ClinVar Miner

List of variants in gene BRCA2 reported by Laboratory of Molecular Diagnosis of Cancer,West China Hospital, Sichuan University

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 74
Download table as spreadsheet
HGVS dbSNP
NM_000059.3(BRCA2):c.10150C>G (p.Arg3384Gly) rs397507568
NM_000059.3(BRCA2):c.1190_1197del (p.Gln397fs) rs886037797
NM_000059.3(BRCA2):c.1211A>G (p.Asn404Ser) rs80358414
NM_000059.3(BRCA2):c.1399A>T (p.Lys467Ter) rs80358427
NM_000059.3(BRCA2):c.1462A>G (p.Ile488Val) rs864622352
NM_000059.3(BRCA2):c.1511C>G (p.Ser504Cys) rs886037807
NM_000059.3(BRCA2):c.1568A>G (p.His523Arg) rs80358443
NM_000059.3(BRCA2):c.1591A>G (p.Lys531Glu) rs876659050
NM_000059.3(BRCA2):c.161del (p.Asn54fs) rs878853297
NM_000059.3(BRCA2):c.171C>T (p.Tyr57=) rs201523522
NM_000059.3(BRCA2):c.1786G>A (p.Asp596Asn) rs56328701
NM_000059.3(BRCA2):c.2059_2063del (p.Leu686_Asp687insTer) rs587782780
NM_000059.3(BRCA2):c.2127G>C (p.Leu709=) rs554040246
NM_000059.3(BRCA2):c.2136G>T (p.Leu712=) rs886037813
NM_000059.3(BRCA2):c.2175dup (p.Val726fs) rs276174819
NM_000059.3(BRCA2):c.2186T>C (p.Ile729Thr) rs431825296
NM_000059.3(BRCA2):c.274C>T (p.Gln92Ter) rs80358529
NM_000059.3(BRCA2):c.2808_2811del (p.Ala938Profs) rs80359351
NM_000059.3(BRCA2):c.3001del (p.Ser1001fs) rs886037801
NM_000059.3(BRCA2):c.3052A>C (p.Lys1018Gln) rs886037810
NM_000059.3(BRCA2):c.3256A>G (p.Ile1086Val) rs80358571
NM_000059.3(BRCA2):c.3473A>G (p.Glu1158Gly) rs886037808
NM_000059.3(BRCA2):c.3475T>G (p.Cys1159Gly) rs886037814
NM_000059.3(BRCA2):c.352C>T (p.Arg118Cys) rs375125172
NM_000059.3(BRCA2):c.3834_3835del (p.His1278fs) rs886037803
NM_000059.3(BRCA2):c.4041_4042del (p.Cys1348fs) rs886037800
NM_000059.3(BRCA2):c.4148_4149del (p.Asp1383fs) rs886037799
NM_000059.3(BRCA2):c.4151del (p.Leu1384fs) rs397507710
NM_000059.3(BRCA2):c.4376A>G (p.Asn1459Ser) rs117187202
NM_000059.3(BRCA2):c.4548C>G (p.Ile1516Met) rs886037815
NM_000059.3(BRCA2):c.454A>G (p.Thr152Ala) rs886037806
NM_000059.3(BRCA2):c.4578A>G (p.Thr1526=) rs202022822
NM_000059.3(BRCA2):c.461A>G (p.Gln154Arg) rs756335278
NM_000059.3(BRCA2):c.4906A>G (p.Lys1636Glu) rs398122788
NM_000059.3(BRCA2):c.4915G>A (p.Val1639Ile) rs80358716
NM_000059.3(BRCA2):c.5206C>T (p.Gln1736Ter) rs886037802
NM_000059.3(BRCA2):c.5345A>G (p.Gln1782Arg) rs758959174
NM_000059.3(BRCA2):c.5487G>T (p.Leu1829Phe) rs779967765
NM_000059.3(BRCA2):c.5590G>A (p.Asp1864Asn) rs587781536
NM_000059.3(BRCA2):c.5645C>A (p.Ser1882Ter) rs80358785
NM_000059.3(BRCA2):c.5683G>A (p.Glu1895Lys) rs146351301
NM_000059.3(BRCA2):c.6148G>A (p.Val2050Ile) rs80358854
NM_000059.3(BRCA2):c.6235G>T (p.Val2079Leu) rs886037812
NM_000059.3(BRCA2):c.6256A>G (p.Ile2086Val) rs886037811
NM_000059.3(BRCA2):c.6325G>A (p.Val2109Ile) rs79456940
NM_000059.3(BRCA2):c.6405_6409del (p.Asn2135fs) rs80359584
NM_000059.3(BRCA2):c.641_643AAG[1] (p.Glu215del) rs80359588
NM_000059.3(BRCA2):c.6532dup (p.His2178fs) rs886037798
NM_000059.3(BRCA2):c.6553del (p.Ala2185fs) rs80359603
NM_000059.3(BRCA2):c.6598T>C (p.Phe2200Leu) rs886037809
NM_000059.3(BRCA2):c.67+1G>C rs81002796
NM_000059.3(BRCA2):c.6952C>T (p.Arg2318Ter) rs80358920
NM_000059.3(BRCA2):c.7188G>A (p.Leu2396=) rs587780871
NM_000059.3(BRCA2):c.7509C>T (p.Val2503=) rs766080516
NM_000059.3(BRCA2):c.7521A>G (p.Pro2507=) rs759383358
NM_000059.3(BRCA2):c.7522G>A (p.Gly2508Ser) rs80358978
NM_000059.3(BRCA2):c.7545A>G (p.Thr2515=) rs767555621
NM_000059.3(BRCA2):c.7672G>C (p.Glu2558Gln) rs886037816
NM_000059.3(BRCA2):c.7772A>G (p.Asn2591Ser) rs80359006
NM_000059.3(BRCA2):c.7967T>C (p.Leu2656Pro) rs886037817
NM_000059.3(BRCA2):c.8322dupT (p.Met2775Tyrfs) rs80359706
NM_000059.3(BRCA2):c.8329A>G (p.Lys2777Glu) rs886037818
NM_000059.3(BRCA2):c.8500A>G (p.Thr2834Ala) rs886037819
NM_000059.3(BRCA2):c.8632G>A (p.Glu2878Lys) rs398122710
NM_000059.3(BRCA2):c.8633_8755del
NM_000059.3(BRCA2):c.9011del (p.Lys3004fs) rs886037804
NM_000059.3(BRCA2):c.9014G>C (p.Arg3005Thr) rs886037821
NM_000059.3(BRCA2):c.9020G>A (p.Arg3007Lys) rs886037820
NM_000059.3(BRCA2):c.9285C>T (p.Asp3095=) rs80359198
NM_000059.3(BRCA2):c.92G>T (p.Trp31Leu) rs397508045
NM_000059.3(BRCA2):c.9318G>A (p.Trp3106Ter) rs771203198
NM_000059.3(BRCA2):c.9382C>T (p.Arg3128Ter) rs80359212
NM_000059.3(BRCA2):c.9401del (p.Gly3134fs) rs80359759
NM_000059.3(BRCA2):c.9753del (p.Lys3251fs) rs886037805

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.