List of variants in gene BRCA2 reported as uncertain significance for Fanconi anemia, complementation group D1

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 108

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HGVS	dbSNP
NM_000059.3(BRCA2):c.*172G>A	rs574944914
NM_000059.3(BRCA2):c.*292A>C	rs886050112
NM_000059.3(BRCA2):c.*390A>G	rs56003538
NM_000059.3(BRCA2):c.*399T>C	rs886050115
NM_000059.3(BRCA2):c.*50A>G	rs761312704
NM_000059.3(BRCA2):c.*545T>C	rs536333595
NM_000059.3(BRCA2):c.*696G>A	rs886050118
NM_000059.3(BRCA2):c.*753C>T	rs190094748
NM_000059.3(BRCA2):c.*854T>C	rs572993583
NM_000059.3(BRCA2):c.1166C>A (p.Pro389Gln)	rs397507263
NM_000059.3(BRCA2):c.1247T>G (p.Ile416Ser)	rs80358418
NM_000059.3(BRCA2):c.1274A>G (p.Glu425Gly)	rs768169574
NM_000059.3(BRCA2):c.1460C>A (p.Ala487Glu)	rs56390402
NM_000059.3(BRCA2):c.1762A>G (p.Asn588Asp)	rs398122731
NM_000059.3(BRCA2):c.1889C>T (p.Thr630Ile)	rs80358479
NM_000059.3(BRCA2):c.2025A>G (p.Thr675=)	rs147381487
NM_000059.3(BRCA2):c.2186T>C (p.Ile729Thr)	rs431825296
NM_000059.3(BRCA2):c.2240A>G (p.Glu747Gly)	rs397507283
NM_000059.3(BRCA2):c.2412A>G (p.Glu804=)	rs587780866
NM_000059.3(BRCA2):c.2526A>G (p.Val842=)	rs770778164
NM_000059.3(BRCA2):c.2596G>A (p.Glu866Lys)	rs864622476
NM_000059.3(BRCA2):c.2606C>T (p.Ser869Leu)	rs80358523
NM_000059.3(BRCA2):c.2803G>C (p.Asp935His)	rs28897716
NM_000059.3(BRCA2):c.316+13A>G	rs773097109
NM_000059.3(BRCA2):c.3226G>A (p.Val1076Ile)	rs431825304
NM_000059.3(BRCA2):c.323A>G (p.Asn108Ser)	rs80358568
NM_000059.3(BRCA2):c.3415A>C (p.Lys1139Gln)	rs747903103
NM_000059.3(BRCA2):c.3447G>A (p.Met1149Ile)	rs876660471
NM_000059.3(BRCA2):c.3495T>C (p.His1165=)	rs776655838
NM_000059.3(BRCA2):c.3497T>A (p.Val1166Asp)	rs762886975
NM_000059.3(BRCA2):c.3824T>C (p.Ile1275Thr)	rs80358625
NM_000059.3(BRCA2):c.4534C>T (p.Arg1512Cys)	rs80358684
NM_000059.3(BRCA2):c.4599A>C (p.Lys1533Asn)	rs80358694
NM_000059.3(BRCA2):c.4686A>G (p.Gln1562=)	rs28897730
NM_000059.3(BRCA2):c.4828G>A (p.Val1610Met)	rs80358705
NM_000059.3(BRCA2):c.506A>G (p.Lys169Arg)	rs80358730
NM_000059.3(BRCA2):c.517-4C>G	rs81002804
NM_000059.3(BRCA2):c.5267T>A (p.Val1756Glu)	rs770664957
NM_000059.3(BRCA2):c.5268A>G (p.Val1756=)	rs199879914
NM_000059.3(BRCA2):c.5414A>G (p.Asn1805Ser)	rs80358765
NM_000059.3(BRCA2):c.5455C>T (p.Pro1819Ser)	rs80358768
NM_000059.3(BRCA2):c.5602G>A (p.Asp1868Asn)	rs80358781
NM_000059.3(BRCA2):c.5604C>T (p.Asp1868=)	rs1401654517
NM_000059.3(BRCA2):c.561G>A (p.Glu187=)	rs754678843
NM_000059.3(BRCA2):c.587G>T (p.Ser196Ile)	rs80358818
NM_000059.3(BRCA2):c.608C>A (p.Thr203Asn)	rs398122547
NM_000059.3(BRCA2):c.6101G>A (p.Arg2034His)	rs80358849
NM_000059.3(BRCA2):c.628A>G (p.Ile210Val)	rs1555281106
NM_000059.3(BRCA2):c.6540G>C (p.Leu2180Phe)	rs398122560
NM_000059.3(BRCA2):c.6560C>T (p.Pro2187Leu)	rs56019712
NM_000059.3(BRCA2):c.6706G>A (p.Glu2236Lys)	rs41293503
NM_000059.3(BRCA2):c.6713A>G (p.Asp2238Gly)	rs80358895
NM_000059.3(BRCA2):c.6785T>G (p.Met2262Arg)	rs80358904
NM_000059.3(BRCA2):c.679G>A (p.Ala227Thr)	rs398122563
NM_000059.3(BRCA2):c.6821G>T (p.Gly2274Val)	rs55712212
NM_000059.3(BRCA2):c.6886A>C (p.Ile2296Leu)	rs576279166
NM_000059.3(BRCA2):c.7034A>G (p.Gln2345Arg)	rs876661187
NM_000059.3(BRCA2):c.7104G>A (p.Leu2368=)	rs764698623
NM_000059.3(BRCA2):c.7188G>A (p.Leu2396=)	rs587780871
NM_000059.3(BRCA2):c.7435+10G>A	rs81002793
NM_000059.3(BRCA2):c.7464A>C (p.Arg2488Ser)	rs80358969
NM_000059.3(BRCA2):c.7976+12G>A	rs81002827
NM_000059.3(BRCA2):c.8042C>G (p.Thr2681Arg)	rs587782519
NM_000059.3(BRCA2):c.8154T>C (p.Ile2718=)	rs148880015
NM_000059.3(BRCA2):c.8215G>A (p.Val2739Ile)	rs80359069
NM_000059.3(BRCA2):c.847A>G (p.Ile283Val)	rs80359097
NM_000059.3(BRCA2):c.8530G>A (p.Glu2844Lys)	rs755783122
NM_000059.3(BRCA2):c.8825C>T (p.Ala2942Val)	rs373227180
NM_000059.3(BRCA2):c.8834A>G (p.Gln2945Arg)	rs587781800
NM_000059.3(BRCA2):c.909T>G (p.Ser303=)	rs757430441
NM_000059.3(BRCA2):c.9106C>G (p.Gln3036Glu)	rs202155613
NM_000059.3(BRCA2):c.9218A>G (p.Asp3073Gly)	rs80359186
NM_000059.3(BRCA2):c.9433G>C (p.Val3145Leu)	rs587776476
NM_000059.3(BRCA2):c.9493A>G (p.Thr3165Ala)	rs587782568
NM_000059.3(BRCA2):c.956A>C (p.Asn319Thr)	rs55939572
NM_000059.3(BRCA2):c.9592T>C (p.Cys3198Arg)	rs80359229
NM_000059.3(BRCA2):c.9606G>A (p.Pro3202=)	rs755890067
NM_000059.3(BRCA2):c.9924C>T (p.Tyr3308=)	rs4987049
NM_000059.4(BRCA2):c.*134C>T
NM_000059.4(BRCA2):c.*271C>A
NM_000059.4(BRCA2):c.*623C>T
NM_000059.4(BRCA2):c.10110G>A (p.Arg3370=)	rs28897762
NM_000059.4(BRCA2):c.1012G>A (p.Ala338Thr)	rs80358396
NM_000059.4(BRCA2):c.10203G>A (p.Thr3401=)	rs147854265
NM_000059.4(BRCA2):c.1144A>C (p.Lys382Gln)	rs371454630
NM_000059.4(BRCA2):c.1151C>T (p.Ser384Phe)	rs41293475
NM_000059.4(BRCA2):c.1224G>A (p.Met408Ile)
NM_000059.4(BRCA2):c.125A>G (p.Tyr42Cys)	rs4987046
NM_000059.4(BRCA2):c.179A>G (p.Asn60Ser)	rs80358463
NM_000059.4(BRCA2):c.184T>C (p.Phe62Leu)
NM_000059.4(BRCA2):c.2416G>C (p.Asp806His)	rs56404215
NM_000059.4(BRCA2):c.2918C>T (p.Ser973Leu)	rs397507296
NM_000059.4(BRCA2):c.2987T>G (p.Leu996Arg)	rs80358545
NM_000059.4(BRCA2):c.3581G>A (p.Gly1194Asp)	rs28897721
NM_000059.4(BRCA2):c.5198C>T (p.Ser1733Phe)	rs55639415
NM_000059.4(BRCA2):c.5312G>A (p.Gly1771Asp)	rs80358755
NM_000059.4(BRCA2):c.5752C>T (p.His1918Tyr)	rs80358803
NM_000059.4(BRCA2):c.6317T>C (p.Leu2106Pro)	rs56172926
NM_000059.4(BRCA2):c.632-3C>T
NM_000059.4(BRCA2):c.7994A>G (p.Asp2665Gly)	rs28897745
NM_000059.4(BRCA2):c.844C>G (p.His282Asp)
NM_000059.4(BRCA2):c.8850G>T (p.Lys2950Asn)	rs28897754
NM_000059.4(BRCA2):c.8905G>A (p.Val2969Met)	rs59004709
NM_000059.4(BRCA2):c.9235G>A (p.Val3079Ile)	rs55933907
NM_000059.4(BRCA2):c.942A>G (p.Lys314=)	rs1384322636
NM_000059.4(BRCA2):c.9502-12T>G	rs81002803
NM_000059.4(BRCA2):c.956A>G (p.Asn319Ser)	rs55939572
NM_000059.4(BRCA2):c.9760A>G (p.Lys3254Glu)

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