ClinVar Miner

List of variants in gene BRCA2 reported as uncertain significance by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 138
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.322A>C (p.Asn108His) rs80358567 0.00034
NM_000059.4(BRCA2):c.2813C>A (p.Ala938Glu) rs55773834 0.00015
NM_000059.4(BRCA2):c.742G>A (p.Ala248Thr) rs55854959 0.00014
NM_000059.4(BRCA2):c.3262C>T (p.Pro1088Ser) rs80358572 0.00009
NM_000059.4(BRCA2):c.8215G>A (p.Val2739Ile) rs80359069 0.00009
NM_000059.4(BRCA2):c.506A>G (p.Lys169Arg) rs80358730 0.00008
NM_000059.4(BRCA2):c.3568C>T (p.Arg1190Trp) rs80358604 0.00007
NM_000059.4(BRCA2):c.841G>A (p.Asp281Asn) rs80359088 0.00007
NM_000059.4(BRCA2):c.2320A>G (p.Thr774Ala) rs55968715 0.00006
NM_000059.4(BRCA2):c.2957A>G (p.Asn986Ser) rs28897718 0.00006
NM_000059.4(BRCA2):c.3073A>G (p.Lys1025Glu) rs80358550 0.00006
NM_000059.4(BRCA2):c.6215C>G (p.Ser2072Cys) rs80358862 0.00006
NM_000059.4(BRCA2):c.6541G>C (p.Gly2181Arg) rs371067421 0.00006
NM_000059.4(BRCA2):c.8125A>G (p.Ser2709Gly) rs398122596 0.00006
NM_000059.4(BRCA2):c.1694C>T (p.Ala565Val) rs55821741 0.00005
NM_000059.4(BRCA2):c.5503A>G (p.Asn1835Asp) rs80358771 0.00005
NM_000059.4(BRCA2):c.5741G>C (p.Ser1914Thr) rs80358801 0.00005
NM_000059.4(BRCA2):c.8807T>C (p.Leu2936Ser) rs398122714 0.00005
NM_000059.4(BRCA2):c.9353T>C (p.Met3118Thr) rs56204128 0.00005
NM_000059.4(BRCA2):c.4531G>A (p.Glu1511Lys) rs376338226 0.00004
NM_000059.4(BRCA2):c.5927G>T (p.Gly1976Val) rs587782751 0.00004
NM_000059.4(BRCA2):c.6290C>T (p.Thr2097Met) rs80358866 0.00004
NM_000059.4(BRCA2):c.6295A>G (p.Arg2099Gly) rs398122551 0.00004
NM_000059.4(BRCA2):c.8755-19A>G rs398122713 0.00004
NM_000059.4(BRCA2):c.9677A>G (p.Tyr3226Cys) rs80359237 0.00004
NM_000059.4(BRCA2):c.1838T>G (p.Leu613Arg) rs587780646 0.00003
NM_000059.4(BRCA2):c.5228G>A (p.Ser1743Asn) rs587782714 0.00003
NM_000059.4(BRCA2):c.9086C>T (p.Ala3029Val) rs80359162 0.00003
NM_000059.4(BRCA2):c.9253A>C (p.Thr3085Pro) rs397507423 0.00003
NM_000059.4(BRCA2):c.10154G>A (p.Arg3385His) rs80358398 0.00002
NM_000059.4(BRCA2):c.2459A>G (p.Asp820Gly) rs80358511 0.00002
NM_000059.4(BRCA2):c.266C>T (p.Pro89Leu) rs748609599 0.00002
NM_000059.4(BRCA2):c.3697G>A (p.Ala1233Thr) rs80358613 0.00002
NM_000059.4(BRCA2):c.5423T>C (p.Ile1808Thr) rs397507350 0.00002
NM_000059.4(BRCA2):c.5428G>A (p.Val1810Ile) rs80358766 0.00002
NM_000059.4(BRCA2):c.5660C>T (p.Thr1887Met) rs397507795 0.00002
NM_000059.4(BRCA2):c.72A>T (p.Leu24Phe) rs397507909 0.00002
NM_000059.4(BRCA2):c.7507G>A (p.Val2503Ile) rs587782191 0.00002
NM_000059.4(BRCA2):c.7618C>A (p.Leu2540Met) rs397507390 0.00002
NM_000059.4(BRCA2):c.7822C>G (p.Pro2608Ala) rs879255308 0.00002
NM_000059.4(BRCA2):c.9728C>T (p.Pro3243Leu) rs80359241 0.00002
NM_000059.4(BRCA2):c.1159G>T (p.Val387Phe) rs869320791 0.00001
NM_000059.4(BRCA2):c.1225G>A (p.Glu409Lys) rs80358416 0.00001
NM_000059.4(BRCA2):c.1315T>G (p.Phe439Val) rs80358420 0.00001
NM_000059.4(BRCA2):c.1955C>G (p.Ser652Cys) rs1593895864 0.00001
NM_000059.4(BRCA2):c.2366A>G (p.Lys789Arg) rs587782062 0.00001
NM_000059.4(BRCA2):c.2933A>G (p.Asn978Ser) rs775890004 0.00001
NM_000059.4(BRCA2):c.3101T>C (p.Ile1034Thr) rs545974734 0.00001
NM_000059.4(BRCA2):c.3188A>G (p.Gln1063Arg) rs775030825 0.00001
NM_000059.4(BRCA2):c.3206C>T (p.Ser1069Phe) rs80358563 0.00001
NM_000059.4(BRCA2):c.3326C>T (p.Ala1109Val) rs41293479 0.00001
NM_000059.4(BRCA2):c.3407T>C (p.Ile1136Thr) rs398122765 0.00001
NM_000059.4(BRCA2):c.3414G>C (p.Gln1138His) rs398122766 0.00001
NM_000059.4(BRCA2):c.3635A>T (p.Asn1212Ile) rs80358609 0.00001
NM_000059.4(BRCA2):c.369A>C (p.Lys123Asn) rs1566218165 0.00001
NM_000059.4(BRCA2):c.4703A>G (p.Lys1568Arg) rs80358699 0.00001
NM_000059.4(BRCA2):c.5225A>T (p.Asn1742Ile) rs756463217 0.00001
NM_000059.4(BRCA2):c.7090G>A (p.Glu2364Lys) rs80358940 0.00001
NM_000059.4(BRCA2):c.7096C>G (p.Leu2366Val) rs80358941 0.00001
NM_000059.4(BRCA2):c.7347T>G (p.Ile2449Met) rs1057520563 0.00001
NM_000059.4(BRCA2):c.7628A>G (p.Tyr2543Cys) rs431825354 0.00001
NM_000059.4(BRCA2):c.7759C>T (p.Leu2587Phe) rs56335340 0.00001
NM_000059.4(BRCA2):c.7916C>T (p.Pro2639Leu) rs774723315 0.00001
NM_000059.4(BRCA2):c.8201C>T (p.Pro2734Leu) rs876658732 0.00001
NM_000059.4(BRCA2):c.8351G>A (p.Arg2784Gln) rs80359076 0.00001
NM_000059.4(BRCA2):c.839A>G (p.Lys280Arg) rs1306507591 0.00001
NM_000059.4(BRCA2):c.8417C>T (p.Ser2806Leu) rs587782785 0.00001
NM_000059.4(BRCA2):c.8867A>C (p.Glu2956Ala) rs151174152 0.00001
NM_000059.4(BRCA2):c.9338T>C (p.Ile3113Thr) rs770003991 0.00001
NM_000059.4(BRCA2):c.9433G>C (p.Val3145Leu) rs587776476 0.00001
NM_000059.4(BRCA2):c.9581C>A (p.Pro3194Gln) rs28897760 0.00001
NM_000059.4(BRCA2):c.971G>C (p.Arg324Thr) rs397507435 0.00001
NM_000059.4(BRCA2):c.9905G>A (p.Arg3302Lys) rs80359249 0.00001
NM_000059.4(BRCA2):c.9997C>G (p.Leu3333Val) rs567476314 0.00001
NM_000059.4(BRCA2):c.10048C>T (p.Gln3350Ter)
NM_000059.4(BRCA2):c.10230C>A (p.Asp3410Glu) rs80358404
NM_000059.4(BRCA2):c.1211A>G (p.Asn404Ser) rs80358414
NM_000059.4(BRCA2):c.1666A>G (p.Asn556Asp) rs587781794
NM_000059.4(BRCA2):c.1963C>A (p.Pro655Thr) rs1566225847
NM_000059.4(BRCA2):c.199A>G (p.Arg67Gly) rs1566215868
NM_000059.4(BRCA2):c.2097G>T (p.Gln699His) rs80358486
NM_000059.4(BRCA2):c.2125C>G (p.Leu709Val) rs80358489
NM_000059.4(BRCA2):c.2245A>G (p.Ser749Gly) rs80358495
NM_000059.4(BRCA2):c.2782G>T (p.Val928Phe)
NM_000059.4(BRCA2):c.2791G>A (p.Gly931Arg) rs1555282848
NM_000059.4(BRCA2):c.2957A>T (p.Asn986Ile) rs28897718
NM_000059.4(BRCA2):c.3179G>A (p.Ser1060Asn) rs2072474262
NM_000059.4(BRCA2):c.3553A>G (p.Thr1185Ala) rs786202485
NM_000059.4(BRCA2):c.3772A>G (p.Ile1258Val) rs587782720
NM_000059.4(BRCA2):c.3826G>A (p.Glu1276Lys) rs878853575
NM_000059.4(BRCA2):c.3966_3968del (p.Asn1322del) rs397507319
NM_000059.4(BRCA2):c.3987A>T (p.Arg1329Ser) rs786203361
NM_000059.4(BRCA2):c.4025G>A (p.Ser1342Asn) rs1270552356
NM_000059.4(BRCA2):c.4143AGA[1] (p.Glu1382del) rs80359432
NM_000059.4(BRCA2):c.4237A>G (p.Lys1413Glu) rs876661198
NM_000059.4(BRCA2):c.4355A>G (p.Gln1452Arg) rs56317927
NM_000059.4(BRCA2):c.4464C>A (p.His1488Gln) rs786203743
NM_000059.4(BRCA2):c.451G>A (p.Val151Ile) rs397507335
NM_000059.4(BRCA2):c.4611A>C (p.Glu1537Asp) rs786202313
NM_000059.4(BRCA2):c.4856A>G (p.Asn1619Ser) rs80358709
NM_000059.4(BRCA2):c.4969A>C (p.Asn1657His) rs587781599
NM_000059.4(BRCA2):c.5368G>C (p.Val1790Leu) rs1566232328
NM_000059.4(BRCA2):c.5492T>C (p.Ile1831Thr) rs587782007
NM_000059.4(BRCA2):c.5629AAC[1] (p.Asn1878del) rs794727015
NM_000059.4(BRCA2):c.5775G>C (p.Gln1925His) rs1593906484
NM_000059.4(BRCA2):c.6099A>G (p.Ile2033Met) rs80358848
NM_000059.4(BRCA2):c.6192G>C (p.Lys2064Asn) rs786202616
NM_000059.4(BRCA2):c.6415_6416delinsAT (p.Glu2139Ile) rs1064795067
NM_000059.4(BRCA2):c.641AAG[1] (p.Glu215del) rs80359588
NM_000059.4(BRCA2):c.6554C>T (p.Ala2185Val) rs980859921
NM_000059.4(BRCA2):c.6787G>A (p.Val2263Ile) rs1566235410
NM_000059.4(BRCA2):c.6871A>G (p.Asn2291Asp) rs80358911
NM_000059.4(BRCA2):c.6957A>C (p.Arg2319Ser) rs398122573
NM_000059.4(BRCA2):c.7045T>C (p.Phe2349Leu) rs1555285984
NM_000059.4(BRCA2):c.7067T>A (p.Phe2356Tyr) rs587781844
NM_000059.4(BRCA2):c.7095T>A (p.His2365Gln) rs370708814
NM_000059.4(BRCA2):c.7426G>A (p.Glu2476Lys) rs879248686
NM_000059.4(BRCA2):c.7600G>A (p.Ala2534Thr) rs1555286305
NM_000059.4(BRCA2):c.7685T>G (p.Phe2562Cys) rs587782715
NM_000059.4(BRCA2):c.793G>A (p.Gly265Arg) rs1403242422
NM_000059.4(BRCA2):c.7953G>T (p.Arg2651Ser) rs752351454
NM_000059.4(BRCA2):c.7992T>G (p.Ile2664Met) rs80359800
NM_000059.4(BRCA2):c.8314G>A (p.Glu2772Lys) rs397507975
NM_000059.4(BRCA2):c.8324T>C (p.Met2775Thr) rs80359073
NM_000059.4(BRCA2):c.8324T>G (p.Met2775Arg) rs80359073
NM_000059.4(BRCA2):c.8368A>T (p.Thr2790Ser) rs80359081
NM_000059.4(BRCA2):c.8378G>A (p.Gly2793Glu) rs80359083
NM_000059.4(BRCA2):c.8789A>G (p.Asn2930Ser) rs397508008
NM_000059.4(BRCA2):c.8825C>T (p.Ala2942Val) rs373227180
NM_000059.4(BRCA2):c.883G>A (p.Val295Ile) rs1254525537
NM_000059.4(BRCA2):c.9019A>G (p.Arg3007Gly) rs397507417
NM_000059.4(BRCA2):c.9040T>G (p.Ser3014Ala)
NM_000059.4(BRCA2):c.9052_9057del (p.3015KS[2]) rs786202063
NM_000059.4(BRCA2):c.9175A>G (p.Lys3059Glu) rs80359174
NM_000059.4(BRCA2):c.9419C>A (p.Ala3140Asp)
NM_000059.4(BRCA2):c.9433G>A (p.Val3145Met) rs587776476
NM_000059.4(BRCA2):c.950C>A (p.Thr317Lys)
NM_000059.4(BRCA2):c.9945del (p.Glu3316fs) rs431825381

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.