Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32359467_32364093delCA2580087377BRCA2c.7805+1538_8331+560del
c.7436+1538_7962+560del
c.272+1538_798+560del
c.7805+1538_8339+560del
c.370+1538_896+560del
c.7709+1538_8235+560del
 ClinVar
13g.32363288_32363304delinsTTGAGCGCAAATATATCCA2082835215BRCA2c.8086_8102delinsTTGAGCGCAAATATATC (p.Leu2696=)
c.7717_7733delinsTTGAGCGCAAATATATC (p.Leu2573=)
c.553_569delinsTTGAGCGCAAATATATC (p.Leu185=)
c.8094_8110delinsTTGAGCGCAAATATATC (n.8094_8110delinsTTGAGCGCAAATATATC)
c.651_667delinsTTGAGCGCAAATATATC
c.7990_8006delinsTTGAGCGCAAATATATC (p.Leu2664=)
13g.32363292_32363307delCA645509332BRCA2c.8090_8105del (p.Ser2697LysfsTer?)
c.7721_7736del (p.Ser2574LysfsTer?)
c.557_572del (p.Ser186LysfsTer?)
c.8098_8113del (n.8098_8113del)
c.655_670del
c.7994_8009del (p.Ser2665LysfsTer?)
 ClinVar dbSNP COSMIC
13g.32363301_32363315delCA2697551769BRCA2c.8099_8113del (p.Ile2700_Ser2704del)
c.7730_7744del (p.Ile2577_Ser2581del)
c.566_580del (p.Ile189_Ser193del)
c.8107_8121del (n.8107_8121del)
c.664_678del
c.8003_8017del (p.Ile2668_Ser2672del)
 ClinVar
13g.32363301delCA2573053825BRCA2c.8099del (p.Ile2700AsnfsTer?)
c.7730del (p.Ile2577AsnfsTer?)
c.566del (p.Ile189AsnfsTer?)
c.8107del (n.8107del)
c.664del
c.8003del (p.Ile2668AsnfsTer?)
 ClinVar dbSNP
13g.32363301T>ACA387749301BRCA2c.8099T>A (p.Ile2700Lys)
c.7730T>A (p.Ile2577Lys)
c.566T>A (p.Ile189Lys)
c.8107T>A (n.8107T>A)
c.664T>A
c.8003T>A (p.Ile2668Lys)
 ClinVar dbSNP
13g.32363301T>CCA025453BRCA2c.8099T>C (p.Ile2700Thr)
c.7730T>C (p.Ile2577Thr)
c.566T>C (p.Ile189Thr)
c.8107T>C (n.8107T>C)
c.664T>C
c.8003T>C (p.Ile2668Thr)
 ClinVar dbSNP
13g.32363301T>GCA387749302BRCA2c.8099T>G (p.Ile2700Arg)
c.7730T>G (p.Ile2577Arg)
c.566T>G (p.Ile189Arg)
c.8107T>G (n.8107T>G)
c.664T>G
c.8003T>G (p.Ile2668Arg)
13g.32363301T=CA2082835293BRCA2c.8099T= (p.Ile2700=)
c.7730T= (p.Ile2577=)
c.566T= (p.Ile189=)
c.8107T= (n.8107T=)
c.664T=
c.8003T= (p.Ile2668=)
13g.32363301dupCA2739277542BRCA2c.8099dup (p.Ser2701IlefsTer2)
c.7730dup (p.Ser2578IlefsTer2)
c.566dup (p.Ser190IlefsTer2)
c.8107dup (n.8107dup)
c.664dup
c.8003dup (p.Ser2669IlefsTer2)
 ClinVar
13g.32363302A=CA2082835303BRCA2c.8100A= (p.Ile2700=)
c.7731A= (p.Ile2577=)
c.567A= (p.Ile189=)
c.8108A= (n.8108A=)
c.665A=
c.8004A= (p.Ile2668=)
13g.32363302A>CCA483439596BRCA2c.8100A>C (p.Ile2700=)
c.7731A>C (p.Ile2577=)
c.567A>C (p.Ile189=)
c.8108A>C (n.8108A>C)
c.665A>C
c.8004A>C (p.Ile2668=)
13g.32363302A>GCA387749304BRCA2c.8100A>G (p.Ile2700Met)
c.7731A>G (p.Ile2577Met)
c.567A>G (p.Ile189Met)
c.8108A>G (n.8108A>G)
c.665A>G
c.8004A>G (p.Ile2668Met)
 ClinVar dbSNP
13g.32363302A>TCA483439600BRCA2c.8100A>T (p.Ile2700=)
c.7731A>T (p.Ile2577=)
c.567A>T (p.Ile189=)
c.8108A>T (n.8108A>T)
c.665A>T
c.8004A>T (p.Ile2668=)
 dbSNP
13g.32363303T>ACA387749306BRCA2c.8101T>A (p.Ser2701Thr)
c.7732T>A (p.Ser2578Thr)
c.568T>A (p.Ser190Thr)
c.8109T>A (n.8109T>A)
c.666T>A
c.8005T>A (p.Ser2669Thr)
 dbSNP
13g.32363303T>CCA025455BRCA2c.8101T>C (p.Ser2701Pro)
c.7732T>C (p.Ser2578Pro)
c.568T>C (p.Ser190Pro)
c.8109T>C (n.8109T>C)
c.666T>C
c.8005T>C (p.Ser2669Pro)
 ClinVar dbSNP gnomAD v4
13g.32363303T>GCA387749309BRCA2c.8101T>G (p.Ser2701Ala)
c.7732T>G (p.Ser2578Ala)
c.568T>G (p.Ser190Ala)
c.8109T>G (n.8109T>G)
c.666T>G
c.8005T>G (p.Ser2669Ala)
13g.32363303T=CA2082835315BRCA2c.8101T= (p.Ser2701=)
c.7732T= (p.Ser2578=)
c.568T= (p.Ser190=)
c.8109T= (n.8109T=)
c.666T=
c.8005T= (p.Ser2669=)
13g.32363304C>ACA387749311BRCA2c.8102C>A (p.Ser2701Tyr)
c.7733C>A (p.Ser2578Tyr)
c.569C>A (p.Ser190Tyr)
c.8110C>A (n.8110C>A)
c.667C>A
c.8006C>A (p.Ser2669Tyr)
13g.32363304C=CA2082835326BRCA2c.8102C= (p.Ser2701=)
c.7733C= (p.Ser2578=)
c.569C= (p.Ser190=)
c.8110C= (n.8110C=)
c.667C=
c.8006C= (p.Ser2669=)
13g.32363304C>GCA10579767BRCA2c.8102C>G (p.Ser2701Cys)
c.7733C>G (p.Ser2578Cys)
c.569C>G (p.Ser190Cys)
c.8110C>G (n.8110C>G)
c.667C>G
c.8006C>G (p.Ser2669Cys)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32363304C>TCA387749314BRCA2c.8102C>T (p.Ser2701Phe)
c.7733C>T (p.Ser2578Phe)
c.569C>T (p.Ser190Phe)
c.8110C>T (n.8110C>T)
c.667C>T
c.8006C>T (p.Ser2669Phe)
 ClinVar dbSNP
13g.32363305T>ACA483439601BRCA2c.8103T>A (p.Ser2701=)
c.7734T>A (p.Ser2578=)
c.570T>A (p.Ser190=)
c.8111T>A (n.8111T>A)
c.668T>A
c.8007T>A (p.Ser2669=)
 dbSNP
13g.32363305T>CCA483439602BRCA2c.8103T>C (p.Ser2701=)
c.7734T>C (p.Ser2578=)
c.570T>C (p.Ser190=)
c.8111T>C (n.8111T>C)
c.668T>C
c.8007T>C (p.Ser2669=)
 ClinVar dbSNP
13g.32363305T>GCA025456BRCA2c.8103T>G (p.Ser2701=)
c.7734T>G (p.Ser2578=)
c.570T>G (p.Ser190=)
c.8111T>G (n.8111T>G)
c.668T>G
c.8007T>G (p.Ser2669=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32363305T=CA2082835333BRCA2c.8103T= (p.Ser2701=)
c.7734T= (p.Ser2578=)
c.570T= (p.Ser190=)
c.8111T= (n.8111T=)
c.668T=
c.8007T= (p.Ser2669=)
13g.32363306G>ACA387749317BRCA2c.8104G>A (p.Glu2702Lys)
c.7735G>A (p.Glu2579Lys)
c.571G>A (p.Glu191Lys)
c.8112G>A (n.8112G>A)
c.669G>A
c.8008G>A (p.Glu2670Lys)
 ClinVar dbSNP
13g.32363306G>CCA247477685BRCA2c.8104G>C (p.Glu2702Gln)
c.7735G>C (p.Glu2579Gln)
c.571G>C (p.Glu191Gln)
c.8112G>C (n.8112G>C)
c.669G>C
c.8008G>C (p.Glu2670Gln)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32363306G=CA2082835360BRCA2c.8104G= (p.Glu2702=)
c.7735G= (p.Glu2579=)
c.571G= (p.Glu191=)
c.8112G= (n.8112G=)
c.669G=
c.8008G= (p.Glu2670=)
13g.32363306G>TCA387749319BRCA2c.8104G>T (p.Glu2702Ter)
c.7735G>T (p.Glu2579Ter)
c.571G>T (p.Glu191Ter)
c.8112G>T (n.8112G>T)
c.669G>T
c.8008G>T (p.Glu2670Ter)
13g.32363307A>CCA387749321BRCA2c.8105A>C (p.Glu2702Ala)
c.7736A>C (p.Glu2579Ala)
c.572A>C (p.Glu191Ala)
c.8113A>C (n.8113A>C)
c.670A>C
c.8009A>C (p.Glu2670Ala)
13g.32363307A>GCA387749323BRCA2c.8105A>G (p.Glu2702Gly)
c.7736A>G (p.Glu2579Gly)
c.572A>G (p.Glu191Gly)
c.8113A>G (n.8113A>G)
c.670A>G
c.8009A>G (p.Glu2670Gly)
13g.32363307A>TCA387749320BRCA2c.8105A>T (p.Glu2702Val)
c.7736A>T (p.Glu2579Val)
c.572A>T (p.Glu191Val)
c.8113A>T (n.8113A>T)
c.670A>T
c.8009A>T (p.Glu2670Val)
 dbSNP
13g.32363308A>CCA387749326BRCA2c.8106A>C (p.Glu2702Asp)
c.7737A>C (p.Glu2579Asp)
c.573A>C (p.Glu191Asp)
c.8114A>C (n.8114A>C)
c.671A>C
c.8010A>C (p.Glu2670Asp)
13g.32363308A>GCA483439607BRCA2c.8106A>G (p.Glu2702=)
c.7737A>G (p.Glu2579=)
c.573A>G (p.Glu191=)
c.8114A>G (n.8114A>G)
c.671A>G
c.8010A>G (p.Glu2670=)
 ClinVar
13g.32363308A>TCA387749327BRCA2c.8106A>T (p.Glu2702Asp)
c.7737A>T (p.Glu2579Asp)
c.573A>T (p.Glu191Asp)
c.8114A>T (n.8114A>T)
c.671A>T
c.8010A>T (p.Glu2670Asp)
 dbSNP
13g.32363309A>CCA387749330BRCA2c.8107A>C (p.Thr2703Pro)
c.7738A>C (p.Thr2580Pro)
c.574A>C (p.Thr192Pro)
c.8115A>C (n.8115A>C)
c.672A>C
c.8011A>C (p.Thr2671Pro)
 dbSNP
13g.32363309A>GCA387749332BRCA2c.8107A>G (p.Thr2703Ala)
c.7738A>G (p.Thr2580Ala)
c.574A>G (p.Thr192Ala)
c.8115A>G (n.8115A>G)
c.672A>G
c.8011A>G (p.Thr2671Ala)
 ClinVar dbSNP gnomAD v4
13g.32363309A>TCA387749333BRCA2c.8107A>T (p.Thr2703Ser)
c.7738A>T (p.Thr2580Ser)
c.574A>T (p.Thr192Ser)
c.8115A>T (n.8115A>T)
c.672A>T
c.8011A>T (p.Thr2671Ser)
 dbSNP
13g.32363310C>ACA387749339BRCA2c.8108C>A (p.Thr2703Asn)
c.7739C>A (p.Thr2580Asn)
c.575C>A (p.Thr192Asn)
c.8116C>A (n.8116C>A)
c.673C>A
c.8012C>A (p.Thr2671Asn)
 ClinVar dbSNP
13g.32363310C>GCA387749337BRCA2c.8108C>G (p.Thr2703Ser)
c.7739C>G (p.Thr2580Ser)
c.575C>G (p.Thr192Ser)
c.8116C>G (n.8116C>G)
c.673C>G
c.8012C>G (p.Thr2671Ser)
 dbSNP
13g.32363310C>TCA387749335BRCA2c.8108C>T (p.Thr2703Ile)
c.7739C>T (p.Thr2580Ile)
c.575C>T (p.Thr192Ile)
c.8116C>T (n.8116C>T)
c.673C>T
c.8012C>T (p.Thr2671Ile)
13g.32363311T>ACA483439611BRCA2c.8109T>A (p.Thr2703=)
c.7740T>A (p.Thr2580=)
c.576T>A (p.Thr192=)
c.8117T>A (n.8117T>A)
c.674T>A
c.8013T>A (p.Thr2671=)
 dbSNP
13g.32363311T>CCA483439610BRCA2c.8109T>C (p.Thr2703=)
c.7740T>C (p.Thr2580=)
c.576T>C (p.Thr192=)
c.8117T>C (n.8117T>C)
c.674T>C
c.8013T>C (p.Thr2671=)
 dbSNP
13g.32363311T>GCA483439609BRCA2c.8109T>G (p.Thr2703=)
c.7740T>G (p.Thr2580=)
c.576T>G (p.Thr192=)
c.8117T>G (n.8117T>G)
c.674T>G
c.8013T>G (p.Thr2671=)
 gnomAD v4
13g.32363311_32363319delinsTTCTAGCAACA2082835393BRCA2c.8109_8117delinsTTCTAGCAA (p.Thr2703=)
c.7740_7748delinsTTCTAGCAA (p.Thr2580=)
c.576_584delinsTTCTAGCAA (p.Thr192=)
c.8117_8125delinsTTCTAGCAA (n.8117_8125delinsTTCTAGCAA)
c.674_682delinsTTCTAGCAA
c.8013_8021delinsTTCTAGCAA (p.Thr2671=)
13g.32363311_32363312insGAAAACAAAAACA2554986632BRCA2c.8109_8110insGAAAACAAAAA (p.Ser2704GlufsTer33)
c.7740_7741insGAAAACAAAAA (p.Ser2581GlufsTer33)
c.576_577insGAAAACAAAAA (p.Ser193GlufsTer33)
c.8117_8118insGAAAACAAAAA (n.8117_8118insGAAAACAAAAA)
c.674_675insGAAAACAAAAA
c.8013_8014insGAAAACAAAAA (p.Ser2672GlufsTer33)
13g.32363312T>ACA387749343BRCA2c.8110T>A (p.Ser2704Thr)
c.7741T>A (p.Ser2581Thr)
c.577T>A (p.Ser193Thr)
c.8118T>A (n.8118T>A)
c.675T>A
c.8014T>A (p.Ser2672Thr)
13g.32363312T>CCA6941188BRCA2c.8110T>C (p.Ser2704Pro)
c.7741T>C (p.Ser2581Pro)
c.577T>C (p.Ser193Pro)
c.8118T>C (n.8118T>C)
c.675T>C
c.8014T>C (p.Ser2672Pro)
 dbSNP ExAC gnomAD v2
13g.32363312T>GCA387749348BRCA2c.8110T>G (p.Ser2704Ala)
c.7741T>G (p.Ser2581Ala)
c.577T>G (p.Ser193Ala)
c.8118T>G (n.8118T>G)
c.675T>G
c.8014T>G (p.Ser2672Ala)
13g.32363312T=CA2082835408BRCA2c.8110T= (p.Ser2704=)
c.7741T= (p.Ser2581=)
c.577T= (p.Ser193=)
c.8118T= (n.8118T=)
c.675T=
c.8014T= (p.Ser2672=)
13g.32363312_32363313delinsTCCA2082835409BRCA2c.8110_8111delinsTC (p.Ser2704=)
c.7741_7742delinsTC (p.Ser2581=)
c.577_578delinsTC (p.Ser193=)
c.8118_8119delinsTC (n.8118_8119delinsTC)
c.675_676delinsTC
c.8014_8015delinsTC (p.Ser2672=)
13g.32363313_32363320delCA658823762BRCA2c.8111_8118del (p.Ser2704Ter)
c.7742_7749del (p.Ser2581Ter)
c.578_585del (p.Ser193Ter)
c.8119_8126del (n.8119_8126del)
c.676_683del
c.8015_8022del (p.Ser2672Ter)
 ClinVar dbSNP
13g.32363312_32363313insAGCAATAAAACTAGTAGTGCAGCTGAAACCA2573149379BRCA2c.8110_8111insAGCAATAAAACTAGTAGTGCAGCTGAAAC (p.Ser2704Ter)
c.7741_7742insAGCAATAAAACTAGTAGTGCAGCTGAAAC (p.Ser2581Ter)
c.577_578insAGCAATAAAACTAGTAGTGCAGCTGAAAC (p.Ser193Ter)
c.8118_8119insAGCAATAAAACTAGTAGTGCAGCTGAAAC (n.8118_8119insAGCAATAAAACTAGTAGTGCAGCTGAAAC)
c.675_676insAGCAATAAAACTAGTAGTGCAGCTGAAAC
c.8014_8015insAGCAATAAAACTAGTAGTGCAGCTGAAAC (p.Ser2672Ter)
 ClinVar dbSNP
13g.32363313C>ACA387749352BRCA2c.8111C>A (p.Ser2704Tyr)
c.7742C>A (p.Ser2581Tyr)
c.578C>A (p.Ser193Tyr)
c.8119C>A (n.8119C>A)
c.676C>A
c.8015C>A (p.Ser2672Tyr)
 dbSNP
13g.32363313C=CA2082835426BRCA2c.8111C= (p.Ser2704=)
c.7742C= (p.Ser2581=)
c.578C= (p.Ser193=)
c.8119C= (n.8119C=)
c.676C=
c.8015C= (p.Ser2672=)
13g.32363313C>GCA387749354BRCA2c.8111C>G (p.Ser2704Cys)
c.7742C>G (p.Ser2581Cys)
c.578C>G (p.Ser193Cys)
c.8119C>G (n.8119C>G)
c.676C>G
c.8015C>G (p.Ser2672Cys)
 gnomAD v4
13g.32363313C>TCA025457BRCA2c.8111C>T (p.Ser2704Phe)
c.7742C>T (p.Ser2581Phe)
c.578C>T (p.Ser193Phe)
c.8119C>T (n.8119C>T)
c.676C>T
c.8015C>T (p.Ser2672Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
13g.32363313delinsAGCAATAAAACTAGTAGTGCAGCTGAAACTCA915946890BRCA2c.8111delinsAGCAATAAAACTAGTAGTGCAGCTGAAACT (p.Ser2704Ter)
c.7742delinsAGCAATAAAACTAGTAGTGCAGCTGAAACT (p.Ser2581Ter)
c.578delinsAGCAATAAAACTAGTAGTGCAGCTGAAACT (p.Ser193Ter)
c.8119delinsAGCAATAAAACTAGTAGTGCAGCTGAAACT (n.8119delinsAGCAATAAAACTAGTAGTGCAGCTGAAACT)
c.676delinsAGCAATAAAACTAGTAGTGCAGCTGAAACT
c.8015delinsAGCAATAAAACTAGTAGTGCAGCTGAAACT (p.Ser2672Ter)
 ClinVar dbSNP
13g.32363314T>ACA483439616BRCA2c.8112T>A (p.Ser2704=)
c.7743T>A (p.Ser2581=)
c.579T>A (p.Ser193=)
c.8120T>A (n.8120T>A)
c.677T>A
c.8016T>A (p.Ser2672=)
 dbSNP
13g.32363314T>CCA483439615BRCA2c.8112T>C (p.Ser2704=)
c.7743T>C (p.Ser2581=)
c.579T>C (p.Ser193=)
c.8120T>C (n.8120T>C)
c.677T>C
c.8016T>C (p.Ser2672=)
 ClinVar
13g.32363314T>GCA483439614BRCA2c.8112T>G (p.Ser2704=)
c.7743T>G (p.Ser2581=)
c.579T>G (p.Ser193=)
c.8120T>G (n.8120T>G)
c.677T>G
c.8016T>G (p.Ser2672=)
13g.32363314T=CA2082835443BRCA2c.8112T= (p.Ser2704=)
c.7743T= (p.Ser2581=)
c.579T= (p.Ser193=)
c.8120T= (n.8120T=)
c.677T=
c.8016T= (p.Ser2672=)
13g.32363315A=CA2082835460BRCA2c.8113A= (p.Ser2705=)
c.7744A= (p.Ser2582=)
c.580A= (p.Ser194=)
c.8121A= (n.8121A=)
c.678A=
c.8017A= (p.Ser2673=)
13g.32363315A>CCA387749356BRCA2c.8113A>C (p.Ser2705Arg)
c.7744A>C (p.Ser2582Arg)
c.580A>C (p.Ser194Arg)
c.8121A>C (n.8121A>C)
c.678A>C
c.8017A>C (p.Ser2673Arg)
13g.32363315A>GCA6941189BRCA2c.8113A>G (p.Ser2705Gly)
c.7744A>G (p.Ser2582Gly)
c.580A>G (p.Ser194Gly)
c.8121A>G (n.8121A>G)
c.678A>G
c.8017A>G (p.Ser2673Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32363315A>TCA387749358BRCA2c.8113A>T (p.Ser2705Cys)
c.7744A>T (p.Ser2582Cys)
c.580A>T (p.Ser194Cys)
c.8121A>T (n.8121A>T)
c.678A>T
c.8017A>T (p.Ser2673Cys)
 dbSNP
13g.32363315dupCA10589468BRCA2c.8113dup (p.Ser2705LysfsTer3)
c.7744dup (p.Ser2582LysfsTer3)
c.580dup (p.Ser194LysfsTer3)
c.8121dup (n.8121dup)
c.678dup
c.8017dup (p.Ser2673LysfsTer3)
 ClinVar dbSNP
13g.32363316G>ACA387749361BRCA2c.8114G>A (p.Ser2705Asn)
c.7745G>A (p.Ser2582Asn)
c.581G>A (p.Ser194Asn)
c.8122G>A (n.8122G>A)
c.679G>A
c.8018G>A (p.Ser2673Asn)
 ClinVar dbSNP gnomAD v4
13g.32363316G>CCA387749364BRCA2c.8114G>C (p.Ser2705Thr)
c.7745G>C (p.Ser2582Thr)
c.581G>C (p.Ser194Thr)
c.8122G>C (n.8122G>C)
c.679G>C
c.8018G>C (p.Ser2673Thr)
 dbSNP gnomAD v4
13g.32363316G=CA2082835479BRCA2c.8114G= (p.Ser2705=)
c.7745G= (p.Ser2582=)
c.581G= (p.Ser194=)
c.8122G= (n.8122G=)
c.679G=
c.8018G= (p.Ser2673=)
13g.32363316G>TCA6941190BRCA2c.8114G>T (p.Ser2705Ile)
c.7745G>T (p.Ser2582Ile)
c.581G>T (p.Ser194Ile)
c.8122G>T (n.8122G>T)
c.679G>T
c.8018G>T (p.Ser2673Ile)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32363317C>ACA387749368BRCA2c.8115C>A (p.Ser2705Arg)
c.7746C>A (p.Ser2582Arg)
c.582C>A (p.Ser194Arg)
c.8123C>A (n.8123C>A)
c.680C>A
c.8019C>A (p.Ser2673Arg)
13g.32363317C=CA2082835488BRCA2c.8115C= (p.Ser2705=)
c.7746C= (p.Ser2582=)
c.582C= (p.Ser194=)
c.8123C= (n.8123C=)
c.680C=
c.8019C= (p.Ser2673=)
13g.32363317C>GCA025458BRCA2c.8115C>G (p.Ser2705Arg)
c.7746C>G (p.Ser2582Arg)
c.582C>G (p.Ser194Arg)
c.8123C>G (n.8123C>G)
c.680C>G
c.8019C>G (p.Ser2673Arg)
 ClinVar dbSNP gnomAD v4
13g.32363317C>TCA483439624BRCA2c.8115C>T (p.Ser2705=)
c.7746C>T (p.Ser2582=)
c.582C>T (p.Ser194=)
c.8123C>T (n.8123C>T)
c.680C>T
c.8019C>T (p.Ser2673=)
13g.32363318A=CA2082835500BRCA2c.8116A= (p.Asn2706=)
c.7747A= (p.Asn2583=)
c.583A= (p.Asn195=)
c.8124A= (n.8124A=)
c.681A=
c.8020A= (p.Asn2674=)
13g.32363318A>CCA387749370BRCA2c.8116A>C (p.Asn2706His)
c.7747A>C (p.Asn2583His)
c.583A>C (p.Asn195His)
c.8124A>C (n.8124A>C)
c.681A>C
c.8020A>C (p.Asn2674His)
13g.32363318A>GCA387749371BRCA2c.8116A>G (p.Asn2706Asp)
c.7747A>G (p.Asn2583Asp)
c.583A>G (p.Asn195Asp)
c.8124A>G (n.8124A>G)
c.681A>G
c.8020A>G (p.Asn2674Asp)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32363318A>TCA387749372BRCA2c.8116A>T (p.Asn2706Tyr)
c.7747A>T (p.Asn2583Tyr)
c.583A>T (p.Asn195Tyr)
c.8124A>T (n.8124A>T)
c.681A>T
c.8020A>T (p.Asn2674Tyr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32363319delCA2825002150BRCA2c.8117del (p.Asn2706IlefsTer27)
c.7748del (p.Asn2583IlefsTer27)
c.584del (p.Asn195IlefsTer27)
c.8125del (n.8125del)
c.682del
c.8021del (p.Asn2674IlefsTer27)
 ClinVar
13g.32363319A=CA2082835505BRCA2c.8117A= (p.Asn2706=)
c.7748A= (p.Asn2583=)
c.584A= (p.Asn195=)
c.8125A= (n.8125A=)
c.682A=
c.8021A= (p.Asn2674=)
13g.32363319A>CCA387749374BRCA2c.8117A>C (p.Asn2706Thr)
c.7748A>C (p.Asn2583Thr)
c.584A>C (p.Asn195Thr)
c.8125A>C (n.8125A>C)
c.682A>C
c.8021A>C (p.Asn2674Thr)
13g.32363319A>GCA025459BRCA2c.8117A>G (p.Asn2706Ser)
c.7748A>G (p.Asn2583Ser)
c.584A>G (p.Asn195Ser)
c.8125A>G (n.8125A>G)
c.682A>G
c.8021A>G (p.Asn2674Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32363319A>TCA387749376BRCA2c.8117A>T (p.Asn2706Ile)
c.7748A>T (p.Asn2583Ile)
c.584A>T (p.Asn195Ile)
c.8125A>T (n.8125A>T)
c.682A>T
c.8021A>T (p.Asn2674Ile)
 dbSNP
13g.32363320T>ACA387749378BRCA2c.8118T>A (p.Asn2706Lys)
c.7749T>A (p.Asn2583Lys)
c.585T>A (p.Asn195Lys)
c.8126T>A (n.8126T>A)
c.683T>A
c.8022T>A (p.Asn2674Lys)
13g.32363320T>CCA025460BRCA2c.8118T>C (p.Asn2706=)
c.7749T>C (p.Asn2583=)
c.585T>C (p.Asn195=)
c.8126T>C (n.8126T>C)
c.683T>C
c.8022T>C (p.Asn2674=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32363320T>GCA387749380BRCA2c.8118T>G (p.Asn2706Lys)
c.7749T>G (p.Asn2583Lys)
c.585T>G (p.Asn195Lys)
c.8126T>G (n.8126T>G)
c.683T>G
c.8022T>G (p.Asn2674Lys)
13g.32363320T=CA2082835510BRCA2c.8118T= (p.Asn2706=)
c.7749T= (p.Asn2583=)
c.585T= (p.Asn195=)
c.8126T= (n.8126T=)
c.683T=
c.8022T= (p.Asn2674=)
13g.32363321A=CA2082835522BRCA2c.8119A= (p.Lys2707=)
c.7750A= (p.Lys2584=)
c.586A= (p.Lys196=)
c.8127A= (n.8127A=)
c.684A=
c.8023A= (p.Lys2675=)
13g.32363321A>CCA387749383BRCA2c.8119A>C (p.Lys2707Gln)
c.7750A>C (p.Lys2584Gln)
c.586A>C (p.Lys196Gln)
c.8127A>C (n.8127A>C)
c.684A>C
c.8023A>C (p.Lys2675Gln)
13g.32363321A>GCA247477722BRCA2c.8119A>G (p.Lys2707Glu)
c.7750A>G (p.Lys2584Glu)
c.586A>G (p.Lys196Glu)
c.8127A>G (n.8127A>G)
c.684A>G
c.8023A>G (p.Lys2675Glu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32363321A>TCA387749385BRCA2c.8119A>T (p.Lys2707Ter)
c.7750A>T (p.Lys2584Ter)
c.586A>T (p.Lys196Ter)
c.8127A>T (n.8127A>T)
c.684A>T
c.8023A>T (p.Lys2675Ter)
 dbSNP
13g.32363324delCA2580610726BRCA2c.8122del (p.Thr2708LeufsTer25)
c.7753del (p.Thr2585LeufsTer25)
c.589del (p.Thr197LeufsTer25)
c.8130del (n.8130del)
c.687del
c.8026del (p.Thr2676LeufsTer25)
13g.32363322A=CA2082835535BRCA2c.8120A= (p.Lys2707=)
c.7751A= (p.Lys2584=)
c.587A= (p.Lys196=)
c.8128A= (n.8128A=)
c.685A=
c.8024A= (p.Lys2675=)
13g.32363322A>CCA387749386BRCA2c.8120A>C (p.Lys2707Thr)
c.7751A>C (p.Lys2584Thr)
c.587A>C (p.Lys196Thr)
c.8128A>C (n.8128A>C)
c.685A>C
c.8024A>C (p.Lys2675Thr)
13g.32363322A>GCA387749387BRCA2c.8120A>G (p.Lys2707Arg)
c.7751A>G (p.Lys2584Arg)
c.587A>G (p.Lys196Arg)
c.8128A>G (n.8128A>G)
c.685A>G
c.8024A>G (p.Lys2675Arg)
 ClinVar dbSNP
13g.32363322A>TCA387749388BRCA2c.8120A>T (p.Lys2707Ile)
c.7751A>T (p.Lys2584Ile)
c.587A>T (p.Lys196Ile)
c.8128A>T (n.8128A>T)
c.685A>T
c.8024A>T (p.Lys2675Ile)
 ClinVar dbSNP
13g.32363323A>CCA387749389BRCA2c.8121A>C (p.Lys2707Asn)
c.7752A>C (p.Lys2584Asn)
c.588A>C (p.Lys196Asn)
c.8129A>C (n.8129A>C)
c.686A>C
c.8025A>C (p.Lys2675Asn)
13g.32363323A>GCA483439636BRCA2c.8121A>G (p.Lys2707=)
c.7752A>G (p.Lys2584=)
c.588A>G (p.Lys196=)
c.8129A>G (n.8129A>G)
c.686A>G
c.8025A>G (p.Lys2675=)
13g.32363323A>TCA387749390BRCA2c.8121A>T (p.Lys2707Asn)
c.7752A>T (p.Lys2584Asn)
c.588A>T (p.Lys196Asn)
c.8129A>T (n.8129A>T)
c.686A>T
c.8025A>T (p.Lys2675Asn)
 dbSNP
13g.32363324A=CA2082835544BRCA2c.8122A= (p.Thr2708=)
c.7753A= (p.Thr2585=)
c.589A= (p.Thr197=)
c.8130A= (n.8130A=)
c.687A=
c.8026A= (p.Thr2676=)
13g.32363324A>CCA387749391BRCA2c.8122A>C (p.Thr2708Pro)
c.7753A>C (p.Thr2585Pro)
c.589A>C (p.Thr197Pro)
c.8130A>C (n.8130A>C)
c.687A>C
c.8026A>C (p.Thr2676Pro)
 dbSNP
13g.32363324A>GCA387749393BRCA2c.8122A>G (p.Thr2708Ala)
c.7753A>G (p.Thr2585Ala)
c.589A>G (p.Thr197Ala)
c.8130A>G (n.8130A>G)
c.687A>G
c.8026A>G (p.Thr2676Ala)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32363324A>TCA387749392BRCA2c.8122A>T (p.Thr2708Ser)
c.7753A>T (p.Thr2585Ser)
c.589A>T (p.Thr197Ser)
c.8130A>T (n.8130A>T)
c.687A>T
c.8026A>T (p.Thr2676Ser)
 ClinVar dbSNP
13g.32363324_32363325insTACTTCA2573149380BRCA2c.8122_8123insTACTT (p.Thr2708IlefsTer27)
c.7753_7754insTACTT (p.Thr2585IlefsTer27)
c.589_590insTACTT (p.Thr197IlefsTer27)
c.8130_8131insTACTT (n.8130_8131insTACTT)
c.687_688insTACTT
c.8026_8027insTACTT (p.Thr2676IlefsTer27)
 dbSNP
13g.32363325C>ACA387749394BRCA2c.8123C>A (p.Thr2708Asn)
c.7754C>A (p.Thr2585Asn)
c.590C>A (p.Thr197Asn)
c.8131C>A (n.8131C>A)
c.688C>A
c.8027C>A (p.Thr2676Asn)
 dbSNP
13g.32363325C=CA2082835560BRCA2c.8123C= (p.Thr2708=)
c.7754C= (p.Thr2585=)
c.590C= (p.Thr197=)
c.8131C= (n.8131C=)
c.688C=
c.8027C= (p.Thr2676=)
13g.32363325C>GCA387749395BRCA2c.8123C>G (p.Thr2708Ser)
c.7754C>G (p.Thr2585Ser)
c.590C>G (p.Thr197Ser)
c.8131C>G (n.8131C>G)
c.688C>G
c.8027C>G (p.Thr2676Ser)
 dbSNP
13g.32363325C>TCA387749396BRCA2c.8123C>T (p.Thr2708Ile)
c.7754C>T (p.Thr2585Ile)
c.590C>T (p.Thr197Ile)
c.8131C>T (n.8131C>T)
c.688C>T
c.8027C>T (p.Thr2676Ile)
 ClinVar dbSNP gnomAD v4
13g.32363326T>ACA483439644BRCA2c.8124T>A (p.Thr2708=)
c.7755T>A (p.Thr2585=)
c.591T>A (p.Thr197=)
c.8132T>A (n.8132T>A)
c.689T>A
c.8028T>A (p.Thr2676=)
 dbSNP
13g.32363326T>CCA483439646BRCA2c.8124T>C (p.Thr2708=)
c.7755T>C (p.Thr2585=)
c.591T>C (p.Thr197=)
c.8132T>C (n.8132T>C)
c.689T>C
c.8028T>C (p.Thr2676=)
 ClinVar gnomAD v4
13g.32363326T>GCA025462BRCA2c.8124T>G (p.Thr2708=)
c.7755T>G (p.Thr2585=)
c.591T>G (p.Thr197=)
c.8132T>G (n.8132T>G)
c.689T>G
c.8028T>G (p.Thr2676=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32363326T=CA2082835569BRCA2c.8124T= (p.Thr2708=)
c.7755T= (p.Thr2585=)
c.591T= (p.Thr197=)
c.8132T= (n.8132T=)
c.689T=
c.8028T= (p.Thr2676=)
13g.32363327A=CA2082835578BRCA2c.8125A= (p.Ser2709=)
c.7756A= (p.Ser2586=)
c.592A= (p.Ser198=)
c.8133A= (n.8133A=)
c.690A=
c.8029A= (p.Ser2677=)
13g.32363327A>CCA387749401BRCA2c.8125A>C (p.Ser2709Arg)
c.7756A>C (p.Ser2586Arg)
c.592A>C (p.Ser198Arg)
c.8133A>C (n.8133A>C)
c.690A>C
c.8029A>C (p.Ser2677Arg)
13g.32363327A>GCA025463BRCA2c.8125A>G (p.Ser2709Gly)
c.7756A>G (p.Ser2586Gly)
c.592A>G (p.Ser198Gly)
c.8133A>G (n.8133A>G)
c.690A>G
c.8029A>G (p.Ser2677Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32363327A>TCA387749403BRCA2c.8125A>T (p.Ser2709Cys)
c.7756A>T (p.Ser2586Cys)
c.592A>T (p.Ser198Cys)
c.8133A>T (n.8133A>T)
c.690A>T
c.8029A>T (p.Ser2677Cys)
 dbSNP
13g.32363328G>ACA387749406BRCA2c.8126G>A (p.Ser2709Asn)
c.7757G>A (p.Ser2586Asn)
c.593G>A (p.Ser198Asn)
c.8134G>A (n.8134G>A)
c.691G>A
c.8030G>A (p.Ser2677Asn)
 dbSNP
13g.32363328G>CCA387749408BRCA2c.8126G>C (p.Ser2709Thr)
c.7757G>C (p.Ser2586Thr)
c.593G>C (p.Ser198Thr)
c.8134G>C (n.8134G>C)
c.691G>C
c.8030G>C (p.Ser2677Thr)
 dbSNP
13g.32363328G>TCA387749409BRCA2c.8126G>T (p.Ser2709Ile)
c.7757G>T (p.Ser2586Ile)
c.593G>T (p.Ser198Ile)
c.8134G>T (n.8134G>T)
c.691G>T
c.8030G>T (p.Ser2677Ile)
 ClinVar
13g.32363329T>ACA387749411BRCA2c.8127T>A (p.Ser2709Arg)
c.7758T>A (p.Ser2586Arg)
c.594T>A (p.Ser198Arg)
c.8135T>A (n.8135T>A)
c.692T>A
c.8031T>A (p.Ser2677Arg)
 dbSNP
13g.32363329T>CCA483439653BRCA2c.8127T>C (p.Ser2709=)
c.7758T>C (p.Ser2586=)
c.594T>C (p.Ser198=)
c.8135T>C (n.8135T>C)
c.692T>C
c.8031T>C (p.Ser2677=)
 ClinVar dbSNP gnomAD v4
13g.32363329T>GCA387749412BRCA2c.8127T>G (p.Ser2709Arg)
c.7758T>G (p.Ser2586Arg)
c.594T>G (p.Ser198Arg)
c.8135T>G (n.8135T>G)
c.692T>G
c.8031T>G (p.Ser2677Arg)
13g.32363329T=CA2082835579BRCA2c.8127T= (p.Ser2709=)
c.7758T= (p.Ser2586=)
c.594T= (p.Ser198=)
c.8135T= (n.8135T=)
c.692T=
c.8031T= (p.Ser2677=)
13g.32363330A=CA2082835583BRCA2c.8128A= (p.Ser2710=)
c.7759A= (p.Ser2587=)
c.595A= (p.Ser199=)
c.8136A= (n.8136A=)
c.693A=
c.8032A= (p.Ser2678=)
13g.32363330A>CCA387749413BRCA2c.8128A>C (p.Ser2710Arg)
c.7759A>C (p.Ser2587Arg)
c.595A>C (p.Ser199Arg)
c.8136A>C (n.8136A>C)
c.693A>C
c.8032A>C (p.Ser2678Arg)
13g.32363330A>GCA025464BRCA2c.8128A>G (p.Ser2710Gly)
c.7759A>G (p.Ser2587Gly)
c.595A>G (p.Ser199Gly)
c.8136A>G (n.8136A>G)
c.693A>G
c.8032A>G (p.Ser2678Gly)
 ClinVar dbSNP
13g.32363330A>TCA387749416BRCA2c.8128A>T (p.Ser2710Cys)
c.7759A>T (p.Ser2587Cys)
c.595A>T (p.Ser199Cys)
c.8136A>T (n.8136A>T)
c.693A>T
c.8032A>T (p.Ser2678Cys)
 dbSNP
13g.32363331G>ACA387749417BRCA2c.8129G>A (p.Ser2710Asn)
c.7760G>A (p.Ser2587Asn)
c.596G>A (p.Ser199Asn)
c.8137G>A (n.8137G>A)
c.694G>A
c.8033G>A (p.Ser2678Asn)
 ClinVar dbSNP gnomAD v4
13g.32363331G>CCA387749422BRCA2c.8129G>C (p.Ser2710Thr)
c.7760G>C (p.Ser2587Thr)
c.596G>C (p.Ser199Thr)
c.8137G>C (n.8137G>C)
c.694G>C
c.8033G>C (p.Ser2678Thr)
13g.32363331G=CA2082835589BRCA2c.8129G= (p.Ser2710=)
c.7760G= (p.Ser2587=)
c.596G= (p.Ser199=)
c.8137G= (n.8137G=)
c.694G=
c.8033G= (p.Ser2678=)
13g.32363331G>TCA387749430BRCA2c.8129G>T (p.Ser2710Ile)
c.7760G>T (p.Ser2587Ile)
c.596G>T (p.Ser199Ile)
c.8137G>T (n.8137G>T)
c.694G>T
c.8033G>T (p.Ser2678Ile)
13g.32363331_32363332delinsGTCA2082835591BRCA2c.8129_8130delinsGT (p.Ser2710=)
c.7760_7761delinsGT (p.Ser2587=)
c.596_597delinsGT (p.Ser199=)
c.8137_8138delinsGT (n.8137_8138delinsGT)
c.694_695delinsGT
c.8033_8034delinsGT (p.Ser2678=)
13g.32363332delCA025465BRCA2c.8130del (p.Ser2710ArgfsTer23)
c.7761del (p.Ser2587ArgfsTer23)
c.597del (p.Ser199ArgfsTer23)
c.8138del (n.8138del)
c.695del
c.8034del (p.Ser2678ArgfsTer23)
 ClinVar dbSNP
13g.32363332T>ACA387749433BRCA2c.8130T>A (p.Ser2710Arg)
c.7761T>A (p.Ser2587Arg)
c.597T>A (p.Ser199Arg)
c.8138T>A (n.8138T>A)
c.695T>A
c.8034T>A (p.Ser2678Arg)
 dbSNP
13g.32363332T>CCA483439545BRCA2c.8130T>C (p.Ser2710=)
c.7761T>C (p.Ser2587=)
c.597T>C (p.Ser199=)
c.8138T>C (n.8138T>C)
c.695T>C
c.8034T>C (p.Ser2678=)
 ClinVar dbSNP
13g.32363332T>GCA387749435BRCA2c.8130T>G (p.Ser2710Arg)
c.7761T>G (p.Ser2587Arg)
c.597T>G (p.Ser199Arg)
c.8138T>G (n.8138T>G)
c.695T>G
c.8034T>G (p.Ser2678Arg)
13g.32363332dupCA2580087483BRCA2c.8130dup (p.Ala2711CysfsTer10)
c.7761dup (p.Ala2588CysfsTer10)
c.597dup (p.Ala200CysfsTer10)
c.8138dup (n.8138dup)
c.695dup
c.8034dup (p.Ala2679CysfsTer10)
 ClinVar
13g.32363333G>ACA16614369BRCA2c.8131G>A (p.Ala2711Thr)
c.7762G>A (p.Ala2588Thr)
c.598G>A (p.Ala200Thr)
c.8139G>A (n.8139G>A)
c.696G>A
c.8035G>A (p.Ala2679Thr)
 ClinVar dbSNP COSMIC COSMIC
13g.32363333G>CCA387749439BRCA2c.8131G>C (p.Ala2711Pro)
c.7762G>C (p.Ala2588Pro)
c.598G>C (p.Ala200Pro)
c.8139G>C (n.8139G>C)
c.696G>C
c.8035G>C (p.Ala2679Pro)
 dbSNP
13g.32363333G=CA2082835615BRCA2c.8131G= (p.Ala2711=)
c.7762G= (p.Ala2588=)
c.598G= (p.Ala200=)
c.8139G= (n.8139G=)
c.696G=
c.8035G= (p.Ala2679=)
13g.32363333G>TCA387749441BRCA2c.8131G>T (p.Ala2711Ser)
c.7762G>T (p.Ala2588Ser)
c.598G>T (p.Ala200Ser)
c.8139G>T (n.8139G>T)
c.696G>T
c.8035G>T (p.Ala2679Ser)
 ClinVar dbSNP gnomAD v4
13g.32363334C>ACA387749443BRCA2c.8132C>A (p.Ala2711Glu)
c.7763C>A (p.Ala2588Glu)
c.599C>A (p.Ala200Glu)
c.8140C>A (n.8140C>A)
c.697C>A
c.8036C>A (p.Ala2679Glu)
 dbSNP
13g.32363334C>GCA387749445BRCA2c.8132C>G (p.Ala2711Gly)
c.7763C>G (p.Ala2588Gly)
c.599C>G (p.Ala200Gly)
c.8140C>G (n.8140C>G)
c.697C>G
c.8036C>G (p.Ala2679Gly)
 dbSNP
13g.32363334C>TCA387749447BRCA2c.8132C>T (p.Ala2711Val)
c.7763C>T (p.Ala2588Val)
c.599C>T (p.Ala200Val)
c.8140C>T (n.8140C>T)
c.697C>T
c.8036C>T (p.Ala2679Val)
 ClinVar dbSNP
13g.32363335A=CA2082835627BRCA2c.8133A= (p.Ala2711=)
c.7764A= (p.Ala2588=)
c.600A= (p.Ala200=)
c.8141A= (n.8141A=)
c.698A=
c.8037A= (p.Ala2679=)
13g.32363335A>CCA483439548BRCA2c.8133A>C (p.Ala2711=)
c.7764A>C (p.Ala2588=)
c.600A>C (p.Ala200=)
c.8141A>C (n.8141A>C)
c.698A>C
c.8037A>C (p.Ala2679=)
13g.32363335A>GCA6941191BRCA2c.8133A>G (p.Ala2711=)
c.7764A>G (p.Ala2588=)
c.600A>G (p.Ala200=)
c.8141A>G (n.8141A>G)
c.698A>G
c.8037A>G (p.Ala2679=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32363335A>TCA483439547BRCA2c.8133A>T (p.Ala2711=)
c.7764A>T (p.Ala2588=)
c.600A>T (p.Ala200=)
c.8141A>T (n.8141A>T)
c.698A>T
c.8037A>T (p.Ala2679=)
 dbSNP
13g.32363336G>ACA025466BRCA2c.8134G>A (p.Asp2712Asn)
c.7765G>A (p.Asp2589Asn)
c.601G>A (p.Asp201Asn)
c.8142G>A (n.8142G>A)
c.699G>A
c.8038G>A (p.Asp2680Asn)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
13g.32363336G>CCA387749452BRCA2c.8134G>C (p.Asp2712His)
c.7765G>C (p.Asp2589His)
c.601G>C (p.Asp201His)
c.8142G>C (n.8142G>C)
c.699G>C
c.8038G>C (p.Asp2680His)
 ClinVar dbSNP
13g.32363336G=CA2082835640BRCA2c.8134G= (p.Asp2712=)
c.7765G= (p.Asp2589=)
c.601G= (p.Asp201=)
c.8142G= (n.8142G=)
c.699G=
c.8038G= (p.Asp2680=)
13g.32363336G>TCA387749453BRCA2c.8134G>T (p.Asp2712Tyr)
c.7765G>T (p.Asp2589Tyr)
c.601G>T (p.Asp201Tyr)
c.8142G>T (n.8142G>T)
c.699G>T
c.8038G>T (p.Asp2680Tyr)
13g.32363337A=CA2082835651BRCA2c.8135A= (p.Asp2712=)
c.7766A= (p.Asp2589=)
c.602A= (p.Asp201=)
c.8143A= (n.8143A=)
c.700A=
c.8039A= (p.Asp2680=)
13g.32363337A>CCA387749455BRCA2c.8135A>C (p.Asp2712Ala)
c.7766A>C (p.Asp2589Ala)
c.602A>C (p.Asp201Ala)
c.8143A>C (n.8143A>C)
c.700A>C
c.8039A>C (p.Asp2680Ala)
 ClinVar dbSNP gnomAD v4
13g.32363337A>GCA387749457BRCA2c.8135A>G (p.Asp2712Gly)
c.7766A>G (p.Asp2589Gly)
c.602A>G (p.Asp201Gly)
c.8143A>G (n.8143A>G)
c.700A>G
c.8039A>G (p.Asp2680Gly)
13g.32363337A>TCA025467BRCA2c.8135A>T (p.Asp2712Val)
c.7766A>T (p.Asp2589Val)
c.602A>T (p.Asp201Val)
c.8143A>T (n.8143A>T)
c.700A>T
c.8039A>T (p.Asp2680Val)
 ClinVar dbSNP gnomAD v4
13g.32363338T>ACA387749461BRCA2c.8136T>A (p.Asp2712Glu)
c.7767T>A (p.Asp2589Glu)
c.603T>A (p.Asp201Glu)
c.8144T>A (n.8144T>A)
c.701T>A
c.8040T>A (p.Asp2680Glu)
13g.32363338T>CCA483439550BRCA2c.8136T>C (p.Asp2712=)
c.7767T>C (p.Asp2589=)
c.603T>C (p.Asp201=)
c.8144T>C (n.8144T>C)
c.701T>C
c.8040T>C (p.Asp2680=)
 gnomAD v4
13g.32363338T>GCA387749462BRCA2c.8136T>G (p.Asp2712Glu)
c.7767T>G (p.Asp2589Glu)
c.603T>G (p.Asp201Glu)
c.8144T>G (n.8144T>G)
c.701T>G
c.8040T>G (p.Asp2680Glu)
 ClinVar dbSNP
13g.32363338T=CA2082835657BRCA2c.8136T= (p.Asp2712=)
c.7767T= (p.Asp2589=)
c.603T= (p.Asp201=)
c.8144T= (n.8144T=)
c.701T=
c.8040T= (p.Asp2680=)
13g.32363339A>CCA387749463BRCA2c.8137A>C (p.Thr2713Pro)
c.7768A>C (p.Thr2590Pro)
c.604A>C (p.Thr202Pro)
c.8145A>C (n.8145A>C)
c.702A>C
c.8041A>C (p.Thr2681Pro)
 dbSNP
13g.32363339A>GCA387749466BRCA2c.8137A>G (p.Thr2713Ala)
c.7768A>G (p.Thr2590Ala)
c.604A>G (p.Thr202Ala)
c.8145A>G (n.8145A>G)
c.702A>G
c.8041A>G (p.Thr2681Ala)
 COSMIC COSMIC
13g.32363339A>TCA387749467BRCA2c.8137A>T (p.Thr2713Ser)
c.7768A>T (p.Thr2590Ser)
c.604A>T (p.Thr202Ser)
c.8145A>T (n.8145A>T)
c.702A>T
c.8041A>T (p.Thr2681Ser)
 dbSNP
13g.32363340C>ACA387749469BRCA2c.8138C>A (p.Thr2713Asn)
c.7769C>A (p.Thr2590Asn)
c.605C>A (p.Thr202Asn)
c.8146C>A (n.8146C>A)
c.703C>A
c.8042C>A (p.Thr2681Asn)
 ClinVar dbSNP gnomAD v4
13g.32363340C=CA2082835664BRCA2c.8138C= (p.Thr2713=)
c.7769C= (p.Thr2590=)
c.605C= (p.Thr202=)
c.8146C= (n.8146C=)
c.703C=
c.8042C= (p.Thr2681=)
13g.32363340C>GCA387749471BRCA2c.8138C>G (p.Thr2713Ser)
c.7769C>G (p.Thr2590Ser)
c.605C>G (p.Thr202Ser)
c.8146C>G (n.8146C>G)
c.703C>G
c.8042C>G (p.Thr2681Ser)
 dbSNP
13g.32363340C>TCA247477752BRCA2c.8138C>T (p.Thr2713Ile)
c.7769C>T (p.Thr2590Ile)
c.605C>T (p.Thr202Ile)
c.8146C>T (n.8146C>T)
c.703C>T
c.8042C>T (p.Thr2681Ile)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32363341C>ACA483439555BRCA2c.8139C>A (p.Thr2713=)
c.7770C>A (p.Thr2590=)
c.606C>A (p.Thr202=)
c.8147C>A (n.8147C>A)
c.704C>A
c.8043C>A (p.Thr2681=)
 ClinVar dbSNP gnomAD v4
13g.32363341C=CA2082835671BRCA2c.8139C= (p.Thr2713=)
c.7770C= (p.Thr2590=)
c.606C= (p.Thr202=)
c.8147C= (n.8147C=)
c.704C=
c.8043C= (p.Thr2681=)
13g.32363341C>GCA483439556BRCA2c.8139C>G (p.Thr2713=)
c.7770C>G (p.Thr2590=)
c.606C>G (p.Thr202=)
c.8147C>G (n.8147C>G)
c.704C>G
c.8043C>G (p.Thr2681=)
 ClinVar dbSNP
13g.32363341C>TCA483439557BRCA2c.8139C>T (p.Thr2713=)
c.7770C>T (p.Thr2590=)
c.606C>T (p.Thr202=)
c.8147C>T (n.8147C>T)
c.704C>T
c.8043C>T (p.Thr2681=)
 dbSNP
13g.32363342C>ACA387749473BRCA2c.8140C>A (p.Gln2714Lys)
c.7771C>A (p.Gln2591Lys)
c.607C>A (p.Gln203Lys)
c.8148C>A (n.8148C>A)
c.705C>A
c.8044C>A (p.Gln2682Lys)
 ClinVar
13g.32363342C=CA2082835684BRCA2c.8140C= (p.Gln2714=)
c.7771C= (p.Gln2591=)
c.607C= (p.Gln203=)
c.8148C= (n.8148C=)
c.705C=
c.8044C= (p.Gln2682=)
13g.32363342C>GCA025468BRCA2c.8140C>G (p.Gln2714Glu)
c.7771C>G (p.Gln2591Glu)
c.607C>G (p.Gln203Glu)
c.8148C>G (n.8148C>G)
c.705C>G
c.8044C>G (p.Gln2682Glu)
 ClinVar dbSNP gnomAD v4
13g.32363342C>TCA025469BRCA2c.8140C>T (p.Gln2714Ter)
c.7771C>T (p.Gln2591Ter)
c.607C>T (p.Gln203Ter)
c.8148C>T (n.8148C>T)
c.705C>T
c.8044C>T (p.Gln2682Ter)
 ClinVar dbSNP
13g.32363342_32363343delinsCACA2082835681BRCA2c.8140_8141delinsCA (p.Gln2714=)
c.7771_7772delinsCA (p.Gln2591=)
c.607_608delinsCA (p.Gln203=)
c.8148_8149delinsCA (n.8148_8149delinsCA)
c.705_706delinsCA
c.8044_8045delinsCA (p.Gln2682=)
13g.32363343A=CA2082835691BRCA2c.8141A= (p.Gln2714=)
c.7772A= (p.Gln2591=)
c.608A= (p.Gln203=)
c.8149A= (n.8149A=)
c.706A=
c.8045A= (p.Gln2682=)
13g.32363343A>CCA387749477BRCA2c.8141A>C (p.Gln2714Pro)
c.7772A>C (p.Gln2591Pro)
c.608A>C (p.Gln203Pro)
c.8149A>C (n.8149A>C)
c.706A>C
c.8045A>C (p.Gln2682Pro)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32363343A>GCA025470BRCA2c.8141A>G (p.Gln2714Arg)
c.7772A>G (p.Gln2591Arg)
c.608A>G (p.Gln203Arg)
c.8149A>G (n.8149A>G)
c.706A>G
c.8045A>G (p.Gln2682Arg)
 ClinVar dbSNP gnomAD v4
13g.32363343A>TCA387749479BRCA2c.8141A>T (p.Gln2714Leu)
c.7772A>T (p.Gln2591Leu)
c.608A>T (p.Gln203Leu)
c.8149A>T (n.8149A>T)
c.706A>T
c.8045A>T (p.Gln2682Leu)
13g.32363343_32363347delCA1139770850BRCA2c.8141_8145del (p.Gln2714ArgfsTer5)
c.7772_7776del (p.Gln2591ArgfsTer5)
c.608_612del (p.Gln203ArgfsTer5)
c.8149_8153del (n.8149_8153del)
c.706_710del
c.8045_8049del (p.Gln2682ArgfsTer5)
13g.32363347delCA645372930BRCA2c.8145del (p.Val2716TrpfsTer17)
c.7776del (p.Val2593TrpfsTer17)
c.612del (p.Val205TrpfsTer17)
c.8153del (n.8153del)
c.710del
c.8049del (p.Val2684TrpfsTer17)
 ClinVar dbSNP
13g.32363344A=CA2082835699BRCA2c.8142A= (p.Gln2714=)
c.7773A= (p.Gln2591=)
c.609A= (p.Gln203=)
c.8150A= (n.8150A=)
c.707A=
c.8046A= (p.Gln2682=)
13g.32363344A>CCA387749481BRCA2c.8142A>C (p.Gln2714His)
c.7773A>C (p.Gln2591His)
c.609A>C (p.Gln203His)
c.8150A>C (n.8150A>C)
c.707A>C
c.8046A>C (p.Gln2682His)
13g.32363344A>GCA483439564BRCA2c.8142A>G (p.Gln2714=)
c.7773A>G (p.Gln2591=)
c.609A>G (p.Gln203=)
c.8150A>G (n.8150A>G)
c.707A>G
c.8046A>G (p.Gln2682=)
 ClinVar dbSNP gnomAD v4
13g.32363344A>TCA387749483BRCA2c.8142A>T (p.Gln2714His)
c.7773A>T (p.Gln2591His)
c.609A>T (p.Gln203His)
c.8150A>T (n.8150A>T)
c.707A>T
c.8046A>T (p.Gln2682His)
 dbSNP
13g.32363345A=CA2082835705BRCA2c.8143A= (p.Lys2715=)
c.7774A= (p.Lys2592=)
c.610A= (p.Lys204=)
c.8151A= (n.8151A=)
c.708A=
c.8047A= (p.Lys2683=)
13g.32363345A>CCA387749485BRCA2c.8143A>C (p.Lys2715Gln)
c.7774A>C (p.Lys2592Gln)
c.610A>C (p.Lys204Gln)
c.8151A>C (n.8151A>C)
c.708A>C
c.8047A>C (p.Lys2683Gln)
 dbSNP
13g.32363345A>GCA387749488BRCA2c.8143A>G (p.Lys2715Glu)
c.7774A>G (p.Lys2592Glu)
c.610A>G (p.Lys204Glu)
c.8151A>G (n.8151A>G)
c.708A>G
c.8047A>G (p.Lys2683Glu)
13g.32363345A>TCA339029BRCA2c.8143A>T (p.Lys2715Ter)
c.7774A>T (p.Lys2592Ter)
c.610A>T (p.Lys204Ter)
c.8151A>T (n.8151A>T)
c.708A>T
c.8047A>T (p.Lys2683Ter)
 ClinVar dbSNP
13g.32363346A=CA2082835714BRCA2c.8144A= (p.Lys2715=)
c.7775A= (p.Lys2592=)
c.611A= (p.Lys204=)
c.8152A= (n.8152A=)
c.709A=
c.8048A= (p.Lys2683=)
13g.32363346A>CCA387749491BRCA2c.8144A>C (p.Lys2715Thr)
c.7775A>C (p.Lys2592Thr)
c.611A>C (p.Lys204Thr)
c.8152A>C (n.8152A>C)
c.709A>C
c.8048A>C (p.Lys2683Thr)
13g.32363346A>GCA6941192BRCA2c.8144A>G (p.Lys2715Arg)
c.7775A>G (p.Lys2592Arg)
c.611A>G (p.Lys204Arg)
c.8152A>G (n.8152A>G)
c.709A>G
c.8048A>G (p.Lys2683Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32363346A>TCA387749493BRCA2c.8144A>T (p.Lys2715Ile)
c.7775A>T (p.Lys2592Ile)
c.611A>T (p.Lys204Ile)
c.8152A>T (n.8152A>T)
c.709A>T
c.8048A>T (p.Lys2683Ile)
13g.32363347A>CCA387749495BRCA2c.8145A>C (p.Lys2715Asn)
c.7776A>C (p.Lys2592Asn)
c.612A>C (p.Lys204Asn)
c.8153A>C (n.8153A>C)
c.710A>C
c.8049A>C (p.Lys2683Asn)
13g.32363347A>GCA483439566BRCA2c.8145A>G (p.Lys2715=)
c.7776A>G (p.Lys2592=)
c.612A>G (p.Lys204=)
c.8153A>G (n.8153A>G)
c.710A>G
c.8049A>G (p.Lys2683=)
13g.32363347A>TCA387749497BRCA2c.8145A>T (p.Lys2715Asn)
c.7776A>T (p.Lys2592Asn)
c.612A>T (p.Lys204Asn)
c.8153A>T (n.8153A>T)
c.710A>T
c.8049A>T (p.Lys2683Asn)
 dbSNP
13g.32363348G>ACA387749499BRCA2c.8146G>A (p.Val2716Met)
c.7777G>A (p.Val2593Met)
c.613G>A (p.Val205Met)
c.8154G>A (n.8154G>A)
c.711G>A
c.8050G>A (p.Val2684Met)
 ClinVar dbSNP
13g.32363348G>CCA387749501BRCA2c.8146G>C (p.Val2716Leu)
c.7777G>C (p.Val2593Leu)
c.613G>C (p.Val205Leu)
c.8154G>C (n.8154G>C)
c.711G>C
c.8050G>C (p.Val2684Leu)
 ClinVar dbSNP
13g.32363348G=CA2082835725BRCA2c.8146G= (p.Val2716=)
c.7777G= (p.Val2593=)
c.613G= (p.Val205=)
c.8154G= (n.8154G=)
c.711G=
c.8050G= (p.Val2684=)
13g.32363348G>TCA6941193BRCA2c.8146G>T (p.Val2716Leu)
c.7777G>T (p.Val2593Leu)
c.613G>T (p.Val205Leu)
c.8154G>T (n.8154G>T)
c.711G>T
c.8050G>T (p.Val2684Leu)
 dbSNP ExAC gnomAD v2
13g.32363348_32363349delinsGTCA2082835726BRCA2c.8146_8147delinsGT (p.Val2716=)
c.7777_7778delinsGT (p.Val2593=)
c.613_614delinsGT (p.Val205=)
c.8154_8155delinsGT (n.8154_8155delinsGT)
c.711_712delinsGT
c.8050_8051delinsGT (p.Val2684=)
13g.32363349delCA891843894BRCA2c.8147del (p.Val2716GlyfsTer17)
c.7778del (p.Val2593GlyfsTer17)
c.614del (p.Val205GlyfsTer17)
c.8155del (n.8155del)
c.712del
c.8051del (p.Val2684GlyfsTer17)
 ClinVar dbSNP
13g.32363349T>ACA387749504BRCA2c.8147T>A (p.Val2716Glu)
c.7778T>A (p.Val2593Glu)
c.614T>A (p.Val205Glu)
c.8155T>A (n.8155T>A)
c.712T>A
c.8051T>A (p.Val2684Glu)
13g.32363349T>CCA387749506BRCA2c.8147T>C (p.Val2716Ala)
c.7778T>C (p.Val2593Ala)
c.614T>C (p.Val205Ala)
c.8155T>C (n.8155T>C)
c.712T>C
c.8051T>C (p.Val2684Ala)
13g.32363349T>GCA387749508BRCA2c.8147T>G (p.Val2716Gly)
c.7778T>G (p.Val2593Gly)
c.614T>G (p.Val205Gly)
c.8155T>G (n.8155T>G)
c.712T>G
c.8051T>G (p.Val2684Gly)
13g.32363350G>ACA483439568BRCA2c.8148G>A (p.Val2716=)
c.7779G>A (p.Val2593=)
c.615G>A (p.Val205=)
c.8156G>A (n.8156G>A)
c.713G>A
c.8052G>A (p.Val2684=)
 ClinVar dbSNP
13g.32363350G>CCA483439569BRCA2c.8148G>C (p.Val2716=)
c.7779G>C (p.Val2593=)
c.615G>C (p.Val205=)
c.8156G>C (n.8156G>C)
c.713G>C
c.8052G>C (p.Val2684=)
 dbSNP
13g.32363350G=CA2082835737BRCA2c.8148G= (p.Val2716=)
c.7779G= (p.Val2593=)
c.615G= (p.Val205=)
c.8156G= (n.8156G=)
c.713G=
c.8052G= (p.Val2684=)
13g.32363350G>TCA483439570BRCA2c.8148G>T (p.Val2716=)
c.7779G>T (p.Val2593=)
c.615G>T (p.Val205=)
c.8156G>T (n.8156G>T)
c.713G>T
c.8052G>T (p.Val2684=)
 ClinVar dbSNP
13g.32363351G>ACA6941194BRCA2c.8149G>A (p.Ala2717Thr)
c.7780G>A (p.Ala2594Thr)
c.616G>A (p.Ala206Thr)
c.8157G>A (n.8157G>A)
c.714G>A
c.8053G>A (p.Ala2685Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32363351G>CCA387749511BRCA2c.8149G>C (p.Ala2717Pro)
c.7780G>C (p.Ala2594Pro)
c.616G>C (p.Ala206Pro)
c.8157G>C (n.8157G>C)
c.714G>C
c.8053G>C (p.Ala2685Pro)
 dbSNP
13g.32363351G=CA2082835750BRCA2c.8149G= (p.Ala2717=)
c.7780G= (p.Ala2594=)
c.616G= (p.Ala206=)
c.8157G= (n.8157G=)
c.714G=
c.8053G= (p.Ala2685=)
13g.32363351G>TCA025471BRCA2c.8149G>T (p.Ala2717Ser)
c.7780G>T (p.Ala2594Ser)
c.616G>T (p.Ala206Ser)
c.8157G>T (n.8157G>T)
c.714G>T
c.8053G>T (p.Ala2685Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32363352C>ACA387749517BRCA2c.8150C>A (p.Ala2717Asp)
c.7781C>A (p.Ala2594Asp)
c.617C>A (p.Ala206Asp)
c.8158C>A (n.8158C>A)
c.715C>A
c.8054C>A (p.Ala2685Asp)
13g.32363352C=CA2082835757BRCA2c.8150C= (p.Ala2717=)
c.7781C= (p.Ala2594=)
c.617C= (p.Ala206=)
c.8158C= (n.8158C=)
c.715C=
c.8054C= (p.Ala2685=)
13g.32363352C>GCA387749515BRCA2c.8150C>G (p.Ala2717Gly)
c.7781C>G (p.Ala2594Gly)
c.617C>G (p.Ala206Gly)
c.8158C>G (n.8158C>G)
c.715C>G
c.8054C>G (p.Ala2685Gly)
 dbSNP
13g.32363352C>TCA10579768BRCA2c.8150C>T (p.Ala2717Val)
c.7781C>T (p.Ala2594Val)
c.617C>T (p.Ala206Val)
c.8158C>T (n.8158C>T)
c.715C>T
c.8054C>T (p.Ala2685Val)
 ClinVar dbSNP COSMIC COSMIC
13g.32363353C>ACA483439573BRCA2c.8151C>A (p.Ala2717=)
c.7782C>A (p.Ala2594=)
c.618C>A (p.Ala206=)
c.8159C>A (n.8159C>A)
c.716C>A
c.8055C>A (p.Ala2685=)
 dbSNP
13g.32363353C=CA2082835763BRCA2c.8151C= (p.Ala2717=)
c.7782C= (p.Ala2594=)
c.618C= (p.Ala206=)
c.8159C= (n.8159C=)
c.716C=
c.8055C= (p.Ala2685=)
13g.32363353C>GCA483439574BRCA2c.8151C>G (p.Ala2717=)
c.7782C>G (p.Ala2594=)
c.618C>G (p.Ala206=)
c.8159C>G (n.8159C>G)
c.716C>G
c.8055C>G (p.Ala2685=)
 dbSNP
13g.32363353C>TCA338963BRCA2c.8151C>T (p.Ala2717=)
c.7782C>T (p.Ala2594=)
c.618C>T (p.Ala206=)
c.8159C>T (n.8159C>T)
c.716C>T
c.8055C>T (p.Ala2685=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32363354A=CA2082835773BRCA2c.8152A= (p.Ile2718=)
c.7783A= (p.Ile2595=)
c.619A= (p.Ile207=)
c.8160A= (n.8160A=)
c.717A=
c.8056A= (p.Ile2686=)
13g.32363354A>CCA387749520BRCA2c.8152A>C (p.Ile2718Leu)
c.7783A>C (p.Ile2595Leu)
c.619A>C (p.Ile207Leu)
c.8160A>C (n.8160A>C)
c.717A>C
c.8056A>C (p.Ile2686Leu)
13g.32363354A>GCA387749521BRCA2c.8152A>G (p.Ile2718Val)
c.7783A>G (p.Ile2595Val)
c.619A>G (p.Ile207Val)
c.8160A>G (n.8160A>G)
c.717A>G
c.8056A>G (p.Ile2686Val)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC
13g.32363354A>TCA387749523BRCA2c.8152A>T (p.Ile2718Phe)
c.7783A>T (p.Ile2595Phe)
c.619A>T (p.Ile207Phe)
c.8160A>T (n.8160A>T)
c.717A>T
c.8056A>T (p.Ile2686Phe)
 dbSNP
13g.32363355T>ACA387749524BRCA2c.8153T>A (p.Ile2718Asn)
c.7784T>A (p.Ile2595Asn)
c.620T>A (p.Ile207Asn)
c.8161T>A (n.8161T>A)
c.718T>A
c.8057T>A (p.Ile2686Asn)
 dbSNP
13g.32363355T>CCA025473BRCA2c.8153T>C (p.Ile2718Thr)
c.7784T>C (p.Ile2595Thr)
c.620T>C (p.Ile207Thr)
c.8161T>C (n.8161T>C)
c.718T>C
c.8057T>C (p.Ile2686Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32363355T>GCA387749526BRCA2c.8153T>G (p.Ile2718Ser)
c.7784T>G (p.Ile2595Ser)
c.620T>G (p.Ile207Ser)
c.8161T>G (n.8161T>G)
c.718T>G
c.8057T>G (p.Ile2686Ser)
 dbSNP
13g.32363355T=CA2082835785BRCA2c.8153T= (p.Ile2718=)
c.7784T= (p.Ile2595=)
c.620T= (p.Ile207=)
c.8161T= (n.8161T=)
c.718T=
c.8057T= (p.Ile2686=)
13g.32363356T>ACA483439575BRCA2c.8154T>A (p.Ile2718=)
c.7785T>A (p.Ile2595=)
c.621T>A (p.Ile207=)
c.8162T>A (n.8162T>A)
c.719T>A
c.8058T>A (p.Ile2686=)
 dbSNP
13g.32363356T>CCA025474BRCA2c.8154T>C (p.Ile2718=)
c.7785T>C (p.Ile2595=)
c.621T>C (p.Ile207=)
c.8162T>C (n.8162T>C)
c.719T>C
c.8058T>C (p.Ile2686=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32363356T>GCA387749530BRCA2c.8154T>G (p.Ile2718Met)
c.7785T>G (p.Ile2595Met)
c.621T>G (p.Ile207Met)
c.8162T>G (n.8162T>G)
c.719T>G
c.8058T>G (p.Ile2686Met)
 dbSNP
13g.32363356T=CA2082835792BRCA2c.8154T= (p.Ile2718=)
c.7785T= (p.Ile2595=)
c.621T= (p.Ile207=)
c.8162T= (n.8162T=)
c.719T=
c.8058T= (p.Ile2686=)
13g.32363357A=CA2082835805BRCA2c.8155A= (p.Ile2719=)
c.7786A= (p.Ile2596=)
c.622A= (p.Ile208=)
c.8163A= (n.8163A=)
c.720A=
c.8059A= (p.Ile2687=)
13g.32363357A>CCA387749532BRCA2c.8155A>C (p.Ile2719Leu)
c.7786A>C (p.Ile2596Leu)
c.622A>C (p.Ile208Leu)
c.8163A>C (n.8163A>C)
c.720A>C
c.8059A>C (p.Ile2687Leu)
13g.32363357A>GCA387749534BRCA2c.8155A>G (p.Ile2719Val)
c.7786A>G (p.Ile2596Val)
c.622A>G (p.Ile208Val)
c.8163A>G (n.8163A>G)
c.720A>G
c.8059A>G (p.Ile2687Val)
 ClinVar dbSNP
13g.32363357A>TCA387749535BRCA2c.8155A>T (p.Ile2719Phe)
c.7786A>T (p.Ile2596Phe)
c.622A>T (p.Ile208Phe)
c.8163A>T (n.8163A>T)
c.720A>T
c.8059A>T (p.Ile2687Phe)
 ClinVar dbSNP
13g.32363358T>ACA387749541BRCA2c.8156T>A (p.Ile2719Asn)
c.7787T>A (p.Ile2596Asn)
c.623T>A (p.Ile208Asn)
c.8164T>A (n.8164T>A)
c.721T>A
c.8060T>A (p.Ile2687Asn)
 dbSNP
13g.32363358T>CCA247477789BRCA2c.8156T>C (p.Ile2719Thr)
c.7787T>C (p.Ile2596Thr)
c.623T>C (p.Ile208Thr)
c.8164T>C (n.8164T>C)
c.721T>C
c.8060T>C (p.Ile2687Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32363358T>GCA387749538BRCA2c.8156T>G (p.Ile2719Ser)
c.7787T>G (p.Ile2596Ser)
c.623T>G (p.Ile208Ser)
c.8164T>G (n.8164T>G)
c.721T>G
c.8060T>G (p.Ile2687Ser)
13g.32363358T=CA2082835809BRCA2c.8156T= (p.Ile2719=)
c.7787T= (p.Ile2596=)
c.623T= (p.Ile208=)
c.8164T= (n.8164T=)
c.721T=
c.8060T= (p.Ile2687=)
13g.32363359delCA2580087486BRCA2c.8157del (p.Ile2719MetfsTer14)
c.7788del (p.Ile2596MetfsTer14)
c.624del (p.Ile208MetfsTer14)
c.8165del (n.8165del)
c.722del
c.8061del (p.Ile2687MetfsTer14)
 ClinVar
13g.32363359T>ACA483439578BRCA2c.8157T>A (p.Ile2719=)
c.7788T>A (p.Ile2596=)
c.624T>A (p.Ile208=)
c.8165T>A (n.8165T>A)
c.722T>A
c.8061T>A (p.Ile2687=)
 dbSNP
13g.32363359T>CCA025475BRCA2c.8157T>C (p.Ile2719=)
c.7788T>C (p.Ile2596=)
c.624T>C (p.Ile208=)
c.8165T>C (n.8165T>C)
c.722T>C
c.8061T>C (p.Ile2687=)
 ClinVar dbSNP
13g.32363359T>GCA025476BRCA2c.8157T>G (p.Ile2719Met)
c.7788T>G (p.Ile2596Met)
c.624T>G (p.Ile208Met)
c.8165T>G (n.8165T>G)
c.722T>G
c.8061T>G (p.Ile2687Met)
 ClinVar dbSNP gnomAD v4
13g.32363359T=CA2082835817BRCA2c.8157T= (p.Ile2719=)
c.7788T= (p.Ile2596=)
c.624T= (p.Ile208=)
c.8165T= (n.8165T=)
c.722T=
c.8061T= (p.Ile2687=)
13g.32363360G>ACA387749545BRCA2c.8158G>A (p.Glu2720Lys)
c.7789G>A (p.Glu2597Lys)
c.625G>A (p.Glu209Lys)
c.8166G>A (n.8166G>A)
c.723G>A
c.8062G>A (p.Glu2688Lys)
 ClinVar dbSNP
13g.32363360G>CCA387749547BRCA2c.8158G>C (p.Glu2720Gln)
c.7789G>C (p.Glu2597Gln)
c.625G>C (p.Glu209Gln)
c.8166G>C (n.8166G>C)
c.723G>C
c.8062G>C (p.Glu2688Gln)
 dbSNP
13g.32363360G=CA2082835828BRCA2c.8158G= (p.Glu2720=)
c.7789G= (p.Glu2597=)
c.625G= (p.Glu209=)
c.8166G= (n.8166G=)
c.723G=
c.8062G= (p.Glu2688=)
13g.32363360G>TCA387749549BRCA2c.8158G>T (p.Glu2720Ter)
c.7789G>T (p.Glu2597Ter)
c.625G>T (p.Glu209Ter)
c.8166G>T (n.8166G>T)
c.723G>T
c.8062G>T (p.Glu2688Ter)
 dbSNP
13g.32363361A>CCA387749551BRCA2c.8159A>C (p.Glu2720Ala)
c.7790A>C (p.Glu2597Ala)
c.626A>C (p.Glu209Ala)
c.8167A>C (n.8167A>C)
c.724A>C
c.8063A>C (p.Glu2688Ala)
 dbSNP
13g.32363361A>GCA387749553BRCA2c.8159A>G (p.Glu2720Gly)
c.7790A>G (p.Glu2597Gly)
c.626A>G (p.Glu209Gly)
c.8167A>G (n.8167A>G)
c.724A>G
c.8063A>G (p.Glu2688Gly)
 dbSNP
13g.32363361A>TCA387749555BRCA2c.8159A>T (p.Glu2720Val)
c.7790A>T (p.Glu2597Val)
c.626A>T (p.Glu209Val)
c.8167A>T (n.8167A>T)
c.724A>T
c.8063A>T (p.Glu2688Val)
 dbSNP
13g.32363362_32363398dupCA10589469BRCA2c.8160_8196dup (p.Asp2733ThrfsTer9)
c.7791_7827dup (p.Asp2610ThrfsTer9)
c.627_663dup (p.Asp222ThrfsTer9)
c.8168_8204dup (n.8168_8204dup)
c.725_761dup
c.8064_8100dup (p.Asp2701ThrfsTer9)
 ClinVar dbSNP
13g.32363362A>CCA387749558BRCA2c.8160A>C (p.Glu2720Asp)
c.7791A>C (p.Glu2597Asp)
c.627A>C (p.Glu209Asp)
c.8168A>C (n.8168A>C)
c.725A>C
c.8064A>C (p.Glu2688Asp)
 dbSNP
13g.32363362A>GCA483439582BRCA2c.8160A>G (p.Glu2720=)
c.7791A>G (p.Glu2597=)
c.627A>G (p.Glu209=)
c.8168A>G (n.8168A>G)
c.725A>G
c.8064A>G (p.Glu2688=)
13g.32363362A>TCA387749560BRCA2c.8160A>T (p.Glu2720Asp)
c.7791A>T (p.Glu2597Asp)
c.627A>T (p.Glu209Asp)
c.8168A>T (n.8168A>T)
c.725A>T
c.8064A>T (p.Glu2688Asp)
13g.32363363C>ACA387749563BRCA2c.8161C>A (p.Leu2721Ile)
c.7792C>A (p.Leu2598Ile)
c.628C>A (p.Leu210Ile)
c.8169C>A (n.8169C>A)
c.726C>A
c.8065C>A (p.Leu2689Ile)
13g.32363363C=CA2082835839BRCA2c.8161C= (p.Leu2721=)
c.7792C= (p.Leu2598=)
c.628C= (p.Leu210=)
c.8169C= (n.8169C=)
c.726C=
c.8065C= (p.Leu2689=)
13g.32363363C>GCA387749564BRCA2c.8161C>G (p.Leu2721Val)
c.7792C>G (p.Leu2598Val)
c.628C>G (p.Leu210Val)
c.8169C>G (n.8169C>G)
c.726C>G
c.8065C>G (p.Leu2689Val)
 ClinVar
13g.32363363C>TCA387749566BRCA2c.8161C>T (p.Leu2721Phe)
c.7792C>T (p.Leu2598Phe)
c.628C>T (p.Leu210Phe)
c.8169C>T (n.8169C>T)
c.726C>T
c.8065C>T (p.Leu2689Phe)
 ClinVar dbSNP
13g.32363364T>ACA025477BRCA2c.8162T>A (p.Leu2721His)
c.7793T>A (p.Leu2598His)
c.629T>A (p.Leu210His)
c.8170T>A (n.8170T>A)
c.727T>A
c.8066T>A (p.Leu2689His)
 ClinVar dbSNP
13g.32363364T>CCA387749568BRCA2c.8162T>C (p.Leu2721Pro)
c.7793T>C (p.Leu2598Pro)
c.629T>C (p.Leu210Pro)
c.8170T>C (n.8170T>C)
c.727T>C
c.8066T>C (p.Leu2689Pro)
 ClinVar dbSNP
13g.32363364T>GCA025478BRCA2c.8162T>G (p.Leu2721Arg)
c.7793T>G (p.Leu2598Arg)
c.629T>G (p.Leu210Arg)
c.8170T>G (n.8170T>G)
c.727T>G
c.8066T>G (p.Leu2689Arg)
 ClinVar dbSNP
13g.32363364T=CA2082835852BRCA2c.8162T= (p.Leu2721=)
c.7793T= (p.Leu2598=)
c.629T= (p.Leu210=)
c.8170T= (n.8170T=)
c.727T=
c.8066T= (p.Leu2689=)
13g.32363365T>ACA483439583BRCA2c.8163T>A (p.Leu2721=)
c.7794T>A (p.Leu2598=)
c.630T>A (p.Leu210=)
c.8171T>A (n.8171T>A)
c.728T>A
c.8067T>A (p.Leu2689=)
 dbSNP
13g.32363365T>CCA025479BRCA2c.8163T>C (p.Leu2721=)
c.7794T>C (p.Leu2598=)
c.630T>C (p.Leu210=)
c.8171T>C (n.8171T>C)
c.728T>C
c.8067T>C (p.Leu2689=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32363365T>GCA483439584BRCA2c.8163T>G (p.Leu2721=)
c.7794T>G (p.Leu2598=)
c.630T>G (p.Leu210=)
c.8171T>G (n.8171T>G)
c.728T>G
c.8067T>G (p.Leu2689=)
13g.32363365T=CA2082835856BRCA2c.8163T= (p.Leu2721=)
c.7794T= (p.Leu2598=)
c.630T= (p.Leu210=)
c.8171T= (n.8171T=)
c.728T=
c.8067T= (p.Leu2689=)
13g.32363365_32363366delinsTACA2082835860BRCA2c.8163_8164delinsTA (p.Leu2721=)
c.7794_7795delinsTA (p.Leu2598=)
c.630_631delinsTA (p.Leu210=)
c.8171_8172delinsTA (n.8171_8172delinsTA)
c.728_729delinsTA
c.8067_8068delinsTA (p.Leu2689=)
13g.32363366delCA10589470BRCA2c.8164del (p.Thr2722GlnfsTer11)
c.7795del (p.Thr2599GlnfsTer11)
c.631del (p.Thr211GlnfsTer11)
c.8172del (n.8172del)
c.729del
c.8068del (p.Thr2690GlnfsTer11)
 ClinVar dbSNP
13g.32363366A=CA2082835873BRCA2c.8164A= (p.Thr2722=)
c.7795A= (p.Thr2599=)
c.631A= (p.Thr211=)
c.8172A= (n.8172A=)
c.729A=
c.8068A= (p.Thr2690=)
13g.32363366A>CCA387749573BRCA2c.8164A>C (p.Thr2722Pro)
c.7795A>C (p.Thr2599Pro)
c.631A>C (p.Thr211Pro)
c.8172A>C (n.8172A>C)
c.729A>C
c.8068A>C (p.Thr2690Pro)
 dbSNP
13g.32363366A>GCA387749574BRCA2c.8164A>G (p.Thr2722Ala)
c.7795A>G (p.Thr2599Ala)
c.631A>G (p.Thr211Ala)
c.8172A>G (n.8172A>G)
c.729A>G
c.8068A>G (p.Thr2690Ala)
 ClinVar dbSNP gnomAD v4
13g.32363366A>TCA387749576BRCA2c.8164A>T (p.Thr2722Ser)
c.7795A>T (p.Thr2599Ser)
c.631A>T (p.Thr211Ser)
c.8172A>T (n.8172A>T)
c.729A>T
c.8068A>T (p.Thr2690Ser)
 dbSNP
13g.32363366dupCA2573149390BRCA2c.8164dup (p.Thr2722AsnfsTer8)
c.7795dup (p.Thr2599AsnfsTer8)
c.631dup (p.Thr211AsnfsTer8)
c.8172dup (n.8172dup)
c.729dup
c.8068dup (p.Thr2690AsnfsTer8)
 ClinVar dbSNP
13g.32363367_32363368delCA2739277543BRCA2c.8165_8166del (p.Thr2722ArgfsTer7)
c.7796_7797del (p.Thr2599ArgfsTer7)
c.632_633del (p.Thr211ArgfsTer7)
c.8173_8174del (n.8173_8174del)
c.730_731del
c.8069_8070del (p.Thr2690ArgfsTer7)
 ClinVar
13g.32363367C>ACA10579769BRCA2c.8165C>A (p.Thr2722Lys)
c.7796C>A (p.Thr2599Lys)
c.632C>A (p.Thr211Lys)
c.8173C>A (n.8173C>A)
c.730C>A
c.8069C>A (p.Thr2690Lys)
 ClinVar dbSNP
13g.32363367C=CA2082835881BRCA2c.8165C= (p.Thr2722=)
c.7796C= (p.Thr2599=)
c.632C= (p.Thr211=)
c.8173C= (n.8173C=)
c.730C=
c.8069C= (p.Thr2690=)
13g.32363367C>GCA025480BRCA2c.8165C>G (p.Thr2722Arg)
c.7796C>G (p.Thr2599Arg)
c.632C>G (p.Thr211Arg)
c.8173C>G (n.8173C>G)
c.730C>G
c.8069C>G (p.Thr2690Arg)
 ClinVar dbSNP
13g.32363367C>TCA387749581BRCA2c.8165C>T (p.Thr2722Ile)
c.7796C>T (p.Thr2599Ile)
c.632C>T (p.Thr211Ile)
c.8173C>T (n.8173C>T)
c.730C>T
c.8069C>T (p.Thr2690Ile)
 ClinVar dbSNP gnomAD v4
13g.32363368A=CA2082835896BRCA2c.8166A= (p.Thr2722=)
c.7797A= (p.Thr2599=)
c.633A= (p.Thr211=)
c.8174A= (n.8174A=)
c.731A=
c.8070A= (p.Thr2690=)
13g.32363368A>CCA025481BRCA2c.8166A>C (p.Thr2722=)
c.7797A>C (p.Thr2599=)
c.633A>C (p.Thr211=)
c.8174A>C (n.8174A>C)
c.731A>C
c.8070A>C (p.Thr2690=)
 ClinVar dbSNP gnomAD v4
13g.32363368A>GCA16606820BRCA2c.8166A>G (p.Thr2722=)
c.7797A>G (p.Thr2599=)
c.633A>G (p.Thr211=)
c.8174A>G (n.8174A>G)
c.731A>G
c.8070A>G (p.Thr2690=)
 ClinVar dbSNP
13g.32363368A>TCA483439586BRCA2c.8166A>T (p.Thr2722=)
c.7797A>T (p.Thr2599=)
c.633A>T (p.Thr211=)
c.8174A>T (n.8174A>T)
c.731A>T
c.8070A>T (p.Thr2690=)
 dbSNP
13g.32363369G>ACA387749585BRCA2c.8167G>A (p.Asp2723Asn)
c.7798G>A (p.Asp2600Asn)
c.634G>A (p.Asp212Asn)
c.8175G>A (n.8175G>A)
c.732G>A
c.8071G>A (p.Asp2691Asn)
 ClinVar dbSNP
13g.32363369G>CCA025482BRCA2c.8167G>C (p.Asp2723His)
c.7798G>C (p.Asp2600His)
c.634G>C (p.Asp212His)
c.8175G>C (n.8175G>C)
c.732G>C
c.8071G>C (p.Asp2691His)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32363369G=CA2082835903BRCA2c.8167G= (p.Asp2723=)
c.7798G= (p.Asp2600=)
c.634G= (p.Asp212=)
c.8175G= (n.8175G=)
c.732G=
c.8071G= (p.Asp2691=)
13g.32363369G>TCA387749586BRCA2c.8167G>T (p.Asp2723Tyr)
c.7798G>T (p.Asp2600Tyr)
c.634G>T (p.Asp212Tyr)
c.8175G>T (n.8175G>T)
c.732G>T
c.8071G>T (p.Asp2691Tyr)
13g.32363370A=CA2082835912BRCA2c.8168A= (p.Asp2723=)
c.7799A= (p.Asp2600=)
c.635A= (p.Asp212=)
c.8176A= (n.8176A=)
c.733A=
c.8072A= (p.Asp2691=)
13g.32363370A>CCA025483BRCA2c.8168A>C (p.Asp2723Ala)
c.7799A>C (p.Asp2600Ala)
c.635A>C (p.Asp212Ala)
c.8176A>C (n.8176A>C)
c.733A>C
c.8072A>C (p.Asp2691Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32363370A>GCA025484BRCA2c.8168A>G (p.Asp2723Gly)
c.7799A>G (p.Asp2600Gly)
c.635A>G (p.Asp212Gly)
c.8176A>G (n.8176A>G)
c.733A>G
c.8072A>G (p.Asp2691Gly)
 ClinVar dbSNP gnomAD v4
13g.32363370A>TCA025485BRCA2c.8168A>T (p.Asp2723Val)
c.7799A>T (p.Asp2600Val)
c.635A>T (p.Asp212Val)
c.8176A>T (n.8176A>T)
c.733A>T
c.8072A>T (p.Asp2691Val)
 ClinVar dbSNP gnomAD v4
13g.32363371T>ACA16614371BRCA2c.8169T>A (p.Asp2723Glu)
c.7800T>A (p.Asp2600Glu)
c.636T>A (p.Asp212Glu)
c.8177T>A (n.8177T>A)
c.734T>A
c.8073T>A (p.Asp2691Glu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32363371T>CCA483439587BRCA2c.8169T>C (p.Asp2723=)
c.7800T>C (p.Asp2600=)
c.636T>C (p.Asp212=)
c.8177T>C (n.8177T>C)
c.734T>C
c.8073T>C (p.Asp2691=)
 ClinVar dbSNP gnomAD v4
13g.32363371T>GCA387749594BRCA2c.8169T>G (p.Asp2723Glu)
c.7800T>G (p.Asp2600Glu)
c.636T>G (p.Asp212Glu)
c.8177T>G (n.8177T>G)
c.734T>G
c.8073T>G (p.Asp2691Glu)
13g.32363371T=CA2082835924BRCA2c.8169T= (p.Asp2723=)
c.7800T= (p.Asp2600=)
c.636T= (p.Asp212=)
c.8177T= (n.8177T=)
c.734T=
c.8073T= (p.Asp2691=)
13g.32363371_32363372delinsTGCA2082835931BRCA2c.8169_8170delinsTG (p.Asp2723=)
c.7800_7801delinsTG (p.Asp2600=)
c.636_637delinsTG (p.Asp212=)
c.8177_8178delinsTG (n.8177_8178delinsTG)
c.734_735delinsTG
c.8073_8074delinsTG (p.Asp2691=)
13g.32363374_32363377dupCA025489BRCA2c.8172_8175dup (p.Tyr2726ValfsTer5)
c.7803_7806dup (p.Tyr2603ValfsTer5)
c.639_642dup (p.Tyr215ValfsTer5)
c.8180_8183dup (n.8180_8183dup)
c.737_740dup
c.8076_8079dup (p.Tyr2694ValfsTer5)
 ClinVar dbSNP
13g.32363372G>ACA387749597BRCA2c.8170G>A (p.Gly2724Arg)
c.7801G>A (p.Gly2601Arg)
c.637G>A (p.Gly213Arg)
c.8178G>A (n.8178G>A)
c.735G>A
c.8074G>A (p.Gly2692Arg)
 ClinVar dbSNP
13g.32363372G>CCA387749599BRCA2c.8170G>C (p.Gly2724Arg)
c.7801G>C (p.Gly2601Arg)
c.637G>C (p.Gly213Arg)
c.8178G>C (n.8178G>C)
c.735G>C
c.8074G>C (p.Gly2692Arg)
 dbSNP
13g.32363372G=CA2082835941BRCA2c.8170G= (p.Gly2724=)
c.7801G= (p.Gly2601=)
c.637G= (p.Gly213=)
c.8178G= (n.8178G=)
c.735G=
c.8074G= (p.Gly2692=)
13g.32363372G>TCA16607488BRCA2c.8170G>T (p.Gly2724Trp)
c.7801G>T (p.Gly2601Trp)
c.637G>T (p.Gly213Trp)
c.8178G>T (n.8178G>T)
c.735G>T
c.8074G>T (p.Gly2692Trp)
 ClinVar dbSNP gnomAD v4
13g.32363374delCA919242797BRCA2c.8172del (p.Trp2725GlyfsTer8)
c.7803del (p.Trp2602GlyfsTer8)
c.639del (p.Trp214GlyfsTer8)
c.8180del (n.8180del)
c.737del
c.8076del (p.Trp2693GlyfsTer8)
 ClinVar dbSNP
13g.32363373G>ACA387749602BRCA2c.8171G>A (p.Gly2724Glu)
c.7802G>A (p.Gly2601Glu)
c.638G>A (p.Gly213Glu)
c.8179G>A (n.8179G>A)
c.736G>A
c.8075G>A (p.Gly2692Glu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32363373G>CCA387749604BRCA2c.8171G>C (p.Gly2724Ala)
c.7802G>C (p.Gly2601Ala)
c.638G>C (p.Gly213Ala)
c.8179G>C (n.8179G>C)
c.736G>C
c.8075G>C (p.Gly2692Ala)
 dbSNP gnomAD v4
13g.32363373G=CA2082835944BRCA2c.8171G= (p.Gly2724=)
c.7802G= (p.Gly2601=)
c.638G= (p.Gly213=)
c.8179G= (n.8179G=)
c.736G=
c.8075G= (p.Gly2692=)
13g.32363373G>TCA025486BRCA2c.8171G>T (p.Gly2724Val)
c.7802G>T (p.Gly2601Val)
c.638G>T (p.Gly213Val)
c.8179G>T (n.8179G>T)
c.736G>T
c.8075G>T (p.Gly2692Val)
 ClinVar dbSNP
13g.32363373_32363383delinsGGTGGTATGCTCA2082835951BRCA2c.8171_8181delinsGGTGGTATGCT (p.Gly2724=)
c.7802_7812delinsGGTGGTATGCT (p.Gly2601=)
c.638_648delinsGGTGGTATGCT (p.Gly213=)
c.8179_8189delinsGGTGGTATGCT (n.8179_8189delinsGGTGGTATGCT)
c.736_746delinsGGTGGTATGCT
c.8075_8085delinsGGTGGTATGCT (p.Gly2692=)
13g.32363374G>ACA10579770BRCA2c.8172G>A (p.Gly2724=)
c.7803G>A (p.Gly2601=)
c.639G>A (p.Gly213=)
c.8180G>A (n.8180G>A)
c.737G>A
c.8076G>A (p.Gly2692=)
 ClinVar dbSNP
13g.32363374G>CCA483439588BRCA2c.8172G>C (p.Gly2724=)
c.7803G>C (p.Gly2601=)
c.639G>C (p.Gly213=)
c.8180G>C (n.8180G>C)
c.737G>C
c.8076G>C (p.Gly2692=)
 dbSNP
13g.32363374G=CA2082835968BRCA2c.8172G= (p.Gly2724=)
c.7803G= (p.Gly2601=)
c.639G= (p.Gly213=)
c.8180G= (n.8180G=)
c.737G=
c.8076G= (p.Gly2692=)
13g.32363374G>TCA483439589BRCA2c.8172G>T (p.Gly2724=)
c.7803G>T (p.Gly2601=)
c.639G>T (p.Gly213=)
c.8180G>T (n.8180G>T)
c.737G>T
c.8076G>T (p.Gly2692=)
 ClinVar dbSNP
13g.32363376_32363385delCA2082835956BRCA2c.8174_8183del (p.Trp2725LeufsTer5)
c.7805_7814del (p.Trp2602LeufsTer5)
c.641_650del (p.Trp214LeufsTer5)
c.8182_8191del (n.8182_8191del)
c.739_748del
c.8078_8087del (p.Trp2693LeufsTer5)
 dbSNP
13g.32363375T>ACA387749608BRCA2c.8173T>A (p.Trp2725Arg)
c.7804T>A (p.Trp2602Arg)
c.640T>A (p.Trp214Arg)
c.8181T>A (n.8181T>A)
c.738T>A
c.8077T>A (p.Trp2693Arg)
13g.32363375T>CCA387749610BRCA2c.8173T>C (p.Trp2725Arg)
c.7804T>C (p.Trp2602Arg)
c.640T>C (p.Trp214Arg)
c.8181T>C (n.8181T>C)
c.738T>C
c.8077T>C (p.Trp2693Arg)
 ClinVar
13g.32363375T>GCA387749612BRCA2c.8173T>G (p.Trp2725Gly)
c.7804T>G (p.Trp2602Gly)
c.640T>G (p.Trp214Gly)
c.8181T>G (n.8181T>G)
c.738T>G
c.8077T>G (p.Trp2693Gly)
 ClinVar dbSNP
13g.32363375_32363384delinsTGGTATGCTGCA2082835976BRCA2c.8173_8182delinsTGGTATGCTG (p.Trp2725=)
c.7804_7813delinsTGGTATGCTG (p.Trp2602=)
c.640_649delinsTGGTATGCTG (p.Trp214=)
c.8181_8190delinsTGGTATGCTG (n.8181_8190delinsTGGTATGCTG)
c.738_747delinsTGGTATGCTG
c.8077_8086delinsTGGTATGCTG (p.Trp2693=)
13g.32363375_32363387delinsTGGTATGCTGTTACA2082835974BRCA2c.8173_8185delinsTGGTATGCTGTTA (p.Trp2725=)
c.7804_7816delinsTGGTATGCTGTTA (p.Trp2602=)
c.640_652delinsTGGTATGCTGTTA (p.Trp214=)
c.8181_8193delinsTGGTATGCTGTTA (n.8181_8193delinsTGGTATGCTGTTA)
c.738_750delinsTGGTATGCTGTTA
c.8077_8089delinsTGGTATGCTGTTA (p.Trp2693=)
13g.32363376G>ACA025488BRCA2c.8174G>A (p.Trp2725Ter)
c.7805G>A (p.Trp2602Ter)
c.641G>A (p.Trp214Ter)
c.8182G>A (n.8182G>A)
c.739G>A
c.8078G>A (p.Trp2693Ter)
 ClinVar dbSNP
13g.32363376G>CCA387749616BRCA2c.8174G>C (p.Trp2725Ser)
c.7805G>C (p.Trp2602Ser)
c.641G>C (p.Trp214Ser)
c.8182G>C (n.8182G>C)
c.739G>C
c.8078G>C (p.Trp2693Ser)
 dbSNP
13g.32363376G=CA2082835989BRCA2c.8174G= (p.Trp2725=)
c.7805G= (p.Trp2602=)
c.641G= (p.Trp214=)
c.8182G= (n.8182G=)
c.739G=
c.8078G= (p.Trp2693=)
13g.32363376G>TCA387749613BRCA2c.8174G>T (p.Trp2725Leu)
c.7805G>T (p.Trp2602Leu)
c.641G>T (p.Trp214Leu)
c.8182G>T (n.8182G>T)
c.739G>T
c.8078G>T (p.Trp2693Leu)
 ClinVar dbSNP
13g.32363377delCA2499222321BRCA2c.8175del (p.Trp2725CysfsTer8)
c.7806del (p.Trp2602CysfsTer8)
c.642del (p.Trp214CysfsTer8)
c.8183del (n.8183del)
c.740del
c.8079del (p.Trp2693CysfsTer8)
 ClinVar
13g.32363376_32363384delCA954700683BRCA2c.8174_8182del (p.Trp2725_Val2728delinsPhe)
c.7805_7813del (p.Trp2602_Val2605delinsPhe)
c.641_649del (p.Trp214_Val217delinsPhe)
c.8182_8190del (n.8182_8190del)
c.739_747del
c.8078_8086del (p.Trp2693_Val2696delinsPhe)
 dbSNP gnomAD v3 gnomAD v4
13g.32363376_32363387delinsTTCA025487BRCA2c.8174_8185delinsTT (p.Trp2725PhefsTer5)
c.7805_7816delinsTT (p.Trp2602PhefsTer5)
c.641_652delinsTT (p.Trp214PhefsTer5)
c.8182_8193delinsTT (n.8182_8193delinsTT)
c.739_750delinsTT
c.8078_8089delinsTT (p.Trp2693PhefsTer5)
 ClinVar dbSNP
13g.32363377G>ACA025490BRCA2c.8175G>A (p.Trp2725Ter)
c.7806G>A (p.Trp2602Ter)
c.642G>A (p.Trp214Ter)
c.8183G>A (n.8183G>A)
c.740G>A
c.8079G>A (p.Trp2693Ter)
 ClinVar dbSNP
13g.32363377G>CCA387749620BRCA2c.8175G>C (p.Trp2725Cys)
c.7806G>C (p.Trp2602Cys)
c.642G>C (p.Trp214Cys)
c.8183G>C (n.8183G>C)
c.740G>C
c.8079G>C (p.Trp2693Cys)
 dbSNP
13g.32363377G=CA2082836011BRCA2c.8175G= (p.Trp2725=)
c.7806G= (p.Trp2602=)
c.642G= (p.Trp214=)
c.8183G= (n.8183G=)
c.740G=
c.8079G= (p.Trp2693=)
13g.32363377G>TCA387749622BRCA2c.8175G>T (p.Trp2725Cys)
c.7806G>T (p.Trp2602Cys)
c.642G>T (p.Trp214Cys)
c.8183G>T (n.8183G>T)
c.740G>T
c.8079G>T (p.Trp2693Cys)
 dbSNP
13g.32363378T>ACA387749624BRCA2c.8176T>A (p.Tyr2726Asn)
c.7807T>A (p.Tyr2603Asn)
c.643T>A (p.Tyr215Asn)
c.8184T>A (n.8184T>A)
c.741T>A
c.8080T>A (p.Tyr2694Asn)
 ClinVar dbSNP gnomAD v4
13g.32363378T>CCA387749626BRCA2c.8176T>C (p.Tyr2726His)
c.7807T>C (p.Tyr2603His)
c.643T>C (p.Tyr215His)
c.8184T>C (n.8184T>C)
c.741T>C
c.8080T>C (p.Tyr2694His)
 dbSNP
13g.32363378T>GCA387749628BRCA2c.8176T>G (p.Tyr2726Asp)
c.7807T>G (p.Tyr2603Asp)
c.643T>G (p.Tyr215Asp)
c.8184T>G (n.8184T>G)
c.741T>G
c.8080T>G (p.Tyr2694Asp)
 dbSNP
13g.32363379A=CA2082836025BRCA2c.8177A= (p.Tyr2726=)
c.7808A= (p.Tyr2603=)
c.644A= (p.Tyr215=)
c.8185A= (n.8185A=)
c.742A=
c.8081A= (p.Tyr2694=)
13g.32363379A>CCA387749630BRCA2c.8177A>C (p.Tyr2726Ser)
c.7808A>C (p.Tyr2603Ser)
c.644A>C (p.Tyr215Ser)
c.8185A>C (n.8185A>C)
c.742A>C
c.8081A>C (p.Tyr2694Ser)
 dbSNP
13g.32363379A>GCA025491BRCA2c.8177A>G (p.Tyr2726Cys)
c.7808A>G (p.Tyr2603Cys)
c.644A>G (p.Tyr215Cys)
c.8185A>G (n.8185A>G)
c.742A>G
c.8081A>G (p.Tyr2694Cys)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32363379A>TCA387749633BRCA2c.8177A>T (p.Tyr2726Phe)
c.7808A>T (p.Tyr2603Phe)
c.644A>T (p.Tyr215Phe)
c.8185A>T (n.8185A>T)
c.742A>T
c.8081A>T (p.Tyr2694Phe)
 ClinVar dbSNP
13g.32363380T>ACA10586587BRCA2c.8178T>A (p.Tyr2726Ter)
c.7809T>A (p.Tyr2603Ter)
c.645T>A (p.Tyr215Ter)
c.8186T>A (n.8186T>A)
c.743T>A
c.8082T>A (p.Tyr2694Ter)
 ClinVar dbSNP
13g.32363380T>CCA6941195BRCA2c.8178T>C (p.Tyr2726=)
c.7809T>C (p.Tyr2603=)
c.645T>C (p.Tyr215=)
c.8186T>C (n.8186T>C)
c.743T>C
c.8082T>C (p.Tyr2694=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32363380T>GCA387749637BRCA2c.8178T>G (p.Tyr2726Ter)
c.7809T>G (p.Tyr2603Ter)
c.645T>G (p.Tyr215Ter)
c.8186T>G (n.8186T>G)
c.743T>G
c.8082T>G (p.Tyr2694Ter)
13g.32363380T=CA2082836042BRCA2c.8178T= (p.Tyr2726=)
c.7809T= (p.Tyr2603=)
c.645T= (p.Tyr215=)
c.8186T= (n.8186T=)
c.743T=
c.8082T= (p.Tyr2694=)
13g.32363380_32363389delinsTGCTGTTAAGCA2082836036BRCA2c.8178_8187delinsTGCTGTTAAG (p.Tyr2726=)
c.7809_7818delinsTGCTGTTAAG (p.Tyr2603=)
c.645_654delinsTGCTGTTAAG (p.Tyr215=)
c.8186_8195delinsTGCTGTTAAG (n.8186_8195delinsTGCTGTTAAG)
c.743_752delinsTGCTGTTAAG
c.8082_8091delinsTGCTGTTAAG (p.Tyr2694=)
13g.32363381G>ACA387749643BRCA2c.8179G>A (p.Ala2727Thr)
c.7810G>A (p.Ala2604Thr)
c.646G>A (p.Ala216Thr)
c.8187G>A (n.8187G>A)
c.744G>A
c.8083G>A (p.Ala2695Thr)
 ClinVar dbSNP
13g.32363381G>CCA387749640BRCA2c.8179G>C (p.Ala2727Pro)
c.7810G>C (p.Ala2604Pro)
c.646G>C (p.Ala216Pro)
c.8187G>C (n.8187G>C)
c.744G>C
c.8083G>C (p.Ala2695Pro)
 dbSNP
13g.32363381G=CA2082836056BRCA2c.8179G= (p.Ala2727=)
c.7810G= (p.Ala2604=)
c.646G= (p.Ala216=)
c.8187G= (n.8187G=)
c.744G=
c.8083G= (p.Ala2695=)
13g.32363381G>TCA025492BRCA2c.8179G>T (p.Ala2727Ser)
c.7810G>T (p.Ala2604Ser)
c.646G>T (p.Ala216Ser)
c.8187G>T (n.8187G>T)
c.744G>T
c.8083G>T (p.Ala2695Ser)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32363383_32363391delCA025493BRCA2c.8181_8189del (p.Val2728_Ala2730del)
c.7812_7820del (p.Val2605_Ala2607del)
c.648_656del (p.Val217_Ala219del)
c.8189_8197del (n.8189_8197del)
c.746_754del
c.8085_8093del (p.Val2696_Ala2698del)
 ClinVar dbSNP
13g.32363382C>ACA387749646BRCA2c.8180C>A (p.Ala2727Asp)
c.7811C>A (p.Ala2604Asp)
c.647C>A (p.Ala216Asp)
c.8188C>A (n.8188C>A)
c.745C>A
c.8084C>A (p.Ala2695Asp)
 dbSNP
13g.32363382C=CA2082836066BRCA2c.8180C= (p.Ala2727=)
c.7811C= (p.Ala2604=)
c.647C= (p.Ala216=)
c.8188C= (n.8188C=)
c.745C=
c.8084C= (p.Ala2695=)
13g.32363382C>GCA10586083BRCA2c.8180C>G (p.Ala2727Gly)
c.7811C>G (p.Ala2604Gly)
c.647C>G (p.Ala216Gly)
c.8188C>G (n.8188C>G)
c.745C>G
c.8084C>G (p.Ala2695Gly)
 ClinVar dbSNP gnomAD v4
13g.32363382C>TCA387749648BRCA2c.8180C>T (p.Ala2727Val)
c.7811C>T (p.Ala2604Val)
c.647C>T (p.Ala216Val)
c.8188C>T (n.8188C>T)
c.745C>T
c.8084C>T (p.Ala2695Val)
 ClinVar dbSNP
13g.32363383delCA2695199720BRCA2c.8181del (p.Val2728LeufsTer5)
c.7812del (p.Val2605LeufsTer5)
c.648del (p.Val217LeufsTer5)
c.8189del (n.8189del)
c.746del
c.8085del (p.Val2696LeufsTer5)
 ClinVar
13g.32363383T>ACA483439593BRCA2c.8181T>A (p.Ala2727=)
c.7812T>A (p.Ala2604=)
c.648T>A (p.Ala216=)
c.8189T>A (n.8189T>A)
c.746T>A
c.8085T>A (p.Ala2695=)
 dbSNP
13g.32363383T>CCA483439594BRCA2c.8181T>C (p.Ala2727=)
c.7812T>C (p.Ala2604=)
c.648T>C (p.Ala216=)
c.8189T>C (n.8189T>C)
c.746T>C
c.8085T>C (p.Ala2695=)
13g.32363383T>GCA483439595BRCA2c.8181T>G (p.Ala2727=)
c.7812T>G (p.Ala2604=)
c.648T>G (p.Ala216=)
c.8189T>G (n.8189T>G)
c.746T>G
c.8085T>G (p.Ala2695=)
13g.32363384G>ACA025494BRCA2c.8182G>A (p.Val2728Ile)
c.7813G>A (p.Val2605Ile)
c.649G>A (p.Val217Ile)
c.8190G>A (n.8190G>A)
c.747G>A
c.8086G>A (p.Val2696Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32363384G>CCA025495BRCA2c.8182G>C (p.Val2728Leu)
c.7813G>C (p.Val2605Leu)
c.649G>C (p.Val217Leu)
c.8190G>C (n.8190G>C)
c.747G>C
c.8086G>C (p.Val2696Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32363384G=CA2082836077BRCA2c.8182G= (p.Val2728=)
c.7813G= (p.Val2605=)
c.649G= (p.Val217=)
c.8190G= (n.8190G=)
c.747G=
c.8086G= (p.Val2696=)
13g.32363384G>TCA387749652BRCA2c.8182G>T (p.Val2728Phe)
c.7813G>T (p.Val2605Phe)
c.649G>T (p.Val217Phe)
c.8190G>T (n.8190G>T)
c.747G>T
c.8086G>T (p.Val2696Phe)
 ClinVar
13g.32363385T>ACA387749655BRCA2c.8183T>A (p.Val2728Asp)
c.7814T>A (p.Val2605Asp)
c.650T>A (p.Val217Asp)
c.8191T>A (n.8191T>A)
c.748T>A
c.8087T>A (p.Val2696Asp)
 dbSNP
13g.32363385T>CCA025496BRCA2c.8183T>C (p.Val2728Ala)
c.7814T>C (p.Val2605Ala)
c.650T>C (p.Val217Ala)
c.8191T>C (n.8191T>C)
c.748T>C
c.8087T>C (p.Val2696Ala)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32363385T>GCA387749657BRCA2c.8183T>G (p.Val2728Gly)
c.7814T>G (p.Val2605Gly)
c.650T>G (p.Val217Gly)
c.8191T>G (n.8191T>G)
c.748T>G
c.8087T>G (p.Val2696Gly)
 dbSNP
13g.32363385T=CA2082836093BRCA2c.8183T= (p.Val2728=)
c.7814T= (p.Val2605=)
c.650T= (p.Val217=)
c.8191T= (n.8191T=)
c.748T=
c.8087T= (p.Val2696=)
13g.32363386T>ACA483439597BRCA2c.8184T>A (p.Val2728=)
c.7815T>A (p.Val2605=)
c.651T>A (p.Val217=)
c.8192T>A (n.8192T>A)
c.749T>A
c.8088T>A (p.Val2696=)
13g.32363386T>CCA483439598BRCA2c.8184T>C (p.Val2728=)
c.7815T>C (p.Val2605=)
c.651T>C (p.Val217=)
c.8192T>C (n.8192T>C)
c.749T>C
c.8088T>C (p.Val2696=)
 ClinVar dbSNP
13g.32363386T>GCA483439599BRCA2c.8184T>G (p.Val2728=)
c.7815T>G (p.Val2605=)
c.651T>G (p.Val217=)
c.8192T>G (n.8192T>G)
c.749T>G
c.8088T>G (p.Val2696=)
13g.32363386_32363387delinsTACA2082836098BRCA2c.8184_8185delinsTA (p.Val2728=)
c.7815_7816delinsTA (p.Val2605=)
c.651_652delinsTA (p.Val217=)
c.8192_8193delinsTA (n.8192_8193delinsTA)
c.749_750delinsTA
c.8088_8089delinsTA (p.Val2696=)
13g.32363387A=CA2082836105BRCA2c.8185A= (p.Lys2729=)
c.7816A= (p.Lys2606=)
c.652A= (p.Lys218=)
c.8193A= (n.8193A=)
c.750A=
c.8089A= (p.Lys2697=)
13g.32363387A>CCA387749660BRCA2c.8185A>C (p.Lys2729Gln)
c.7816A>C (p.Lys2606Gln)
c.652A>C (p.Lys218Gln)
c.8193A>C (n.8193A>C)
c.750A>C
c.8089A>C (p.Lys2697Gln)
13g.32363387A>GCA387749662BRCA2c.8185A>G (p.Lys2729Glu)
c.7816A>G (p.Lys2606Glu)
c.652A>G (p.Lys218Glu)
c.8193A>G (n.8193A>G)
c.750A>G
c.8089A>G (p.Lys2697Glu)
13g.32363387A>TCA387749663BRCA2c.8185A>T (p.Lys2729Ter)
c.7816A>T (p.Lys2606Ter)
c.652A>T (p.Lys218Ter)
c.8193A>T (n.8193A>T)
c.750A>T
c.8089A>T (p.Lys2697Ter)
 dbSNP
13g.32363388delCA954700713BRCA2c.8186del (p.Lys2729ArgfsTer4)
c.7817del (p.Lys2606ArgfsTer4)
c.653del (p.Lys218ArgfsTer4)
c.8194del (n.8194del)
c.751del
c.8090del (p.Lys2697ArgfsTer4)
 dbSNP gnomAD v3 gnomAD v4
13g.32363388A=CA2082836107BRCA2c.8186A= (p.Lys2729=)
c.7817A= (p.Lys2606=)
c.653A= (p.Lys218=)
c.8194A= (n.8194A=)
c.751A=
c.8090A= (p.Lys2697=)
13g.32363388A>CCA387749668BRCA2c.8186A>C (p.Lys2729Thr)
c.7817A>C (p.Lys2606Thr)
c.653A>C (p.Lys218Thr)
c.8194A>C (n.8194A>C)
c.751A>C
c.8090A>C (p.Lys2697Thr)
13g.32363388A>GCA6941196BRCA2c.8186A>G (p.Lys2729Arg)
c.7817A>G (p.Lys2606Arg)
c.653A>G (p.Lys218Arg)
c.8194A>G (n.8194A>G)
c.751A>G
c.8090A>G (p.Lys2697Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32363388A>TCA387749666BRCA2c.8186A>T (p.Lys2729Met)
c.7817A>T (p.Lys2606Met)
c.653A>T (p.Lys218Met)
c.8194A>T (n.8194A>T)
c.751A>T
c.8090A>T (p.Lys2697Met)
13g.32363389G>ACA025497BRCA2c.8187G>A (p.Lys2729=)
c.7818G>A (p.Lys2606=)
c.654G>A (p.Lys218=)
c.8195G>A (n.8195G>A)
c.752G>A
c.8091G>A (p.Lys2697=)
 ClinVar dbSNP gnomAD v4
13g.32363389G>CCA387749672BRCA2c.8187G>C (p.Lys2729Asn)
c.7818G>C (p.Lys2606Asn)
c.654G>C (p.Lys218Asn)
c.8195G>C (n.8195G>C)
c.752G>C
c.8091G>C (p.Lys2697Asn)
 dbSNP
13g.32363389G=CA2082836122BRCA2c.8187G= (p.Lys2729=)
c.7818G= (p.Lys2606=)
c.654G= (p.Lys218=)
c.8195G= (n.8195G=)
c.752G=
c.8091G= (p.Lys2697=)
13g.32363389G>TCA025498BRCA2c.8187G>T (p.Lys2729Asn)
c.7818G>T (p.Lys2606Asn)
c.654G>T (p.Lys218Asn)
c.8195G>T (n.8195G>T)
c.752G>T
c.8091G>T (p.Lys2697Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32363390G>ACA387749675BRCA2c.8188G>A (p.Ala2730Thr)
c.7819G>A (p.Ala2607Thr)
c.655G>A (p.Ala219Thr)
c.8196G>A (n.8196G>A)
c.753G>A
c.8092G>A (p.Ala2698Thr)
 ClinVar dbSNP
13g.32363390G>CCA025499BRCA2c.8188G>C (p.Ala2730Pro)
c.7819G>C (p.Ala2607Pro)
c.655G>C (p.Ala219Pro)
c.8196G>C (n.8196G>C)
c.753G>C
c.8092G>C (p.Ala2698Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32363390G=CA2082836131BRCA2c.8188G= (p.Ala2730=)
c.7819G= (p.Ala2607=)
c.655G= (p.Ala219=)
c.8196G= (n.8196G=)
c.753G=
c.8092G= (p.Ala2698=)
13g.32363390G>TCA387749677BRCA2c.8188G>T (p.Ala2730Ser)
c.7819G>T (p.Ala2607Ser)
c.655G>T (p.Ala219Ser)
c.8196G>T (n.8196G>T)
c.753G>T
c.8092G>T (p.Ala2698Ser)
 ClinVar dbSNP gnomAD v4
13g.32363390_32363391delinsGCCA2082836140BRCA2c.8188_8189delinsGC (p.Ala2730=)
c.7819_7820delinsGC (p.Ala2607=)
c.655_656delinsGC (p.Ala219=)
c.8196_8197delinsGC (n.8196_8197delinsGC)
c.753_754delinsGC
c.8092_8093delinsGC (p.Ala2698=)
13g.32363391C>ACA387749680BRCA2c.8189C>A (p.Ala2730Asp)
c.7820C>A (p.Ala2607Asp)
c.656C>A (p.Ala219Asp)
c.8197C>A (n.8197C>A)
c.754C>A
c.8093C>A (p.Ala2698Asp)
 dbSNP
13g.32363391C=CA2082836152BRCA2c.8189C= (p.Ala2730=)
c.7820C= (p.Ala2607=)
c.656C= (p.Ala219=)
c.8197C= (n.8197C=)
c.754C=
c.8093C= (p.Ala2698=)
13g.32363391C>GCA387749682BRCA2c.8189C>G (p.Ala2730Gly)
c.7820C>G (p.Ala2607Gly)
c.656C>G (p.Ala219Gly)
c.8197C>G (n.8197C>G)
c.754C>G
c.8093C>G (p.Ala2698Gly)
 ClinVar dbSNP
13g.32363391C>TCA025500BRCA2c.8189C>T (p.Ala2730Val)
c.7820C>T (p.Ala2607Val)
c.656C>T (p.Ala219Val)
c.8197C>T (n.8197C>T)
c.754C>T
c.8093C>T (p.Ala2698Val)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32363393delCA658798132BRCA2c.8191del (p.Gln2731SerfsTer2)
c.7822del (p.Gln2608SerfsTer2)
c.658del (p.Gln220SerfsTer2)
c.8199del (n.8199del)
c.756del
c.8095del (p.Gln2699SerfsTer2)
 ClinVar dbSNP
13g.32363392C>ACA483439603BRCA2c.8190C>A (p.Ala2730=)
c.7821C>A (p.Ala2607=)
c.657C>A (p.Ala219=)
c.8198C>A (n.8198C>A)
c.755C>A
c.8094C>A (p.Ala2698=)
 dbSNP
13g.32363392C>GCA483439604BRCA2c.8190C>G (p.Ala2730=)
c.7821C>G (p.Ala2607=)
c.657C>G (p.Ala219=)
c.8198C>G (n.8198C>G)
c.755C>G
c.8094C>G (p.Ala2698=)
 dbSNP
13g.32363392C>TCA483439605BRCA2c.8190C>T (p.Ala2730=)
c.7821C>T (p.Ala2607=)
c.657C>T (p.Ala219=)
c.8198C>T (n.8198C>T)
c.755C>T
c.8094C>T (p.Ala2698=)
 dbSNP
13g.32363393C>ACA387749685BRCA2c.8191C>A (p.Gln2731Lys)
c.7822C>A (p.Gln2608Lys)
c.658C>A (p.Gln220Lys)
c.8199C>A (n.8199C>A)
c.756C>A
c.8095C>A (p.Gln2699Lys)
 ClinVar
13g.32363393C=CA2082836158BRCA2c.8191C= (p.Gln2731=)
c.7822C= (p.Gln2608=)
c.658C= (p.Gln220=)
c.8199C= (n.8199C=)
c.756C=
c.8095C= (p.Gln2699=)
13g.32363393C>GCA10583138BRCA2c.8191C>G (p.Gln2731Glu)
c.7822C>G (p.Gln2608Glu)
c.658C>G (p.Gln220Glu)
c.8199C>G (n.8199C>G)
c.756C>G
c.8095C>G (p.Gln2699Glu)
 ClinVar dbSNP gnomAD v4
13g.32363393C>TCA025503BRCA2c.8191C>T (p.Gln2731Ter)
c.7822C>T (p.Gln2608Ter)
c.658C>T (p.Gln220Ter)
c.8199C>T (n.8199C>T)
c.756C>T
c.8095C>T (p.Gln2699Ter)
 ClinVar dbSNP
13g.32363394A=CA2082836167BRCA2c.8192A= (p.Gln2731=)
c.7823A= (p.Gln2608=)
c.659A= (p.Gln220=)
c.8200A= (n.8200A=)
c.757A=
c.8096A= (p.Gln2699=)
13g.32363394A>CCA387749689BRCA2c.8192A>C (p.Gln2731Pro)
c.7823A>C (p.Gln2608Pro)
c.659A>C (p.Gln220Pro)
c.8200A>C (n.8200A>C)
c.757A>C
c.8096A>C (p.Gln2699Pro)
13g.32363394A>GCA6941197BRCA2c.8192A>G (p.Gln2731Arg)
c.7823A>G (p.Gln2608Arg)
c.659A>G (p.Gln220Arg)
c.8200A>G (n.8200A>G)
c.757A>G
c.8096A>G (p.Gln2699Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32363394A>TCA387749691BRCA2c.8192A>T (p.Gln2731Leu)
c.7823A>T (p.Gln2608Leu)
c.659A>T (p.Gln220Leu)
c.8200A>T (n.8200A>T)
c.757A>T
c.8096A>T (p.Gln2699Leu)
 dbSNP
13g.32363395G>ACA483439606BRCA2c.8193G>A (p.Gln2731=)
c.7824G>A (p.Gln2608=)
c.660G>A (p.Gln220=)
c.8201G>A (n.8201G>A)
c.758G>A
c.8097G>A (p.Gln2699=)
 ClinVar dbSNP gnomAD v4
13g.32363395G>CCA387749694BRCA2c.8193G>C (p.Gln2731His)
c.7824G>C (p.Gln2608His)
c.660G>C (p.Gln220His)
c.8201G>C (n.8201G>C)
c.758G>C
c.8097G>C (p.Gln2699His)
 ClinVar dbSNP
13g.32363395G=CA2082836181BRCA2c.8193G= (p.Gln2731=)
c.7824G= (p.Gln2608=)
c.660G= (p.Gln220=)
c.8201G= (n.8201G=)
c.758G=
c.8097G= (p.Gln2699=)
13g.32363395G>TCA387749695BRCA2c.8193G>T (p.Gln2731His)
c.7824G>T (p.Gln2608His)
c.660G>T (p.Gln220His)
c.8201G>T (n.8201G>T)
c.758G>T
c.8097G>T (p.Gln2699His)
13g.32363395_32363403delinsGTTAGATCCCA2082836178BRCA2c.8193_8201delinsGTTAGATCC (p.Gln2731=)
c.7824_7832delinsGTTAGATCC (p.Gln2608=)
c.660_668delinsGTTAGATCC (p.Gln220=)
c.8201_8209delinsGTTAGATCC (n.8201_8209delinsGTTAGATCC)
c.758_766delinsGTTAGATCC
c.8097_8105delinsGTTAGATCC (p.Gln2699=)
13g.32363396T>ACA387749697BRCA2c.8194T>A (p.Leu2732Ile)
c.7825T>A (p.Leu2609Ile)
c.661T>A (p.Leu221Ile)
c.8202T>A (n.8202T>A)
c.759T>A
c.8098T>A (p.Leu2700Ile)
 dbSNP
13g.32363396T>CCA16613955BRCA2c.8194T>C (p.Leu2732=)
c.7825T>C (p.Leu2609=)
c.661T>C (p.Leu221=)
c.8202T>C (n.8202T>C)
c.759T>C
c.8098T>C (p.Leu2700=)
 ClinVar dbSNP
13g.32363396T>GCA387749699BRCA2c.8194T>G (p.Leu2732Val)
c.7825T>G (p.Leu2609Val)
c.661T>G (p.Leu221Val)
c.8202T>G (n.8202T>G)
c.759T>G
c.8098T>G (p.Leu2700Val)
 ClinVar dbSNP
13g.32363396T=CA2082836196BRCA2c.8194T= (p.Leu2732=)
c.7825T= (p.Leu2609=)
c.661T= (p.Leu221=)
c.8202T= (n.8202T=)
c.759T=
c.8098T= (p.Leu2700=)
13g.32363397_32363404delCA10589472BRCA2c.8195_8202del (p.Leu2732SerfsTer29)
c.7826_7833del (p.Leu2609SerfsTer29)
c.662_669del (p.Leu221SerfsTer29)
c.8203_8210del (n.8203_8210del)
c.760_767del
c.8099_8106del (p.Leu2700SerfsTer29)
 ClinVar dbSNP
13g.32363397T>ACA10589471BRCA2c.8195T>A (p.Leu2732Ter)
c.7826T>A (p.Leu2609Ter)
c.662T>A (p.Leu221Ter)
c.8203T>A (n.8203T>A)
c.760T>A
c.8099T>A (p.Leu2700Ter)
 ClinVar dbSNP
13g.32363397T>CCA387749702BRCA2c.8195T>C (p.Leu2732Ser)
c.7826T>C (p.Leu2609Ser)
c.662T>C (p.Leu221Ser)
c.8203T>C (n.8203T>C)
c.760T>C
c.8099T>C (p.Leu2700Ser)
 gnomAD v4
13g.32363397T>GCA025504BRCA2c.8195T>G (p.Leu2732Ter)
c.7826T>G (p.Leu2609Ter)
c.662T>G (p.Leu221Ter)
c.8203T>G (n.8203T>G)
c.760T>G
c.8099T>G (p.Leu2700Ter)
 ClinVar dbSNP
13g.32363397T=CA2082836206BRCA2c.8195T= (p.Leu2732=)
c.7826T= (p.Leu2609=)
c.662T= (p.Leu221=)
c.8203T= (n.8203T=)
c.760T=
c.8099T= (p.Leu2700=)
13g.32363398A=CA2082836213BRCA2c.8196A= (p.Leu2732=)
c.7827A= (p.Leu2609=)
c.663A= (p.Leu221=)
c.8204A= (n.8204A=)
c.761A=
c.8100A= (p.Leu2700=)
13g.32363398A>CCA387749707BRCA2c.8196A>C (p.Leu2732Phe)
c.7827A>C (p.Leu2609Phe)
c.663A>C (p.Leu221Phe)
c.8204A>C (n.8204A>C)
c.761A>C
c.8100A>C (p.Leu2700Phe)
13g.32363398A>GCA483439608BRCA2c.8196A>G (p.Leu2732=)
c.7827A>G (p.Leu2609=)
c.663A>G (p.Leu221=)
c.8204A>G (n.8204A>G)
c.761A>G
c.8100A>G (p.Leu2700=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32363398A>TCA387749705BRCA2c.8196A>T (p.Leu2732Phe)
c.7827A>T (p.Leu2609Phe)
c.663A>T (p.Leu221Phe)
c.8204A>T (n.8204A>T)
c.761A>T
c.8100A>T (p.Leu2700Phe)
 dbSNP
13g.32363399G>ACA387749709BRCA2c.8197G>A (p.Asp2733Asn)
c.7828G>A (p.Asp2610Asn)
c.664G>A (p.Asp222Asn)
c.8205G>A (n.8205G>A)
c.762G>A
c.8101G>A (p.Asp2701Asn)
 dbSNP gnomAD v2 gnomAD v4
13g.32363399G>CCA387749711BRCA2c.8197G>C (p.Asp2733His)
c.7828G>C (p.Asp2610His)
c.664G>C (p.Asp222His)
c.8205G>C (n.8205G>C)
c.762G>C
c.8101G>C (p.Asp2701His)
 ClinVar dbSNP gnomAD v4
13g.32363399G=CA2082836218BRCA2c.8197G= (p.Asp2733=)
c.7828G= (p.Asp2610=)
c.664G= (p.Asp222=)
c.8205G= (n.8205G=)
c.762G=
c.8101G= (p.Asp2701=)
13g.32363399G>TCA387749713BRCA2c.8197G>T (p.Asp2733Tyr)
c.7828G>T (p.Asp2610Tyr)
c.664G>T (p.Asp222Tyr)
c.8205G>T (n.8205G>T)
c.762G>T
c.8101G>T (p.Asp2701Tyr)
 dbSNP
13g.32363400A=CA2082836244BRCA2c.8198A= (p.Asp2733=)
c.7829A= (p.Asp2610=)
c.665A= (p.Asp222=)
c.8206A= (n.8206A=)
c.763A=
c.8102A= (p.Asp2701=)
13g.32363400A>CCA387749716BRCA2c.8198A>C (p.Asp2733Ala)
c.7829A>C (p.Asp2610Ala)
c.665A>C (p.Asp222Ala)
c.8206A>C (n.8206A>C)
c.763A>C
c.8102A>C (p.Asp2701Ala)
13g.32363400A>GCA387749717BRCA2c.8198A>G (p.Asp2733Gly)
c.7829A>G (p.Asp2610Gly)
c.665A>G (p.Asp222Gly)
c.8206A>G (n.8206A>G)
c.763A>G
c.8102A>G (p.Asp2701Gly)
 ClinVar dbSNP gnomAD v4
13g.32363400A>TCA387749719BRCA2c.8198A>T (p.Asp2733Val)
c.7829A>T (p.Asp2610Val)
c.665A>T (p.Asp222Val)
c.8206A>T (n.8206A>T)
c.763A>T
c.8102A>T (p.Asp2701Val)
 dbSNP
13g.32363400_32363410delinsATCCTCCCCTCCA2082836223BRCA2c.8198_8208delinsATCCTCCCCTC (p.Asp2733=)
c.7829_7839delinsATCCTCCCCTC (p.Asp2610=)
c.665_675delinsATCCTCCCCTC (p.Asp222=)
c.8206_8216delinsATCCTCCCCTC (n.8206_8216delinsATCCTCCCCTC)
c.763_773delinsATCCTCCCCTC
c.8102_8112delinsATCCTCCCCTC (p.Asp2701=)
13g.32363401T>ACA387749722BRCA2c.8199T>A (p.Asp2733Glu)
c.7830T>A (p.Asp2610Glu)
c.666T>A (p.Asp222Glu)
c.8207T>A (n.8207T>A)
c.764T>A
c.8103T>A (p.Asp2701Glu)
13g.32363401T>CCA483439612BRCA2c.8199T>C (p.Asp2733=)
c.7830T>C (p.Asp2610=)
c.666T>C (p.Asp222=)
c.8207T>C (n.8207T>C)
c.764T>C
c.8103T>C (p.Asp2701=)
 ClinVar dbSNP
13g.32363401T>GCA387749725BRCA2c.8199T>G (p.Asp2733Glu)
c.7830T>G (p.Asp2610Glu)
c.666T>G (p.Asp222Glu)
c.8207T>G (n.8207T>G)
c.764T>G
c.8103T>G (p.Asp2701Glu)
13g.32363401_32363402delinsTCCA2082836258BRCA2c.8199_8200delinsTC (p.Asp2733=)
c.7830_7831delinsTC (p.Asp2610=)
c.666_667delinsTC (p.Asp222=)
c.8207_8208delinsTC (n.8207_8208delinsTC)
c.764_765delinsTC
c.8103_8104delinsTC (p.Asp2701=)
13g.32363402_32363411delCA025507BRCA2c.8200_8209del (p.Pro2734Ter)
c.7831_7840del (p.Pro2611Ter)
c.667_676del (p.Pro223Ter)
c.8208_8217del (n.8208_8217del)
c.765_774del
c.8104_8113del (p.Pro2702Ter)
 ClinVar dbSNP

Number of alleles fetched