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NM_007294.4(BRCA1):c.3205C>T (p.Gln1069Ter) AND Hereditary breast ovarian cancer syndrome

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Jun 4, 2023
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:
RCV001381235.15

Allele description [Variation Report for NM_007294.4(BRCA1):c.3205C>T (p.Gln1069Ter)]

NM_007294.4(BRCA1):c.3205C>T (p.Gln1069Ter)

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.3205C>T (p.Gln1069Ter)
HGVS:
  • NC_000017.11:g.43092326G>A
  • NG_005905.2:g.125658C>T
  • NG_087068.1:g.1308G>A
  • NM_001407571.1:c.2992C>T
  • NM_001407581.1:c.3205C>T
  • NM_001407582.1:c.3205C>T
  • NM_001407583.1:c.3205C>T
  • NM_001407585.1:c.3205C>T
  • NM_001407587.1:c.3202C>T
  • NM_001407590.1:c.3202C>T
  • NM_001407591.1:c.3202C>T
  • NM_001407593.1:c.3205C>T
  • NM_001407594.1:c.3205C>T
  • NM_001407596.1:c.3205C>T
  • NM_001407597.1:c.3205C>T
  • NM_001407598.1:c.3205C>T
  • NM_001407602.1:c.3205C>T
  • NM_001407603.1:c.3205C>T
  • NM_001407605.1:c.3205C>T
  • NM_001407610.1:c.3202C>T
  • NM_001407611.1:c.3202C>T
  • NM_001407612.1:c.3202C>T
  • NM_001407613.1:c.3202C>T
  • NM_001407614.1:c.3202C>T
  • NM_001407615.1:c.3202C>T
  • NM_001407616.1:c.3205C>T
  • NM_001407617.1:c.3205C>T
  • NM_001407618.1:c.3205C>T
  • NM_001407619.1:c.3205C>T
  • NM_001407620.1:c.3205C>T
  • NM_001407621.1:c.3205C>T
  • NM_001407622.1:c.3205C>T
  • NM_001407623.1:c.3205C>T
  • NM_001407624.1:c.3205C>T
  • NM_001407625.1:c.3205C>T
  • NM_001407626.1:c.3205C>T
  • NM_001407627.1:c.3202C>T
  • NM_001407628.1:c.3202C>T
  • NM_001407629.1:c.3202C>T
  • NM_001407630.1:c.3202C>T
  • NM_001407631.1:c.3202C>T
  • NM_001407632.1:c.3202C>T
  • NM_001407633.1:c.3202C>T
  • NM_001407634.1:c.3202C>T
  • NM_001407635.1:c.3202C>T
  • NM_001407636.1:c.3202C>T
  • NM_001407637.1:c.3202C>T
  • NM_001407638.1:c.3202C>T
  • NM_001407639.1:c.3205C>T
  • NM_001407640.1:c.3205C>T
  • NM_001407641.1:c.3205C>T
  • NM_001407642.1:c.3205C>T
  • NM_001407644.1:c.3202C>T
  • NM_001407645.1:c.3202C>T
  • NM_001407646.1:c.3196C>T
  • NM_001407647.1:c.3196C>T
  • NM_001407648.1:c.3082C>T
  • NM_001407649.1:c.3079C>T
  • NM_001407652.1:c.3205C>T
  • NM_001407653.1:c.3127C>T
  • NM_001407654.1:c.3127C>T
  • NM_001407655.1:c.3127C>T
  • NM_001407656.1:c.3127C>T
  • NM_001407657.1:c.3127C>T
  • NM_001407658.1:c.3127C>T
  • NM_001407659.1:c.3124C>T
  • NM_001407660.1:c.3124C>T
  • NM_001407661.1:c.3124C>T
  • NM_001407662.1:c.3124C>T
  • NM_001407663.1:c.3127C>T
  • NM_001407664.1:c.3082C>T
  • NM_001407665.1:c.3082C>T
  • NM_001407666.1:c.3082C>T
  • NM_001407667.1:c.3082C>T
  • NM_001407668.1:c.3082C>T
  • NM_001407669.1:c.3082C>T
  • NM_001407670.1:c.3079C>T
  • NM_001407671.1:c.3079C>T
  • NM_001407672.1:c.3079C>T
  • NM_001407673.1:c.3079C>T
  • NM_001407674.1:c.3082C>T
  • NM_001407675.1:c.3082C>T
  • NM_001407676.1:c.3082C>T
  • NM_001407677.1:c.3082C>T
  • NM_001407678.1:c.3082C>T
  • NM_001407679.1:c.3082C>T
  • NM_001407680.1:c.3082C>T
  • NM_001407681.1:c.3082C>T
  • NM_001407682.1:c.3082C>T
  • NM_001407683.1:c.3082C>T
  • NM_001407684.1:c.3205C>T
  • NM_001407685.1:c.3079C>T
  • NM_001407686.1:c.3079C>T
  • NM_001407687.1:c.3079C>T
  • NM_001407688.1:c.3079C>T
  • NM_001407689.1:c.3079C>T
  • NM_001407690.1:c.3079C>T
  • NM_001407691.1:c.3079C>T
  • NM_001407692.1:c.3064C>T
  • NM_001407694.1:c.3064C>T
  • NM_001407695.1:c.3064C>T
  • NM_001407696.1:c.3064C>T
  • NM_001407697.1:c.3064C>T
  • NM_001407698.1:c.3064C>T
  • NM_001407724.1:c.3064C>T
  • NM_001407725.1:c.3064C>T
  • NM_001407726.1:c.3064C>T
  • NM_001407727.1:c.3064C>T
  • NM_001407728.1:c.3064C>T
  • NM_001407729.1:c.3064C>T
  • NM_001407730.1:c.3064C>T
  • NM_001407731.1:c.3064C>T
  • NM_001407732.1:c.3064C>T
  • NM_001407733.1:c.3064C>T
  • NM_001407734.1:c.3064C>T
  • NM_001407735.1:c.3064C>T
  • NM_001407736.1:c.3064C>T
  • NM_001407737.1:c.3064C>T
  • NM_001407738.1:c.3064C>T
  • NM_001407739.1:c.3064C>T
  • NM_001407740.1:c.3061C>T
  • NM_001407741.1:c.3061C>T
  • NM_001407742.1:c.3061C>T
  • NM_001407743.1:c.3061C>T
  • NM_001407744.1:c.3061C>T
  • NM_001407745.1:c.3061C>T
  • NM_001407746.1:c.3061C>T
  • NM_001407747.1:c.3061C>T
  • NM_001407748.1:c.3061C>T
  • NM_001407749.1:c.3061C>T
  • NM_001407750.1:c.3064C>T
  • NM_001407751.1:c.3064C>T
  • NM_001407752.1:c.3064C>T
  • NM_001407838.1:c.3061C>T
  • NM_001407839.1:c.3061C>T
  • NM_001407841.1:c.3061C>T
  • NM_001407842.1:c.3061C>T
  • NM_001407843.1:c.3061C>T
  • NM_001407844.1:c.3061C>T
  • NM_001407845.1:c.3061C>T
  • NM_001407846.1:c.3061C>T
  • NM_001407847.1:c.3061C>T
  • NM_001407848.1:c.3061C>T
  • NM_001407849.1:c.3061C>T
  • NM_001407850.1:c.3064C>T
  • NM_001407851.1:c.3064C>T
  • NM_001407852.1:c.3064C>T
  • NM_001407853.1:c.2992C>T
  • NM_001407854.1:c.3205C>T
  • NM_001407858.1:c.3205C>T
  • NM_001407859.1:c.3205C>T
  • NM_001407860.1:c.3202C>T
  • NM_001407861.1:c.3202C>T
  • NM_001407862.1:c.3004C>T
  • NM_001407863.1:c.3082C>T
  • NM_001407874.1:c.3001C>T
  • NM_001407875.1:c.3001C>T
  • NM_001407879.1:c.2995C>T
  • NM_001407881.1:c.2995C>T
  • NM_001407882.1:c.2995C>T
  • NM_001407884.1:c.2995C>T
  • NM_001407885.1:c.2995C>T
  • NM_001407886.1:c.2995C>T
  • NM_001407887.1:c.2995C>T
  • NM_001407889.1:c.2995C>T
  • NM_001407894.1:c.2992C>T
  • NM_001407895.1:c.2992C>T
  • NM_001407896.1:c.2992C>T
  • NM_001407897.1:c.2992C>T
  • NM_001407898.1:c.2992C>T
  • NM_001407899.1:c.2992C>T
  • NM_001407900.1:c.2995C>T
  • NM_001407902.1:c.2995C>T
  • NM_001407904.1:c.2995C>T
  • NM_001407906.1:c.2995C>T
  • NM_001407907.1:c.2995C>T
  • NM_001407908.1:c.2995C>T
  • NM_001407909.1:c.2995C>T
  • NM_001407910.1:c.2995C>T
  • NM_001407915.1:c.2992C>T
  • NM_001407916.1:c.2992C>T
  • NM_001407917.1:c.2992C>T
  • NM_001407918.1:c.2992C>T
  • NM_001407919.1:c.3082C>T
  • NM_001407920.1:c.2941C>T
  • NM_001407921.1:c.2941C>T
  • NM_001407922.1:c.2941C>T
  • NM_001407923.1:c.2941C>T
  • NM_001407924.1:c.2941C>T
  • NM_001407925.1:c.2941C>T
  • NM_001407926.1:c.2941C>T
  • NM_001407927.1:c.2941C>T
  • NM_001407928.1:c.2941C>T
  • NM_001407929.1:c.2941C>T
  • NM_001407930.1:c.2938C>T
  • NM_001407931.1:c.2938C>T
  • NM_001407932.1:c.2938C>T
  • NM_001407933.1:c.2941C>T
  • NM_001407934.1:c.2938C>T
  • NM_001407935.1:c.2941C>T
  • NM_001407936.1:c.2938C>T
  • NM_001407937.1:c.3082C>T
  • NM_001407938.1:c.3082C>T
  • NM_001407939.1:c.3082C>T
  • NM_001407940.1:c.3079C>T
  • NM_001407941.1:c.3079C>T
  • NM_001407942.1:c.3064C>T
  • NM_001407943.1:c.3061C>T
  • NM_001407944.1:c.3064C>T
  • NM_001407945.1:c.3064C>T
  • NM_001407946.1:c.2872C>T
  • NM_001407947.1:c.2872C>T
  • NM_001407948.1:c.2872C>T
  • NM_001407949.1:c.2872C>T
  • NM_001407950.1:c.2872C>T
  • NM_001407951.1:c.2872C>T
  • NM_001407952.1:c.2872C>T
  • NM_001407953.1:c.2872C>T
  • NM_001407954.1:c.2869C>T
  • NM_001407955.1:c.2869C>T
  • NM_001407956.1:c.2869C>T
  • NM_001407957.1:c.2872C>T
  • NM_001407958.1:c.2869C>T
  • NM_001407959.1:c.2824C>T
  • NM_001407960.1:c.2824C>T
  • NM_001407962.1:c.2821C>T
  • NM_001407963.1:c.2824C>T
  • NM_001407964.1:c.3061C>T
  • NM_001407965.1:c.2701C>T
  • NM_001407966.1:c.2317C>T
  • NM_001407967.1:c.2317C>T
  • NM_001407968.1:c.788-187C>T
  • NM_001407969.1:c.788-187C>T
  • NM_001407970.1:c.788-1294C>T
  • NM_001407971.1:c.788-1294C>T
  • NM_001407972.1:c.785-1294C>T
  • NM_001407973.1:c.788-1294C>T
  • NM_001407974.1:c.788-1294C>T
  • NM_001407975.1:c.788-1294C>T
  • NM_001407976.1:c.788-1294C>T
  • NM_001407977.1:c.788-1294C>T
  • NM_001407978.1:c.788-1294C>T
  • NM_001407979.1:c.788-1294C>T
  • NM_001407980.1:c.788-1294C>T
  • NM_001407981.1:c.788-1294C>T
  • NM_001407982.1:c.788-1294C>T
  • NM_001407983.1:c.788-1294C>T
  • NM_001407984.1:c.785-1294C>T
  • NM_001407985.1:c.785-1294C>T
  • NM_001407986.1:c.785-1294C>T
  • NM_001407990.1:c.788-1294C>T
  • NM_001407991.1:c.785-1294C>T
  • NM_001407992.1:c.785-1294C>T
  • NM_001407993.1:c.788-1294C>T
  • NM_001408392.1:c.785-1294C>T
  • NM_001408396.1:c.785-1294C>T
  • NM_001408397.1:c.785-1294C>T
  • NM_001408398.1:c.785-1294C>T
  • NM_001408399.1:c.785-1294C>T
  • NM_001408400.1:c.785-1294C>T
  • NM_001408401.1:c.785-1294C>T
  • NM_001408402.1:c.785-1294C>T
  • NM_001408403.1:c.788-1294C>T
  • NM_001408404.1:c.788-1294C>T
  • NM_001408406.1:c.791-1303C>T
  • NM_001408407.1:c.785-1294C>T
  • NM_001408408.1:c.779-1294C>T
  • NM_001408409.1:c.710-1294C>T
  • NM_001408410.1:c.647-1294C>T
  • NM_001408411.1:c.710-1294C>T
  • NM_001408412.1:c.710-1294C>T
  • NM_001408413.1:c.707-1294C>T
  • NM_001408414.1:c.710-1294C>T
  • NM_001408415.1:c.710-1294C>T
  • NM_001408416.1:c.707-1294C>T
  • NM_001408418.1:c.671-1294C>T
  • NM_001408419.1:c.671-1294C>T
  • NM_001408420.1:c.671-1294C>T
  • NM_001408421.1:c.668-1294C>T
  • NM_001408422.1:c.671-1294C>T
  • NM_001408423.1:c.671-1294C>T
  • NM_001408424.1:c.668-1294C>T
  • NM_001408425.1:c.665-1294C>T
  • NM_001408426.1:c.665-1294C>T
  • NM_001408427.1:c.665-1294C>T
  • NM_001408428.1:c.665-1294C>T
  • NM_001408429.1:c.665-1294C>T
  • NM_001408430.1:c.665-1294C>T
  • NM_001408431.1:c.668-1294C>T
  • NM_001408432.1:c.662-1294C>T
  • NM_001408433.1:c.662-1294C>T
  • NM_001408434.1:c.662-1294C>T
  • NM_001408435.1:c.662-1294C>T
  • NM_001408436.1:c.665-1294C>T
  • NM_001408437.1:c.665-1294C>T
  • NM_001408438.1:c.665-1294C>T
  • NM_001408439.1:c.665-1294C>T
  • NM_001408440.1:c.665-1294C>T
  • NM_001408441.1:c.665-1294C>T
  • NM_001408442.1:c.665-1294C>T
  • NM_001408443.1:c.665-1294C>T
  • NM_001408444.1:c.665-1294C>T
  • NM_001408445.1:c.662-1294C>T
  • NM_001408446.1:c.662-1294C>T
  • NM_001408447.1:c.662-1294C>T
  • NM_001408448.1:c.662-1294C>T
  • NM_001408450.1:c.662-1294C>T
  • NM_001408451.1:c.653-1294C>T
  • NM_001408452.1:c.647-1294C>T
  • NM_001408453.1:c.647-1294C>T
  • NM_001408454.1:c.647-1294C>T
  • NM_001408455.1:c.647-1294C>T
  • NM_001408456.1:c.647-1294C>T
  • NM_001408457.1:c.647-1294C>T
  • NM_001408458.1:c.647-1294C>T
  • NM_001408459.1:c.647-1294C>T
  • NM_001408460.1:c.647-1294C>T
  • NM_001408461.1:c.647-1294C>T
  • NM_001408462.1:c.644-1294C>T
  • NM_001408463.1:c.644-1294C>T
  • NM_001408464.1:c.644-1294C>T
  • NM_001408465.1:c.644-1294C>T
  • NM_001408466.1:c.647-1294C>T
  • NM_001408467.1:c.647-1294C>T
  • NM_001408468.1:c.644-1294C>T
  • NM_001408469.1:c.647-1294C>T
  • NM_001408470.1:c.644-1294C>T
  • NM_001408472.1:c.788-1294C>T
  • NM_001408473.1:c.785-1294C>T
  • NM_001408474.1:c.587-1294C>T
  • NM_001408475.1:c.584-1294C>T
  • NM_001408476.1:c.587-1294C>T
  • NM_001408478.1:c.578-1294C>T
  • NM_001408479.1:c.578-1294C>T
  • NM_001408480.1:c.578-1294C>T
  • NM_001408481.1:c.578-1294C>T
  • NM_001408482.1:c.578-1294C>T
  • NM_001408483.1:c.578-1294C>T
  • NM_001408484.1:c.578-1294C>T
  • NM_001408485.1:c.578-1294C>T
  • NM_001408489.1:c.578-1294C>T
  • NM_001408490.1:c.575-1294C>T
  • NM_001408491.1:c.575-1294C>T
  • NM_001408492.1:c.578-1294C>T
  • NM_001408493.1:c.575-1294C>T
  • NM_001408494.1:c.548-1294C>T
  • NM_001408495.1:c.545-1294C>T
  • NM_001408496.1:c.524-1294C>T
  • NM_001408497.1:c.524-1294C>T
  • NM_001408498.1:c.524-1294C>T
  • NM_001408499.1:c.524-1294C>T
  • NM_001408500.1:c.524-1294C>T
  • NM_001408501.1:c.524-1294C>T
  • NM_001408502.1:c.455-1294C>T
  • NM_001408503.1:c.521-1294C>T
  • NM_001408504.1:c.521-1294C>T
  • NM_001408505.1:c.521-1294C>T
  • NM_001408506.1:c.461-1294C>T
  • NM_001408507.1:c.461-1294C>T
  • NM_001408508.1:c.452-1294C>T
  • NM_001408509.1:c.452-1294C>T
  • NM_001408510.1:c.407-1294C>T
  • NM_001408511.1:c.404-1294C>T
  • NM_001408512.1:c.284-1294C>T
  • NM_001408513.1:c.578-1294C>T
  • NM_001408514.1:c.578-1294C>T
  • NM_007294.4:c.3205C>TMANE SELECT
  • NM_007297.4:c.3064C>T
  • NM_007298.4:c.788-1294C>T
  • NM_007299.4:c.788-1294C>T
  • NM_007300.4:c.3205C>T
  • NP_001394500.1:p.Gln998Ter
  • NP_001394510.1:p.Gln1069Ter
  • NP_001394511.1:p.Gln1069Ter
  • NP_001394512.1:p.Gln1069Ter
  • NP_001394514.1:p.Gln1069Ter
  • NP_001394516.1:p.Gln1068Ter
  • NP_001394519.1:p.Gln1068Ter
  • NP_001394520.1:p.Gln1068Ter
  • NP_001394522.1:p.Gln1069Ter
  • NP_001394523.1:p.Gln1069Ter
  • NP_001394525.1:p.Gln1069Ter
  • NP_001394526.1:p.Gln1069Ter
  • NP_001394527.1:p.Gln1069Ter
  • NP_001394531.1:p.Gln1069Ter
  • NP_001394532.1:p.Gln1069Ter
  • NP_001394534.1:p.Gln1069Ter
  • NP_001394539.1:p.Gln1068Ter
  • NP_001394540.1:p.Gln1068Ter
  • NP_001394541.1:p.Gln1068Ter
  • NP_001394542.1:p.Gln1068Ter
  • NP_001394543.1:p.Gln1068Ter
  • NP_001394544.1:p.Gln1068Ter
  • NP_001394545.1:p.Gln1069Ter
  • NP_001394546.1:p.Gln1069Ter
  • NP_001394547.1:p.Gln1069Ter
  • NP_001394548.1:p.Gln1069Ter
  • NP_001394549.1:p.Gln1069Ter
  • NP_001394550.1:p.Gln1069Ter
  • NP_001394551.1:p.Gln1069Ter
  • NP_001394552.1:p.Gln1069Ter
  • NP_001394553.1:p.Gln1069Ter
  • NP_001394554.1:p.Gln1069Ter
  • NP_001394555.1:p.Gln1069Ter
  • NP_001394556.1:p.Gln1068Ter
  • NP_001394557.1:p.Gln1068Ter
  • NP_001394558.1:p.Gln1068Ter
  • NP_001394559.1:p.Gln1068Ter
  • NP_001394560.1:p.Gln1068Ter
  • NP_001394561.1:p.Gln1068Ter
  • NP_001394562.1:p.Gln1068Ter
  • NP_001394563.1:p.Gln1068Ter
  • NP_001394564.1:p.Gln1068Ter
  • NP_001394565.1:p.Gln1068Ter
  • NP_001394566.1:p.Gln1068Ter
  • NP_001394567.1:p.Gln1068Ter
  • NP_001394568.1:p.Gln1069Ter
  • NP_001394569.1:p.Gln1069Ter
  • NP_001394570.1:p.Gln1069Ter
  • NP_001394571.1:p.Gln1069Ter
  • NP_001394573.1:p.Gln1068Ter
  • NP_001394574.1:p.Gln1068Ter
  • NP_001394575.1:p.Gln1066Ter
  • NP_001394576.1:p.Gln1066Ter
  • NP_001394577.1:p.Gln1028Ter
  • NP_001394578.1:p.Gln1027Ter
  • NP_001394581.1:p.Gln1069Ter
  • NP_001394582.1:p.Gln1043Ter
  • NP_001394583.1:p.Gln1043Ter
  • NP_001394584.1:p.Gln1043Ter
  • NP_001394585.1:p.Gln1043Ter
  • NP_001394586.1:p.Gln1043Ter
  • NP_001394587.1:p.Gln1043Ter
  • NP_001394588.1:p.Gln1042Ter
  • NP_001394589.1:p.Gln1042Ter
  • NP_001394590.1:p.Gln1042Ter
  • NP_001394591.1:p.Gln1042Ter
  • NP_001394592.1:p.Gln1043Ter
  • NP_001394593.1:p.Gln1028Ter
  • NP_001394594.1:p.Gln1028Ter
  • NP_001394595.1:p.Gln1028Ter
  • NP_001394596.1:p.Gln1028Ter
  • NP_001394597.1:p.Gln1028Ter
  • NP_001394598.1:p.Gln1028Ter
  • NP_001394599.1:p.Gln1027Ter
  • NP_001394600.1:p.Gln1027Ter
  • NP_001394601.1:p.Gln1027Ter
  • NP_001394602.1:p.Gln1027Ter
  • NP_001394603.1:p.Gln1028Ter
  • NP_001394604.1:p.Gln1028Ter
  • NP_001394605.1:p.Gln1028Ter
  • NP_001394606.1:p.Gln1028Ter
  • NP_001394607.1:p.Gln1028Ter
  • NP_001394608.1:p.Gln1028Ter
  • NP_001394609.1:p.Gln1028Ter
  • NP_001394610.1:p.Gln1028Ter
  • NP_001394611.1:p.Gln1028Ter
  • NP_001394612.1:p.Gln1028Ter
  • NP_001394613.1:p.Gln1069Ter
  • NP_001394614.1:p.Gln1027Ter
  • NP_001394615.1:p.Gln1027Ter
  • NP_001394616.1:p.Gln1027Ter
  • NP_001394617.1:p.Gln1027Ter
  • NP_001394618.1:p.Gln1027Ter
  • NP_001394619.1:p.Gln1027Ter
  • NP_001394620.1:p.Gln1027Ter
  • NP_001394621.1:p.Gln1022Ter
  • NP_001394623.1:p.Gln1022Ter
  • NP_001394624.1:p.Gln1022Ter
  • NP_001394625.1:p.Gln1022Ter
  • NP_001394626.1:p.Gln1022Ter
  • NP_001394627.1:p.Gln1022Ter
  • NP_001394653.1:p.Gln1022Ter
  • NP_001394654.1:p.Gln1022Ter
  • NP_001394655.1:p.Gln1022Ter
  • NP_001394656.1:p.Gln1022Ter
  • NP_001394657.1:p.Gln1022Ter
  • NP_001394658.1:p.Gln1022Ter
  • NP_001394659.1:p.Gln1022Ter
  • NP_001394660.1:p.Gln1022Ter
  • NP_001394661.1:p.Gln1022Ter
  • NP_001394662.1:p.Gln1022Ter
  • NP_001394663.1:p.Gln1022Ter
  • NP_001394664.1:p.Gln1022Ter
  • NP_001394665.1:p.Gln1022Ter
  • NP_001394666.1:p.Gln1022Ter
  • NP_001394667.1:p.Gln1022Ter
  • NP_001394668.1:p.Gln1022Ter
  • NP_001394669.1:p.Gln1021Ter
  • NP_001394670.1:p.Gln1021Ter
  • NP_001394671.1:p.Gln1021Ter
  • NP_001394672.1:p.Gln1021Ter
  • NP_001394673.1:p.Gln1021Ter
  • NP_001394674.1:p.Gln1021Ter
  • NP_001394675.1:p.Gln1021Ter
  • NP_001394676.1:p.Gln1021Ter
  • NP_001394677.1:p.Gln1021Ter
  • NP_001394678.1:p.Gln1021Ter
  • NP_001394679.1:p.Gln1022Ter
  • NP_001394680.1:p.Gln1022Ter
  • NP_001394681.1:p.Gln1022Ter
  • NP_001394767.1:p.Gln1021Ter
  • NP_001394768.1:p.Gln1021Ter
  • NP_001394770.1:p.Gln1021Ter
  • NP_001394771.1:p.Gln1021Ter
  • NP_001394772.1:p.Gln1021Ter
  • NP_001394773.1:p.Gln1021Ter
  • NP_001394774.1:p.Gln1021Ter
  • NP_001394775.1:p.Gln1021Ter
  • NP_001394776.1:p.Gln1021Ter
  • NP_001394777.1:p.Gln1021Ter
  • NP_001394778.1:p.Gln1021Ter
  • NP_001394779.1:p.Gln1022Ter
  • NP_001394780.1:p.Gln1022Ter
  • NP_001394781.1:p.Gln1022Ter
  • NP_001394782.1:p.Gln998Ter
  • NP_001394783.1:p.Gln1069Ter
  • NP_001394787.1:p.Gln1069Ter
  • NP_001394788.1:p.Gln1069Ter
  • NP_001394789.1:p.Gln1068Ter
  • NP_001394790.1:p.Gln1068Ter
  • NP_001394791.1:p.Gln1002Ter
  • NP_001394792.1:p.Gln1028Ter
  • NP_001394803.1:p.Gln1001Ter
  • NP_001394804.1:p.Gln1001Ter
  • NP_001394808.1:p.Gln999Ter
  • NP_001394810.1:p.Gln999Ter
  • NP_001394811.1:p.Gln999Ter
  • NP_001394813.1:p.Gln999Ter
  • NP_001394814.1:p.Gln999Ter
  • NP_001394815.1:p.Gln999Ter
  • NP_001394816.1:p.Gln999Ter
  • NP_001394818.1:p.Gln999Ter
  • NP_001394823.1:p.Gln998Ter
  • NP_001394824.1:p.Gln998Ter
  • NP_001394825.1:p.Gln998Ter
  • NP_001394826.1:p.Gln998Ter
  • NP_001394827.1:p.Gln998Ter
  • NP_001394828.1:p.Gln998Ter
  • NP_001394829.1:p.Gln999Ter
  • NP_001394831.1:p.Gln999Ter
  • NP_001394833.1:p.Gln999Ter
  • NP_001394835.1:p.Gln999Ter
  • NP_001394836.1:p.Gln999Ter
  • NP_001394837.1:p.Gln999Ter
  • NP_001394838.1:p.Gln999Ter
  • NP_001394839.1:p.Gln999Ter
  • NP_001394844.1:p.Gln998Ter
  • NP_001394845.1:p.Gln998Ter
  • NP_001394846.1:p.Gln998Ter
  • NP_001394847.1:p.Gln998Ter
  • NP_001394848.1:p.Gln1028Ter
  • NP_001394849.1:p.Gln981Ter
  • NP_001394850.1:p.Gln981Ter
  • NP_001394851.1:p.Gln981Ter
  • NP_001394852.1:p.Gln981Ter
  • NP_001394853.1:p.Gln981Ter
  • NP_001394854.1:p.Gln981Ter
  • NP_001394855.1:p.Gln981Ter
  • NP_001394856.1:p.Gln981Ter
  • NP_001394857.1:p.Gln981Ter
  • NP_001394858.1:p.Gln981Ter
  • NP_001394859.1:p.Gln980Ter
  • NP_001394860.1:p.Gln980Ter
  • NP_001394861.1:p.Gln980Ter
  • NP_001394862.1:p.Gln981Ter
  • NP_001394863.1:p.Gln980Ter
  • NP_001394864.1:p.Gln981Ter
  • NP_001394865.1:p.Gln980Ter
  • NP_001394866.1:p.Gln1028Ter
  • NP_001394867.1:p.Gln1028Ter
  • NP_001394868.1:p.Gln1028Ter
  • NP_001394869.1:p.Gln1027Ter
  • NP_001394870.1:p.Gln1027Ter
  • NP_001394871.1:p.Gln1022Ter
  • NP_001394872.1:p.Gln1021Ter
  • NP_001394873.1:p.Gln1022Ter
  • NP_001394874.1:p.Gln1022Ter
  • NP_001394875.1:p.Gln958Ter
  • NP_001394876.1:p.Gln958Ter
  • NP_001394877.1:p.Gln958Ter
  • NP_001394878.1:p.Gln958Ter
  • NP_001394879.1:p.Gln958Ter
  • NP_001394880.1:p.Gln958Ter
  • NP_001394881.1:p.Gln958Ter
  • NP_001394882.1:p.Gln958Ter
  • NP_001394883.1:p.Gln957Ter
  • NP_001394884.1:p.Gln957Ter
  • NP_001394885.1:p.Gln957Ter
  • NP_001394886.1:p.Gln958Ter
  • NP_001394887.1:p.Gln957Ter
  • NP_001394888.1:p.Gln942Ter
  • NP_001394889.1:p.Gln942Ter
  • NP_001394891.1:p.Gln941Ter
  • NP_001394892.1:p.Gln942Ter
  • NP_001394893.1:p.Gln1021Ter
  • NP_001394894.1:p.Gln901Ter
  • NP_001394895.1:p.Gln773Ter
  • NP_001394896.1:p.Gln773Ter
  • NP_009225.1:p.Gln1069Ter
  • NP_009225.1:p.Gln1069Ter
  • NP_009228.2:p.Gln1022Ter
  • NP_009231.2:p.Gln1069Ter
  • LRG_292t1:c.3205C>T
  • LRG_292:g.125658C>T
  • LRG_292p1:p.Gln1069Ter
  • NC_000017.10:g.41244343G>A
  • NM_007294.3:c.3205C>T
  • NR_027676.1:n.3341C>T
Protein change:
Q1001*
Links:
dbSNP: rs2053627043
NCBI 1000 Genomes Browser:
rs2053627043
Molecular consequence:
  • NM_001407968.1:c.788-187C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407969.1:c.788-187C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407970.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407971.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407972.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407973.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407974.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407975.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407976.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407977.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407978.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407979.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407980.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407981.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407982.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407983.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407984.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407985.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407986.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407990.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407991.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407992.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407993.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408392.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408396.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408397.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408398.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408399.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408400.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408401.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408402.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408403.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408404.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408406.1:c.791-1303C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408407.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408408.1:c.779-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408409.1:c.710-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408410.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408411.1:c.710-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408412.1:c.710-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408413.1:c.707-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408414.1:c.710-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408415.1:c.710-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408416.1:c.707-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408418.1:c.671-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408419.1:c.671-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408420.1:c.671-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408421.1:c.668-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408422.1:c.671-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408423.1:c.671-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408424.1:c.668-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408425.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408426.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408427.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408428.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408429.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408430.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408431.1:c.668-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408432.1:c.662-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408433.1:c.662-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408434.1:c.662-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408435.1:c.662-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408436.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408437.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408438.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408439.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408440.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408441.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408442.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408443.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408444.1:c.665-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408445.1:c.662-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408446.1:c.662-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408447.1:c.662-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408448.1:c.662-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408450.1:c.662-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408451.1:c.653-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408452.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408453.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408454.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408455.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408456.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408457.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408458.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408459.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408460.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408461.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408462.1:c.644-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408463.1:c.644-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408464.1:c.644-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408465.1:c.644-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408466.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408467.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408468.1:c.644-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408469.1:c.647-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408470.1:c.644-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408472.1:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408473.1:c.785-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408474.1:c.587-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408475.1:c.584-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408476.1:c.587-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408478.1:c.578-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408479.1:c.578-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408480.1:c.578-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408481.1:c.578-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408482.1:c.578-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408483.1:c.578-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408484.1:c.578-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408485.1:c.578-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408489.1:c.578-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408490.1:c.575-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408491.1:c.575-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408492.1:c.578-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408493.1:c.575-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408494.1:c.548-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408495.1:c.545-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408496.1:c.524-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408497.1:c.524-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408498.1:c.524-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408499.1:c.524-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408500.1:c.524-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408501.1:c.524-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408502.1:c.455-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408503.1:c.521-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408504.1:c.521-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408505.1:c.521-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408506.1:c.461-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408507.1:c.461-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408508.1:c.452-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408509.1:c.452-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408510.1:c.407-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408511.1:c.404-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408512.1:c.284-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408513.1:c.578-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408514.1:c.578-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.4:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.788-1294C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407571.1:c.2992C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407581.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407582.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407583.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407585.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407587.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407590.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407591.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407593.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407594.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407596.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407597.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407598.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407602.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407603.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407605.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407610.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407611.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407612.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407613.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407614.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407615.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407616.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407617.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407618.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407619.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407620.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407621.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407622.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407623.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407624.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407625.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407626.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407627.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407628.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407629.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407630.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407631.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407632.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407633.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407634.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407635.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407636.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407637.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407638.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407639.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407640.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407641.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407642.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407644.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407645.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407646.1:c.3196C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407647.1:c.3196C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407648.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407649.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407652.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407653.1:c.3127C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407654.1:c.3127C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407655.1:c.3127C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407656.1:c.3127C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407657.1:c.3127C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407658.1:c.3127C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407659.1:c.3124C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407660.1:c.3124C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407661.1:c.3124C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407662.1:c.3124C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407663.1:c.3127C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407664.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407665.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407666.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407667.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407668.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407669.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407670.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407671.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407672.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407673.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407674.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407675.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407676.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407677.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407678.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407679.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407680.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407681.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407682.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407683.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407684.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407685.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407686.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407687.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407688.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407689.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407690.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407691.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407692.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407694.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407695.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407696.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407697.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407698.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407724.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407725.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407726.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407727.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407728.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407729.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407730.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407731.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407732.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407733.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407734.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407735.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407736.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407737.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407738.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407739.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407740.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407741.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407742.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407743.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407744.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407745.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407746.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407747.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407748.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407749.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407750.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407751.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407752.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407838.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407839.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407841.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407842.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407843.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407844.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407845.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407846.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407847.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407848.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407849.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407850.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407851.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407852.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407853.1:c.2992C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407854.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407858.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407859.1:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407860.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407861.1:c.3202C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407862.1:c.3004C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407863.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407874.1:c.3001C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407875.1:c.3001C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407879.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407881.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407882.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407884.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407885.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407886.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407887.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407889.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407894.1:c.2992C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407895.1:c.2992C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407896.1:c.2992C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407897.1:c.2992C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407898.1:c.2992C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407899.1:c.2992C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407900.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407902.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407904.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407906.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407907.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407908.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407909.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407910.1:c.2995C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407915.1:c.2992C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407916.1:c.2992C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407917.1:c.2992C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407918.1:c.2992C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407919.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407920.1:c.2941C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407921.1:c.2941C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407922.1:c.2941C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407923.1:c.2941C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407924.1:c.2941C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407925.1:c.2941C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407926.1:c.2941C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407927.1:c.2941C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407928.1:c.2941C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407929.1:c.2941C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407930.1:c.2938C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407931.1:c.2938C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407932.1:c.2938C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407933.1:c.2941C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407934.1:c.2938C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407935.1:c.2941C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407936.1:c.2938C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407937.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407938.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407939.1:c.3082C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407940.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407941.1:c.3079C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407942.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407943.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407944.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407945.1:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407946.1:c.2872C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407947.1:c.2872C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407948.1:c.2872C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407949.1:c.2872C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407950.1:c.2872C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407951.1:c.2872C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407952.1:c.2872C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407953.1:c.2872C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407954.1:c.2869C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407955.1:c.2869C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407956.1:c.2869C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407957.1:c.2872C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407958.1:c.2869C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407959.1:c.2824C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407960.1:c.2824C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407962.1:c.2821C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407963.1:c.2824C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407964.1:c.3061C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407965.1:c.2701C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407966.1:c.2317C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001407967.1:c.2317C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_007294.4:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_007297.4:c.3064C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_007300.4:c.3205C>T - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

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

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001579546Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Pathogenic
(Jun 4, 2023)
germlineclinical testing

PubMed (3)
[See all records that cite these PMIDs]

Summary from all submissions

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

Citations

PubMed

Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study.

Borg A, Haile RW, Malone KE, Capanu M, Diep A, Törngren T, Teraoka S, Begg CB, Thomas DC, Concannon P, Mellemkjaer L, Bernstein L, Tellhed L, Xue S, Olson ER, Liang X, Dolle J, Børresen-Dale AL, Bernstein JL.

Hum Mutat. 2010 Mar;31(3):E1200-40. doi: 10.1002/humu.21202.

PubMed [citation]
PMID:
20104584
PMCID:
PMC2928257

Molecular characterization and clinical interpretation of BRCA1/BRCA2 variants in families from Murcia (south-eastern Spain) with hereditary breast and ovarian cancer: clinical-pathological features in BRCA carriers and non-carriers.

Gabaldó Barrios X, Sarabia Meseguer MD, Marín Vera M, Sánchez Bermúdez AI, Macías Cerrolaza JA, Sánchez Henarejos P, Zafra Poves M, García Hernández MR, Cuevas Tortosa E, Aliaga Baño Á, Castillo Guardiola V, Martínez Hernández P, Tovar Zapata I, Martínez Barba E, Ayala de la Peña F, Alonso Romero JL, Noguera Velasco JA, Ruiz Espejo F.

Fam Cancer. 2017 Oct;16(4):477-489. doi: 10.1007/s10689-017-9985-x.

PubMed [citation]
PMID:
28477318
See all PubMed Citations (3)

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV001579546.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (3)

Description

This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Gln1069*) in the BRCA1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in BRCA1 are known to be pathogenic (PMID: 20104584). This premature translational stop signal has been observed in individual(s) with hereditary breast and ovarian cancer syndrome (PMID: 28477318). For these reasons, this variant has been classified as Pathogenic. ClinVar contains an entry for this variant (Variation ID: 923489).

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

Last Updated: Nov 10, 2024