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NM_007294.4(BRCA1):c.2993T>G (p.Leu998Arg) AND Hereditary breast ovarian cancer syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 31, 2020
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
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:
RCV000803204.7

Allele description

NM_007294.4(BRCA1):c.2993T>G (p.Leu998Arg)

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.2993T>G (p.Leu998Arg)
HGVS:
  • NC_000017.11:g.43092538A>C
  • NG_005905.2:g.125446T>G
  • NM_001407571.1:c.2780T>G
  • NM_001407581.1:c.2993T>G
  • NM_001407582.1:c.2993T>G
  • NM_001407583.1:c.2993T>G
  • NM_001407585.1:c.2993T>G
  • NM_001407587.1:c.2990T>G
  • NM_001407590.1:c.2990T>G
  • NM_001407591.1:c.2990T>G
  • NM_001407593.1:c.2993T>G
  • NM_001407594.1:c.2993T>G
  • NM_001407596.1:c.2993T>G
  • NM_001407597.1:c.2993T>G
  • NM_001407598.1:c.2993T>G
  • NM_001407602.1:c.2993T>G
  • NM_001407603.1:c.2993T>G
  • NM_001407605.1:c.2993T>G
  • NM_001407610.1:c.2990T>G
  • NM_001407611.1:c.2990T>G
  • NM_001407612.1:c.2990T>G
  • NM_001407613.1:c.2990T>G
  • NM_001407614.1:c.2990T>G
  • NM_001407615.1:c.2990T>G
  • NM_001407616.1:c.2993T>G
  • NM_001407617.1:c.2993T>G
  • NM_001407618.1:c.2993T>G
  • NM_001407619.1:c.2993T>G
  • NM_001407620.1:c.2993T>G
  • NM_001407621.1:c.2993T>G
  • NM_001407622.1:c.2993T>G
  • NM_001407623.1:c.2993T>G
  • NM_001407624.1:c.2993T>G
  • NM_001407625.1:c.2993T>G
  • NM_001407626.1:c.2993T>G
  • NM_001407627.1:c.2990T>G
  • NM_001407628.1:c.2990T>G
  • NM_001407629.1:c.2990T>G
  • NM_001407630.1:c.2990T>G
  • NM_001407631.1:c.2990T>G
  • NM_001407632.1:c.2990T>G
  • NM_001407633.1:c.2990T>G
  • NM_001407634.1:c.2990T>G
  • NM_001407635.1:c.2990T>G
  • NM_001407636.1:c.2990T>G
  • NM_001407637.1:c.2990T>G
  • NM_001407638.1:c.2990T>G
  • NM_001407639.1:c.2993T>G
  • NM_001407640.1:c.2993T>G
  • NM_001407641.1:c.2993T>G
  • NM_001407642.1:c.2993T>G
  • NM_001407644.1:c.2990T>G
  • NM_001407645.1:c.2990T>G
  • NM_001407646.1:c.2984T>G
  • NM_001407647.1:c.2984T>G
  • NM_001407648.1:c.2870T>G
  • NM_001407649.1:c.2867T>G
  • NM_001407652.1:c.2993T>G
  • NM_001407653.1:c.2915T>G
  • NM_001407654.1:c.2915T>G
  • NM_001407655.1:c.2915T>G
  • NM_001407656.1:c.2915T>G
  • NM_001407657.1:c.2915T>G
  • NM_001407658.1:c.2915T>G
  • NM_001407659.1:c.2912T>G
  • NM_001407660.1:c.2912T>G
  • NM_001407661.1:c.2912T>G
  • NM_001407662.1:c.2912T>G
  • NM_001407663.1:c.2915T>G
  • NM_001407664.1:c.2870T>G
  • NM_001407665.1:c.2870T>G
  • NM_001407666.1:c.2870T>G
  • NM_001407667.1:c.2870T>G
  • NM_001407668.1:c.2870T>G
  • NM_001407669.1:c.2870T>G
  • NM_001407670.1:c.2867T>G
  • NM_001407671.1:c.2867T>G
  • NM_001407672.1:c.2867T>G
  • NM_001407673.1:c.2867T>G
  • NM_001407674.1:c.2870T>G
  • NM_001407675.1:c.2870T>G
  • NM_001407676.1:c.2870T>G
  • NM_001407677.1:c.2870T>G
  • NM_001407678.1:c.2870T>G
  • NM_001407679.1:c.2870T>G
  • NM_001407680.1:c.2870T>G
  • NM_001407681.1:c.2870T>G
  • NM_001407682.1:c.2870T>G
  • NM_001407683.1:c.2870T>G
  • NM_001407684.1:c.2993T>G
  • NM_001407685.1:c.2867T>G
  • NM_001407686.1:c.2867T>G
  • NM_001407687.1:c.2867T>G
  • NM_001407688.1:c.2867T>G
  • NM_001407689.1:c.2867T>G
  • NM_001407690.1:c.2867T>G
  • NM_001407691.1:c.2867T>G
  • NM_001407692.1:c.2852T>G
  • NM_001407694.1:c.2852T>G
  • NM_001407695.1:c.2852T>G
  • NM_001407696.1:c.2852T>G
  • NM_001407697.1:c.2852T>G
  • NM_001407698.1:c.2852T>G
  • NM_001407724.1:c.2852T>G
  • NM_001407725.1:c.2852T>G
  • NM_001407726.1:c.2852T>G
  • NM_001407727.1:c.2852T>G
  • NM_001407728.1:c.2852T>G
  • NM_001407729.1:c.2852T>G
  • NM_001407730.1:c.2852T>G
  • NM_001407731.1:c.2852T>G
  • NM_001407732.1:c.2852T>G
  • NM_001407733.1:c.2852T>G
  • NM_001407734.1:c.2852T>G
  • NM_001407735.1:c.2852T>G
  • NM_001407736.1:c.2852T>G
  • NM_001407737.1:c.2852T>G
  • NM_001407738.1:c.2852T>G
  • NM_001407739.1:c.2852T>G
  • NM_001407740.1:c.2849T>G
  • NM_001407741.1:c.2849T>G
  • NM_001407742.1:c.2849T>G
  • NM_001407743.1:c.2849T>G
  • NM_001407744.1:c.2849T>G
  • NM_001407745.1:c.2849T>G
  • NM_001407746.1:c.2849T>G
  • NM_001407747.1:c.2849T>G
  • NM_001407748.1:c.2849T>G
  • NM_001407749.1:c.2849T>G
  • NM_001407750.1:c.2852T>G
  • NM_001407751.1:c.2852T>G
  • NM_001407752.1:c.2852T>G
  • NM_001407838.1:c.2849T>G
  • NM_001407839.1:c.2849T>G
  • NM_001407841.1:c.2849T>G
  • NM_001407842.1:c.2849T>G
  • NM_001407843.1:c.2849T>G
  • NM_001407844.1:c.2849T>G
  • NM_001407845.1:c.2849T>G
  • NM_001407846.1:c.2849T>G
  • NM_001407847.1:c.2849T>G
  • NM_001407848.1:c.2849T>G
  • NM_001407849.1:c.2849T>G
  • NM_001407850.1:c.2852T>G
  • NM_001407851.1:c.2852T>G
  • NM_001407852.1:c.2852T>G
  • NM_001407853.1:c.2780T>G
  • NM_001407854.1:c.2993T>G
  • NM_001407858.1:c.2993T>G
  • NM_001407859.1:c.2993T>G
  • NM_001407860.1:c.2990T>G
  • NM_001407861.1:c.2990T>G
  • NM_001407862.1:c.2792T>G
  • NM_001407863.1:c.2870T>G
  • NM_001407874.1:c.2789T>G
  • NM_001407875.1:c.2789T>G
  • NM_001407879.1:c.2783T>G
  • NM_001407881.1:c.2783T>G
  • NM_001407882.1:c.2783T>G
  • NM_001407884.1:c.2783T>G
  • NM_001407885.1:c.2783T>G
  • NM_001407886.1:c.2783T>G
  • NM_001407887.1:c.2783T>G
  • NM_001407889.1:c.2783T>G
  • NM_001407894.1:c.2780T>G
  • NM_001407895.1:c.2780T>G
  • NM_001407896.1:c.2780T>G
  • NM_001407897.1:c.2780T>G
  • NM_001407898.1:c.2780T>G
  • NM_001407899.1:c.2780T>G
  • NM_001407900.1:c.2783T>G
  • NM_001407902.1:c.2783T>G
  • NM_001407904.1:c.2783T>G
  • NM_001407906.1:c.2783T>G
  • NM_001407907.1:c.2783T>G
  • NM_001407908.1:c.2783T>G
  • NM_001407909.1:c.2783T>G
  • NM_001407910.1:c.2783T>G
  • NM_001407915.1:c.2780T>G
  • NM_001407916.1:c.2780T>G
  • NM_001407917.1:c.2780T>G
  • NM_001407918.1:c.2780T>G
  • NM_001407919.1:c.2870T>G
  • NM_001407920.1:c.2729T>G
  • NM_001407921.1:c.2729T>G
  • NM_001407922.1:c.2729T>G
  • NM_001407923.1:c.2729T>G
  • NM_001407924.1:c.2729T>G
  • NM_001407925.1:c.2729T>G
  • NM_001407926.1:c.2729T>G
  • NM_001407927.1:c.2729T>G
  • NM_001407928.1:c.2729T>G
  • NM_001407929.1:c.2729T>G
  • NM_001407930.1:c.2726T>G
  • NM_001407931.1:c.2726T>G
  • NM_001407932.1:c.2726T>G
  • NM_001407933.1:c.2729T>G
  • NM_001407934.1:c.2726T>G
  • NM_001407935.1:c.2729T>G
  • NM_001407936.1:c.2726T>G
  • NM_001407937.1:c.2870T>G
  • NM_001407938.1:c.2870T>G
  • NM_001407939.1:c.2870T>G
  • NM_001407940.1:c.2867T>G
  • NM_001407941.1:c.2867T>G
  • NM_001407942.1:c.2852T>G
  • NM_001407943.1:c.2849T>G
  • NM_001407944.1:c.2852T>G
  • NM_001407945.1:c.2852T>G
  • NM_001407946.1:c.2660T>G
  • NM_001407947.1:c.2660T>G
  • NM_001407948.1:c.2660T>G
  • NM_001407949.1:c.2660T>G
  • NM_001407950.1:c.2660T>G
  • NM_001407951.1:c.2660T>G
  • NM_001407952.1:c.2660T>G
  • NM_001407953.1:c.2660T>G
  • NM_001407954.1:c.2657T>G
  • NM_001407955.1:c.2657T>G
  • NM_001407956.1:c.2657T>G
  • NM_001407957.1:c.2660T>G
  • NM_001407958.1:c.2657T>G
  • NM_001407959.1:c.2612T>G
  • NM_001407960.1:c.2612T>G
  • NM_001407962.1:c.2609T>G
  • NM_001407963.1:c.2612T>G
  • NM_001407964.1:c.2849T>G
  • NM_001407965.1:c.2489T>G
  • NM_001407966.1:c.2105T>G
  • NM_001407967.1:c.2105T>G
  • NM_001407968.1:c.788-399T>G
  • NM_001407969.1:c.788-399T>G
  • NM_001407970.1:c.788-1506T>G
  • NM_001407971.1:c.788-1506T>G
  • NM_001407972.1:c.785-1506T>G
  • NM_001407973.1:c.788-1506T>G
  • NM_001407974.1:c.788-1506T>G
  • NM_001407975.1:c.788-1506T>G
  • NM_001407976.1:c.788-1506T>G
  • NM_001407977.1:c.788-1506T>G
  • NM_001407978.1:c.788-1506T>G
  • NM_001407979.1:c.788-1506T>G
  • NM_001407980.1:c.788-1506T>G
  • NM_001407981.1:c.788-1506T>G
  • NM_001407982.1:c.788-1506T>G
  • NM_001407983.1:c.788-1506T>G
  • NM_001407984.1:c.785-1506T>G
  • NM_001407985.1:c.785-1506T>G
  • NM_001407986.1:c.785-1506T>G
  • NM_001407990.1:c.788-1506T>G
  • NM_001407991.1:c.785-1506T>G
  • NM_001407992.1:c.785-1506T>G
  • NM_001407993.1:c.788-1506T>G
  • NM_001408392.1:c.785-1506T>G
  • NM_001408396.1:c.785-1506T>G
  • NM_001408397.1:c.785-1506T>G
  • NM_001408398.1:c.785-1506T>G
  • NM_001408399.1:c.785-1506T>G
  • NM_001408400.1:c.785-1506T>G
  • NM_001408401.1:c.785-1506T>G
  • NM_001408402.1:c.785-1506T>G
  • NM_001408403.1:c.788-1506T>G
  • NM_001408404.1:c.788-1506T>G
  • NM_001408406.1:c.791-1515T>G
  • NM_001408407.1:c.785-1506T>G
  • NM_001408408.1:c.779-1506T>G
  • NM_001408409.1:c.710-1506T>G
  • NM_001408410.1:c.647-1506T>G
  • NM_001408411.1:c.710-1506T>G
  • NM_001408412.1:c.710-1506T>G
  • NM_001408413.1:c.707-1506T>G
  • NM_001408414.1:c.710-1506T>G
  • NM_001408415.1:c.710-1506T>G
  • NM_001408416.1:c.707-1506T>G
  • NM_001408418.1:c.671-1506T>G
  • NM_001408419.1:c.671-1506T>G
  • NM_001408420.1:c.671-1506T>G
  • NM_001408421.1:c.668-1506T>G
  • NM_001408422.1:c.671-1506T>G
  • NM_001408423.1:c.671-1506T>G
  • NM_001408424.1:c.668-1506T>G
  • NM_001408425.1:c.665-1506T>G
  • NM_001408426.1:c.665-1506T>G
  • NM_001408427.1:c.665-1506T>G
  • NM_001408428.1:c.665-1506T>G
  • NM_001408429.1:c.665-1506T>G
  • NM_001408430.1:c.665-1506T>G
  • NM_001408431.1:c.668-1506T>G
  • NM_001408432.1:c.662-1506T>G
  • NM_001408433.1:c.662-1506T>G
  • NM_001408434.1:c.662-1506T>G
  • NM_001408435.1:c.662-1506T>G
  • NM_001408436.1:c.665-1506T>G
  • NM_001408437.1:c.665-1506T>G
  • NM_001408438.1:c.665-1506T>G
  • NM_001408439.1:c.665-1506T>G
  • NM_001408440.1:c.665-1506T>G
  • NM_001408441.1:c.665-1506T>G
  • NM_001408442.1:c.665-1506T>G
  • NM_001408443.1:c.665-1506T>G
  • NM_001408444.1:c.665-1506T>G
  • NM_001408445.1:c.662-1506T>G
  • NM_001408446.1:c.662-1506T>G
  • NM_001408447.1:c.662-1506T>G
  • NM_001408448.1:c.662-1506T>G
  • NM_001408450.1:c.662-1506T>G
  • NM_001408451.1:c.653-1506T>G
  • NM_001408452.1:c.647-1506T>G
  • NM_001408453.1:c.647-1506T>G
  • NM_001408454.1:c.647-1506T>G
  • NM_001408455.1:c.647-1506T>G
  • NM_001408456.1:c.647-1506T>G
  • NM_001408457.1:c.647-1506T>G
  • NM_001408458.1:c.647-1506T>G
  • NM_001408459.1:c.647-1506T>G
  • NM_001408460.1:c.647-1506T>G
  • NM_001408461.1:c.647-1506T>G
  • NM_001408462.1:c.644-1506T>G
  • NM_001408463.1:c.644-1506T>G
  • NM_001408464.1:c.644-1506T>G
  • NM_001408465.1:c.644-1506T>G
  • NM_001408466.1:c.647-1506T>G
  • NM_001408467.1:c.647-1506T>G
  • NM_001408468.1:c.644-1506T>G
  • NM_001408469.1:c.647-1506T>G
  • NM_001408470.1:c.644-1506T>G
  • NM_001408472.1:c.788-1506T>G
  • NM_001408473.1:c.785-1506T>G
  • NM_001408474.1:c.587-1506T>G
  • NM_001408475.1:c.584-1506T>G
  • NM_001408476.1:c.587-1506T>G
  • NM_001408478.1:c.578-1506T>G
  • NM_001408479.1:c.578-1506T>G
  • NM_001408480.1:c.578-1506T>G
  • NM_001408481.1:c.578-1506T>G
  • NM_001408482.1:c.578-1506T>G
  • NM_001408483.1:c.578-1506T>G
  • NM_001408484.1:c.578-1506T>G
  • NM_001408485.1:c.578-1506T>G
  • NM_001408489.1:c.578-1506T>G
  • NM_001408490.1:c.575-1506T>G
  • NM_001408491.1:c.575-1506T>G
  • NM_001408492.1:c.578-1506T>G
  • NM_001408493.1:c.575-1506T>G
  • NM_001408494.1:c.548-1506T>G
  • NM_001408495.1:c.545-1506T>G
  • NM_001408496.1:c.524-1506T>G
  • NM_001408497.1:c.524-1506T>G
  • NM_001408498.1:c.524-1506T>G
  • NM_001408499.1:c.524-1506T>G
  • NM_001408500.1:c.524-1506T>G
  • NM_001408501.1:c.524-1506T>G
  • NM_001408502.1:c.455-1506T>G
  • NM_001408503.1:c.521-1506T>G
  • NM_001408504.1:c.521-1506T>G
  • NM_001408505.1:c.521-1506T>G
  • NM_001408506.1:c.461-1506T>G
  • NM_001408507.1:c.461-1506T>G
  • NM_001408508.1:c.452-1506T>G
  • NM_001408509.1:c.452-1506T>G
  • NM_001408510.1:c.407-1506T>G
  • NM_001408511.1:c.404-1506T>G
  • NM_001408512.1:c.284-1506T>G
  • NM_001408513.1:c.578-1506T>G
  • NM_001408514.1:c.578-1506T>G
  • NM_007294.4:c.2993T>GMANE SELECT
  • NM_007297.4:c.2852T>G
  • NM_007298.4:c.788-1506T>G
  • NM_007299.4:c.788-1506T>G
  • NM_007300.4:c.2993T>G
  • NP_001394500.1:p.Leu927Arg
  • NP_001394510.1:p.Leu998Arg
  • NP_001394511.1:p.Leu998Arg
  • NP_001394512.1:p.Leu998Arg
  • NP_001394514.1:p.Leu998Arg
  • NP_001394516.1:p.Leu997Arg
  • NP_001394519.1:p.Leu997Arg
  • NP_001394520.1:p.Leu997Arg
  • NP_001394522.1:p.Leu998Arg
  • NP_001394523.1:p.Leu998Arg
  • NP_001394525.1:p.Leu998Arg
  • NP_001394526.1:p.Leu998Arg
  • NP_001394527.1:p.Leu998Arg
  • NP_001394531.1:p.Leu998Arg
  • NP_001394532.1:p.Leu998Arg
  • NP_001394534.1:p.Leu998Arg
  • NP_001394539.1:p.Leu997Arg
  • NP_001394540.1:p.Leu997Arg
  • NP_001394541.1:p.Leu997Arg
  • NP_001394542.1:p.Leu997Arg
  • NP_001394543.1:p.Leu997Arg
  • NP_001394544.1:p.Leu997Arg
  • NP_001394545.1:p.Leu998Arg
  • NP_001394546.1:p.Leu998Arg
  • NP_001394547.1:p.Leu998Arg
  • NP_001394548.1:p.Leu998Arg
  • NP_001394549.1:p.Leu998Arg
  • NP_001394550.1:p.Leu998Arg
  • NP_001394551.1:p.Leu998Arg
  • NP_001394552.1:p.Leu998Arg
  • NP_001394553.1:p.Leu998Arg
  • NP_001394554.1:p.Leu998Arg
  • NP_001394555.1:p.Leu998Arg
  • NP_001394556.1:p.Leu997Arg
  • NP_001394557.1:p.Leu997Arg
  • NP_001394558.1:p.Leu997Arg
  • NP_001394559.1:p.Leu997Arg
  • NP_001394560.1:p.Leu997Arg
  • NP_001394561.1:p.Leu997Arg
  • NP_001394562.1:p.Leu997Arg
  • NP_001394563.1:p.Leu997Arg
  • NP_001394564.1:p.Leu997Arg
  • NP_001394565.1:p.Leu997Arg
  • NP_001394566.1:p.Leu997Arg
  • NP_001394567.1:p.Leu997Arg
  • NP_001394568.1:p.Leu998Arg
  • NP_001394569.1:p.Leu998Arg
  • NP_001394570.1:p.Leu998Arg
  • NP_001394571.1:p.Leu998Arg
  • NP_001394573.1:p.Leu997Arg
  • NP_001394574.1:p.Leu997Arg
  • NP_001394575.1:p.Leu995Arg
  • NP_001394576.1:p.Leu995Arg
  • NP_001394577.1:p.Leu957Arg
  • NP_001394578.1:p.Leu956Arg
  • NP_001394581.1:p.Leu998Arg
  • NP_001394582.1:p.Leu972Arg
  • NP_001394583.1:p.Leu972Arg
  • NP_001394584.1:p.Leu972Arg
  • NP_001394585.1:p.Leu972Arg
  • NP_001394586.1:p.Leu972Arg
  • NP_001394587.1:p.Leu972Arg
  • NP_001394588.1:p.Leu971Arg
  • NP_001394589.1:p.Leu971Arg
  • NP_001394590.1:p.Leu971Arg
  • NP_001394591.1:p.Leu971Arg
  • NP_001394592.1:p.Leu972Arg
  • NP_001394593.1:p.Leu957Arg
  • NP_001394594.1:p.Leu957Arg
  • NP_001394595.1:p.Leu957Arg
  • NP_001394596.1:p.Leu957Arg
  • NP_001394597.1:p.Leu957Arg
  • NP_001394598.1:p.Leu957Arg
  • NP_001394599.1:p.Leu956Arg
  • NP_001394600.1:p.Leu956Arg
  • NP_001394601.1:p.Leu956Arg
  • NP_001394602.1:p.Leu956Arg
  • NP_001394603.1:p.Leu957Arg
  • NP_001394604.1:p.Leu957Arg
  • NP_001394605.1:p.Leu957Arg
  • NP_001394606.1:p.Leu957Arg
  • NP_001394607.1:p.Leu957Arg
  • NP_001394608.1:p.Leu957Arg
  • NP_001394609.1:p.Leu957Arg
  • NP_001394610.1:p.Leu957Arg
  • NP_001394611.1:p.Leu957Arg
  • NP_001394612.1:p.Leu957Arg
  • NP_001394613.1:p.Leu998Arg
  • NP_001394614.1:p.Leu956Arg
  • NP_001394615.1:p.Leu956Arg
  • NP_001394616.1:p.Leu956Arg
  • NP_001394617.1:p.Leu956Arg
  • NP_001394618.1:p.Leu956Arg
  • NP_001394619.1:p.Leu956Arg
  • NP_001394620.1:p.Leu956Arg
  • NP_001394621.1:p.Leu951Arg
  • NP_001394623.1:p.Leu951Arg
  • NP_001394624.1:p.Leu951Arg
  • NP_001394625.1:p.Leu951Arg
  • NP_001394626.1:p.Leu951Arg
  • NP_001394627.1:p.Leu951Arg
  • NP_001394653.1:p.Leu951Arg
  • NP_001394654.1:p.Leu951Arg
  • NP_001394655.1:p.Leu951Arg
  • NP_001394656.1:p.Leu951Arg
  • NP_001394657.1:p.Leu951Arg
  • NP_001394658.1:p.Leu951Arg
  • NP_001394659.1:p.Leu951Arg
  • NP_001394660.1:p.Leu951Arg
  • NP_001394661.1:p.Leu951Arg
  • NP_001394662.1:p.Leu951Arg
  • NP_001394663.1:p.Leu951Arg
  • NP_001394664.1:p.Leu951Arg
  • NP_001394665.1:p.Leu951Arg
  • NP_001394666.1:p.Leu951Arg
  • NP_001394667.1:p.Leu951Arg
  • NP_001394668.1:p.Leu951Arg
  • NP_001394669.1:p.Leu950Arg
  • NP_001394670.1:p.Leu950Arg
  • NP_001394671.1:p.Leu950Arg
  • NP_001394672.1:p.Leu950Arg
  • NP_001394673.1:p.Leu950Arg
  • NP_001394674.1:p.Leu950Arg
  • NP_001394675.1:p.Leu950Arg
  • NP_001394676.1:p.Leu950Arg
  • NP_001394677.1:p.Leu950Arg
  • NP_001394678.1:p.Leu950Arg
  • NP_001394679.1:p.Leu951Arg
  • NP_001394680.1:p.Leu951Arg
  • NP_001394681.1:p.Leu951Arg
  • NP_001394767.1:p.Leu950Arg
  • NP_001394768.1:p.Leu950Arg
  • NP_001394770.1:p.Leu950Arg
  • NP_001394771.1:p.Leu950Arg
  • NP_001394772.1:p.Leu950Arg
  • NP_001394773.1:p.Leu950Arg
  • NP_001394774.1:p.Leu950Arg
  • NP_001394775.1:p.Leu950Arg
  • NP_001394776.1:p.Leu950Arg
  • NP_001394777.1:p.Leu950Arg
  • NP_001394778.1:p.Leu950Arg
  • NP_001394779.1:p.Leu951Arg
  • NP_001394780.1:p.Leu951Arg
  • NP_001394781.1:p.Leu951Arg
  • NP_001394782.1:p.Leu927Arg
  • NP_001394783.1:p.Leu998Arg
  • NP_001394787.1:p.Leu998Arg
  • NP_001394788.1:p.Leu998Arg
  • NP_001394789.1:p.Leu997Arg
  • NP_001394790.1:p.Leu997Arg
  • NP_001394791.1:p.Leu931Arg
  • NP_001394792.1:p.Leu957Arg
  • NP_001394803.1:p.Leu930Arg
  • NP_001394804.1:p.Leu930Arg
  • NP_001394808.1:p.Leu928Arg
  • NP_001394810.1:p.Leu928Arg
  • NP_001394811.1:p.Leu928Arg
  • NP_001394813.1:p.Leu928Arg
  • NP_001394814.1:p.Leu928Arg
  • NP_001394815.1:p.Leu928Arg
  • NP_001394816.1:p.Leu928Arg
  • NP_001394818.1:p.Leu928Arg
  • NP_001394823.1:p.Leu927Arg
  • NP_001394824.1:p.Leu927Arg
  • NP_001394825.1:p.Leu927Arg
  • NP_001394826.1:p.Leu927Arg
  • NP_001394827.1:p.Leu927Arg
  • NP_001394828.1:p.Leu927Arg
  • NP_001394829.1:p.Leu928Arg
  • NP_001394831.1:p.Leu928Arg
  • NP_001394833.1:p.Leu928Arg
  • NP_001394835.1:p.Leu928Arg
  • NP_001394836.1:p.Leu928Arg
  • NP_001394837.1:p.Leu928Arg
  • NP_001394838.1:p.Leu928Arg
  • NP_001394839.1:p.Leu928Arg
  • NP_001394844.1:p.Leu927Arg
  • NP_001394845.1:p.Leu927Arg
  • NP_001394846.1:p.Leu927Arg
  • NP_001394847.1:p.Leu927Arg
  • NP_001394848.1:p.Leu957Arg
  • NP_001394849.1:p.Leu910Arg
  • NP_001394850.1:p.Leu910Arg
  • NP_001394851.1:p.Leu910Arg
  • NP_001394852.1:p.Leu910Arg
  • NP_001394853.1:p.Leu910Arg
  • NP_001394854.1:p.Leu910Arg
  • NP_001394855.1:p.Leu910Arg
  • NP_001394856.1:p.Leu910Arg
  • NP_001394857.1:p.Leu910Arg
  • NP_001394858.1:p.Leu910Arg
  • NP_001394859.1:p.Leu909Arg
  • NP_001394860.1:p.Leu909Arg
  • NP_001394861.1:p.Leu909Arg
  • NP_001394862.1:p.Leu910Arg
  • NP_001394863.1:p.Leu909Arg
  • NP_001394864.1:p.Leu910Arg
  • NP_001394865.1:p.Leu909Arg
  • NP_001394866.1:p.Leu957Arg
  • NP_001394867.1:p.Leu957Arg
  • NP_001394868.1:p.Leu957Arg
  • NP_001394869.1:p.Leu956Arg
  • NP_001394870.1:p.Leu956Arg
  • NP_001394871.1:p.Leu951Arg
  • NP_001394872.1:p.Leu950Arg
  • NP_001394873.1:p.Leu951Arg
  • NP_001394874.1:p.Leu951Arg
  • NP_001394875.1:p.Leu887Arg
  • NP_001394876.1:p.Leu887Arg
  • NP_001394877.1:p.Leu887Arg
  • NP_001394878.1:p.Leu887Arg
  • NP_001394879.1:p.Leu887Arg
  • NP_001394880.1:p.Leu887Arg
  • NP_001394881.1:p.Leu887Arg
  • NP_001394882.1:p.Leu887Arg
  • NP_001394883.1:p.Leu886Arg
  • NP_001394884.1:p.Leu886Arg
  • NP_001394885.1:p.Leu886Arg
  • NP_001394886.1:p.Leu887Arg
  • NP_001394887.1:p.Leu886Arg
  • NP_001394888.1:p.Leu871Arg
  • NP_001394889.1:p.Leu871Arg
  • NP_001394891.1:p.Leu870Arg
  • NP_001394892.1:p.Leu871Arg
  • NP_001394893.1:p.Leu950Arg
  • NP_001394894.1:p.Leu830Arg
  • NP_001394895.1:p.Leu702Arg
  • NP_001394896.1:p.Leu702Arg
  • NP_009225.1:p.Leu998Arg
  • NP_009225.1:p.Leu998Arg
  • NP_009228.2:p.Leu951Arg
  • NP_009231.2:p.Leu998Arg
  • LRG_292t1:c.2993T>G
  • LRG_292:g.125446T>G
  • LRG_292p1:p.Leu998Arg
  • NC_000017.10:g.41244555A>C
  • NM_007294.3:c.2993T>G
  • NR_027676.1:n.3129T>G
Protein change:
L702R
Links:
dbSNP: rs1567793330
NCBI 1000 Genomes Browser:
rs1567793330
Molecular consequence:
  • NM_001407968.1:c.788-399T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407969.1:c.788-399T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407970.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407971.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407972.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407973.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407974.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407975.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407976.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407977.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407978.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407979.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407980.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407981.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407982.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407983.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407984.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407985.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407986.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407990.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407991.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407992.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407993.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408392.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408396.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408397.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408398.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408399.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408400.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408401.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408402.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408403.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408404.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408406.1:c.791-1515T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408407.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408408.1:c.779-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408409.1:c.710-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408410.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408411.1:c.710-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408412.1:c.710-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408413.1:c.707-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408414.1:c.710-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408415.1:c.710-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408416.1:c.707-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408418.1:c.671-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408419.1:c.671-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408420.1:c.671-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408421.1:c.668-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408422.1:c.671-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408423.1:c.671-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408424.1:c.668-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408425.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408426.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408427.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408428.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408429.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408430.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408431.1:c.668-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408432.1:c.662-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408433.1:c.662-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408434.1:c.662-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408435.1:c.662-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408436.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408437.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408438.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408439.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408440.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408441.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408442.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408443.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408444.1:c.665-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408445.1:c.662-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408446.1:c.662-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408447.1:c.662-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408448.1:c.662-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408450.1:c.662-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408451.1:c.653-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408452.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408453.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408454.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408455.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408456.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408457.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408458.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408459.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408460.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408461.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408462.1:c.644-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408463.1:c.644-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408464.1:c.644-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408465.1:c.644-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408466.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408467.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408468.1:c.644-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408469.1:c.647-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408470.1:c.644-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408472.1:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408473.1:c.785-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408474.1:c.587-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408475.1:c.584-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408476.1:c.587-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408478.1:c.578-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408479.1:c.578-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408480.1:c.578-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408481.1:c.578-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408482.1:c.578-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408483.1:c.578-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408484.1:c.578-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408485.1:c.578-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408489.1:c.578-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408490.1:c.575-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408491.1:c.575-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408492.1:c.578-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408493.1:c.575-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408494.1:c.548-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408495.1:c.545-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408496.1:c.524-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408497.1:c.524-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408498.1:c.524-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408499.1:c.524-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408500.1:c.524-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408501.1:c.524-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408502.1:c.455-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408503.1:c.521-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408504.1:c.521-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408505.1:c.521-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408506.1:c.461-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408507.1:c.461-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408508.1:c.452-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408509.1:c.452-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408510.1:c.407-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408511.1:c.404-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408512.1:c.284-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408513.1:c.578-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408514.1:c.578-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.4:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.788-1506T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407571.1:c.2780T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.2984T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.2984T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.2915T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.2915T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.2915T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.2915T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.2915T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.2915T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.2912T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.2912T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.2912T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.2912T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.2915T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407732.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407733.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407734.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407735.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407736.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407737.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407738.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407739.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407838.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407839.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407841.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407842.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407843.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407844.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407845.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407846.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407850.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407851.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407852.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.2780T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.2990T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.2792T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.2789T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.2789T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.2780T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.2780T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.2780T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.2780T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.2780T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.2780T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407900.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407902.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407904.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407906.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.2783T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.2780T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407916.1:c.2780T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407917.1:c.2780T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407918.1:c.2780T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.2729T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.2729T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.2729T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.2729T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.2729T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.2729T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.2729T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407927.1:c.2729T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407928.1:c.2729T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407929.1:c.2729T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.2726T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.2726T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.2726T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.2729T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.2726T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407935.1:c.2729T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407936.1:c.2726T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.2870T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.2867T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407942.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407943.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407944.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407945.1:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.2660T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.2660T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.2660T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.2660T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407950.1:c.2660T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407951.1:c.2660T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.2660T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.2660T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.2657T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.2657T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.2657T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407957.1:c.2660T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407958.1:c.2657T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.2612T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407960.1:c.2612T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.2609T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407963.1:c.2612T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407964.1:c.2849T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.2489T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.2105T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407967.1:c.2105T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.2852T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.2993T>G - missense variant - [Sequence Ontology: SO:0001583]

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

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000943066Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Dec 31, 2020) 		germlineclinical testing

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

Help

Summary from all submissions

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

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

Details of each submission

From Invitae, SCV000943066.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with BRCA1-related disease. This variant is not present in population databases (ExAC no frequency). This sequence change replaces leucine with arginine at codon 998 of the BRCA1 protein (p.Leu998Arg). The leucine residue is moderately conserved and there is a moderate physicochemical difference between leucine and arginine.

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

Last Updated: Jul 15, 2024