ClinVar Miner

List of variants in gene BRCA2 reported as uncertain significance by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
Download table as spreadsheet
HGVS dbSNP
NM_000059.3(BRCA2):c.10076A>G (p.Glu3359Gly) rs80358389
NM_000059.3(BRCA2):c.10176del (p.Glu3393fs) rs80359258
NM_000059.3(BRCA2):c.121C>T (p.Pro41Ser) rs80358415
NM_000059.3(BRCA2):c.1368G>C (p.Glu456Asp) rs747489126
NM_000059.3(BRCA2):c.136C>T (p.Pro46Ser) rs80358425
NM_000059.3(BRCA2):c.165_167del rs11571587
NM_000059.3(BRCA2):c.1744A>G (p.Thr582Ala) rs80358457
NM_000059.3(BRCA2):c.1910-6G>A rs1555282344
NM_000059.3(BRCA2):c.2459A>G (p.Asp820Gly) rs80358511
NM_000059.3(BRCA2):c.2484T>C (p.Tyr828=) rs45619134
NM_000059.3(BRCA2):c.3032C>G (p.Thr1011Arg) rs80358548
NM_000059.3(BRCA2):c.3392G>A (p.Arg1131Lys) rs1555283214
NM_000059.3(BRCA2):c.3731T>C (p.Ile1244Thr) rs730881526
NM_000059.3(BRCA2):c.3788G>A (p.Ser1263Asn) rs1555283398
NM_000059.3(BRCA2):c.4315G>A (p.Ala1439Thr) rs80358666
NM_000059.3(BRCA2):c.4570T>G (p.Phe1524Val) rs56386506
NM_000059.3(BRCA2):c.5479A>G (p.Ile1827Val) rs80358770
NM_000059.3(BRCA2):c.5552T>G (p.Ile1851Ser) rs80358776
NM_000059.3(BRCA2):c.602C>T (p.Pro201Leu) rs397507822
NM_000059.3(BRCA2):c.6115T>A (p.Leu2039Ile) rs370026879
NM_000059.3(BRCA2):c.622G>C (p.Val208Leu) rs1593887544
NM_000059.3(BRCA2):c.66A>T (p.Ala22=) rs1555280115
NM_000059.3(BRCA2):c.673_675ACT[1] (p.Thr226del) rs1566220661
NM_000059.3(BRCA2):c.7056T>A (p.Pro2352=) rs276174888
NM_000059.3(BRCA2):c.7417T>C (p.Cys2473Arg) rs786202720
NM_000059.3(BRCA2):c.7601C>T (p.Ala2534Val) rs74047012
NM_000059.3(BRCA2):c.7661G>A (p.Ser2554Asn) rs398122588
NM_000059.3(BRCA2):c.8166A>G (p.Thr2722=) rs786201640
NM_000059.3(BRCA2):c.8416T>C (p.Ser2806Pro) rs1280487930
NM_000059.3(BRCA2):c.8775G>C (p.Gln2925His) rs80359136
NM_000059.3(BRCA2):c.9104A>G (p.Tyr3035Cys) rs80359165
NM_000059.3(BRCA2):c.9689T>C (p.Leu3230Ser) rs1476814134
NM_000059.3(BRCA2):c.9932C>T (p.Pro3311Leu) rs1060502416
NM_000059.4(BRCA2):c.10202C>T (p.Thr3401Met) rs55853199
NM_000059.4(BRCA2):c.2281T>C (p.Tyr761His) rs80358499
NM_000059.4(BRCA2):c.4928T>C (p.Val1643Ala) rs28897731
NM_000059.4(BRCA2):c.5634C>G (p.Asn1878Lys) rs80358784
NM_000059.4(BRCA2):c.5678G>A (p.Cys1893Tyr)
NM_000059.4(BRCA2):c.5869A>G (p.Ile1957Val) rs80358817
NM_000059.4(BRCA2):c.5870T>C (p.Ile1957Thr) rs587782320
NM_000059.4(BRCA2):c.5897A>G (p.His1966Arg) rs80358823
NM_000059.4(BRCA2):c.6263C>T (p.Thr2088Ile) rs767567428
NM_000059.4(BRCA2):c.68-7T>A rs81002830
NM_000059.4(BRCA2):c.7448G>A (p.Ser2483Asn) rs80358967
NM_000059.4(BRCA2):c.9244G>A (p.Val3082Met)
NM_000059.4(BRCA2):c.9501+3A>T rs61757642

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.