ClinVar Miner

List of variants in gene BRCA2 reported as likely benign for breast carcinoma

Included ClinVar conditions (60):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 116
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HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.10234A>G (p.Ile3412Val) rs1801426 0.03864
NM_000059.4(BRCA2):c.7469T>C (p.Ile2490Thr) rs11571707 0.00868
NM_000059.4(BRCA2):c.3264T>C (p.Pro1088=) rs36060526 0.00793
NM_000059.4(BRCA2):c.5199C>T (p.Ser1733=) rs28897734 0.00488
NM_000059.4(BRCA2):c.4068G>A (p.Leu1356=) rs28897724 0.00295
NM_000059.4(BRCA2):c.68-7T>A rs81002830 0.00277
NM_000059.4(BRCA2):c.8182G>A (p.Val2728Ile) rs28897749 0.00239
NM_000059.4(BRCA2):c.8503T>C (p.Ser2835Pro) rs11571746 0.00202
NM_000059.4(BRCA2):c.1792A>G (p.Thr598Ala) rs28897710 0.00182
NM_000059.4(BRCA2):c.1938C>T (p.Ser646=) rs28897711 0.00096
NM_000059.4(BRCA2):c.978C>A (p.Ser326Arg) rs28897706 0.00082
NM_000059.4(BRCA2):c.1151C>T (p.Ser384Phe) rs41293475 0.00074
NM_000059.4(BRCA2):c.5198C>T (p.Ser1733Phe) rs55639415 0.00069
NM_000059.4(BRCA2):c.1964C>G (p.Pro655Arg) rs28897712 0.00054
NM_000059.4(BRCA2):c.2803G>A (p.Asp935Asn) rs28897716 0.00054
NM_000059.4(BRCA2):c.8187G>T (p.Lys2729Asn) rs80359065 0.00032
NM_000059.4(BRCA2):c.5785A>G (p.Ile1929Val) rs79538375 0.00031
NM_000059.4(BRCA2):c.1395A>C (p.Val465=) rs11571641 0.00026
NM_000059.4(BRCA2):c.1786G>C (p.Asp596His) rs56328701 0.00025
NM_000059.4(BRCA2):c.440A>G (p.Gln147Arg) rs80358674 0.00025
NM_000059.4(BRCA2):c.9876G>A (p.Pro3292=) rs369047997 0.00025
NM_000059.4(BRCA2):c.6322C>T (p.Arg2108Cys) rs55794205 0.00019
NM_000059.4(BRCA2):c.2350A>G (p.Met784Val) rs11571653 0.00018
NM_000059.4(BRCA2):c.3445A>G (p.Met1149Val) rs80358589 0.00013
NM_000059.4(BRCA2):c.943T>A (p.Cys315Ser) rs79483201 0.00011
NM_000059.4(BRCA2):c.5414A>G (p.Asn1805Ser) rs80358765 0.00010
NM_000059.4(BRCA2):c.1568A>G (p.His523Arg) rs80358443 0.00009
NM_000059.4(BRCA2):c.4656T>C (p.Gly1552=) rs41293491 0.00009
NM_000059.4(BRCA2):c.5455C>T (p.Pro1819Ser) rs80358768 0.00009
NM_000059.4(BRCA2):c.1662T>G (p.Cys554Trp) rs80358451 0.00006
NM_000059.4(BRCA2):c.6325G>A (p.Val2109Ile) rs79456940 0.00006
NM_000059.4(BRCA2):c.7052C>G (p.Ala2351Gly) rs80358932 0.00005
NM_000059.4(BRCA2):c.8090G>A (p.Ser2697Asn) rs80359051 0.00005
NM_000059.4(BRCA2):c.8092G>A (p.Ala2698Thr) rs80359052 0.00005
NM_000059.4(BRCA2):c.6739A>G (p.Ser2247Gly) rs80358896 0.00004
NM_000059.4(BRCA2):c.7102T>G (p.Leu2368Val) rs397507382 0.00004
NM_000059.4(BRCA2):c.8702G>A (p.Gly2901Asp) rs80359129 0.00004
NM_000059.4(BRCA2):c.1744A>C (p.Thr582Pro) rs80358457 0.00003
NM_000059.4(BRCA2):c.3910A>G (p.Thr1304Ala) rs28897723 0.00003
NM_000059.4(BRCA2):c.6847C>G (p.Pro2283Ala) rs80358909 0.00003
NM_000059.4(BRCA2):c.6935A>T (p.Asp2312Val) rs80358916 0.00003
NM_000059.4(BRCA2):c.1538A>G (p.Lys513Arg) rs28897709 0.00002
NM_000059.4(BRCA2):c.179A>G (p.Asn60Ser) rs80358463 0.00002
NM_000059.4(BRCA2):c.353G>A (p.Arg118His) rs80358603 0.00002
NM_000059.4(BRCA2):c.6550C>G (p.Gln2184Glu) rs80358887 0.00002
NM_000059.4(BRCA2):c.7986G>A (p.Thr2662=) rs1057522378 0.00002
NM_000059.4(BRCA2):c.10054C>G (p.Leu3352Val) rs1475702169 0.00001
NM_000059.4(BRCA2):c.10111A>G (p.Thr3371Ala) rs80358393 0.00001
NM_000059.4(BRCA2):c.10113T>C (p.Thr3371=) rs779075029 0.00001
NM_000059.4(BRCA2):c.10150C>T (p.Arg3384Ter) rs397507568 0.00001
NM_000059.4(BRCA2):c.1124C>T (p.Pro375Leu) rs80358409 0.00001
NM_000059.4(BRCA2):c.1159G>T (p.Val387Phe) rs869320791 0.00001
NM_000059.4(BRCA2):c.1179T>C (p.Cys393=) rs786201237 0.00001
NM_000059.4(BRCA2):c.2599A>G (p.Thr867Ala) rs80358522 0.00001
NM_000059.4(BRCA2):c.3085A>G (p.Met1029Val) rs80358553 0.00001
NM_000059.4(BRCA2):c.4685A>C (p.Gln1562Pro) rs544688816 0.00001
NM_000059.4(BRCA2):c.5028T>C (p.Ser1676=) rs762458631 0.00001
NM_000059.4(BRCA2):c.5225A>T (p.Asn1742Ile) rs756463217 0.00001
NM_000059.4(BRCA2):c.5487G>T (p.Leu1829Phe) rs779967765 0.00001
NM_000059.4(BRCA2):c.5683G>A (p.Glu1895Lys) rs146351301 0.00001
NM_000059.4(BRCA2):c.6264T>C (p.Thr2088=) rs750651726 0.00001
NM_000059.4(BRCA2):c.6458C>T (p.Pro2153Leu) rs276174873 0.00001
NM_000059.4(BRCA2):c.6467C>T (p.Ser2156Phe) rs765575482 0.00001
NM_000059.4(BRCA2):c.6772G>A (p.Glu2258Lys) rs730881549 0.00001
NM_000059.4(BRCA2):c.7222C>T (p.Pro2408Ser) rs398122577 0.00001
NM_000059.4(BRCA2):c.7633G>A (p.Val2545Ile) rs80358990 0.00001
NM_000059.4(BRCA2):c.8798G>C (p.Arg2933Thr) rs553440338 0.00001
NM_000059.4(BRCA2):c.959T>C (p.Leu320Pro) rs1334767632 0.00001
NM_000059.4(BRCA2):c.9983T>G (p.Phe3328Cys) rs770826575 0.00001
NM_000059.4(BRCA2):c.10013C>A (p.Ser3338Ter) rs1593202166
NM_000059.4(BRCA2):c.10072G>A (p.Gly3358Arg) rs1593202253
NM_000059.4(BRCA2):c.1117C>A (p.Gln373Lys)
NM_000059.4(BRCA2):c.1166C>T (p.Pro389Leu) rs397507263
NM_000059.4(BRCA2):c.1942T>A (p.Ser648Thr) rs1593895835
NM_000059.4(BRCA2):c.2024C>G (p.Thr675Arg) rs80358484
NM_000059.4(BRCA2):c.2091A>C (p.Lys697Asn) rs876659230
NM_000059.4(BRCA2):c.2515T>C (p.Tyr839His) rs587778125
NM_000059.4(BRCA2):c.2743A>T (p.Thr915Ser)
NM_000059.4(BRCA2):c.2779A>G (p.Met927Val) rs786201837
NM_000059.4(BRCA2):c.305A>G (p.Lys102Arg) rs80358549
NM_000059.4(BRCA2):c.3503T>C (p.Met1168Thr) rs80358598
NM_000059.4(BRCA2):c.3521G>A (p.Gly1174Asp) rs1555283272
NM_000059.4(BRCA2):c.3524A>G (p.Gln1175Arg)
NM_000059.4(BRCA2):c.362A>T (p.Lys121Ile)
NM_000059.4(BRCA2):c.3762G>T (p.Glu1254Asp) rs777028631
NM_000059.4(BRCA2):c.3767A>G (p.His1256Arg) rs80358618
NM_000059.4(BRCA2):c.3836A>G (p.Asn1279Ser) rs1060502384
NM_000059.4(BRCA2):c.397C>A (p.Pro133Thr) rs571823764
NM_000059.4(BRCA2):c.4028A>G (p.Lys1343Arg)
NM_000059.4(BRCA2):c.4059A>C (p.Glu1353Asp)
NM_000059.4(BRCA2):c.454A>G (p.Thr152Ala) rs886037806
NM_000059.4(BRCA2):c.4644A>C (p.Glu1548Asp)
NM_000059.4(BRCA2):c.464G>A (p.Arg155Lys) rs377639990
NM_000059.4(BRCA2):c.5025T>C (p.Cys1675=) rs370591460
NM_000059.4(BRCA2):c.5081G>A (p.Arg1694Lys) rs753721331
NM_000059.4(BRCA2):c.5386G>T (p.Asp1796Tyr) rs1064793715
NM_000059.4(BRCA2):c.5661G>A (p.Thr1887=) rs80359793
NM_000059.4(BRCA2):c.5860A>G (p.Thr1954Ala) rs1566233345
NM_000059.4(BRCA2):c.5987C>G (p.Ala1996Gly) rs80358834
NM_000059.4(BRCA2):c.6030C>A (p.Val2010=) rs786201328
NM_000059.4(BRCA2):c.6034T>C (p.Ser2012Pro)
NM_000059.4(BRCA2):c.6144T>G (p.Asn2048Lys) rs587782775
NM_000059.4(BRCA2):c.622G>C (p.Val208Leu) rs1593887544
NM_000059.4(BRCA2):c.631+7A>G rs431825339
NM_000059.4(BRCA2):c.6469C>G (p.Gln2157Glu) rs397507859
NM_000059.4(BRCA2):c.6742C>T (p.His2248Tyr)
NM_000059.4(BRCA2):c.68-7dup rs276174878
NM_000059.4(BRCA2):c.6842G>T (p.Gly2281Val) rs80358908
NM_000059.4(BRCA2):c.6884G>C (p.Arg2295Thr) rs1555285151
NM_000059.4(BRCA2):c.6916G>C (p.Ala2306Pro) rs730881550
NM_000059.4(BRCA2):c.6941C>T (p.Thr2314Ile) rs1177474377
NM_000059.4(BRCA2):c.7033C>G (p.Gln2345Glu) rs886040685
NM_000059.4(BRCA2):c.7095T>A (p.His2365Gln) rs370708814
NM_000059.4(BRCA2):c.9613_9614delinsCT (p.Ala3205Leu) rs276174926
NM_000059.4(BRCA2):c.9749C>T (p.Ser3250Leu)
NM_000059.4(BRCA2):c.9998T>C (p.Leu3333Pro) rs1555290016

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