
  • NM_001408504.1:c.959G>T
  • NM_001408505.1:c.956G>T
  • NM_001408506.1:c.899G>T
  • NM_001408507.1:c.896G>T
  • NM_001408508.1:c.887G>T
  • NM_001408509.1:c.884G>T
  • NM_001408510.1:c.845G>T
  • NM_001408511.1:c.842G>T
  • NM_001408512.1:c.722G>T
  • NM_007294.4:c.4535G>TMANE SELECT
  • NM_007297.4:c.4394G>T
  • NM_007298.4:c.1223G>T
  • NM_007299.4:c.1223G>T
  • NM_007300.4:c.4598G>T
  • NM_007304.2:c.1223G>T
  • NP_001394500.1:p.Ser1441Ile
  • NP_001394510.1:p.Ser1534Ile
  • NP_001394511.1:p.Ser1534Ile
  • NP_001394512.1:p.Ser1533Ile
  • NP_001394514.1:p.Ser1533Ile
  • NP_001394516.1:p.Ser1533Ile
  • NP_001394519.1:p.Ser1532Ile
  • NP_001394520.1:p.Ser1532Ile
  • NP_001394522.1:p.Ser1512Ile
  • NP_001394523.1:p.Ser1512Ile
  • NP_001394525.1:p.Ser1512Ile
  • NP_001394526.1:p.Ser1512Ile
  • NP_001394527.1:p.Ser1512Ile
  • NP_001394531.1:p.Ser1512Ile
  • NP_001394532.1:p.Ser1512Ile
  • NP_001394534.1:p.Ser1512Ile
  • NP_001394539.1:p.Ser1511Ile
  • NP_001394540.1:p.Ser1511Ile
  • NP_001394541.1:p.Ser1511Ile
  • NP_001394542.1:p.Ser1511Ile
  • NP_001394543.1:p.Ser1511Ile
  • NP_001394544.1:p.Ser1511Ile
  • NP_001394545.1:p.Ser1511Ile
  • NP_001394546.1:p.Ser1511Ile
  • NP_001394547.1:p.Ser1511Ile
  • NP_001394548.1:p.Ser1511Ile
  • NP_001394549.1:p.Ser1511Ile
  • NP_001394550.1:p.Ser1511Ile
  • NP_001394551.1:p.Ser1511Ile
  • NP_001394552.1:p.Ser1511Ile
  • NP_001394553.1:p.Ser1511Ile
  • NP_001394554.1:p.Ser1511Ile
  • NP_001394555.1:p.Ser1511Ile
  • NP_001394556.1:p.Ser1510Ile
  • NP_001394557.1:p.Ser1510Ile
  • NP_001394558.1:p.Ser1510Ile
  • NP_001394559.1:p.Ser1510Ile
  • NP_001394560.1:p.Ser1510Ile
  • NP_001394561.1:p.Ser1510Ile
  • NP_001394562.1:p.Ser1510Ile
  • NP_001394563.1:p.Ser1510Ile
  • NP_001394564.1:p.Ser1510Ile
  • NP_001394565.1:p.Ser1510Ile
  • NP_001394566.1:p.Ser1510Ile
  • NP_001394567.1:p.Ser1510Ile
  • NP_001394568.1:p.Ser1510Ile
  • NP_001394569.1:p.Ser1510Ile
  • NP_001394570.1:p.Ser1510Ile
  • NP_001394571.1:p.Ser1510Ile
  • NP_001394573.1:p.Ser1509Ile
  • NP_001394574.1:p.Ser1509Ile
  • NP_001394575.1:p.Ser1508Ile
  • NP_001394576.1:p.Ser1507Ile
  • NP_001394577.1:p.Ser1493Ile
  • NP_001394578.1:p.Ser1492Ile
  • NP_001394581.1:p.Ser1512Ile
  • NP_001394582.1:p.Ser1486Ile
  • NP_001394583.1:p.Ser1486Ile
  • NP_001394584.1:p.Ser1486Ile
  • NP_001394585.1:p.Ser1485Ile
  • NP_001394586.1:p.Ser1485Ile
  • NP_001394587.1:p.Ser1485Ile
  • NP_001394588.1:p.Ser1484Ile
  • NP_001394589.1:p.Ser1484Ile
  • NP_001394590.1:p.Ser1484Ile
  • NP_001394591.1:p.Ser1484Ile
  • NP_001394592.1:p.Ser1484Ile
  • NP_001394593.1:p.Ser1471Ile
  • NP_001394594.1:p.Ser1471Ile
  • NP_001394595.1:p.Ser1471Ile
  • NP_001394596.1:p.Ser1471Ile
  • NP_001394597.1:p.Ser1471Ile
  • NP_001394598.1:p.Ser1471Ile
  • NP_001394599.1:p.Ser1470Ile
  • NP_001394600.1:p.Ser1470Ile
  • NP_001394601.1:p.Ser1470Ile
  • NP_001394602.1:p.Ser1470Ile
  • NP_001394603.1:p.Ser1470Ile
  • NP_001394604.1:p.Ser1470Ile
  • NP_001394605.1:p.Ser1470Ile
  • NP_001394606.1:p.Ser1470Ile
  • NP_001394607.1:p.Ser1470Ile
  • NP_001394608.1:p.Ser1470Ile
  • NP_001394609.1:p.Ser1470Ile
  • NP_001394610.1:p.Ser1469Ile
  • NP_001394611.1:p.Ser1469Ile
  • NP_001394612.1:p.Ser1469Ile
  • NP_001394613.1:p.Ser1512Ile
  • NP_001394614.1:p.Ser1469Ile
  • NP_001394615.1:p.Ser1469Ile
  • NP_001394616.1:p.Ser1469Ile
  • NP_001394617.1:p.Ser1469Ile
  • NP_001394618.1:p.Ser1469Ile
  • NP_001394619.1:p.Ser1468Ile
  • NP_001394620.1:p.Ser1468Ile
  • NP_001394621.1:p.Ser1465Ile
  • NP_001394623.1:p.Ser1465Ile
  • NP_001394624.1:p.Ser1465Ile
  • NP_001394625.1:p.Ser1465Ile
  • NP_001394626.1:p.Ser1465Ile
  • NP_001394627.1:p.Ser1465Ile
  • NP_001394653.1:p.Ser1465Ile
  • NP_001394654.1:p.Ser1465Ile
  • NP_001394655.1:p.Ser1465Ile
  • NP_001394656.1:p.Ser1465Ile
  • NP_001394657.1:p.Ser1465Ile
  • NP_001394658.1:p.Ser1465Ile
  • NP_001394659.1:p.Ser1465Ile
  • NP_001394660.1:p.Ser1465Ile
  • NP_001394661.1:p.Ser1464Ile
  • NP_001394662.1:p.Ser1464Ile
  • NP_001394663.1:p.Ser1464Ile
  • NP_001394664.1:p.Ser1464Ile
  • NP_001394665.1:p.Ser1464Ile
  • NP_001394666.1:p.Ser1464Ile
  • NP_001394667.1:p.Ser1464Ile
  • NP_001394668.1:p.Ser1464Ile
  • NP_001394669.1:p.Ser1464Ile
  • NP_001394670.1:p.Ser1464Ile
  • NP_001394671.1:p.Ser1464Ile
  • NP_001394672.1:p.Ser1464Ile
  • NP_001394673.1:p.Ser1464Ile
  • NP_001394674.1:p.Ser1464Ile
  • NP_001394675.1:p.Ser1464Ile
  • NP_001394676.1:p.Ser1464Ile
  • NP_001394677.1:p.Ser1464Ile
  • NP_001394678.1:p.Ser1464Ile
  • NP_001394679.1:p.Ser1464Ile
  • NP_001394680.1:p.Ser1464Ile
  • NP_001394681.1:p.Ser1464Ile
  • NP_001394767.1:p.Ser1463Ile
  • NP_001394768.1:p.Ser1463Ile
  • NP_001394770.1:p.Ser1463Ile
  • NP_001394771.1:p.Ser1463Ile
  • NP_001394772.1:p.Ser1463Ile
  • NP_001394773.1:p.Ser1463Ile
  • NP_001394774.1:p.Ser1463Ile
  • NP_001394775.1:p.Ser1463Ile
  • NP_001394776.1:p.Ser1463Ile
  • NP_001394777.1:p.Ser1463Ile
  • NP_001394778.1:p.Ser1463Ile
  • NP_001394779.1:p.Ser1463Ile
  • NP_001394780.1:p.Ser1463Ile
  • NP_001394781.1:p.Ser1463Ile
  • NP_001394782.1:p.Ser1463Ile
  • NP_001394783.1:p.Ser1512Ile
  • NP_001394787.1:p.Ser1511Ile
  • NP_001394788.1:p.Ser1511Ile
  • NP_001394789.1:p.Ser1511Ile
  • NP_001394790.1:p.Ser1510Ile
  • NP_001394791.1:p.Ser1445Ile
  • NP_001394792.1:p.Ser1470Ile
  • NP_001394803.1:p.Ser1443Ile
  • NP_001394804.1:p.Ser1443Ile
  • NP_001394808.1:p.Ser1442Ile
  • NP_001394810.1:p.Ser1442Ile
  • NP_001394811.1:p.Ser1442Ile
  • NP_001394813.1:p.Ser1442Ile
  • NP_001394814.1:p.Ser1442Ile
  • NP_001394815.1:p.Ser1442Ile
  • NP_001394816.1:p.Ser1442Ile
  • NP_001394818.1:p.Ser1442Ile
  • NP_001394823.1:p.Ser1441Ile
  • NP_001394824.1:p.Ser1441Ile
  • NP_001394825.1:p.Ser1441Ile
  • NP_001394826.1:p.Ser1441Ile
  • NP_001394827.1:p.Ser1441Ile
  • NP_001394828.1:p.Ser1441Ile
  • NP_001394829.1:p.Ser1441Ile
  • NP_001394831.1:p.Ser1441Ile
  • NP_001394833.1:p.Ser1441Ile
  • NP_001394835.1:p.Ser1441Ile
  • NP_001394836.1:p.Ser1441Ile
  • NP_001394837.1:p.Ser1441Ile
  • NP_001394838.1:p.Ser1441Ile
  • NP_001394839.1:p.Ser1441Ile
  • NP_001394844.1:p.Ser1440Ile
  • NP_001394845.1:p.Ser1440Ile
  • NP_001394846.1:p.Ser1440Ile
  • NP_001394847.1:p.Ser1440Ile
  • NP_001394848.1:p.Ser1471Ile
  • NP_001394849.1:p.Ser1424Ile
  • NP_001394850.1:p.Ser1424Ile
  • NP_001394851.1:p.Ser1424Ile
  • NP_001394852.1:p.Ser1424Ile
  • NP_001394853.1:p.Ser1424Ile
  • NP_001394854.1:p.Ser1424Ile
  • NP_001394855.1:p.Ser1424Ile
  • NP_001394856.1:p.Ser1423Ile
  • NP_001394857.1:p.Ser1423Ile
  • NP_001394858.1:p.Ser1423Ile
  • NP_001394859.1:p.Ser1423Ile
  • NP_001394860.1:p.Ser1423Ile
  • NP_001394861.1:p.Ser1423Ile
  • NP_001394862.1:p.Ser1423Ile
  • NP_001394863.1:p.Ser1422Ile
  • NP_001394864.1:p.Ser1422Ile
  • NP_001394865.1:p.Ser1422Ile
  • NP_001394866.1:p.Ser1471Ile
  • NP_001394867.1:p.Ser1471Ile
  • NP_001394868.1:p.Ser1470Ile
  • NP_001394869.1:p.Ser1470Ile
  • NP_001394870.1:p.Ser1469Ile
  • NP_001394871.1:p.Ser1465Ile
  • NP_001394872.1:p.Ser1464Ile
  • NP_001394873.1:p.Ser1464Ile
  • NP_001394874.1:p.Ser1464Ile
  • NP_001394875.1:p.Ser1401Ile
  • NP_001394876.1:p.Ser1401Ile
  • NP_001394877.1:p.Ser1401Ile
  • NP_001394878.1:p.Ser1401Ile
  • NP_001394879.1:p.Ser1400Ile
  • NP_001394880.1:p.Ser1400Ile
  • NP_001394881.1:p.Ser1400Ile
  • NP_001394882.1:p.Ser1400Ile
  • NP_001394883.1:p.Ser1400Ile
  • NP_001394884.1:p.Ser1400Ile
  • NP_001394885.1:p.Ser1399Ile
  • NP_001394886.1:p.Ser1399Ile
  • NP_001394887.1:p.Ser1399Ile
  • NP_001394888.1:p.Ser1385Ile
  • NP_001394889.1:p.Ser1384Ile
  • NP_001394891.1:p.Ser1384Ile
  • NP_001394892.1:p.Ser1383Ile
  • NP_001394894.1:p.Ser1343Ile
  • NP_001394895.1:p.Ser1216Ile
  • NP_001394896.1:p.Ser1215Ile
  • NP_001394897.1:p.Ser644Ile
  • NP_001394898.1:p.Ser643Ile
  • NP_001394899.1:p.Ser431Ile
  • NP_001394900.1:p.Ser431Ile
  • NP_001394901.1:p.Ser430Ile
  • NP_001394902.1:p.Ser409Ile
  • NP_001394903.1:p.Ser409Ile
  • NP_001394904.1:p.Ser409Ile
  • NP_001394905.1:p.Ser409Ile
  • NP_001394906.1:p.Ser409Ile
  • NP_001394907.1:p.Ser409Ile
  • NP_001394908.1:p.Ser408Ile
  • NP_001394909.1:p.Ser408Ile
  • NP_001394910.1:p.Ser408Ile
  • NP_001394911.1:p.Ser408Ile
  • NP_001394912.1:p.Ser408Ile
  • NP_001394913.1:p.Ser408Ile
  • NP_001394914.1:p.Ser408Ile
  • NP_001394915.1:p.Ser408Ile
  • NP_001394919.1:p.Ser408Ile
  • NP_001394920.1:p.Ser408Ile
  • NP_001394921.1:p.Ser408Ile
  • NP_001394922.1:p.Ser408Ile
  • NP_001395321.1:p.Ser407Ile
  • NP_001395325.1:p.Ser407Ile
  • NP_001395326.1:p.Ser407Ile
  • NP_001395327.1:p.Ser407Ile
  • NP_001395328.1:p.Ser407Ile
  • NP_001395329.1:p.Ser407Ile
  • NP_001395330.1:p.Ser407Ile
  • NP_001395331.1:p.Ser407Ile
  • NP_001395332.1:p.Ser407Ile
  • NP_001395333.1:p.Ser407Ile
  • NP_001395335.1:p.Ser406Ile
  • NP_001395336.1:p.Ser406Ile
  • NP_001395337.1:p.Ser406Ile
  • NP_001395338.1:p.Ser405Ile
  • NP_001395339.1:p.Ser384Ile
  • NP_001395340.1:p.Ser383Ile
  • NP_001395341.1:p.Ser382Ile
  • NP_001395342.1:p.Ser382Ile
  • NP_001395343.1:p.Ser382Ile
  • NP_001395344.1:p.Ser382Ile
  • NP_001395345.1:p.Ser382Ile
  • NP_001395347.1:p.Ser370Ile
  • NP_001395348.1:p.Ser370Ile
  • NP_001395349.1:p.Ser370Ile
  • NP_001395350.1:p.Ser369Ile
  • NP_001395351.1:p.Ser369Ile
  • NP_001395352.1:p.Ser369Ile
  • NP_001395353.1:p.Ser369Ile
  • NP_001395354.1:p.Ser368Ile
  • NP_001395355.1:p.Ser368Ile
  • NP_001395356.1:p.Ser368Ile
  • NP_001395357.1:p.Ser368Ile
  • NP_001395358.1:p.Ser368Ile
  • NP_001395359.1:p.Ser368Ile
  • NP_001395360.1:p.Ser368Ile
  • NP_001395361.1:p.Ser367Ile
  • NP_001395362.1:p.Ser367Ile
  • NP_001395363.1:p.Ser367Ile
  • NP_001395364.1:p.Ser367Ile
  • NP_001395365.1:p.Ser367Ile
  • NP_001395366.1:p.Ser367Ile
  • NP_001395367.1:p.Ser367Ile
  • NP_001395368.1:p.Ser367Ile
  • NP_001395369.1:p.Ser367Ile
  • NP_001395370.1:p.Ser367Ile
  • NP_001395371.1:p.Ser367Ile
  • NP_001395372.1:p.Ser367Ile
  • NP_001395373.1:p.Ser367Ile
  • NP_001395374.1:p.Ser366Ile
  • NP_001395375.1:p.Ser366Ile
  • NP_001395376.1:p.Ser366Ile
  • NP_001395377.1:p.Ser366Ile
  • NP_001395379.1:p.Ser366Ile
  • NP_001395380.1:p.Ser364Ile
  • NP_001395381.1:p.Ser362Ile
  • NP_001395382.1:p.Ser362Ile
  • NP_001395383.1:p.Ser362Ile
  • NP_001395384.1:p.Ser362Ile
  • NP_001395385.1:p.Ser362Ile
  • NP_001395386.1:p.Ser362Ile
  • NP_001395387.1:p.Ser361Ile
  • NP_001395388.1:p.Ser361Ile
  • NP_001395389.1:p.Ser361Ile
  • NP_001395390.1:p.Ser361Ile
  • NP_001395391.1:p.Ser361Ile
  • NP_001395392.1:p.Ser361Ile
  • NP_001395393.1:p.Ser361Ile
  • NP_001395394.1:p.Ser361Ile
  • NP_001395395.1:p.Ser361Ile
  • NP_001395396.1:p.Ser361Ile
  • NP_001395397.1:p.Ser360Ile
  • NP_001395398.1:p.Ser360Ile
  • NP_001395399.1:p.Ser360Ile
  • NP_001395401.1:p.Ser408Ile
  • NP_001395402.1:p.Ser407Ile
  • NP_001395403.1:p.Ser342Ile
  • NP_001395404.1:p.Ser341Ile
  • NP_001395405.1:p.Ser341Ile
  • NP_001395407.1:p.Ser339Ile
  • NP_001395408.1:p.Ser339Ile
  • NP_001395409.1:p.Ser339Ile
  • NP_001395410.1:p.Ser338Ile
  • NP_001395411.1:p.Ser338Ile
  • NP_001395412.1:p.Ser338Ile
  • NP_001395413.1:p.Ser338Ile
  • NP_001395414.1:p.Ser338Ile
  • NP_001395418.1:p.Ser338Ile
  • NP_001395419.1:p.Ser338Ile
  • NP_001395420.1:p.Ser338Ile
  • NP_001395421.1:p.Ser337Ile
  • NP_001395422.1:p.Ser337Ile
  • NP_001395423.1:p.Ser329Ile
  • NP_001395424.1:p.Ser327Ile
  • NP_001395425.1:p.Ser321Ile
  • NP_001395426.1:p.Ser321Ile
  • NP_001395427.1:p.Ser321Ile
  • NP_001395428.1:p.Ser321Ile
  • NP_001395429.1:p.Ser321Ile
  • NP_001395430.1:p.Ser321Ile
  • NP_001395431.1:p.Ser320Ile
  • NP_001395432.1:p.Ser320Ile
  • NP_001395433.1:p.Ser320Ile
  • NP_001395434.1:p.Ser319Ile
  • NP_001395435.1:p.Ser300Ile
  • NP_001395436.1:p.Ser299Ile
  • NP_001395437.1:p.Ser296Ile
  • NP_001395438.1:p.Ser295Ile
  • NP_001395439.1:p.Ser282Ile
  • NP_001395440.1:p.Ser281Ile
  • NP_001395441.1:p.Ser241Ile
  • NP_009225.1:p.Ser1512Ile
  • NP_009225.1:p.Ser1512Ile
  • NP_009228.2:p.Ser1465Ile
  • NP_009229.2:p.Ser408Ile
  • NP_009229.2:p.Ser408Ile
  • NP_009230.2:p.Ser408Ile
  • NP_009231.2:p.Ser1533Ile
  • NP_009235.2:p.Ser408Ile
  • LRG_292t1:c.4535G>T
  • LRG_292:g.143513G>T
  • LRG_292p1:p.Ser1512Ile
  • NC_000017.10:g.41226488C>A
  • NM_007294.2:c.4535G>T
  • NM_007294.3:c.4535G>T
  • NM_007294.4:c.4535G>T
  • NM_007298.3:c.1223G>T
  • NM_007299.3:c.1223G>T
  • NM_007300.3:c.4598G>T
  • NR_027676.2:n.4712G>T
  • P38398:p.Ser1512Ile
  • U14680.1:n.4654G>T
  • p.S1512I
Nucleotide change:
4654G>T
Protein change:
S1215I
Links:
BRCA1-HCI: BRCA1_00016; UniProtKB: P38398#VAR_007788; dbSNP: rs1800744
NCBI 1000 Genomes Browser:
rs1800744
Molecular consequence:
  • NM_001407571.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.4601G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.4601G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.4598G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.4598G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.4598G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.4595G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.4595G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.4535G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.4535G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.4535G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.4535G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.4535G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.4535G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.4535G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.4535G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.4526G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.4526G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.4523G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.4520G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.4478G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.4475G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.4535G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.4457G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.4457G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.4457G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.4454G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.4454G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.4454G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.4451G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.4451G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.4451G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.4451G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.4451G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.4412G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.4412G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.4412G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.4412G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.4412G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.4412G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.4406G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.4406G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.4406G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.4535G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.4406G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.4406G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.4406G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.4406G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.4406G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.4403G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.4403G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407732.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407733.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407734.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407735.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407736.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407737.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407738.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407739.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407838.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407839.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407841.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407842.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407843.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407844.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407845.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407846.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407850.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407851.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407852.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.4388G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.4535G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.4532G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.4529G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.4334G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.4328G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.4328G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.4325G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.4325G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.4325G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.4325G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.4325G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.4325G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.4325G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.4325G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407900.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407902.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407904.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407906.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.4322G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.4319G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407916.1:c.4319G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407917.1:c.4319G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407918.1:c.4319G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.4412G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.4271G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.4271G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.4271G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.4271G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.4271G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.4271G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.4271G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407927.1:c.4268G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407928.1:c.4268G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407929.1:c.4268G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.4268G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.4268G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.4268G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.4268G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.4265G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407935.1:c.4265G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407936.1:c.4265G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.4412G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.4412G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.4409G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.4406G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407942.1:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407943.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407944.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407945.1:c.4391G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.4202G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.4202G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.4202G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.4202G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407950.1:c.4199G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407951.1:c.4199G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.4199G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.4199G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.4199G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.4199G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.4196G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407957.1:c.4196G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407958.1:c.4196G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.4154G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407960.1:c.4151G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.4151G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407963.1:c.4148G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.4028G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.3647G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407967.1:c.3644G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407968.1:c.1931G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407969.1:c.1928G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407970.1:c.1292G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407971.1:c.1292G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407972.1:c.1289G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407973.1:c.1226G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407974.1:c.1226G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407975.1:c.1226G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407976.1:c.1226G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407977.1:c.1226G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407978.1:c.1226G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407979.1:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407980.1:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407981.1:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407982.1:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407983.1:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407984.1:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407985.1:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407986.1:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407990.1:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407991.1:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407992.1:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407993.1:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408392.1:c.1220G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408396.1:c.1220G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408397.1:c.1220G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408398.1:c.1220G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408399.1:c.1220G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408400.1:c.1220G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408401.1:c.1220G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408402.1:c.1220G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408403.1:c.1220G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408404.1:c.1220G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408406.1:c.1217G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408407.1:c.1217G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408408.1:c.1217G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408409.1:c.1214G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408410.1:c.1151G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408411.1:c.1148G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408412.1:c.1145G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408413.1:c.1145G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408414.1:c.1145G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408415.1:c.1145G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408416.1:c.1145G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408418.1:c.1109G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408419.1:c.1109G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408420.1:c.1109G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408421.1:c.1106G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408422.1:c.1106G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408423.1:c.1106G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408424.1:c.1106G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408425.1:c.1103G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408426.1:c.1103G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408427.1:c.1103G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408428.1:c.1103G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408429.1:c.1103G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408430.1:c.1103G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408431.1:c.1103G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408432.1:c.1100G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408433.1:c.1100G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408434.1:c.1100G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408435.1:c.1100G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408436.1:c.1100G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408437.1:c.1100G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408438.1:c.1100G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408439.1:c.1100G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408440.1:c.1100G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408441.1:c.1100G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408442.1:c.1100G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408443.1:c.1100G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408444.1:c.1100G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408445.1:c.1097G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408446.1:c.1097G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408447.1:c.1097G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408448.1:c.1097G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408450.1:c.1097G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408451.1:c.1091G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408452.1:c.1085G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408453.1:c.1085G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408454.1:c.1085G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408455.1:c.1085G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408456.1:c.1085G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408457.1:c.1085G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408458.1:c.1082G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408459.1:c.1082G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408460.1:c.1082G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408461.1:c.1082G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408462.1:c.1082G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408463.1:c.1082G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408464.1:c.1082G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408465.1:c.1082G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408466.1:c.1082G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408467.1:c.1082G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408468.1:c.1079G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408469.1:c.1079G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408470.1:c.1079G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408472.1:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408473.1:c.1220G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408474.1:c.1025G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408475.1:c.1022G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408476.1:c.1022G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408478.1:c.1016G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408479.1:c.1016G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408480.1:c.1016G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408481.1:c.1013G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408482.1:c.1013G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408483.1:c.1013G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408484.1:c.1013G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408485.1:c.1013G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408489.1:c.1013G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408490.1:c.1013G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408491.1:c.1013G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408492.1:c.1010G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408493.1:c.1010G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408494.1:c.986G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408495.1:c.980G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408496.1:c.962G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408497.1:c.962G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408498.1:c.962G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408499.1:c.962G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408500.1:c.962G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408501.1:c.962G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408502.1:c.959G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408503.1:c.959G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408504.1:c.959G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408505.1:c.956G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408506.1:c.899G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408507.1:c.896G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408508.1:c.887G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408509.1:c.884G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408510.1:c.845G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408511.1:c.842G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408512.1:c.722G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.4535G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.4394G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007298.4:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007299.4:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.4598G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007304.2:c.1223G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NR_027676.2:n.4712G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Observations:
3

Condition(s)

Name:
Hereditary breast ovarian cancer syndrome
Synonyms:
Hereditary breast and ovarian cancer syndrome; Hereditary breast and ovarian cancer; Hereditary breast and ovarian cancer syndrome (HBOC); See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0003582; MeSH: D061325; MedGen: C0677776; Orphanet: 145

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000076604Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Benign
(Feb 1, 2024)
germlineclinical testing

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

SCV000494296Women's Health and Genetics/Laboratory Corporation of America, LabCorp
criteria provided, single submitter

(LabCorp Variant Classification Summary - May 2015)
Benign
(Jan 24, 2014)
germlineclinical testing

PubMed (12)
[See all records that cite these PMIDs]

LabCorp Variant Classification Summary - May 2015.docx,

Citation Link,

SCV001977041Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C.
no assertion criteria provided
Benign
(Sep 27, 2021)
germlineclinical testing

SCV002025932National Health Laboratory Service, Universitas Academic Hospital and University of the Free State
criteria provided, single submitter

(ACMG Guidelines, 2015)
Benign
(Apr 19, 2022)
germlineclinical testing

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

SCV002515214Genetics Program, Instituto Nacional de Cancer
criteria provided, single submitter

(ACMG Guidelines, 2015)
Likely benign
(Nov 1, 2021)
germlineresearch

PubMed (2)
[See all records that cite these PMIDs]

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing
not providedgermlineyes3not providednot providednot providednot providedclinical testing, research

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group, Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.

Johnston JJ, Rubinstein WS, Facio FM, Ng D, Singh LN, Teer JK, Mullikin JC, Biesecker LG.

Am J Hum Genet. 2012 Jul 13;91(1):97-108. doi: 10.1016/j.ajhg.2012.05.021. Epub 2012 Jun 14.

PubMed [citation]
PMID:
22703879
PMCID:
PMC3397257
See all PubMed Citations (15)

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV000076604.14

#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 Women's Health and Genetics/Laboratory Corporation of America, LabCorp, SCV000494296.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (12)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

From Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C., SCV001977041.1

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

From National Health Laboratory Service, Universitas Academic Hospital and University of the Free State, SCV002025932.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided3not providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided3not providednot providednot provided

From Genetics Program, Instituto Nacional de Cancer, SCV002515214.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedresearch PubMed (2)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Nov 24, 2024