ClinVar Miner

List of variants reported as uncertain significance for Breast-ovarian cancer, familial 2 by Michigan Medical Genetics Laboratories,University of Michigan

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Total variants: 34
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HGVS dbSNP
NM_000059.3(BRCA2):c.1159G>T (p.Val387Phe) rs869320791
NM_000059.3(BRCA2):c.1355T>C (p.Leu452Pro) rs753512842
NM_000059.3(BRCA2):c.1594G>A (p.Glu532Lys) rs138734772
NM_000059.3(BRCA2):c.2152G>A (p.Glu718Lys) rs397507281
NM_000059.3(BRCA2):c.2184_2195dup (p.Asp728_Glu731dup) rs869320792
NM_000059.3(BRCA2):c.2695A>G (p.Asn899Asp) rs564197624
NM_000059.3(BRCA2):c.2813C>A (p.Ala938Glu) rs55773834
NM_000059.3(BRCA2):c.3437A>T (p.Glu1146Val) rs80358588
NM_000059.3(BRCA2):c.4271C>G (p.Ser1424Cys) rs80358664
NM_000059.3(BRCA2):c.4574A>G (p.His1525Arg) rs397507336
NM_000059.3(BRCA2):c.4648G>C (p.Glu1550Gln) rs80358695
NM_000059.3(BRCA2):c.4741G>A (p.Glu1581Lys) rs368952892
NM_000059.3(BRCA2):c.476-9dup rs276174849
NM_000059.3(BRCA2):c.4957A>G (p.Thr1653Ala) rs587782186
NM_000059.3(BRCA2):c.5244C>A (p.Ser1748Arg) rs398122528
NM_000059.3(BRCA2):c.5536A>G (p.Ile1846Val) rs587782375
NM_000059.3(BRCA2):c.5985C>T (p.Asn1995=) rs374620036
NM_000059.3(BRCA2):c.59A>G (p.Asn20Ser) rs398122544
NM_000059.3(BRCA2):c.6196G>A (p.Val2066Ile) rs397507365
NM_000059.3(BRCA2):c.6601T>C (p.Ser2201Pro) rs869320796
NM_000059.3(BRCA2):c.67+4T>C rs373546450
NM_000059.3(BRCA2):c.6803G>A (p.Arg2268Lys) rs80358906
NM_000059.3(BRCA2):c.682-25T>C rs373984939
NM_000059.3(BRCA2):c.694T>C (p.Tyr232His) rs398122572
NM_000059.3(BRCA2):c.7006C>T (p.Arg2336Cys) rs431825347
NM_000059.3(BRCA2):c.7007+31A>T rs555236509
NM_000059.3(BRCA2):c.7008-20_7008-17del rs276174887
NM_000059.3(BRCA2):c.7008-21T>C rs761989332
NM_000059.3(BRCA2):c.7618-19G>T rs371417084
NM_000059.3(BRCA2):c.7865A>G (p.Asn2622Ser) rs142899125
NM_000059.3(BRCA2):c.8435G>A (p.Gly2812Glu) rs80359091
NM_000059.3(BRCA2):c.8953+34T>C rs201726150
NM_000059.3(BRCA2):c.9256+7C>T rs373697701
NM_000059.3(BRCA2):c.9501+3A>T rs61757642

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