ClinVar Miner

List of variants in gene BRCA2 reported as uncertain significance by PreventionGenetics

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Gene type:
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Total variants: 42
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HGVS dbSNP
NM_000059.3(BRCA2):c.10095delinsGAATTATATCT (p.Ser3366fs) rs276174803
NM_000059.3(BRCA2):c.10230C>A (p.Asp3410Glu) rs80358404
NM_000059.3(BRCA2):c.1225G>A (p.Glu409Lys) rs80358416
NM_000059.3(BRCA2):c.1963C>A (p.Pro655Thr) rs1566225847
NM_000059.3(BRCA2):c.199A>G (p.Arg67Gly) rs1566215868
NM_000059.3(BRCA2):c.2097G>T (p.Gln699His) rs80358486
NM_000059.3(BRCA2):c.223G>C (p.Ala75Pro) rs28897701
NM_000059.3(BRCA2):c.2366A>G (p.Lys789Arg) rs587782062
NM_000059.3(BRCA2):c.2957A>T (p.Asn986Ile) rs28897718
NM_000059.3(BRCA2):c.3073A>G (p.Lys1025Glu) rs80358550
NM_000059.3(BRCA2):c.3101T>C (p.Ile1034Thr) rs545974734
NM_000059.3(BRCA2):c.3262C>T (p.Pro1088Ser) rs80358572
NM_000059.3(BRCA2):c.3326C>T (p.Ala1109Val) rs41293479
NM_000059.3(BRCA2):c.3568C>T (p.Arg1190Trp) rs80358604
NM_000059.3(BRCA2):c.3635A>T (p.Asn1212Ile) rs80358609
NM_000059.3(BRCA2):c.4531G>A (p.Glu1511Lys) rs376338226
NM_000059.3(BRCA2):c.4611A>C (p.Glu1537Asp) rs786202313
NM_000059.3(BRCA2):c.502C>A (p.Pro168Thr) rs80358726
NM_000059.3(BRCA2):c.5225A>T (p.Asn1742Ile) rs756463217
NM_000059.3(BRCA2):c.5368G>C (p.Val1790Leu) rs1566232328
NM_000059.3(BRCA2):c.5423T>C (p.Ile1808Thr) rs397507350
NM_000059.3(BRCA2):c.5428G>A (p.Val1810Ile) rs80358766
NM_000059.3(BRCA2):c.6290C>T (p.Thr2097Met) rs80358866
NM_000059.3(BRCA2):c.6323G>A (p.Arg2108His) rs35029074
NM_000059.3(BRCA2):c.641_643AAG[1] (p.Glu215del) rs80359588
NM_000059.3(BRCA2):c.6541G>C (p.Gly2181Arg) rs371067421
NM_000059.3(BRCA2):c.6957A>C (p.Arg2319Ser) rs398122573
NM_000059.3(BRCA2):c.7096C>G (p.Leu2366Val) rs80358941
NM_000059.3(BRCA2):c.7426G>A (p.Glu2476Lys)
NM_000059.3(BRCA2):c.742G>A (p.Ala248Thr) rs55854959
NM_000059.3(BRCA2):c.7916C>T (p.Pro2639Leu) rs774723315
NM_000059.3(BRCA2):c.793G>A (p.Gly265Arg) rs1403242422
NM_000059.3(BRCA2):c.7953G>T (p.Arg2651Ser) rs752351454
NM_000059.3(BRCA2):c.7992T>G (p.Ile2664Met) rs80359800
NM_000059.3(BRCA2):c.8368A>T (p.Thr2790Ser) rs80359081
NM_000059.3(BRCA2):c.8378G>A (p.Gly2793Glu) rs80359083
NM_000059.3(BRCA2):c.8417C>T (p.Ser2806Leu) rs587782785
NM_000059.3(BRCA2):c.841G>A (p.Asp281Asn) rs80359088
NM_000059.3(BRCA2):c.8755-19A>G rs398122713
NM_000059.3(BRCA2):c.9338T>C (p.Ile3113Thr) rs770003991
NM_000059.3(BRCA2):c.9699_9702del (p.Cys3233fs) rs80359775
NM_000059.3(BRCA2):c.9997C>G (p.Leu3333Val) rs567476314

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