ClinVar Miner

List of variants in gene BRCA2 reported as uncertain significance by Research Molecular Genetics Laboratory,Women's College Hospital, University of Toronto

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Total variants: 34
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HGVS dbSNP
NM_000059.3(BRCA2):c.1354C>A (p.Leu452Ile) rs80358424
NM_000059.3(BRCA2):c.2056C>T (p.Leu686Phe) rs1135401896
NM_000059.3(BRCA2):c.2198T>G (p.Val733Gly) rs1135401897
NM_000059.3(BRCA2):c.2963A>C (p.Asp988Ala) rs876659509
NM_000059.3(BRCA2):c.426-12_426-8del5 rs276174844
NM_000059.3(BRCA2):c.467A>G (p.Asp156Gly) rs68071147
NM_000059.3(BRCA2):c.476-9_476-8insT rs276174849
NM_000059.3(BRCA2):c.4850G>A (p.Ser1617Asn) rs397507341
NM_000059.3(BRCA2):c.5051C>G (p.Thr1684Ser) rs80358729
NM_000059.3(BRCA2):c.5609T>A (p.Phe1870Tyr) rs1135401908
NM_000059.3(BRCA2):c.5680_5682delTAC (p.Tyr1894del) rs1135401909
NM_000059.3(BRCA2):c.5870T>C (p.Ile1957Thr) rs587782320
NM_000059.3(BRCA2):c.6361G>A (p.Glu2121Lys) rs587782183
NM_000059.3(BRCA2):c.6413T>A (p.Val2138Asp) rs80358877
NM_000059.3(BRCA2):c.6441C>G (p.His2147Gln) rs80358879
NM_000059.3(BRCA2):c.68-7T>A rs81002830
NM_000059.3(BRCA2):c.7435+6G>A rs81002852
NM_000059.3(BRCA2):c.7799T>G (p.Phe2600Cys) rs1135401920
NM_000059.3(BRCA2):c.7805+3A>C rs81002810
NM_000059.3(BRCA2):c.7806-9T>G rs397507939
NM_000059.3(BRCA2):c.7868A>G (p.His2623Arg) rs80359012
NM_000059.3(BRCA2):c.7976+5G>A rs786201180
NM_000059.3(BRCA2):c.8009C>T (p.Ser2670Leu) rs80359035
NM_000059.3(BRCA2):c.8032A>G (p.Arg2678Gly) rs80359039
NM_000059.3(BRCA2):c.8229_8243del15 (p.Arg2744_Gly2748del) rs80359698
NM_000059.3(BRCA2):c.8332-9T>G rs1135401926
NM_000059.3(BRCA2):c.8364G>C (p.Trp2788Cys) rs397507981
NM_000059.3(BRCA2):c.8377G>A (p.Gly2793Arg) rs80359082
NM_000059.3(BRCA2):c.8473G>A (p.Ala2825Thr) rs587782874
NM_000059.3(BRCA2):c.86T>G (p.Leu29Arg) rs1135401889
NM_000059.3(BRCA2):c.9257-18C>A rs81002807
NM_000059.3(BRCA2):c.9271G>A (p.Val3091Ile) rs80359194
NM_000059.3(BRCA2):c.9338T>C (p.Ile3113Thr) rs770003991
NM_000059.3(BRCA2):c.9491A>T (p.Asn3164Ile) rs1135401930

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