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NM_007294.4(BRCA1):c.3132T>G (p.Ile1044Met) AND Hereditary cancer-predisposing syndrome

Germline classification:
Conflicting interpretations of pathogenicity (2 submissions)
Last evaluated:
Mar 23, 2023
Review status:
criteria provided, conflicting classifications
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:
RCV000510120.7

Allele description [Variation Report for NM_007294.4(BRCA1):c.3132T>G (p.Ile1044Met)]

NM_007294.4(BRCA1):c.3132T>G (p.Ile1044Met)

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.3132T>G (p.Ile1044Met)
HGVS:
  • NC_000017.11:g.43092399A>C
  • NG_005905.2:g.125585T>G
  • NG_087068.1:g.1381A>C
  • NM_001407571.1:c.2919T>G
  • NM_001407581.1:c.3132T>G
  • NM_001407582.1:c.3132T>G
  • NM_001407583.1:c.3132T>G
  • NM_001407585.1:c.3132T>G
  • NM_001407587.1:c.3129T>G
  • NM_001407590.1:c.3129T>G
  • NM_001407591.1:c.3129T>G
  • NM_001407593.1:c.3132T>G
  • NM_001407594.1:c.3132T>G
  • NM_001407596.1:c.3132T>G
  • NM_001407597.1:c.3132T>G
  • NM_001407598.1:c.3132T>G
  • NM_001407602.1:c.3132T>G
  • NM_001407603.1:c.3132T>G
  • NM_001407605.1:c.3132T>G
  • NM_001407610.1:c.3129T>G
  • NM_001407611.1:c.3129T>G
  • NM_001407612.1:c.3129T>G
  • NM_001407613.1:c.3129T>G
  • NM_001407614.1:c.3129T>G
  • NM_001407615.1:c.3129T>G
  • NM_001407616.1:c.3132T>G
  • NM_001407617.1:c.3132T>G
  • NM_001407618.1:c.3132T>G
  • NM_001407619.1:c.3132T>G
  • NM_001407620.1:c.3132T>G
  • NM_001407621.1:c.3132T>G
  • NM_001407622.1:c.3132T>G
  • NM_001407623.1:c.3132T>G
  • NM_001407624.1:c.3132T>G
  • NM_001407625.1:c.3132T>G
  • NM_001407626.1:c.3132T>G
  • NM_001407627.1:c.3129T>G
  • NM_001407628.1:c.3129T>G
  • NM_001407629.1:c.3129T>G
  • NM_001407630.1:c.3129T>G
  • NM_001407631.1:c.3129T>G
  • NM_001407632.1:c.3129T>G
  • NM_001407633.1:c.3129T>G
  • NM_001407634.1:c.3129T>G
  • NM_001407635.1:c.3129T>G
  • NM_001407636.1:c.3129T>G
  • NM_001407637.1:c.3129T>G
  • NM_001407638.1:c.3129T>G
  • NM_001407639.1:c.3132T>G
  • NM_001407640.1:c.3132T>G
  • NM_001407641.1:c.3132T>G
  • NM_001407642.1:c.3132T>G
  • NM_001407644.1:c.3129T>G
  • NM_001407645.1:c.3129T>G
  • NM_001407646.1:c.3123T>G
  • NM_001407647.1:c.3123T>G
  • NM_001407648.1:c.3009T>G
  • NM_001407649.1:c.3006T>G
  • NM_001407652.1:c.3132T>G
  • NM_001407653.1:c.3054T>G
  • NM_001407654.1:c.3054T>G
  • NM_001407655.1:c.3054T>G
  • NM_001407656.1:c.3054T>G
  • NM_001407657.1:c.3054T>G
  • NM_001407658.1:c.3054T>G
  • NM_001407659.1:c.3051T>G
  • NM_001407660.1:c.3051T>G
  • NM_001407661.1:c.3051T>G
  • NM_001407662.1:c.3051T>G
  • NM_001407663.1:c.3054T>G
  • NM_001407664.1:c.3009T>G
  • NM_001407665.1:c.3009T>G
  • NM_001407666.1:c.3009T>G
  • NM_001407667.1:c.3009T>G
  • NM_001407668.1:c.3009T>G
  • NM_001407669.1:c.3009T>G
  • NM_001407670.1:c.3006T>G
  • NM_001407671.1:c.3006T>G
  • NM_001407672.1:c.3006T>G
  • NM_001407673.1:c.3006T>G
  • NM_001407674.1:c.3009T>G
  • NM_001407675.1:c.3009T>G
  • NM_001407676.1:c.3009T>G
  • NM_001407677.1:c.3009T>G
  • NM_001407678.1:c.3009T>G
  • NM_001407679.1:c.3009T>G
  • NM_001407680.1:c.3009T>G
  • NM_001407681.1:c.3009T>G
  • NM_001407682.1:c.3009T>G
  • NM_001407683.1:c.3009T>G
  • NM_001407684.1:c.3132T>G
  • NM_001407685.1:c.3006T>G
  • NM_001407686.1:c.3006T>G
  • NM_001407687.1:c.3006T>G
  • NM_001407688.1:c.3006T>G
  • NM_001407689.1:c.3006T>G
  • NM_001407690.1:c.3006T>G
  • NM_001407691.1:c.3006T>G
  • NM_001407692.1:c.2991T>G
  • NM_001407694.1:c.2991T>G
  • NM_001407695.1:c.2991T>G
  • NM_001407696.1:c.2991T>G
  • NM_001407697.1:c.2991T>G
  • NM_001407698.1:c.2991T>G
  • NM_001407724.1:c.2991T>G
  • NM_001407725.1:c.2991T>G
  • NM_001407726.1:c.2991T>G
  • NM_001407727.1:c.2991T>G
  • NM_001407728.1:c.2991T>G
  • NM_001407729.1:c.2991T>G
  • NM_001407730.1:c.2991T>G
  • NM_001407731.1:c.2991T>G
  • NM_001407732.1:c.2991T>G
  • NM_001407733.1:c.2991T>G
  • NM_001407734.1:c.2991T>G
  • NM_001407735.1:c.2991T>G
  • NM_001407736.1:c.2991T>G
  • NM_001407737.1:c.2991T>G
  • NM_001407738.1:c.2991T>G
  • NM_001407739.1:c.2991T>G
  • NM_001407740.1:c.2988T>G
  • NM_001407741.1:c.2988T>G
  • NM_001407742.1:c.2988T>G
  • NM_001407743.1:c.2988T>G
  • NM_001407744.1:c.2988T>G
  • NM_001407745.1:c.2988T>G
  • NM_001407746.1:c.2988T>G
  • NM_001407747.1:c.2988T>G
  • NM_001407748.1:c.2988T>G
  • NM_001407749.1:c.2988T>G
  • NM_001407750.1:c.2991T>G
  • NM_001407751.1:c.2991T>G
  • NM_001407752.1:c.2991T>G
  • NM_001407838.1:c.2988T>G
  • NM_001407839.1:c.2988T>G
  • NM_001407841.1:c.2988T>G
  • NM_001407842.1:c.2988T>G
  • NM_001407843.1:c.2988T>G
  • NM_001407844.1:c.2988T>G
  • NM_001407845.1:c.2988T>G
  • NM_001407846.1:c.2988T>G
  • NM_001407847.1:c.2988T>G
  • NM_001407848.1:c.2988T>G
  • NM_001407849.1:c.2988T>G
  • NM_001407850.1:c.2991T>G
  • NM_001407851.1:c.2991T>G
  • NM_001407852.1:c.2991T>G
  • NM_001407853.1:c.2919T>G
  • NM_001407854.1:c.3132T>G
  • NM_001407858.1:c.3132T>G
  • NM_001407859.1:c.3132T>G
  • NM_001407860.1:c.3129T>G
  • NM_001407861.1:c.3129T>G
  • NM_001407862.1:c.2931T>G
  • NM_001407863.1:c.3009T>G
  • NM_001407874.1:c.2928T>G
  • NM_001407875.1:c.2928T>G
  • NM_001407879.1:c.2922T>G
  • NM_001407881.1:c.2922T>G
  • NM_001407882.1:c.2922T>G
  • NM_001407884.1:c.2922T>G
  • NM_001407885.1:c.2922T>G
  • NM_001407886.1:c.2922T>G
  • NM_001407887.1:c.2922T>G
  • NM_001407889.1:c.2922T>G
  • NM_001407894.1:c.2919T>G
  • NM_001407895.1:c.2919T>G
  • NM_001407896.1:c.2919T>G
  • NM_001407897.1:c.2919T>G
  • NM_001407898.1:c.2919T>G
  • NM_001407899.1:c.2919T>G
  • NM_001407900.1:c.2922T>G
  • NM_001407902.1:c.2922T>G
  • NM_001407904.1:c.2922T>G
  • NM_001407906.1:c.2922T>G
  • NM_001407907.1:c.2922T>G
  • NM_001407908.1:c.2922T>G
  • NM_001407909.1:c.2922T>G
  • NM_001407910.1:c.2922T>G
  • NM_001407915.1:c.2919T>G
  • NM_001407916.1:c.2919T>G
  • NM_001407917.1:c.2919T>G
  • NM_001407918.1:c.2919T>G
  • NM_001407919.1:c.3009T>G
  • NM_001407920.1:c.2868T>G
  • NM_001407921.1:c.2868T>G
  • NM_001407922.1:c.2868T>G
  • NM_001407923.1:c.2868T>G
  • NM_001407924.1:c.2868T>G
  • NM_001407925.1:c.2868T>G
  • NM_001407926.1:c.2868T>G
  • NM_001407927.1:c.2868T>G
  • NM_001407928.1:c.2868T>G
  • NM_001407929.1:c.2868T>G
  • NM_001407930.1:c.2865T>G
  • NM_001407931.1:c.2865T>G
  • NM_001407932.1:c.2865T>G
  • NM_001407933.1:c.2868T>G
  • NM_001407934.1:c.2865T>G
  • NM_001407935.1:c.2868T>G
  • NM_001407936.1:c.2865T>G
  • NM_001407937.1:c.3009T>G
  • NM_001407938.1:c.3009T>G
  • NM_001407939.1:c.3009T>G
  • NM_001407940.1:c.3006T>G
  • NM_001407941.1:c.3006T>G
  • NM_001407942.1:c.2991T>G
  • NM_001407943.1:c.2988T>G
  • NM_001407944.1:c.2991T>G
  • NM_001407945.1:c.2991T>G
  • NM_001407946.1:c.2799T>G
  • NM_001407947.1:c.2799T>G
  • NM_001407948.1:c.2799T>G
  • NM_001407949.1:c.2799T>G
  • NM_001407950.1:c.2799T>G
  • NM_001407951.1:c.2799T>G
  • NM_001407952.1:c.2799T>G
  • NM_001407953.1:c.2799T>G
  • NM_001407954.1:c.2796T>G
  • NM_001407955.1:c.2796T>G
  • NM_001407956.1:c.2796T>G
  • NM_001407957.1:c.2799T>G
  • NM_001407958.1:c.2796T>G
  • NM_001407959.1:c.2751T>G
  • NM_001407960.1:c.2751T>G
  • NM_001407962.1:c.2748T>G
  • NM_001407963.1:c.2751T>G
  • NM_001407964.1:c.2988T>G
  • NM_001407965.1:c.2628T>G
  • NM_001407966.1:c.2244T>G
  • NM_001407967.1:c.2244T>G
  • NM_001407968.1:c.788-260T>G
  • NM_001407969.1:c.788-260T>G
  • NM_001407970.1:c.788-1367T>G
  • NM_001407971.1:c.788-1367T>G
  • NM_001407972.1:c.785-1367T>G
  • NM_001407973.1:c.788-1367T>G
  • NM_001407974.1:c.788-1367T>G
  • NM_001407975.1:c.788-1367T>G
  • NM_001407976.1:c.788-1367T>G
  • NM_001407977.1:c.788-1367T>G
  • NM_001407978.1:c.788-1367T>G
  • NM_001407979.1:c.788-1367T>G
  • NM_001407980.1:c.788-1367T>G
  • NM_001407981.1:c.788-1367T>G
  • NM_001407982.1:c.788-1367T>G
  • NM_001407983.1:c.788-1367T>G
  • NM_001407984.1:c.785-1367T>G
  • NM_001407985.1:c.785-1367T>G
  • NM_001407986.1:c.785-1367T>G
  • NM_001407990.1:c.788-1367T>G
  • NM_001407991.1:c.785-1367T>G
  • NM_001407992.1:c.785-1367T>G
  • NM_001407993.1:c.788-1367T>G
  • NM_001408392.1:c.785-1367T>G
  • NM_001408396.1:c.785-1367T>G
  • NM_001408397.1:c.785-1367T>G
  • NM_001408398.1:c.785-1367T>G
  • NM_001408399.1:c.785-1367T>G
  • NM_001408400.1:c.785-1367T>G
  • NM_001408401.1:c.785-1367T>G
  • NM_001408402.1:c.785-1367T>G
  • NM_001408403.1:c.788-1367T>G
  • NM_001408404.1:c.788-1367T>G
  • NM_001408406.1:c.791-1376T>G
  • NM_001408407.1:c.785-1367T>G
  • NM_001408408.1:c.779-1367T>G
  • NM_001408409.1:c.710-1367T>G
  • NM_001408410.1:c.647-1367T>G
  • NM_001408411.1:c.710-1367T>G
  • NM_001408412.1:c.710-1367T>G
  • NM_001408413.1:c.707-1367T>G
  • NM_001408414.1:c.710-1367T>G
  • NM_001408415.1:c.710-1367T>G
  • NM_001408416.1:c.707-1367T>G
  • NM_001408418.1:c.671-1367T>G
  • NM_001408419.1:c.671-1367T>G
  • NM_001408420.1:c.671-1367T>G
  • NM_001408421.1:c.668-1367T>G
  • NM_001408422.1:c.671-1367T>G
  • NM_001408423.1:c.671-1367T>G
  • NM_001408424.1:c.668-1367T>G
  • NM_001408425.1:c.665-1367T>G
  • NM_001408426.1:c.665-1367T>G
  • NM_001408427.1:c.665-1367T>G
  • NM_001408428.1:c.665-1367T>G
  • NM_001408429.1:c.665-1367T>G
  • NM_001408430.1:c.665-1367T>G
  • NM_001408431.1:c.668-1367T>G
  • NM_001408432.1:c.662-1367T>G
  • NM_001408433.1:c.662-1367T>G
  • NM_001408434.1:c.662-1367T>G
  • NM_001408435.1:c.662-1367T>G
  • NM_001408436.1:c.665-1367T>G
  • NM_001408437.1:c.665-1367T>G
  • NM_001408438.1:c.665-1367T>G
  • NM_001408439.1:c.665-1367T>G
  • NM_001408440.1:c.665-1367T>G
  • NM_001408441.1:c.665-1367T>G
  • NM_001408442.1:c.665-1367T>G
  • NM_001408443.1:c.665-1367T>G
  • NM_001408444.1:c.665-1367T>G
  • NM_001408445.1:c.662-1367T>G
  • NM_001408446.1:c.662-1367T>G
  • NM_001408447.1:c.662-1367T>G
  • NM_001408448.1:c.662-1367T>G
  • NM_001408450.1:c.662-1367T>G
  • NM_001408451.1:c.653-1367T>G
  • NM_001408452.1:c.647-1367T>G
  • NM_001408453.1:c.647-1367T>G
  • NM_001408454.1:c.647-1367T>G
  • NM_001408455.1:c.647-1367T>G
  • NM_001408456.1:c.647-1367T>G
  • NM_001408457.1:c.647-1367T>G
  • NM_001408458.1:c.647-1367T>G
  • NM_001408459.1:c.647-1367T>G
  • NM_001408460.1:c.647-1367T>G
  • NM_001408461.1:c.647-1367T>G
  • NM_001408462.1:c.644-1367T>G
  • NM_001408463.1:c.644-1367T>G
  • NM_001408464.1:c.644-1367T>G
  • NM_001408465.1:c.644-1367T>G
  • NM_001408466.1:c.647-1367T>G
  • NM_001408467.1:c.647-1367T>G
  • NM_001408468.1:c.644-1367T>G
  • NM_001408469.1:c.647-1367T>G
  • NM_001408470.1:c.644-1367T>G
  • NM_001408472.1:c.788-1367T>G
  • NM_001408473.1:c.785-1367T>G
  • NM_001408474.1:c.587-1367T>G
  • NM_001408475.1:c.584-1367T>G
  • NM_001408476.1:c.587-1367T>G
  • NM_001408478.1:c.578-1367T>G
  • NM_001408479.1:c.578-1367T>G
  • NM_001408480.1:c.578-1367T>G
  • NM_001408481.1:c.578-1367T>G
  • NM_001408482.1:c.578-1367T>G
  • NM_001408483.1:c.578-1367T>G
  • NM_001408484.1:c.578-1367T>G
  • NM_001408485.1:c.578-1367T>G
  • NM_001408489.1:c.578-1367T>G
  • NM_001408490.1:c.575-1367T>G
  • NM_001408491.1:c.575-1367T>G
  • NM_001408492.1:c.578-1367T>G
  • NM_001408493.1:c.575-1367T>G
  • NM_001408494.1:c.548-1367T>G
  • NM_001408495.1:c.545-1367T>G
  • NM_001408496.1:c.524-1367T>G
  • NM_001408497.1:c.524-1367T>G
  • NM_001408498.1:c.524-1367T>G
  • NM_001408499.1:c.524-1367T>G
  • NM_001408500.1:c.524-1367T>G
  • NM_001408501.1:c.524-1367T>G
  • NM_001408502.1:c.455-1367T>G
  • NM_001408503.1:c.521-1367T>G
  • NM_001408504.1:c.521-1367T>G
  • NM_001408505.1:c.521-1367T>G
  • NM_001408506.1:c.461-1367T>G
  • NM_001408507.1:c.461-1367T>G
  • NM_001408508.1:c.452-1367T>G
  • NM_001408509.1:c.452-1367T>G
  • NM_001408510.1:c.407-1367T>G
  • NM_001408511.1:c.404-1367T>G
  • NM_001408512.1:c.284-1367T>G
  • NM_001408513.1:c.578-1367T>G
  • NM_001408514.1:c.578-1367T>G
  • NM_007294.4:c.3132T>GMANE SELECT
  • NM_007297.4:c.2991T>G
  • NM_007298.4:c.788-1367T>G
  • NM_007299.4:c.788-1367T>G
  • NM_007300.4:c.3132T>G
  • NP_001394500.1:p.Ile973Met
  • NP_001394510.1:p.Ile1044Met
  • NP_001394511.1:p.Ile1044Met
  • NP_001394512.1:p.Ile1044Met
  • NP_001394514.1:p.Ile1044Met
  • NP_001394516.1:p.Ile1043Met
  • NP_001394519.1:p.Ile1043Met
  • NP_001394520.1:p.Ile1043Met
  • NP_001394522.1:p.Ile1044Met
  • NP_001394523.1:p.Ile1044Met
  • NP_001394525.1:p.Ile1044Met
  • NP_001394526.1:p.Ile1044Met
  • NP_001394527.1:p.Ile1044Met
  • NP_001394531.1:p.Ile1044Met
  • NP_001394532.1:p.Ile1044Met
  • NP_001394534.1:p.Ile1044Met
  • NP_001394539.1:p.Ile1043Met
  • NP_001394540.1:p.Ile1043Met
  • NP_001394541.1:p.Ile1043Met
  • NP_001394542.1:p.Ile1043Met
  • NP_001394543.1:p.Ile1043Met
  • NP_001394544.1:p.Ile1043Met
  • NP_001394545.1:p.Ile1044Met
  • NP_001394546.1:p.Ile1044Met
  • NP_001394547.1:p.Ile1044Met
  • NP_001394548.1:p.Ile1044Met
  • NP_001394549.1:p.Ile1044Met
  • NP_001394550.1:p.Ile1044Met
  • NP_001394551.1:p.Ile1044Met
  • NP_001394552.1:p.Ile1044Met
  • NP_001394553.1:p.Ile1044Met
  • NP_001394554.1:p.Ile1044Met
  • NP_001394555.1:p.Ile1044Met
  • NP_001394556.1:p.Ile1043Met
  • NP_001394557.1:p.Ile1043Met
  • NP_001394558.1:p.Ile1043Met
  • NP_001394559.1:p.Ile1043Met
  • NP_001394560.1:p.Ile1043Met
  • NP_001394561.1:p.Ile1043Met
  • NP_001394562.1:p.Ile1043Met
  • NP_001394563.1:p.Ile1043Met
  • NP_001394564.1:p.Ile1043Met
  • NP_001394565.1:p.Ile1043Met
  • NP_001394566.1:p.Ile1043Met
  • NP_001394567.1:p.Ile1043Met
  • NP_001394568.1:p.Ile1044Met
  • NP_001394569.1:p.Ile1044Met
  • NP_001394570.1:p.Ile1044Met
  • NP_001394571.1:p.Ile1044Met
  • NP_001394573.1:p.Ile1043Met
  • NP_001394574.1:p.Ile1043Met
  • NP_001394575.1:p.Ile1041Met
  • NP_001394576.1:p.Ile1041Met
  • NP_001394577.1:p.Ile1003Met
  • NP_001394578.1:p.Ile1002Met
  • NP_001394581.1:p.Ile1044Met
  • NP_001394582.1:p.Ile1018Met
  • NP_001394583.1:p.Ile1018Met
  • NP_001394584.1:p.Ile1018Met
  • NP_001394585.1:p.Ile1018Met
  • NP_001394586.1:p.Ile1018Met
  • NP_001394587.1:p.Ile1018Met
  • NP_001394588.1:p.Ile1017Met
  • NP_001394589.1:p.Ile1017Met
  • NP_001394590.1:p.Ile1017Met
  • NP_001394591.1:p.Ile1017Met
  • NP_001394592.1:p.Ile1018Met
  • NP_001394593.1:p.Ile1003Met
  • NP_001394594.1:p.Ile1003Met
  • NP_001394595.1:p.Ile1003Met
  • NP_001394596.1:p.Ile1003Met
  • NP_001394597.1:p.Ile1003Met
  • NP_001394598.1:p.Ile1003Met
  • NP_001394599.1:p.Ile1002Met
  • NP_001394600.1:p.Ile1002Met
  • NP_001394601.1:p.Ile1002Met
  • NP_001394602.1:p.Ile1002Met
  • NP_001394603.1:p.Ile1003Met
  • NP_001394604.1:p.Ile1003Met
  • NP_001394605.1:p.Ile1003Met
  • NP_001394606.1:p.Ile1003Met
  • NP_001394607.1:p.Ile1003Met
  • NP_001394608.1:p.Ile1003Met
  • NP_001394609.1:p.Ile1003Met
  • NP_001394610.1:p.Ile1003Met
  • NP_001394611.1:p.Ile1003Met
  • NP_001394612.1:p.Ile1003Met
  • NP_001394613.1:p.Ile1044Met
  • NP_001394614.1:p.Ile1002Met
  • NP_001394615.1:p.Ile1002Met
  • NP_001394616.1:p.Ile1002Met
  • NP_001394617.1:p.Ile1002Met
  • NP_001394618.1:p.Ile1002Met
  • NP_001394619.1:p.Ile1002Met
  • NP_001394620.1:p.Ile1002Met
  • NP_001394621.1:p.Ile997Met
  • NP_001394623.1:p.Ile997Met
  • NP_001394624.1:p.Ile997Met
  • NP_001394625.1:p.Ile997Met
  • NP_001394626.1:p.Ile997Met
  • NP_001394627.1:p.Ile997Met
  • NP_001394653.1:p.Ile997Met
  • NP_001394654.1:p.Ile997Met
  • NP_001394655.1:p.Ile997Met
  • NP_001394656.1:p.Ile997Met
  • NP_001394657.1:p.Ile997Met
  • NP_001394658.1:p.Ile997Met
  • NP_001394659.1:p.Ile997Met
  • NP_001394660.1:p.Ile997Met
  • NP_001394661.1:p.Ile997Met
  • NP_001394662.1:p.Ile997Met
  • NP_001394663.1:p.Ile997Met
  • NP_001394664.1:p.Ile997Met
  • NP_001394665.1:p.Ile997Met
  • NP_001394666.1:p.Ile997Met
  • NP_001394667.1:p.Ile997Met
  • NP_001394668.1:p.Ile997Met
  • NP_001394669.1:p.Ile996Met
  • NP_001394670.1:p.Ile996Met
  • NP_001394671.1:p.Ile996Met
  • NP_001394672.1:p.Ile996Met
  • NP_001394673.1:p.Ile996Met
  • NP_001394674.1:p.Ile996Met
  • NP_001394675.1:p.Ile996Met
  • NP_001394676.1:p.Ile996Met
  • NP_001394677.1:p.Ile996Met
  • NP_001394678.1:p.Ile996Met
  • NP_001394679.1:p.Ile997Met
  • NP_001394680.1:p.Ile997Met
  • NP_001394681.1:p.Ile997Met
  • NP_001394767.1:p.Ile996Met
  • NP_001394768.1:p.Ile996Met
  • NP_001394770.1:p.Ile996Met
  • NP_001394771.1:p.Ile996Met
  • NP_001394772.1:p.Ile996Met
  • NP_001394773.1:p.Ile996Met
  • NP_001394774.1:p.Ile996Met
  • NP_001394775.1:p.Ile996Met
  • NP_001394776.1:p.Ile996Met
  • NP_001394777.1:p.Ile996Met
  • NP_001394778.1:p.Ile996Met
  • NP_001394779.1:p.Ile997Met
  • NP_001394780.1:p.Ile997Met
  • NP_001394781.1:p.Ile997Met
  • NP_001394782.1:p.Ile973Met
  • NP_001394783.1:p.Ile1044Met
  • NP_001394787.1:p.Ile1044Met
  • NP_001394788.1:p.Ile1044Met
  • NP_001394789.1:p.Ile1043Met
  • NP_001394790.1:p.Ile1043Met
  • NP_001394791.1:p.Ile977Met
  • NP_001394792.1:p.Ile1003Met
  • NP_001394803.1:p.Ile976Met
  • NP_001394804.1:p.Ile976Met
  • NP_001394808.1:p.Ile974Met
  • NP_001394810.1:p.Ile974Met
  • NP_001394811.1:p.Ile974Met
  • NP_001394813.1:p.Ile974Met
  • NP_001394814.1:p.Ile974Met
  • NP_001394815.1:p.Ile974Met
  • NP_001394816.1:p.Ile974Met
  • NP_001394818.1:p.Ile974Met
  • NP_001394823.1:p.Ile973Met
  • NP_001394824.1:p.Ile973Met
  • NP_001394825.1:p.Ile973Met
  • NP_001394826.1:p.Ile973Met
  • NP_001394827.1:p.Ile973Met
  • NP_001394828.1:p.Ile973Met
  • NP_001394829.1:p.Ile974Met
  • NP_001394831.1:p.Ile974Met
  • NP_001394833.1:p.Ile974Met
  • NP_001394835.1:p.Ile974Met
  • NP_001394836.1:p.Ile974Met
  • NP_001394837.1:p.Ile974Met
  • NP_001394838.1:p.Ile974Met
  • NP_001394839.1:p.Ile974Met
  • NP_001394844.1:p.Ile973Met
  • NP_001394845.1:p.Ile973Met
  • NP_001394846.1:p.Ile973Met
  • NP_001394847.1:p.Ile973Met
  • NP_001394848.1:p.Ile1003Met
  • NP_001394849.1:p.Ile956Met
  • NP_001394850.1:p.Ile956Met
  • NP_001394851.1:p.Ile956Met
  • NP_001394852.1:p.Ile956Met
  • NP_001394853.1:p.Ile956Met
  • NP_001394854.1:p.Ile956Met
  • NP_001394855.1:p.Ile956Met
  • NP_001394856.1:p.Ile956Met
  • NP_001394857.1:p.Ile956Met
  • NP_001394858.1:p.Ile956Met
  • NP_001394859.1:p.Ile955Met
  • NP_001394860.1:p.Ile955Met
  • NP_001394861.1:p.Ile955Met
  • NP_001394862.1:p.Ile956Met
  • NP_001394863.1:p.Ile955Met
  • NP_001394864.1:p.Ile956Met
  • NP_001394865.1:p.Ile955Met
  • NP_001394866.1:p.Ile1003Met
  • NP_001394867.1:p.Ile1003Met
  • NP_001394868.1:p.Ile1003Met
  • NP_001394869.1:p.Ile1002Met
  • NP_001394870.1:p.Ile1002Met
  • NP_001394871.1:p.Ile997Met
  • NP_001394872.1:p.Ile996Met
  • NP_001394873.1:p.Ile997Met
  • NP_001394874.1:p.Ile997Met
  • NP_001394875.1:p.Ile933Met
  • NP_001394876.1:p.Ile933Met
  • NP_001394877.1:p.Ile933Met
  • NP_001394878.1:p.Ile933Met
  • NP_001394879.1:p.Ile933Met
  • NP_001394880.1:p.Ile933Met
  • NP_001394881.1:p.Ile933Met
  • NP_001394882.1:p.Ile933Met
  • NP_001394883.1:p.Ile932Met
  • NP_001394884.1:p.Ile932Met
  • NP_001394885.1:p.Ile932Met
  • NP_001394886.1:p.Ile933Met
  • NP_001394887.1:p.Ile932Met
  • NP_001394888.1:p.Ile917Met
  • NP_001394889.1:p.Ile917Met
  • NP_001394891.1:p.Ile916Met
  • NP_001394892.1:p.Ile917Met
  • NP_001394893.1:p.Ile996Met
  • NP_001394894.1:p.Ile876Met
  • NP_001394895.1:p.Ile748Met
  • NP_001394896.1:p.Ile748Met
  • NP_009225.1:p.Ile1044Met
  • NP_009225.1:p.Ile1044Met
  • NP_009228.2:p.Ile997Met
  • NP_009231.2:p.Ile1044Met
  • LRG_292t1:c.3132T>G
  • LRG_292:g.125585T>G
  • LRG_292p1:p.Ile1044Met
  • NC_000017.10:g.41244416A>C
  • NM_007294.3:c.3132T>G
  • NR_027676.1:n.3268T>G
Protein change:
I1002M
Links:
dbSNP: rs1555588333
NCBI 1000 Genomes Browser:
rs1555588333
Molecular consequence:
  • NM_001407968.1:c.788-260T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407969.1:c.788-260T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407970.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407971.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407972.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407973.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407974.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407975.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407976.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407977.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407978.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407979.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407980.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407981.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407982.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407983.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407984.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407985.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407986.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407990.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407991.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407992.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407993.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408392.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408396.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408397.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408398.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408399.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408400.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408401.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408402.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408403.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408404.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408406.1:c.791-1376T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408407.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408408.1:c.779-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408409.1:c.710-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408410.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408411.1:c.710-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408412.1:c.710-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408413.1:c.707-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408414.1:c.710-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408415.1:c.710-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408416.1:c.707-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408418.1:c.671-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408419.1:c.671-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408420.1:c.671-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408421.1:c.668-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408422.1:c.671-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408423.1:c.671-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408424.1:c.668-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408425.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408426.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408427.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408428.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408429.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408430.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408431.1:c.668-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408432.1:c.662-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408433.1:c.662-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408434.1:c.662-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408435.1:c.662-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408436.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408437.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408438.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408439.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408440.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408441.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408442.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408443.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408444.1:c.665-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408445.1:c.662-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408446.1:c.662-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408447.1:c.662-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408448.1:c.662-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408450.1:c.662-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408451.1:c.653-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408452.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408453.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408454.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408455.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408456.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408457.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408458.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408459.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408460.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408461.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408462.1:c.644-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408463.1:c.644-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408464.1:c.644-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408465.1:c.644-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408466.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408467.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408468.1:c.644-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408469.1:c.647-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408470.1:c.644-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408472.1:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408473.1:c.785-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408474.1:c.587-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408475.1:c.584-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408476.1:c.587-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408478.1:c.578-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408479.1:c.578-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408480.1:c.578-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408481.1:c.578-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408482.1:c.578-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408483.1:c.578-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408484.1:c.578-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408485.1:c.578-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408489.1:c.578-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408490.1:c.575-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408491.1:c.575-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408492.1:c.578-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408493.1:c.575-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408494.1:c.548-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408495.1:c.545-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408496.1:c.524-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408497.1:c.524-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408498.1:c.524-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408499.1:c.524-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408500.1:c.524-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408501.1:c.524-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408502.1:c.455-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408503.1:c.521-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408504.1:c.521-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408505.1:c.521-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408506.1:c.461-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408507.1:c.461-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408508.1:c.452-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408509.1:c.452-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408510.1:c.407-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408511.1:c.404-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408512.1:c.284-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408513.1:c.578-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408514.1:c.578-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.4:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.788-1367T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407571.1:c.2919T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.3123T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.3123T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.3054T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.3054T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.3054T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.3054T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.3054T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.3054T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.3051T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.3051T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.3051T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.3051T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.3054T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407732.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407733.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407734.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407735.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407736.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407737.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407738.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407739.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407838.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407839.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407841.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407842.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407843.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407844.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407845.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407846.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407850.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407851.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407852.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.2919T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.3129T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.2931T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.2928T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.2928T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.2919T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.2919T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.2919T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.2919T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.2919T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.2919T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407900.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407902.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407904.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407906.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.2922T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.2919T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407916.1:c.2919T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407917.1:c.2919T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407918.1:c.2919T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.2868T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.2868T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.2868T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.2868T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.2868T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.2868T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.2868T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407927.1:c.2868T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407928.1:c.2868T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407929.1:c.2868T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.2865T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.2865T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.2865T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.2868T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.2865T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407935.1:c.2868T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407936.1:c.2865T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.3009T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.3006T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407942.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407943.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407944.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407945.1:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.2799T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.2799T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.2799T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.2799T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407950.1:c.2799T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407951.1:c.2799T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.2799T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.2799T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.2796T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.2796T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.2796T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407957.1:c.2799T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407958.1:c.2796T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.2751T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407960.1:c.2751T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.2748T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407963.1:c.2751T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407964.1:c.2988T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.2628T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.2244T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407967.1:c.2244T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.2991T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.3132T>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000608117Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(May 26, 2016) 		germlineclinical testing

Citation Link,

SCV003847499University of Washington Department of Laboratory Medicine, University of Washington
criteria provided, single submitter

(Dines et al. (Genet Med. 2020))		Likely benign
(Mar 23, 2023) 		germlinecuration

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, curation

Citations

PubMed

Systematic misclassification of missense variants in BRCA1 and BRCA2 "coldspots".

Dines JN, Shirts BH, Slavin TP, Walsh T, King MC, Fowler DM, Pritchard CC.

Genet Med. 2020 May;22(5):825-830. doi: 10.1038/s41436-019-0740-6. Epub 2020 Jan 8.

PubMed [citation]
PMID:
31911673
PMCID:
PMC7200594

Details of each submission

From Ambry Genetics, SCV000608117.4

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

Description

The p.I1044M variant (also known as c.3132T>G), located in coding exon 9 of the BRCA1 gene, results from a T to G substitution at nucleotide position 3132. The isoleucine at codon 1044 is replaced by methionine, an amino acid with highly similar properties. This variant was not reported in population based cohorts in the following databases: Database of Single Nucleotide Polymorphisms (dbSNP), NHLBI Exome Sequencing Project (ESP), and 1000 Genomes Project. In the ESP, this variant was not observed in 6502 samples (13004 alleles) with coverage at this position. To date, this alteration has been detected with an allele frequency of approximately 0.0003% (greater than 300000 alleles tested) in our clinical cohort. This amino acid position is poorly conserved in available vertebrate species. In addition, this alteration is predicted to be possibly damaging and deleterious by PolyPhen and SIFT in silico analyses, respectively. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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

From University of Washington Department of Laboratory Medicine, University of Washington, SCV003847499.1

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

Description

Missense variant in a coldspot region where missense variants are very unlikely to be pathogenic (PMID:31911673).

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

Last Updated: May 7, 2024