Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32357226_32357777delCA2580087492BRCA2c.7618-516_7653del
c.7249-516_7284del
c.85-516_120del
c.183-516_218del
n.7618-516_7653del
c.7522-516_7557del
 ClinVar
13g.32357740_32357767delinsGTGTTATTTTGTTTTATTCA2580087327BRCA2c.7618-2_7643delinsGTGTTATTTTGTTTTATT
c.7249-2_7274delinsGTGTTATTTTGTTTTATT
c.85-2_110delinsGTGTTATTTTGTTTTATT
c.183-2_208delinsGTGTTATTTTGTTTTATT
n.7618-2_7643delinsGTGTTATTTTGTTTTATT
c.7522-2_7547delinsGTGTTATTTTGTTTTATT
 ClinVar
13g.32357757_32357767delinsGTTTCTAAACACA2082817628BRCA2c.7633_7643delinsGTTTCTAAACA (p.Val2545=)
c.7264_7274delinsGTTTCTAAACA (p.Val2422=)
c.100_110delinsGTTTCTAAACA (p.Val34=)
c.198_208delinsGTTTCTAAACA
n.7633_7643delinsGTTTCTAAACA
c.7537_7547delinsGTTTCTAAACA (p.Val2513=)
13g.32357760_32357769delCA025203BRCA2c.7636_7645del (p.Ser2546AlafsTer2)
c.7267_7276del (p.Ser2423AlafsTer2)
c.103_112del (p.Ser35AlafsTer2)
c.201_210del
n.7636_7645del
c.7540_7549del (p.Ser2514AlafsTer2)
 ClinVar dbSNP
13g.32357760_32357770delinsTCTAAACATTGCA2082817653BRCA2c.7636_7646delinsTCTAAACATTG (p.Ser2546=)
c.7267_7277delinsTCTAAACATTG (p.Ser2423=)
c.103_113delinsTCTAAACATTG (p.Ser35=)
c.201_211delinsTCTAAACATTG
n.7636_7646delinsTCTAAACATTG
c.7540_7550delinsTCTAAACATTG (p.Ser2514=)
13g.32357762_32357771delCA10589443BRCA2c.7638_7647del (p.Lys2547Ter)
c.7269_7278del (p.Lys2424Ter)
c.105_114del (p.Lys36Ter)
c.203_212del
n.7638_7647del
c.7542_7551del (p.Lys2515Ter)
 ClinVar dbSNP
13g.32357766C>ACA387744862BRCA2c.7642C>A (p.His2548Asn)
c.7273C>A (p.His2425Asn)
c.109C>A (p.His37Asn)
c.207C>A
n.7642C>A
c.7546C>A (p.His2516Asn)
13g.32357766C>GCA387744863BRCA2c.7642C>G (p.His2548Asp)
c.7273C>G (p.His2425Asp)
c.109C>G (p.His37Asp)
c.207C>G
n.7642C>G
c.7546C>G (p.His2516Asp)
 dbSNP
13g.32357766C>TCA387744865BRCA2c.7642C>T (p.His2548Tyr)
c.7273C>T (p.His2425Tyr)
c.109C>T (p.His37Tyr)
c.207C>T
n.7642C>T
c.7546C>T (p.His2516Tyr)
13g.32357766_32357768delinsCATCA2082817724BRCA2c.7642_7644delinsCAT (p.His2548=)
c.7273_7275delinsCAT (p.His2425=)
c.109_111delinsCAT (p.His37=)
c.207_209delinsCAT
n.7642_7644delinsCAT
c.7546_7548delinsCAT (p.His2516=)
13g.32357767A=CA2082817736BRCA2c.7643A= (p.His2548=)
c.7274A= (p.His2425=)
c.110A= (p.His37=)
c.208A=
n.7643A=
c.7547A= (p.His2516=)
13g.32357767A>CCA387744869BRCA2c.7643A>C (p.His2548Pro)
c.7274A>C (p.His2425Pro)
c.110A>C (p.His37Pro)
c.208A>C
n.7643A>C
c.7547A>C (p.His2516Pro)
13g.32357767A>GCA025208BRCA2c.7643A>G (p.His2548Arg)
c.7274A>G (p.His2425Arg)
c.110A>G (p.His37Arg)
c.208A>G
n.7643A>G
c.7547A>G (p.His2516Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32357767A>TCA025209BRCA2c.7643A>T (p.His2548Leu)
c.7274A>T (p.His2425Leu)
c.110A>T (p.His37Leu)
c.208A>T
n.7643A>T
c.7547A>T (p.His2516Leu)
 ClinVar dbSNP
13g.32357767_32357768delCA10589444BRCA2c.7643_7644del (p.His2548LeufsTer5)
c.7274_7275del (p.His2425LeufsTer5)
c.110_111del (p.His37LeufsTer5)
c.208_209del
n.7643_7644del
c.7547_7548del (p.His2516LeufsTer5)
 ClinVar dbSNP
13g.32357768T>ACA387744876BRCA2c.7644T>A (p.His2548Gln)
c.7275T>A (p.His2425Gln)
c.111T>A (p.His37Gln)
c.209T>A
n.7644T>A
c.7548T>A (p.His2516Gln)
 dbSNP
13g.32357768T>CCA247470895BRCA2c.7644T>C (p.His2548=)
c.7275T>C (p.His2425=)
c.111T>C (p.His37=)
c.209T>C
n.7644T>C
c.7548T>C (p.His2516=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357768T>GCA387744877BRCA2c.7644T>G (p.His2548Gln)
c.7275T>G (p.His2425Gln)
c.111T>G (p.His37Gln)
c.209T>G
n.7644T>G
c.7548T>G (p.His2516Gln)
13g.32357768T=CA2082817746BRCA2c.7644T= (p.His2548=)
c.7275T= (p.His2425=)
c.111T= (p.His37=)
c.209T=
n.7644T=
c.7548T= (p.His2516=)
13g.32357769dupCA2695217916BRCA2c.7645dup (p.Cys2549LeufsTer5)
c.7276dup (p.Cys2426LeufsTer5)
c.112dup (p.Cys38LeufsTer5)
c.210dup
n.7645dup
c.7549dup (p.Cys2517LeufsTer5)
13g.32357769T>ACA387744886BRCA2c.7645T>A (p.Cys2549Ser)
c.7276T>A (p.Cys2426Ser)
c.112T>A (p.Cys38Ser)
c.210T>A
n.7645T>A
c.7549T>A (p.Cys2517Ser)
 dbSNP
13g.32357769T>CCA387744884BRCA2c.7645T>C (p.Cys2549Arg)
c.7276T>C (p.Cys2426Arg)
c.112T>C (p.Cys38Arg)
c.210T>C
n.7645T>C
c.7549T>C (p.Cys2517Arg)
13g.32357769T>GCA387744881BRCA2c.7645T>G (p.Cys2549Gly)
c.7276T>G (p.Cys2426Gly)
c.112T>G (p.Cys38Gly)
c.210T>G
n.7645T>G
c.7549T>G (p.Cys2517Gly)
 ClinVar dbSNP
13g.32357769T=CA2082817747BRCA2c.7645T= (p.Cys2549=)
c.7276T= (p.Cys2426=)
c.112T= (p.Cys38=)
c.210T=
n.7645T=
c.7549T= (p.Cys2517=)
13g.32357770G>ACA387744890BRCA2c.7646G>A (p.Cys2549Tyr)
c.7277G>A (p.Cys2426Tyr)
c.113G>A (p.Cys38Tyr)
c.211G>A
n.7646G>A
c.7550G>A (p.Cys2517Tyr)
 dbSNP gnomAD v4
13g.32357770G>CCA387744892BRCA2c.7646G>C (p.Cys2549Ser)
c.7277G>C (p.Cys2426Ser)
c.113G>C (p.Cys38Ser)
c.211G>C
n.7646G>C
c.7550G>C (p.Cys2517Ser)
 ClinVar dbSNP
13g.32357770G=CA2082817748BRCA2c.7646G= (p.Cys2549=)
c.7277G= (p.Cys2426=)
c.113G= (p.Cys38=)
c.211G=
n.7646G=
c.7550G= (p.Cys2517=)
13g.32357770G>TCA387744895BRCA2c.7646G>T (p.Cys2549Phe)
c.7277G>T (p.Cys2426Phe)
c.113G>T (p.Cys38Phe)
c.211G>T
n.7646G>T
c.7550G>T (p.Cys2517Phe)
 dbSNP
13g.32357771C>ACA025210BRCA2c.7647C>A (p.Cys2549Ter)
c.7278C>A (p.Cys2426Ter)
c.114C>A (p.Cys38Ter)
c.212C>A
n.7647C>A
c.7551C>A (p.Cys2517Ter)
 ClinVar dbSNP
13g.32357771C=CA2082817769BRCA2c.7647C= (p.Cys2549=)
c.7278C= (p.Cys2426=)
c.114C= (p.Cys38=)
c.212C=
n.7647C=
c.7551C= (p.Cys2517=)
13g.32357771C>GCA387744899BRCA2c.7647C>G (p.Cys2549Trp)
c.7278C>G (p.Cys2426Trp)
c.114C>G (p.Cys38Trp)
c.212C>G
n.7647C>G
c.7551C>G (p.Cys2517Trp)
 dbSNP
13g.32357771C>TCA483439151BRCA2c.7647C>T (p.Cys2549=)
c.7278C>T (p.Cys2426=)
c.114C>T (p.Cys38=)
c.212C>T
n.7647C>T
c.7551C>T (p.Cys2517=)
 ClinVar dbSNP gnomAD v4
13g.32357772A=CA2082817780BRCA2c.7648A= (p.Ile2550=)
c.7279A= (p.Ile2427=)
c.115A= (p.Ile39=)
c.213A=
n.7648A=
c.7552A= (p.Ile2518=)
13g.32357772A>CCA247470908BRCA2c.7648A>C (p.Ile2550Leu)
c.7279A>C (p.Ile2427Leu)
c.115A>C (p.Ile39Leu)
c.213A>C
n.7648A>C
c.7552A>C (p.Ile2518Leu)
 ClinVar dbSNP gnomAD v4
13g.32357772A>GCA025211BRCA2c.7648A>G (p.Ile2550Val)
c.7279A>G (p.Ile2427Val)
c.115A>G (p.Ile39Val)
c.213A>G
n.7648A>G
c.7552A>G (p.Ile2518Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357772A>TCA387744907BRCA2c.7648A>T (p.Ile2550Leu)
c.7279A>T (p.Ile2427Leu)
c.115A>T (p.Ile39Leu)
c.213A>T
n.7648A>T
c.7552A>T (p.Ile2518Leu)
 ClinVar dbSNP
13g.32357773T>ACA387744909BRCA2c.7649T>A (p.Ile2550Lys)
c.7280T>A (p.Ile2427Lys)
c.116T>A (p.Ile39Lys)
c.214T>A
n.7649T>A
c.7553T>A (p.Ile2518Lys)
 ClinVar dbSNP
13g.32357773T>CCA387744910BRCA2c.7649T>C (p.Ile2550Thr)
c.7280T>C (p.Ile2427Thr)
c.116T>C (p.Ile39Thr)
c.214T>C
n.7649T>C
c.7553T>C (p.Ile2518Thr)
13g.32357773T>GCA387744912BRCA2c.7649T>G (p.Ile2550Arg)
c.7280T>G (p.Ile2427Arg)
c.116T>G (p.Ile39Arg)
c.214T>G
n.7649T>G
c.7553T>G (p.Ile2518Arg)
13g.32357773T=CA2082817794BRCA2c.7649T= (p.Ile2550=)
c.7280T= (p.Ile2427=)
c.116T= (p.Ile39=)
c.214T=
n.7649T=
c.7553T= (p.Ile2518=)
13g.32357774A=CA2082817805BRCA2c.7650A= (p.Ile2550=)
c.7281A= (p.Ile2427=)
c.117A= (p.Ile39=)
c.215A=
n.7650A=
c.7554A= (p.Ile2518=)
13g.32357774A>CCA483439152BRCA2c.7650A>C (p.Ile2550=)
c.7281A>C (p.Ile2427=)
c.117A>C (p.Ile39=)
c.215A>C
n.7650A>C
c.7554A>C (p.Ile2518=)
13g.32357774A>GCA387744916BRCA2c.7650A>G (p.Ile2550Met)
c.7281A>G (p.Ile2427Met)
c.117A>G (p.Ile39Met)
c.215A>G
n.7650A>G
c.7554A>G (p.Ile2518Met)
 COSMIC COSMIC
13g.32357774A>TCA025212BRCA2c.7650A>T (p.Ile2550=)
c.7281A>T (p.Ile2427=)
c.117A>T (p.Ile39=)
c.215A>T
n.7650A>T
c.7554A>T (p.Ile2518=)
 ClinVar dbSNP gnomAD v4
13g.32357778dupCA10586078BRCA2c.7654dup (p.Ile2552AsnfsTer2)
c.7285dup (p.Ile2429AsnfsTer2)
c.121dup (p.Ile41AsnfsTer2)
c.219dup
n.7654dup
c.7558dup (p.Ile2520AsnfsTer2)
 ClinVar dbSNP
13g.32357778delCA891842180BRCA2c.7654del (p.Ile2552LeufsTer?)
c.7285del (p.Ile2429LeufsTer?)
c.121del (p.Ile41LeufsTer?)
c.219del
n.7654del
c.7558del (p.Ile2520LeufsTer?)
 ClinVar dbSNP gnomAD v4
13g.32357775A=CA2082817814BRCA2c.7651A= (p.Lys2551=)
c.7282A= (p.Lys2428=)
c.118A= (p.Lys40=)
c.216A=
n.7651A=
c.7555A= (p.Lys2519=)
13g.32357775A>CCA025213BRCA2c.7651A>C (p.Lys2551Gln)
c.7282A>C (p.Lys2428Gln)
c.118A>C (p.Lys40Gln)
c.216A>C
n.7651A>C
c.7555A>C (p.Lys2519Gln)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32357775A>GCA387744922BRCA2c.7651A>G (p.Lys2551Glu)
c.7282A>G (p.Lys2428Glu)
c.118A>G (p.Lys40Glu)
c.216A>G
n.7651A>G
c.7555A>G (p.Lys2519Glu)
 ClinVar dbSNP
13g.32357775A>TCA387744920BRCA2c.7651A>T (p.Lys2551Ter)
c.7282A>T (p.Lys2428Ter)
c.118A>T (p.Lys40Ter)
c.216A>T
n.7651A>T
c.7555A>T (p.Lys2519Ter)
 dbSNP
13g.32357776A>CCA387744927BRCA2c.7652A>C (p.Lys2551Thr)
c.7283A>C (p.Lys2428Thr)
c.119A>C (p.Lys40Thr)
c.217A>C
n.7652A>C
c.7556A>C (p.Lys2519Thr)
13g.32357776A>GCA387744930BRCA2c.7652A>G (p.Lys2551Arg)
c.7283A>G (p.Lys2428Arg)
c.119A>G (p.Lys40Arg)
c.217A>G
n.7652A>G
c.7556A>G (p.Lys2519Arg)
13g.32357776A>TCA387744932BRCA2c.7652A>T (p.Lys2551Ile)
c.7283A>T (p.Lys2428Ile)
c.119A>T (p.Lys40Ile)
c.217A>T
n.7652A>T
c.7556A>T (p.Lys2519Ile)
13g.32357776_32357780delinsAAATTCA2082817826BRCA2c.7652_7656delinsAAATT (p.Lys2551=)
c.7283_7287delinsAAATT (p.Lys2428=)
c.119_123delinsAAATT (p.Lys40=)
c.217_221delinsAAATT
n.7652_7656delinsAAATT
c.7556_7560delinsAAATT (p.Lys2519=)
13g.32357777A>CCA387744936BRCA2c.7653A>C (p.Lys2551Asn)
c.7284A>C (p.Lys2428Asn)
c.120A>C (p.Lys40Asn)
c.218A>C
n.7653A>C
c.7557A>C (p.Lys2519Asn)
13g.32357777A>GCA483439153BRCA2c.7653A>G (p.Lys2551=)
c.7284A>G (p.Lys2428=)
c.120A>G (p.Lys40=)
c.218A>G
n.7653A>G
c.7557A>G (p.Lys2519=)
13g.32357777A>TCA387744939BRCA2c.7653A>T (p.Lys2551Asn)
c.7284A>T (p.Lys2428Asn)
c.120A>T (p.Lys40Asn)
c.218A>T
n.7653A>T
c.7557A>T (p.Lys2519Asn)
13g.32357779_32357782delCA025214BRCA2c.7655_7658del (p.Ile2552ThrfsTer?)
c.7286_7289del (p.Ile2429ThrfsTer?)
c.122_125del (p.Ile41ThrfsTer?)
c.220_223del
n.7655_7658del
c.7559_7562del (p.Ile2520ThrfsTer?)
 ClinVar dbSNP gnomAD v4
13g.32357778A>CCA387744943BRCA2c.7654A>C (p.Ile2552Leu)
c.7285A>C (p.Ile2429Leu)
c.121A>C (p.Ile41Leu)
c.219A>C
n.7654A>C
c.7558A>C (p.Ile2520Leu)
13g.32357778A>GCA387744946BRCA2c.7654A>G (p.Ile2552Val)
c.7285A>G (p.Ile2429Val)
c.121A>G (p.Ile41Val)
c.219A>G
n.7654A>G
c.7558A>G (p.Ile2520Val)
 ClinVar dbSNP
13g.32357778A>TCA387744949BRCA2c.7654A>T (p.Ile2552Phe)
c.7285A>T (p.Ile2429Phe)
c.121A>T (p.Ile41Phe)
c.219A>T
n.7654A>T
c.7558A>T (p.Ile2520Phe)
13g.32357779T>ACA387744952BRCA2c.7655T>A (p.Ile2552Asn)
c.7286T>A (p.Ile2429Asn)
c.122T>A (p.Ile41Asn)
c.220T>A
n.7655T>A
c.7559T>A (p.Ile2520Asn)
 dbSNP
13g.32357779T>CCA387744955BRCA2c.7655T>C (p.Ile2552Thr)
c.7286T>C (p.Ile2429Thr)
c.122T>C (p.Ile41Thr)
c.220T>C
n.7655T>C
c.7559T>C (p.Ile2520Thr)
 ClinVar dbSNP
13g.32357779T>GCA387744958BRCA2c.7655T>G (p.Ile2552Ser)
c.7286T>G (p.Ile2429Ser)
c.122T>G (p.Ile41Ser)
c.220T>G
n.7655T>G
c.7559T>G (p.Ile2520Ser)
13g.32357779T=CA2082817837BRCA2c.7655T= (p.Ile2552=)
c.7286T= (p.Ile2429=)
c.122T= (p.Ile41=)
c.220T=
n.7655T=
c.7559T= (p.Ile2520=)
13g.32357780T>ACA247470927BRCA2c.7656T>A (p.Ile2552=)
c.7287T>A (p.Ile2429=)
c.123T>A (p.Ile41=)
c.221T>A
n.7656T>A
c.7560T>A (p.Ile2520=)
 ClinVar dbSNP gnomAD v4
13g.32357780T>CCA483439154BRCA2c.7656T>C (p.Ile2552=)
c.7287T>C (p.Ile2429=)
c.123T>C (p.Ile41=)
c.221T>C
n.7656T>C
c.7560T>C (p.Ile2520=)
13g.32357780T>GCA387744962BRCA2c.7656T>G (p.Ile2552Met)
c.7287T>G (p.Ile2429Met)
c.123T>G (p.Ile41Met)
c.221T>G
n.7656T>G
c.7560T>G (p.Ile2520Met)
13g.32357780T=CA2082817846BRCA2c.7656T= (p.Ile2552=)
c.7287T= (p.Ile2429=)
c.123T= (p.Ile41=)
c.221T=
n.7656T=
c.7560T= (p.Ile2520=)
13g.32357780_32357781delinsTACA2082817851BRCA2c.7656_7657delinsTA (p.Ile2552=)
c.7287_7288delinsTA (p.Ile2429=)
c.123_124delinsTA (p.Ile41=)
c.221_222delinsTA
n.7656_7657delinsTA
c.7560_7561delinsTA (p.Ile2520=)
13g.32357780_32357783delinsTAACCA2082817844BRCA2c.7656_7659delinsTAAC (p.Ile2552=)
c.7287_7290delinsTAAC (p.Ile2429=)
c.123_126delinsTAAC (p.Ile41=)
c.221_224delinsTAAC
n.7656_7659delinsTAAC
c.7560_7563delinsTAAC (p.Ile2520=)
13g.32357781A=CA2082817869BRCA2c.7657A= (p.Asn2553=)
c.7288A= (p.Asn2430=)
c.124A= (p.Asn42=)
c.222A=
n.7657A=
c.7561A= (p.Asn2521=)
13g.32357781A>CCA387744966BRCA2c.7657A>C (p.Asn2553His)
c.7288A>C (p.Asn2430His)
c.124A>C (p.Asn42His)
c.222A>C
n.7657A>C
c.7561A>C (p.Asn2521His)
13g.32357781A>GCA387744969BRCA2c.7657A>G (p.Asn2553Asp)
c.7288A>G (p.Asn2430Asp)
c.124A>G (p.Asn42Asp)
c.222A>G
n.7657A>G
c.7561A>G (p.Asn2521Asp)
 ClinVar dbSNP
13g.32357781A>TCA387744971BRCA2c.7657A>T (p.Asn2553Tyr)
c.7288A>T (p.Asn2430Tyr)
c.124A>T (p.Asn42Tyr)
c.222A>T
n.7657A>T
c.7561A>T (p.Asn2521Tyr)
 dbSNP
13g.32357782delCA1139663200BRCA2c.7658del (p.Asn2553ThrfsTer?)
c.7289del (p.Asn2430ThrfsTer?)
c.125del (p.Asn42ThrfsTer?)
c.223del
n.7658del
c.7562del (p.Asn2521ThrfsTer?)
 ClinVar dbSNP
13g.32357782_32357784delCA6941127BRCA2c.7658_7660del (p.Asn2553del)
c.7289_7291del (p.Asn2430del)
c.125_127del (p.Asn42del)
c.223_225del
n.7658_7660del
c.7562_7564del (p.Asn2521del)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357782A=CA2082817875BRCA2c.7658A= (p.Asn2553=)
c.7289A= (p.Asn2430=)
c.125A= (p.Asn42=)
c.223A=
n.7658A=
c.7562A= (p.Asn2521=)
13g.32357782A>CCA387744976BRCA2c.7658A>C (p.Asn2553Thr)
c.7289A>C (p.Asn2430Thr)
c.125A>C (p.Asn42Thr)
c.223A>C
n.7658A>C
c.7562A>C (p.Asn2521Thr)
13g.32357782A>GCA387744972BRCA2c.7658A>G (p.Asn2553Ser)
c.7289A>G (p.Asn2430Ser)
c.125A>G (p.Asn42Ser)
c.223A>G
n.7658A>G
c.7562A>G (p.Asn2521Ser)
 ClinVar dbSNP
13g.32357782A>TCA387744974BRCA2c.7658A>T (p.Asn2553Ile)
c.7289A>T (p.Asn2430Ile)
c.125A>T (p.Asn42Ile)
c.223A>T
n.7658A>T
c.7562A>T (p.Asn2521Ile)
 dbSNP
13g.32357783delCA2695199697BRCA2c.7659del (p.Asn2553LysfsTer?)
c.7290del (p.Asn2430LysfsTer?)
c.126del (p.Asn42LysfsTer?)
c.224del
n.7659del
c.7563del (p.Asn2521LysfsTer?)
 ClinVar
13g.32357783C>ACA387744977BRCA2c.7659C>A (p.Asn2553Lys)
c.7290C>A (p.Asn2430Lys)
c.126C>A (p.Asn42Lys)
c.224C>A
n.7659C>A
c.7563C>A (p.Asn2521Lys)
 dbSNP
13g.32357783C=CA2082817889BRCA2c.7659C= (p.Asn2553=)
c.7290C= (p.Asn2430=)
c.126C= (p.Asn42=)
c.224C=
n.7659C=
c.7563C= (p.Asn2521=)
13g.32357783C>GCA387744980BRCA2c.7659C>G (p.Asn2553Lys)
c.7290C>G (p.Asn2430Lys)
c.126C>G (p.Asn42Lys)
c.224C>G
n.7659C>G
c.7563C>G (p.Asn2521Lys)
 ClinVar dbSNP
13g.32357783C>TCA483439156BRCA2c.7659C>T (p.Asn2553=)
c.7290C>T (p.Asn2430=)
c.126C>T (p.Asn42=)
c.224C>T
n.7659C>T
c.7563C>T (p.Asn2521=)
 dbSNP gnomAD v4
13g.32357784A=CA2082817900BRCA2c.7660A= (p.Ser2554=)
c.7291A= (p.Ser2431=)
c.127A= (p.Ser43=)
c.225A=
n.7660A=
c.7564A= (p.Ser2522=)
13g.32357784A>CCA387744983BRCA2c.7660A>C (p.Ser2554Arg)
c.7291A>C (p.Ser2431Arg)
c.127A>C (p.Ser43Arg)
c.225A>C
n.7660A>C
c.7564A>C (p.Ser2522Arg)
13g.32357784A>GCA10586079BRCA2c.7660A>G (p.Ser2554Gly)
c.7291A>G (p.Ser2431Gly)
c.127A>G (p.Ser43Gly)
c.225A>G
n.7660A>G
c.7564A>G (p.Ser2522Gly)
 ClinVar dbSNP gnomAD v4
13g.32357784A>TCA387744987BRCA2c.7660A>T (p.Ser2554Cys)
c.7291A>T (p.Ser2431Cys)
c.127A>T (p.Ser43Cys)
c.225A>T
n.7660A>T
c.7564A>T (p.Ser2522Cys)
 dbSNP
13g.32357785G>ACA025215BRCA2c.7661G>A (p.Ser2554Asn)
c.7292G>A (p.Ser2431Asn)
c.128G>A (p.Ser43Asn)
c.226G>A
n.7661G>A
c.7565G>A (p.Ser2522Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357785G>CCA387744991BRCA2c.7661G>C (p.Ser2554Thr)
c.7292G>C (p.Ser2431Thr)
c.128G>C (p.Ser43Thr)
c.226G>C
n.7661G>C
c.7565G>C (p.Ser2522Thr)
 ClinVar dbSNP
13g.32357785G=CA2082817925BRCA2c.7661G= (p.Ser2554=)
c.7292G= (p.Ser2431=)
c.128G= (p.Ser43=)
c.226G=
n.7661G=
c.7565G= (p.Ser2522=)
13g.32357785G>TCA387744994BRCA2c.7661G>T (p.Ser2554Ile)
c.7292G>T (p.Ser2431Ile)
c.128G>T (p.Ser43Ile)
c.226G>T
n.7661G>T
c.7565G>T (p.Ser2522Ile)
 dbSNP
13g.32357786C>ACA387744997BRCA2c.7662C>A (p.Ser2554Arg)
c.7293C>A (p.Ser2431Arg)
c.129C>A (p.Ser43Arg)
c.227C>A
n.7662C>A
c.7566C>A (p.Ser2522Arg)
13g.32357786C=CA2082817942BRCA2c.7662C= (p.Ser2554=)
c.7293C= (p.Ser2431=)
c.129C= (p.Ser43=)
c.227C=
n.7662C=
c.7566C= (p.Ser2522=)
13g.32357786C>GCA387744999BRCA2c.7662C>G (p.Ser2554Arg)
c.7293C>G (p.Ser2431Arg)
c.129C>G (p.Ser43Arg)
c.227C>G
n.7662C>G
c.7566C>G (p.Ser2522Arg)
13g.32357786C>TCA483439158BRCA2c.7662C>T (p.Ser2554=)
c.7293C>T (p.Ser2431=)
c.129C>T (p.Ser43=)
c.227C>T
n.7662C>T
c.7566C>T (p.Ser2522=)
13g.32357786_32357787delinsCACA2082817946BRCA2c.7662_7663delinsCA (p.Ser2554=)
c.7293_7294delinsCA (p.Ser2431=)
c.129_130delinsCA (p.Ser43=)
c.227_228delinsCA
n.7662_7663delinsCA
c.7566_7567delinsCA (p.Ser2522=)
13g.32357787A=CA2082817961BRCA2c.7663A= (p.Lys2555=)
c.7294A= (p.Lys2432=)
c.130A= (p.Lys44=)
c.228A=
n.7663A=
c.7567A= (p.Lys2523=)
13g.32357787A>CCA387745006BRCA2c.7663A>C (p.Lys2555Gln)
c.7294A>C (p.Lys2432Gln)
c.130A>C (p.Lys44Gln)
c.228A>C
n.7663A>C
c.7567A>C (p.Lys2523Gln)
13g.32357787A>GCA387745002BRCA2c.7663A>G (p.Lys2555Glu)
c.7294A>G (p.Lys2432Glu)
c.130A>G (p.Lys44Glu)
c.228A>G
n.7663A>G
c.7567A>G (p.Lys2523Glu)
 ClinVar dbSNP gnomAD v4
13g.32357787A>TCA387745005BRCA2c.7663A>T (p.Lys2555Ter)
c.7294A>T (p.Lys2432Ter)
c.130A>T (p.Lys44Ter)
c.228A>T
n.7663A>T
c.7567A>T (p.Lys2523Ter)
 ClinVar
13g.32357791dupCA10581592BRCA2c.7667dup (p.Asn2556LysfsTer10)
c.7298dup (p.Asn2433LysfsTer10)
c.134dup (p.Asn45LysfsTer10)
c.232dup
n.7667dup
c.7571dup (p.Asn2524LysfsTer10)
 ClinVar dbSNP
13g.32357790_32357791dupCA10589445BRCA2c.7666_7667dup (p.Asn2556LysfsTer?)
c.7297_7298dup (p.Asn2433LysfsTer?)
c.133_134dup (p.Asn45LysfsTer?)
c.231_232dup
n.7666_7667dup
c.7570_7571dup (p.Asn2524LysfsTer?)
 ClinVar dbSNP
13g.32357791delCA1139663201BRCA2c.7667del (p.Asn2556MetfsTer?)
c.7298del (p.Asn2433MetfsTer?)
c.134del (p.Asn45MetfsTer?)
c.232del
n.7667del
c.7571del (p.Asn2524MetfsTer?)
 ClinVar dbSNP
13g.32357788A=CA2082817978BRCA2c.7664A= (p.Lys2555=)
c.7295A= (p.Lys2432=)
c.131A= (p.Lys44=)
c.229A=
n.7664A=
c.7568A= (p.Lys2523=)
13g.32357788A>CCA387745007BRCA2c.7664A>C (p.Lys2555Thr)
c.7295A>C (p.Lys2432Thr)
c.131A>C (p.Lys44Thr)
c.229A>C
n.7664A>C
c.7568A>C (p.Lys2523Thr)
13g.32357788A>GCA387745008BRCA2c.7664A>G (p.Lys2555Arg)
c.7295A>G (p.Lys2432Arg)
c.131A>G (p.Lys44Arg)
c.229A>G
n.7664A>G
c.7568A>G (p.Lys2523Arg)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357788A>TCA387745009BRCA2c.7664A>T (p.Lys2555Ile)
c.7295A>T (p.Lys2432Ile)
c.131A>T (p.Lys44Ile)
c.229A>T
n.7664A>T
c.7568A>T (p.Lys2523Ile)
 dbSNP
13g.32357789A=CA2082817990BRCA2c.7665A= (p.Lys2555=)
c.7296A= (p.Lys2432=)
c.132A= (p.Lys44=)
c.230A=
n.7665A=
c.7569A= (p.Lys2523=)
13g.32357789A>CCA387745010BRCA2c.7665A>C (p.Lys2555Asn)
c.7296A>C (p.Lys2432Asn)
c.132A>C (p.Lys44Asn)
c.230A>C
n.7665A>C
c.7569A>C (p.Lys2523Asn)
13g.32357789A>GCA16606439BRCA2c.7665A>G (p.Lys2555=)
c.7296A>G (p.Lys2432=)
c.132A>G (p.Lys44=)
c.230A>G
n.7665A>G
c.7569A>G (p.Lys2523=)
 ClinVar dbSNP
13g.32357789A>TCA387745011BRCA2c.7665A>T (p.Lys2555Asn)
c.7296A>T (p.Lys2432Asn)
c.132A>T (p.Lys44Asn)
c.230A>T
n.7665A>T
c.7569A>T (p.Lys2523Asn)
13g.32357790A>CCA387745013BRCA2c.7666A>C (p.Asn2556His)
c.7297A>C (p.Asn2433His)
c.133A>C (p.Asn45His)
c.231A>C
n.7666A>C
c.7570A>C (p.Asn2524His)
13g.32357790A>GCA387745016BRCA2c.7666A>G (p.Asn2556Asp)
c.7297A>G (p.Asn2433Asp)
c.133A>G (p.Asn45Asp)
c.231A>G
n.7666A>G
c.7570A>G (p.Asn2524Asp)
13g.32357790A>TCA387745023BRCA2c.7666A>T (p.Asn2556Tyr)
c.7297A>T (p.Asn2433Tyr)
c.133A>T (p.Asn45Tyr)
c.231A>T
n.7666A>T
c.7570A>T (p.Asn2524Tyr)
 dbSNP
13g.32357791A>CCA387745025BRCA2c.7667A>C (p.Asn2556Thr)
c.7298A>C (p.Asn2433Thr)
c.134A>C (p.Asn45Thr)
c.232A>C
n.7667A>C
c.7571A>C (p.Asn2524Thr)
 gnomAD v4
13g.32357791A>GCA387745027BRCA2c.7667A>G (p.Asn2556Ser)
c.7298A>G (p.Asn2433Ser)
c.134A>G (p.Asn45Ser)
c.232A>G
n.7667A>G
c.7571A>G (p.Asn2524Ser)
13g.32357791A>TCA387745028BRCA2c.7667A>T (p.Asn2556Ile)
c.7298A>T (p.Asn2433Ile)
c.134A>T (p.Asn45Ile)
c.232A>T
n.7667A>T
c.7571A>T (p.Asn2524Ile)
 dbSNP gnomAD v4
13g.32357791_32357792insAGAAAAACAATTTAAAGTAAACACA2517010024BRCA2c.7667_7668insAGAAAAACAATTTAAAGTAAACA (p.Asn2556LysfsTer?)
c.7298_7299insAGAAAAACAATTTAAAGTAAACA (p.Asn2433LysfsTer?)
c.134_135insAGAAAAACAATTTAAAGTAAACA (p.Asn45LysfsTer?)
c.232_233insAGAAAAACAATTTAAAGTAAACA
n.7667_7668insAGAAAAACAATTTAAAGTAAACA
c.7571_7572insAGAAAAACAATTTAAAGTAAACA (p.Asn2524LysfsTer?)
13g.32357792T>ACA387745029BRCA2c.7668T>A (p.Asn2556Lys)
c.7299T>A (p.Asn2433Lys)
c.135T>A (p.Asn45Lys)
c.233T>A
n.7668T>A
c.7572T>A (p.Asn2524Lys)
 dbSNP
13g.32357792T>CCA483439162BRCA2c.7668T>C (p.Asn2556=)
c.7299T>C (p.Asn2433=)
c.135T>C (p.Asn45=)
c.233T>C
n.7668T>C
c.7572T>C (p.Asn2524=)
13g.32357792T>GCA387745036BRCA2c.7668T>G (p.Asn2556Lys)
c.7299T>G (p.Asn2433Lys)
c.135T>G (p.Asn45Lys)
c.233T>G
n.7668T>G
c.7572T>G (p.Asn2524Lys)
13g.32357792T=CA2082817992BRCA2c.7668T= (p.Asn2556=)
c.7299T= (p.Asn2433=)
c.135T= (p.Asn45=)
c.233T=
n.7668T=
c.7572T= (p.Asn2524=)
13g.32357792_32357793insACA10589446BRCA2c.7668_7669insA (p.Ala2557SerfsTer9)
c.7299_7300insA (p.Ala2434SerfsTer9)
c.135_136insA (p.Ala46SerfsTer9)
c.233_234insA
n.7668_7669insA
c.7572_7573insA (p.Ala2525SerfsTer9)
 ClinVar dbSNP
13g.32357793G>ACA10579747BRCA2c.7669G>A (p.Ala2557Thr)
c.7300G>A (p.Ala2434Thr)
c.136G>A (p.Ala46Thr)
c.234G>A
n.7669G>A
c.7573G>A (p.Ala2525Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32357793G>CCA387745041BRCA2c.7669G>C (p.Ala2557Pro)
c.7300G>C (p.Ala2434Pro)
c.136G>C (p.Ala46Pro)
c.234G>C
n.7669G>C
c.7573G>C (p.Ala2525Pro)
 dbSNP
13g.32357793G=CA2082818001BRCA2c.7669G= (p.Ala2557=)
c.7300G= (p.Ala2434=)
c.136G= (p.Ala46=)
c.234G=
n.7669G=
c.7573G= (p.Ala2525=)
13g.32357793G>TCA387745044BRCA2c.7669G>T (p.Ala2557Ser)
c.7300G>T (p.Ala2434Ser)
c.136G>T (p.Ala46Ser)
c.234G>T
n.7669G>T
c.7573G>T (p.Ala2525Ser)
13g.32357793_32357794insTATCACACAATAAAAACAATTATAACAAACA2501501461BRCA2c.7669_7670insTATCACACAATAAAAACAATTATAACAAA (p.Ala2557ValfsTer?)
c.7300_7301insTATCACACAATAAAAACAATTATAACAAA (p.Ala2434ValfsTer?)
c.136_137insTATCACACAATAAAAACAATTATAACAAA (p.Ala46ValfsTer?)
c.234_235insTATCACACAATAAAAACAATTATAACAAA
n.7669_7670insTATCACACAATAAAAACAATTATAACAAA
c.7573_7574insTATCACACAATAAAAACAATTATAACAAA (p.Ala2525ValfsTer?)
13g.32357794C>ACA387745046BRCA2c.7670C>A (p.Ala2557Glu)
c.7301C>A (p.Ala2434Glu)
c.137C>A (p.Ala46Glu)
c.235C>A
n.7670C>A
c.7574C>A (p.Ala2525Glu)
 ClinVar
13g.32357794C=CA2082818022BRCA2c.7670C= (p.Ala2557=)
c.7301C= (p.Ala2434=)
c.137C= (p.Ala46=)
c.235C=
n.7670C=
c.7574C= (p.Ala2525=)
13g.32357794C>GCA387745047BRCA2c.7670C>G (p.Ala2557Gly)
c.7301C>G (p.Ala2434Gly)
c.137C>G (p.Ala46Gly)
c.235C>G
n.7670C>G
c.7574C>G (p.Ala2525Gly)
 dbSNP
13g.32357794C>TCA6941128BRCA2c.7670C>T (p.Ala2557Val)
c.7301C>T (p.Ala2434Val)
c.137C>T (p.Ala46Val)
c.235C>T
n.7670C>T
c.7574C>T (p.Ala2525Val)
 ClinVar dbSNP ExAC gnomAD v2 COSMIC COSMIC
13g.32357794_32357795delinsCACA2082818011BRCA2c.7670_7671delinsCA (p.Ala2557=)
c.7301_7302delinsCA (p.Ala2434=)
c.137_138delinsCA (p.Ala46=)
c.235_236delinsCA
n.7670_7671delinsCA
c.7574_7575delinsCA (p.Ala2525=)
13g.32357794_32357796delinsCAGCA2082818010BRCA2c.7670_7672delinsCAG (p.Ala2557=)
c.7301_7303delinsCAG (p.Ala2434=)
c.137_139delinsCAG (p.Ala46=)
c.235_237delinsCAG
n.7670_7672delinsCAG
c.7574_7576delinsCAG (p.Ala2525=)
13g.32357795delCA025216BRCA2c.7671del (p.Glu2558SerfsTer?)
c.7302del (p.Glu2435SerfsTer?)
c.138del (p.Glu47SerfsTer?)
c.236del
n.7671del
c.7575del (p.Glu2526SerfsTer?)
 ClinVar dbSNP
13g.32357795A=CA2082818045BRCA2c.7671A= (p.Ala2557=)
c.7302A= (p.Ala2434=)
c.138A= (p.Ala46=)
c.236A=
n.7671A=
c.7575A= (p.Ala2525=)
13g.32357795A>CCA483439166BRCA2c.7671A>C (p.Ala2557=)
c.7302A>C (p.Ala2434=)
c.138A>C (p.Ala46=)
c.236A>C
n.7671A>C
c.7575A>C (p.Ala2525=)
 ClinVar
13g.32357795A>GCA16607482BRCA2c.7671A>G (p.Ala2557=)
c.7302A>G (p.Ala2434=)
c.138A>G (p.Ala46=)
c.236A>G
n.7671A>G
c.7575A>G (p.Ala2525=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357795A>TCA483439165BRCA2c.7671A>T (p.Ala2557=)
c.7302A>T (p.Ala2434=)
c.138A>T (p.Ala46=)
c.236A>T
n.7671A>T
c.7575A>T (p.Ala2525=)
 dbSNP
13g.32357797_32357798dupCA6941129BRCA2c.7673_7674dup (p.Phe2560LeufsTer?)
c.7304_7305dup (p.Phe2437LeufsTer?)
c.140_141dup (p.Phe49LeufsTer?)
c.238_239dup
n.7673_7674dup
c.7577_7578dup (p.Phe2528LeufsTer?)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357797_32357798delCA025217BRCA2c.7673_7674del (p.Glu2558ValfsTer7)
c.7304_7305del (p.Glu2435ValfsTer7)
c.140_141del (p.Glu47ValfsTer7)
c.238_239del
n.7673_7674del
c.7577_7578del (p.Glu2526ValfsTer7)
 ClinVar dbSNP gnomAD v4
13g.32357796G>ACA387745055BRCA2c.7672G>A (p.Glu2558Lys)
c.7303G>A (p.Glu2435Lys)
c.139G>A (p.Glu47Lys)
c.237G>A
n.7672G>A
c.7576G>A (p.Glu2526Lys)
 ClinVar
13g.32357796G>CCA10575928BRCA2c.7672G>C (p.Glu2558Gln)
c.7303G>C (p.Glu2435Gln)
c.139G>C (p.Glu47Gln)
c.237G>C
n.7672G>C
c.7576G>C (p.Glu2526Gln)
 ClinVar dbSNP
13g.32357796G=CA2082818059BRCA2c.7672G= (p.Glu2558=)
c.7303G= (p.Glu2435=)
c.139G= (p.Glu47=)
c.237G=
n.7672G=
c.7576G= (p.Glu2526=)
13g.32357796G>TCA387745058BRCA2c.7672G>T (p.Glu2558Ter)
c.7303G>T (p.Glu2435Ter)
c.139G>T (p.Glu47Ter)
c.237G>T
n.7672G>T
c.7576G>T (p.Glu2526Ter)
13g.32357796_32357797delinsGACA2082818056BRCA2c.7672_7673delinsGA (p.Glu2558=)
c.7303_7304delinsGA (p.Glu2435=)
c.139_140delinsGA (p.Glu47=)
c.237_238delinsGA
n.7672_7673delinsGA
c.7576_7577delinsGA (p.Glu2526=)
13g.32357797delCA10583134BRCA2c.7673del (p.Glu2558GlyfsTer?)
c.7304del (p.Glu2435GlyfsTer?)
c.140del (p.Glu47GlyfsTer?)
c.238del
n.7673del
c.7577del (p.Glu2526GlyfsTer?)
 ClinVar dbSNP
13g.32357797A=CA2082818074BRCA2c.7673A= (p.Glu2558=)
c.7304A= (p.Glu2435=)
c.140A= (p.Glu47=)
c.238A=
n.7673A=
c.7577A= (p.Glu2526=)
13g.32357797A>CCA387745072BRCA2c.7673A>C (p.Glu2558Ala)
c.7304A>C (p.Glu2435Ala)
c.140A>C (p.Glu47Ala)
c.238A>C
n.7673A>C
c.7577A>C (p.Glu2526Ala)
 dbSNP
13g.32357797A>GCA387745064BRCA2c.7673A>G (p.Glu2558Gly)
c.7304A>G (p.Glu2435Gly)
c.140A>G (p.Glu47Gly)
c.238A>G
n.7673A>G
c.7577A>G (p.Glu2526Gly)
13g.32357797A>TCA025218BRCA2c.7673A>T (p.Glu2558Val)
c.7304A>T (p.Glu2435Val)
c.140A>T (p.Glu47Val)
c.238A>T
n.7673A>T
c.7577A>T (p.Glu2526Val)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357798G>ACA483439168BRCA2c.7674G>A (p.Glu2558=)
c.7305G>A (p.Glu2435=)
c.141G>A (p.Glu47=)
c.239G>A
n.7674G>A
c.7578G>A (p.Glu2526=)
 dbSNP
13g.32357798G>CCA025219BRCA2c.7674G>C (p.Glu2558Asp)
c.7305G>C (p.Glu2435Asp)
c.141G>C (p.Glu47Asp)
c.239G>C
n.7674G>C
c.7578G>C (p.Glu2526Asp)
 ClinVar dbSNP
13g.32357798G=CA2082818094BRCA2c.7674G= (p.Glu2558=)
c.7305G= (p.Glu2435=)
c.141G= (p.Glu47=)
c.239G=
n.7674G=
c.7578G= (p.Glu2526=)
13g.32357798G>TCA387745077BRCA2c.7674G>T (p.Glu2558Asp)
c.7305G>T (p.Glu2435Asp)
c.141G>T (p.Glu47Asp)
c.239G>T
n.7674G>T
c.7578G>T (p.Glu2526Asp)
13g.32357798_32357800delinsGTCCA2082818099BRCA2c.7674_7676delinsGTC (p.Glu2558=)
c.7305_7307delinsGTC (p.Glu2435=)
c.141_143delinsGTC (p.Glu47=)
c.239_241delinsGTC
n.7674_7676delinsGTC
c.7578_7580delinsGTC (p.Glu2526=)
13g.32357798_32357803delinsGTCTTTCA2082818097BRCA2c.7674_7679delinsGTCTTT (p.Glu2558=)
c.7305_7310delinsGTCTTT (p.Glu2435=)
c.141_146delinsGTCTTT (p.Glu47=)
c.239_244delinsGTCTTT
n.7674_7679delinsGTCTTT
c.7578_7583delinsGTCTTT (p.Glu2526=)
13g.32357798_32357799insAAACCA658823753BRCA2c.7674_7675insAAAC (p.Ser2559LysfsTer8)
c.7305_7306insAAAC (p.Ser2436LysfsTer8)
c.141_142insAAAC (p.Ser48LysfsTer8)
c.239_240insAAAC
n.7674_7675insAAAC
c.7578_7579insAAAC (p.Ser2527LysfsTer8)
 ClinVar dbSNP
13g.32357799T>ACA387745084BRCA2c.7675T>A (p.Ser2559Thr)
c.7306T>A (p.Ser2436Thr)
c.142T>A (p.Ser48Thr)
c.240T>A
n.7675T>A
c.7579T>A (p.Ser2527Thr)
 ClinVar dbSNP
13g.32357799T>CCA387745087BRCA2c.7675T>C (p.Ser2559Pro)
c.7306T>C (p.Ser2436Pro)
c.142T>C (p.Ser48Pro)
c.240T>C
n.7675T>C
c.7579T>C (p.Ser2527Pro)
 COSMIC COSMIC
13g.32357799T>GCA387745090BRCA2c.7675T>G (p.Ser2559Ala)
c.7306T>G (p.Ser2436Ala)
c.142T>G (p.Ser48Ala)
c.240T>G
n.7675T>G
c.7579T>G (p.Ser2527Ala)
 dbSNP
13g.32357799T=CA2082818116BRCA2c.7675T= (p.Ser2559=)
c.7306T= (p.Ser2436=)
c.142T= (p.Ser48=)
c.240T=
n.7675T=
c.7579T= (p.Ser2527=)
13g.32357800_32357801delCA915946875BRCA2c.7676_7677del (p.Ser2559PhefsTer6)
c.7307_7308del (p.Ser2436PhefsTer6)
c.143_144del (p.Ser48PhefsTer6)
c.241_242del
n.7676_7677del
c.7580_7581del (p.Ser2527PhefsTer6)
 ClinVar dbSNP
13g.32357801_32357805delCA2082818117BRCA2c.7677_7681del (p.Phe2560ValfsTer4)
c.7308_7312del (p.Phe2437ValfsTer4)
c.144_148del (p.Phe49ValfsTer4)
c.242_246del
n.7677_7681del
c.7581_7585del (p.Phe2528ValfsTer4)
 dbSNP
13g.32357799_32357800insAAACCA025220BRCA2c.7675_7676insAAAC (p.Ser2559Ter)
c.7306_7307insAAAC (p.Ser2436Ter)
c.142_143insAAAC (p.Ser48Ter)
c.240_241insAAAC
n.7675_7676insAAAC
c.7579_7580insAAAC (p.Ser2527Ter)
 ClinVar dbSNP
13g.32357800C>ACA387745094BRCA2c.7676C>A (p.Ser2559Tyr)
c.7307C>A (p.Ser2436Tyr)
c.143C>A (p.Ser48Tyr)
c.241C>A
n.7676C>A
c.7580C>A (p.Ser2527Tyr)
 COSMIC COSMIC
13g.32357800C=CA2082818141BRCA2c.7676C= (p.Ser2559=)
c.7307C= (p.Ser2436=)
c.143C= (p.Ser48=)
c.241C=
n.7676C=
c.7580C= (p.Ser2527=)
13g.32357800C>GCA16614210BRCA2c.7676C>G (p.Ser2559Cys)
c.7307C>G (p.Ser2436Cys)
c.143C>G (p.Ser48Cys)
c.241C>G
n.7676C>G
c.7580C>G (p.Ser2527Cys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32357800C>TCA387745097BRCA2c.7676C>T (p.Ser2559Phe)
c.7307C>T (p.Ser2436Phe)
c.143C>T (p.Ser48Phe)
c.241C>T
n.7676C>T
c.7580C>T (p.Ser2527Phe)
 ClinVar dbSNP
13g.32357800_32357802delinsCTTCA2082818134BRCA2c.7676_7678delinsCTT (p.Ser2559=)
c.7307_7309delinsCTT (p.Ser2436=)
c.143_145delinsCTT (p.Ser48=)
c.241_243delinsCTT
n.7676_7678delinsCTT
c.7580_7582delinsCTT (p.Ser2527=)
13g.32357801T>ACA483439170BRCA2c.7677T>A (p.Ser2559=)
c.7308T>A (p.Ser2436=)
c.144T>A (p.Ser48=)
c.242T>A
n.7677T>A
c.7581T>A (p.Ser2527=)
 dbSNP
13g.32357801T>CCA483439171BRCA2c.7677T>C (p.Ser2559=)
c.7308T>C (p.Ser2436=)
c.144T>C (p.Ser48=)
c.242T>C
n.7677T>C
c.7581T>C (p.Ser2527=)
13g.32357801T>GCA483439172BRCA2c.7677T>G (p.Ser2559=)
c.7308T>G (p.Ser2436=)
c.144T>G (p.Ser48=)
c.242T>G
n.7677T>G
c.7581T>G (p.Ser2527=)
13g.32357804dupCA025225BRCA2c.7680dup (p.Gln2561SerfsTer5)
c.7311dup (p.Gln2438SerfsTer5)
c.147dup (p.Gln50SerfsTer5)
c.245dup
n.7680dup
c.7584dup (p.Gln2529SerfsTer5)
 ClinVar dbSNP
13g.32357804delCA025226BRCA2c.7680del (p.Gln2561SerfsTer?)
c.7311del (p.Gln2438SerfsTer?)
c.147del (p.Gln50SerfsTer?)
c.245del
n.7680del
c.7584del (p.Gln2529SerfsTer?)
 ClinVar dbSNP
13g.32357803_32357804delCA025223BRCA2c.7679_7680del (p.Phe2560SerfsTer5)
c.7310_7311del (p.Phe2437SerfsTer5)
c.146_147del (p.Phe49SerfsTer5)
c.244_245del
n.7679_7680del
c.7583_7584del (p.Phe2528SerfsTer5)
 ClinVar dbSNP gnomAD v4
13g.32357802T>ACA387745109BRCA2c.7678T>A (p.Phe2560Ile)
c.7309T>A (p.Phe2437Ile)
c.145T>A (p.Phe49Ile)
c.243T>A
n.7678T>A
c.7582T>A (p.Phe2528Ile)
13g.32357802T>CCA387745107BRCA2c.7678T>C (p.Phe2560Leu)
c.7309T>C (p.Phe2437Leu)
c.145T>C (p.Phe49Leu)
c.243T>C
n.7678T>C
c.7582T>C (p.Phe2528Leu)
 ClinVar dbSNP
13g.32357802T>GCA387745105BRCA2c.7678T>G (p.Phe2560Val)
c.7309T>G (p.Phe2437Val)
c.145T>G (p.Phe49Val)
c.243T>G
n.7678T>G
c.7582T>G (p.Phe2528Val)
13g.32357802T=CA2082818166BRCA2c.7678T= (p.Phe2560=)
c.7309T= (p.Phe2437=)
c.145T= (p.Phe49=)
c.243T=
n.7678T=
c.7582T= (p.Phe2528=)
13g.32357803T>ACA387745118BRCA2c.7679T>A (p.Phe2560Tyr)
c.7310T>A (p.Phe2437Tyr)
c.146T>A (p.Phe49Tyr)
c.244T>A
n.7679T>A
c.7583T>A (p.Phe2528Tyr)
 dbSNP
13g.32357803T>CCA6941130BRCA2c.7679T>C (p.Phe2560Ser)
c.7310T>C (p.Phe2437Ser)
c.146T>C (p.Phe49Ser)
c.244T>C
n.7679T>C
c.7583T>C (p.Phe2528Ser)
 ClinVar dbSNP ExAC
13g.32357803T>GCA387745117BRCA2c.7679T>G (p.Phe2560Cys)
c.7310T>G (p.Phe2437Cys)
c.146T>G (p.Phe49Cys)
c.244T>G
n.7679T>G
c.7583T>G (p.Phe2528Cys)
 dbSNP
13g.32357803T=CA2082818174BRCA2c.7679T= (p.Phe2560=)
c.7310T= (p.Phe2437=)
c.146T= (p.Phe49=)
c.244T=
n.7679T=
c.7583T= (p.Phe2528=)
13g.32357804T>ACA387745119BRCA2c.7680T>A (p.Phe2560Leu)
c.7311T>A (p.Phe2437Leu)
c.147T>A (p.Phe49Leu)
c.245T>A
n.7680T>A
c.7584T>A (p.Phe2528Leu)
13g.32357804T>CCA483439176BRCA2c.7680T>C (p.Phe2560=)
c.7311T>C (p.Phe2437=)
c.147T>C (p.Phe49=)
c.245T>C
n.7680T>C
c.7584T>C (p.Phe2528=)
 ClinVar dbSNP
13g.32357804T>GCA387745120BRCA2c.7680T>G (p.Phe2560Leu)
c.7311T>G (p.Phe2437Leu)
c.147T>G (p.Phe49Leu)
c.245T>G
n.7680T>G
c.7584T>G (p.Phe2528Leu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357804T=CA2082818178BRCA2c.7680T= (p.Phe2560=)
c.7311T= (p.Phe2437=)
c.147T= (p.Phe49=)
c.245T=
n.7680T=
c.7584T= (p.Phe2528=)
13g.32357805C>ACA387745121BRCA2c.7681C>A (p.Gln2561Lys)
c.7312C>A (p.Gln2438Lys)
c.148C>A (p.Gln50Lys)
c.246C>A
n.7681C>A
c.7585C>A (p.Gln2529Lys)
 ClinVar
13g.32357805C=CA2082818186BRCA2c.7681C= (p.Gln2561=)
c.7312C= (p.Gln2438=)
c.148C= (p.Gln50=)
c.246C=
n.7681C=
c.7585C= (p.Gln2529=)
13g.32357805C>GCA387745124BRCA2c.7681C>G (p.Gln2561Glu)
c.7312C>G (p.Gln2438Glu)
c.148C>G (p.Gln50Glu)
c.246C>G
n.7681C>G
c.7585C>G (p.Gln2529Glu)
 dbSNP
13g.32357805C>TCA025228BRCA2c.7681C>T (p.Gln2561Ter)
c.7312C>T (p.Gln2438Ter)
c.148C>T (p.Gln50Ter)
c.246C>T
n.7681C>T
c.7585C>T (p.Gln2529Ter)
 ClinVar dbSNP gnomAD v4
13g.32357805_32357806insTCA025227BRCA2c.7681_7682insT (p.Gln2561LeufsTer5)
c.7312_7313insT (p.Gln2438LeufsTer5)
c.148_149insT (p.Gln50LeufsTer5)
c.246_247insT
n.7681_7682insT
c.7585_7586insT (p.Gln2529LeufsTer5)
 ClinVar dbSNP
13g.32357806A=CA2082818201BRCA2c.7682A= (p.Gln2561=)
c.7313A= (p.Gln2438=)
c.149A= (p.Gln50=)
c.247A=
n.7682A=
c.7586A= (p.Gln2529=)
13g.32357806A>CCA387745132BRCA2c.7682A>C (p.Gln2561Pro)
c.7313A>C (p.Gln2438Pro)
c.149A>C (p.Gln50Pro)
c.247A>C
n.7682A>C
c.7586A>C (p.Gln2529Pro)
 ClinVar dbSNP
13g.32357806A>GCA336029BRCA2c.7682A>G (p.Gln2561Arg)
c.7313A>G (p.Gln2438Arg)
c.149A>G (p.Gln50Arg)
c.247A>G
n.7682A>G
c.7586A>G (p.Gln2529Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32357806A>TCA387745129BRCA2c.7682A>T (p.Gln2561Leu)
c.7313A>T (p.Gln2438Leu)
c.149A>T (p.Gln50Leu)
c.247A>T
n.7682A>T
c.7586A>T (p.Gln2529Leu)
 ClinVar dbSNP gnomAD v4
13g.32357806_32357808delinsAGTCA2082818206BRCA2c.7682_7684delinsAGT (p.Gln2561=)
c.7313_7315delinsAGT (p.Gln2438=)
c.149_151delinsAGT (p.Gln50=)
c.247_249delinsAGT
n.7682_7684delinsAGT
c.7586_7588delinsAGT (p.Gln2529=)
13g.32357807G>ACA025229BRCA2c.7683G>A (p.Gln2561=)
c.7314G>A (p.Gln2438=)
c.150G>A (p.Gln50=)
c.248G>A
n.7683G>A
c.7587G>A (p.Gln2529=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357807G>CCA10579748BRCA2c.7683G>C (p.Gln2561His)
c.7314G>C (p.Gln2438His)
c.150G>C (p.Gln50His)
c.248G>C
n.7683G>C
c.7587G>C (p.Gln2529His)
 ClinVar dbSNP
13g.32357807G=CA2082818223BRCA2c.7683G= (p.Gln2561=)
c.7314G= (p.Gln2438=)
c.150G= (p.Gln50=)
c.248G=
n.7683G=
c.7587G= (p.Gln2529=)
13g.32357807G>TCA387745144BRCA2c.7683G>T (p.Gln2561His)
c.7314G>T (p.Gln2438His)
c.150G>T (p.Gln50His)
c.248G>T
n.7683G>T
c.7587G>T (p.Gln2529His)
13g.32357807_32357808delCA6941131BRCA2c.7683_7684del (p.Gln2561HisfsTer4)
c.7314_7315del (p.Gln2438HisfsTer4)
c.150_151del (p.Gln50HisfsTer4)
c.248_249del
n.7683_7684del
c.7587_7588del (p.Gln2529HisfsTer4)
 ClinVar dbSNP ExAC
13g.32357808T>ACA387745150BRCA2c.7684T>A (p.Phe2562Ile)
c.7315T>A (p.Phe2439Ile)
c.151T>A (p.Phe51Ile)
c.249T>A
n.7684T>A
c.7588T>A (p.Phe2530Ile)
 ClinVar dbSNP
13g.32357808T>CCA025230BRCA2c.7684T>C (p.Phe2562Leu)
c.7315T>C (p.Phe2439Leu)
c.151T>C (p.Phe51Leu)
c.249T>C
n.7684T>C
c.7588T>C (p.Phe2530Leu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357808T>GCA025231BRCA2c.7684T>G (p.Phe2562Val)
c.7315T>G (p.Phe2439Val)
c.151T>G (p.Phe51Val)
c.249T>G
n.7684T>G
c.7588T>G (p.Phe2530Val)
 ClinVar dbSNP
13g.32357808T=CA2082818243BRCA2c.7684T= (p.Phe2562=)
c.7315T= (p.Phe2439=)
c.151T= (p.Phe51=)
c.249T=
n.7684T=
c.7588T= (p.Phe2530=)
13g.32357809T>ACA387745152BRCA2c.7685T>A (p.Phe2562Tyr)
c.7316T>A (p.Phe2439Tyr)
c.152T>A (p.Phe51Tyr)
c.250T>A
n.7685T>A
c.7589T>A (p.Phe2530Tyr)
 dbSNP
13g.32357809T>CCA387745154BRCA2c.7685T>C (p.Phe2562Ser)
c.7316T>C (p.Phe2439Ser)
c.152T>C (p.Phe51Ser)
c.250T>C
n.7685T>C
c.7589T>C (p.Phe2530Ser)
13g.32357809T>GCA025232BRCA2c.7685T>G (p.Phe2562Cys)
c.7316T>G (p.Phe2439Cys)
c.152T>G (p.Phe51Cys)
c.250T>G
n.7685T>G
c.7589T>G (p.Phe2530Cys)
 ClinVar dbSNP
13g.32357809T=CA2082818253BRCA2c.7685T= (p.Phe2562=)
c.7316T= (p.Phe2439=)
c.152T= (p.Phe51=)
c.250T=
n.7685T=
c.7589T= (p.Phe2530=)
13g.32357810T>ACA387745159BRCA2c.7686T>A (p.Phe2562Leu)
c.7317T>A (p.Phe2439Leu)
c.153T>A (p.Phe51Leu)
c.251T>A
n.7686T>A
c.7590T>A (p.Phe2530Leu)
13g.32357810T>CCA483439180BRCA2c.7686T>C (p.Phe2562=)
c.7317T>C (p.Phe2439=)
c.153T>C (p.Phe51=)
c.251T>C
n.7686T>C
c.7590T>C (p.Phe2530=)
13g.32357810T>GCA387745161BRCA2c.7686T>G (p.Phe2562Leu)
c.7317T>G (p.Phe2439Leu)
c.153T>G (p.Phe51Leu)
c.251T>G
n.7686T>G
c.7590T>G (p.Phe2530Leu)
 ClinVar dbSNP
13g.32357811C>ACA387745165BRCA2c.7687C>A (p.His2563Asn)
c.7318C>A (p.His2440Asn)
c.154C>A (p.His52Asn)
c.252C>A
n.7687C>A
c.7591C>A (p.His2531Asn)
13g.32357811C>GCA387745163BRCA2c.7687C>G (p.His2563Asp)
c.7318C>G (p.His2440Asp)
c.154C>G (p.His52Asp)
c.252C>G
n.7687C>G
c.7591C>G (p.His2531Asp)
13g.32357811C>TCA387745162BRCA2c.7687C>T (p.His2563Tyr)
c.7318C>T (p.His2440Tyr)
c.154C>T (p.His52Tyr)
c.252C>T
n.7687C>T
c.7591C>T (p.His2531Tyr)
 ClinVar dbSNP
13g.32357814_32357815delCA2580614660BRCA2c.7690_7691del (p.Thr2564Ter)
c.7321_7322del (p.Thr2441Ter)
c.157_158del (p.Thr53Ter)
c.255_256del
n.7690_7691del
c.7594_7595del (p.Thr2532Ter)
 ClinVar
13g.32357812A>CCA387745168BRCA2c.7688A>C (p.His2563Pro)
c.7319A>C (p.His2440Pro)
c.155A>C (p.His52Pro)
c.253A>C
n.7688A>C
c.7592A>C (p.His2531Pro)
13g.32357812A>GCA387745173BRCA2c.7688A>G (p.His2563Arg)
c.7319A>G (p.His2440Arg)
c.155A>G (p.His52Arg)
c.253A>G
n.7688A>G
c.7592A>G (p.His2531Arg)
 gnomAD v4
13g.32357812A>TCA387745174BRCA2c.7688A>T (p.His2563Leu)
c.7319A>T (p.His2440Leu)
c.155A>T (p.His52Leu)
c.253A>T
n.7688A>T
c.7592A>T (p.His2531Leu)
 dbSNP
13g.32357812_32357813delinsACCA2082818264BRCA2c.7688_7689delinsAC (p.His2563=)
c.7319_7320delinsAC (p.His2440=)
c.155_156delinsAC (p.His52=)
c.253_254delinsAC
n.7688_7689delinsAC
c.7592_7593delinsAC (p.His2531=)
13g.32357813delCA025233BRCA2c.7689del (p.His2563GlnfsTer?)
c.7320del (p.His2440GlnfsTer?)
c.156del (p.His52GlnfsTer?)
c.254del
n.7689del
c.7593del (p.His2531GlnfsTer?)
 ClinVar dbSNP
13g.32357813C>ACA387745176BRCA2c.7689C>A (p.His2563Gln)
c.7320C>A (p.His2440Gln)
c.156C>A (p.His52Gln)
c.254C>A
n.7689C>A
c.7593C>A (p.His2531Gln)
 dbSNP
13g.32357813C=CA2082818274BRCA2c.7689C= (p.His2563=)
c.7320C= (p.His2440=)
c.156C= (p.His52=)
c.254C=
n.7689C=
c.7593C= (p.His2531=)
13g.32357813C>GCA387745178BRCA2c.7689C>G (p.His2563Gln)
c.7320C>G (p.His2440Gln)
c.156C>G (p.His52Gln)
c.254C>G
n.7689C>G
c.7593C>G (p.His2531Gln)
 dbSNP
13g.32357813C>TCA10583135BRCA2c.7689C>T (p.His2563=)
c.7320C>T (p.His2440=)
c.156C>T (p.His52=)
c.254C>T
n.7689C>T
c.7593C>T (p.His2531=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32357814A=CA2082818279BRCA2c.7690A= (p.Thr2564=)
c.7321A= (p.Thr2441=)
c.157A= (p.Thr53=)
c.255A=
n.7690A=
c.7594A= (p.Thr2532=)
13g.32357814A>CCA387745185BRCA2c.7690A>C (p.Thr2564Pro)
c.7321A>C (p.Thr2441Pro)
c.157A>C (p.Thr53Pro)
c.255A>C
n.7690A>C
c.7594A>C (p.Thr2532Pro)
 ClinVar dbSNP gnomAD v4
13g.32357814A>GCA387745187BRCA2c.7690A>G (p.Thr2564Ala)
c.7321A>G (p.Thr2441Ala)
c.157A>G (p.Thr53Ala)
c.255A>G
n.7690A>G
c.7594A>G (p.Thr2532Ala)
13g.32357814A>TCA387745188BRCA2c.7690A>T (p.Thr2564Ser)
c.7321A>T (p.Thr2441Ser)
c.157A>T (p.Thr53Ser)
c.255A>T
n.7690A>T
c.7594A>T (p.Thr2532Ser)
 dbSNP
13g.32357815C>ACA387745191BRCA2c.7691C>A (p.Thr2564Asn)
c.7322C>A (p.Thr2441Asn)
c.158C>A (p.Thr53Asn)
c.256C>A
n.7691C>A
c.7595C>A (p.Thr2532Asn)
 dbSNP
13g.32357815C=CA2082818287BRCA2c.7691C= (p.Thr2564=)
c.7322C= (p.Thr2441=)
c.158C= (p.Thr53=)
c.256C=
n.7691C=
c.7595C= (p.Thr2532=)
13g.32357815C>GCA6941132BRCA2c.7691C>G (p.Thr2564Ser)
c.7322C>G (p.Thr2441Ser)
c.158C>G (p.Thr53Ser)
c.256C>G
n.7691C>G
c.7595C>G (p.Thr2532Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357815C>TCA025234BRCA2c.7691C>T (p.Thr2564Ile)
c.7322C>T (p.Thr2441Ile)
c.158C>T (p.Thr53Ile)
c.256C>T
n.7691C>T
c.7595C>T (p.Thr2532Ile)
 ClinVar dbSNP
13g.32357816T>ACA483439185BRCA2c.7692T>A (p.Thr2564=)
c.7323T>A (p.Thr2441=)
c.159T>A (p.Thr53=)
c.257T>A
n.7692T>A
c.7596T>A (p.Thr2532=)
 dbSNP gnomAD v2
13g.32357816T>CCA483439187BRCA2c.7692T>C (p.Thr2564=)
c.7323T>C (p.Thr2441=)
c.159T>C (p.Thr53=)
c.257T>C
n.7692T>C
c.7596T>C (p.Thr2532=)
 ClinVar dbSNP gnomAD v4
13g.32357816T>GCA483439186BRCA2c.7692T>G (p.Thr2564=)
c.7323T>G (p.Thr2441=)
c.159T>G (p.Thr53=)
c.257T>G
n.7692T>G
c.7596T>G (p.Thr2532=)
 ClinVar
13g.32357816T=CA2082818295BRCA2c.7692T= (p.Thr2564=)
c.7323T= (p.Thr2441=)
c.159T= (p.Thr53=)
c.257T=
n.7692T=
c.7596T= (p.Thr2532=)
13g.32357817G>ACA6941133BRCA2c.7693G>A (p.Glu2565Lys)
c.7324G>A (p.Glu2442Lys)
c.160G>A (p.Glu54Lys)
c.258G>A
n.7693G>A
c.7597G>A (p.Glu2533Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357817G>CCA387745197BRCA2c.7693G>C (p.Glu2565Gln)
c.7324G>C (p.Glu2442Gln)
c.160G>C (p.Glu54Gln)
c.258G>C
n.7693G>C
c.7597G>C (p.Glu2533Gln)
 dbSNP
13g.32357817G=CA2082818301BRCA2c.7693G= (p.Glu2565=)
c.7324G= (p.Glu2442=)
c.160G= (p.Glu54=)
c.258G=
n.7693G=
c.7597G= (p.Glu2533=)
13g.32357817G>TCA387745194BRCA2c.7693G>T (p.Glu2565Ter)
c.7324G>T (p.Glu2442Ter)
c.160G>T (p.Glu54Ter)
c.258G>T
n.7693G>T
c.7597G>T (p.Glu2533Ter)
13g.32357818A>CCA387745204BRCA2c.7694A>C (p.Glu2565Ala)
c.7325A>C (p.Glu2442Ala)
c.161A>C (p.Glu54Ala)
c.259A>C
n.7694A>C
c.7598A>C (p.Glu2533Ala)
 gnomAD v4
13g.32357818A>GCA387745202BRCA2c.7694A>G (p.Glu2565Gly)
c.7325A>G (p.Glu2442Gly)
c.161A>G (p.Glu54Gly)
c.259A>G
n.7694A>G
c.7598A>G (p.Glu2533Gly)
13g.32357818A>TCA387745203BRCA2c.7694A>T (p.Glu2565Val)
c.7325A>T (p.Glu2442Val)
c.161A>T (p.Glu54Val)
c.259A>T
n.7694A>T
c.7598A>T (p.Glu2533Val)
 dbSNP
13g.32357819A>CCA387745205BRCA2c.7695A>C (p.Glu2565Asp)
c.7326A>C (p.Glu2442Asp)
c.162A>C (p.Glu54Asp)
c.260A>C
n.7695A>C
c.7599A>C (p.Glu2533Asp)
13g.32357819A>GCA483439188BRCA2c.7695A>G (p.Glu2565=)
c.7326A>G (p.Glu2442=)
c.162A>G (p.Glu54=)
c.260A>G
n.7695A>G
c.7599A>G (p.Glu2533=)
13g.32357819A>TCA387745206BRCA2c.7695A>T (p.Glu2565Asp)
c.7326A>T (p.Glu2442Asp)
c.162A>T (p.Glu54Asp)
c.260A>T
n.7695A>T
c.7599A>T (p.Glu2533Asp)
13g.32357820G>ACA387745208BRCA2c.7696G>A (p.Asp2566Asn)
c.7327G>A (p.Asp2443Asn)
c.163G>A (p.Asp55Asn)
c.261G>A
n.7696G>A
c.7600G>A (p.Asp2534Asn)
 ClinVar dbSNP
13g.32357820G>CCA387745209BRCA2c.7696G>C (p.Asp2566His)
c.7327G>C (p.Asp2443His)
c.163G>C (p.Asp55His)
c.261G>C
n.7696G>C
c.7600G>C (p.Asp2534His)
 dbSNP
13g.32357820G=CA2082818309BRCA2c.7696G= (p.Asp2566=)
c.7327G= (p.Asp2443=)
c.163G= (p.Asp55=)
c.261G=
n.7696G=
c.7600G= (p.Asp2534=)
13g.32357820G>TCA025235BRCA2c.7696G>T (p.Asp2566Tyr)
c.7327G>T (p.Asp2443Tyr)
c.163G>T (p.Asp55Tyr)
c.261G>T
n.7696G>T
c.7600G>T (p.Asp2534Tyr)
 ClinVar dbSNP gnomAD v4
13g.32357821A>CCA387745216BRCA2c.7697A>C (p.Asp2566Ala)
c.7328A>C (p.Asp2443Ala)
c.164A>C (p.Asp55Ala)
c.262A>C
n.7697A>C
c.7601A>C (p.Asp2534Ala)
13g.32357821A>GCA387745220BRCA2c.7697A>G (p.Asp2566Gly)
c.7328A>G (p.Asp2443Gly)
c.164A>G (p.Asp55Gly)
c.262A>G
n.7697A>G
c.7601A>G (p.Asp2534Gly)
 ClinVar
13g.32357821A>TCA387745228BRCA2c.7697A>T (p.Asp2566Val)
c.7328A>T (p.Asp2443Val)
c.164A>T (p.Asp55Val)
c.262A>T
n.7697A>T
c.7601A>T (p.Asp2534Val)
 gnomAD v4
13g.32357821dupCA025236BRCA2c.7697dup (p.Asp2566GlufsTer5)
c.7328dup (p.Asp2443GlufsTer5)
c.164dup (p.Asp55GlufsTer5)
c.262dup
n.7697dup
c.7601dup (p.Asp2534GlufsTer5)
 ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
13g.32357822T>ACA387745232BRCA2c.7698T>A (p.Asp2566Glu)
c.7329T>A (p.Asp2443Glu)
c.165T>A (p.Asp55Glu)
c.263T>A
n.7698T>A
c.7602T>A (p.Asp2534Glu)
 dbSNP
13g.32357822T>CCA483439189BRCA2c.7698T>C (p.Asp2566=)
c.7329T>C (p.Asp2443=)
c.165T>C (p.Asp55=)
c.263T>C
n.7698T>C
c.7602T>C (p.Asp2534=)
13g.32357822T>GCA387745234BRCA2c.7698T>G (p.Asp2566Glu)
c.7329T>G (p.Asp2443Glu)
c.165T>G (p.Asp55Glu)
c.263T>G
n.7698T>G
c.7602T>G (p.Asp2534Glu)
 ClinVar dbSNP
13g.32357822T=CA2082818324BRCA2c.7698T= (p.Asp2566=)
c.7329T= (p.Asp2443=)
c.165T= (p.Asp55=)
c.263T=
n.7698T=
c.7602T= (p.Asp2534=)
13g.32357823T>ACA387745242BRCA2c.7699T>A (p.Tyr2567Asn)
c.7330T>A (p.Tyr2444Asn)
c.166T>A (p.Tyr56Asn)
c.264T>A
n.7699T>A
c.7603T>A (p.Tyr2535Asn)
13g.32357823T>CCA387745237BRCA2c.7699T>C (p.Tyr2567His)
c.7330T>C (p.Tyr2444His)
c.166T>C (p.Tyr56His)
c.264T>C
n.7699T>C
c.7603T>C (p.Tyr2535His)
 ClinVar dbSNP
13g.32357823T>GCA387745240BRCA2c.7699T>G (p.Tyr2567Asp)
c.7330T>G (p.Tyr2444Asp)
c.166T>G (p.Tyr56Asp)
c.264T>G
n.7699T>G
c.7603T>G (p.Tyr2535Asp)
 ClinVar dbSNP gnomAD v4
13g.32357823T=CA2082818337BRCA2c.7699T= (p.Tyr2567=)
c.7330T= (p.Tyr2444=)
c.166T= (p.Tyr56=)
c.264T=
n.7699T=
c.7603T= (p.Tyr2535=)
13g.32357824delCA2580087341BRCA2c.7700del (p.Tyr2567PhefsTer?)
c.7331del (p.Tyr2444PhefsTer?)
c.167del (p.Tyr56PhefsTer?)
c.265del
n.7700del
c.7604del (p.Tyr2535PhefsTer?)
 ClinVar
13g.32357824A=CA2082818351BRCA2c.7700A= (p.Tyr2567=)
c.7331A= (p.Tyr2444=)
c.167A= (p.Tyr56=)
c.265A=
n.7700A=
c.7604A= (p.Tyr2535=)
13g.32357824A>CCA387745245BRCA2c.7700A>C (p.Tyr2567Ser)
c.7331A>C (p.Tyr2444Ser)
c.167A>C (p.Tyr56Ser)
c.265A>C
n.7700A>C
c.7604A>C (p.Tyr2535Ser)
13g.32357824A>GCA387745247BRCA2c.7700A>G (p.Tyr2567Cys)
c.7331A>G (p.Tyr2444Cys)
c.167A>G (p.Tyr56Cys)
c.265A>G
n.7700A>G
c.7604A>G (p.Tyr2535Cys)
13g.32357824A>TCA025237BRCA2c.7700A>T (p.Tyr2567Phe)
c.7331A>T (p.Tyr2444Phe)
c.167A>T (p.Tyr56Phe)
c.265A>T
n.7700A>T
c.7604A>T (p.Tyr2535Phe)
 ClinVar dbSNP gnomAD v4
13g.32357825T>ACA387745255BRCA2c.7701T>A (p.Tyr2567Ter)
c.7332T>A (p.Tyr2444Ter)
c.168T>A (p.Tyr56Ter)
c.266T>A
n.7701T>A
c.7605T>A (p.Tyr2535Ter)
 ClinVar dbSNP
13g.32357825T>CCA483439191BRCA2c.7701T>C (p.Tyr2567=)
c.7332T>C (p.Tyr2444=)
c.168T>C (p.Tyr56=)
c.266T>C
n.7701T>C
c.7605T>C (p.Tyr2535=)
 ClinVar dbSNP
13g.32357825T>GCA387745258BRCA2c.7701T>G (p.Tyr2567Ter)
c.7332T>G (p.Tyr2444Ter)
c.168T>G (p.Tyr56Ter)
c.266T>G
n.7701T>G
c.7605T>G (p.Tyr2535Ter)
 ClinVar dbSNP
13g.32357825T=CA2082818357BRCA2c.7701T= (p.Tyr2567=)
c.7332T= (p.Tyr2444=)
c.168T= (p.Tyr56=)
c.266T=
n.7701T=
c.7605T= (p.Tyr2535=)
13g.32357828dupCA2580087344BRCA2c.7704dup (p.Gly2569TrpfsTer2)
c.7335dup (p.Gly2446TrpfsTer2)
c.171dup (p.Gly58TrpfsTer2)
c.269dup
n.7704dup
c.7608dup (p.Gly2537TrpfsTer2)
 ClinVar
13g.32357828delCA2580087345BRCA2c.7704del (p.Phe2568LeufsTer?)
c.7335del (p.Phe2445LeufsTer?)
c.171del (p.Phe57LeufsTer?)
c.269del
n.7704del
c.7608del (p.Phe2536LeufsTer?)
 ClinVar
13g.32357827_32357828delCA2499222303BRCA2c.7703_7704del (p.Phe2568TrpfsTer2)
c.7334_7335del (p.Phe2445TrpfsTer2)
c.170_171del (p.Phe57TrpfsTer2)
c.268_269del
n.7703_7704del
c.7607_7608del (p.Phe2536TrpfsTer2)
13g.32357826T>ACA387745262BRCA2c.7702T>A (p.Phe2568Ile)
c.7333T>A (p.Phe2445Ile)
c.169T>A (p.Phe57Ile)
c.267T>A
n.7702T>A
c.7606T>A (p.Phe2536Ile)
13g.32357826T>CCA387745263BRCA2c.7702T>C (p.Phe2568Leu)
c.7333T>C (p.Phe2445Leu)
c.169T>C (p.Phe57Leu)
c.267T>C
n.7702T>C
c.7606T>C (p.Phe2536Leu)
13g.32357826T>GCA387745264BRCA2c.7702T>G (p.Phe2568Val)
c.7333T>G (p.Phe2445Val)
c.169T>G (p.Phe57Val)
c.267T>G
n.7702T>G
c.7606T>G (p.Phe2536Val)
13g.32357826_32357827insGCA2695217920BRCA2c.7702_7703insG (p.Phe2568CysfsTer3)
c.7333_7334insG (p.Phe2445CysfsTer3)
c.169_170insG (p.Phe57CysfsTer3)
c.267_268insG
n.7702_7703insG
c.7606_7607insG (p.Phe2536CysfsTer3)
13g.32357827T>ACA387745265BRCA2c.7703T>A (p.Phe2568Tyr)
c.7334T>A (p.Phe2445Tyr)
c.170T>A (p.Phe57Tyr)
c.268T>A
n.7703T>A
c.7607T>A (p.Phe2536Tyr)
13g.32357827T>CCA387745266BRCA2c.7703T>C (p.Phe2568Ser)
c.7334T>C (p.Phe2445Ser)
c.170T>C (p.Phe57Ser)
c.268T>C
n.7703T>C
c.7607T>C (p.Phe2536Ser)
13g.32357827T>GCA387745271BRCA2c.7703T>G (p.Phe2568Cys)
c.7334T>G (p.Phe2445Cys)
c.170T>G (p.Phe57Cys)
c.268T>G
n.7703T>G
c.7607T>G (p.Phe2536Cys)
 COSMIC COSMIC
13g.32357828T>ACA387745273BRCA2c.7704T>A (p.Phe2568Leu)
c.7335T>A (p.Phe2445Leu)
c.171T>A (p.Phe57Leu)
c.269T>A
n.7704T>A
c.7608T>A (p.Phe2536Leu)
13g.32357828T>CCA483439193BRCA2c.7704T>C (p.Phe2568=)
c.7335T>C (p.Phe2445=)
c.171T>C (p.Phe57=)
c.269T>C
n.7704T>C
c.7608T>C (p.Phe2536=)
13g.32357828T>GCA387745278BRCA2c.7704T>G (p.Phe2568Leu)
c.7335T>G (p.Phe2445Leu)
c.171T>G (p.Phe57Leu)
c.269T>G
n.7704T>G
c.7608T>G (p.Phe2536Leu)
13g.32357828_32357829delinsTGCA2082818366BRCA2c.7704_7705delinsTG (p.Phe2568=)
c.7335_7336delinsTG (p.Phe2445=)
c.171_172delinsTG (p.Phe57=)
c.269_270delinsTG
n.7704_7705delinsTG
c.7608_7609delinsTG (p.Phe2536=)
13g.32357829G>ACA387745284BRCA2c.7705G>A (p.Gly2569Ser)
c.7336G>A (p.Gly2446Ser)
c.172G>A (p.Gly58Ser)
c.270G>A
n.7705G>A
c.7609G>A (p.Gly2537Ser)
 ClinVar dbSNP
13g.32357829G>CCA387745290BRCA2c.7705G>C (p.Gly2569Arg)
c.7336G>C (p.Gly2446Arg)
c.172G>C (p.Gly58Arg)
c.270G>C
n.7705G>C
c.7609G>C (p.Gly2537Arg)
 dbSNP
13g.32357829G=CA2082818377BRCA2c.7705G= (p.Gly2569=)
c.7336G= (p.Gly2446=)
c.172G= (p.Gly58=)
c.270G=
n.7705G=
c.7609G= (p.Gly2537=)
13g.32357829G>TCA387745286BRCA2c.7705G>T (p.Gly2569Cys)
c.7336G>T (p.Gly2446Cys)
c.172G>T (p.Gly58Cys)
c.270G>T
n.7705G>T
c.7609G>T (p.Gly2537Cys)
 ClinVar dbSNP
13g.32357830delCA10586580BRCA2c.7706del (p.Gly2569ValfsTer?)
c.7337del (p.Gly2446ValfsTer?)
c.173del (p.Gly58ValfsTer?)
c.271del
n.7706del
c.7610del (p.Gly2537ValfsTer?)
 ClinVar dbSNP
13g.32357829_32357838delinsGGTAAGGAAACA2082818379BRCA2c.7705_7714delinsGGTAAGGAAA (p.Gly2569=)
c.7336_7345delinsGGTAAGGAAA (p.Gly2446=)
c.172_181delinsGGTAAGGAAA (p.Gly58=)
c.270_279delinsGGTAAGGAAA
n.7705_7714delinsGGTAAGGAAA
c.7609_7618delinsGGTAAGGAAA (p.Gly2537=)
13g.32357830G>ACA025238BRCA2c.7706G>A (p.Gly2569Asp)
c.7337G>A (p.Gly2446Asp)
c.173G>A (p.Gly58Asp)
c.271G>A
n.7706G>A
c.7610G>A (p.Gly2537Asp)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32357830G>CCA387745306BRCA2c.7706G>C (p.Gly2569Ala)
c.7337G>C (p.Gly2446Ala)
c.173G>C (p.Gly58Ala)
c.271G>C
n.7706G>C
c.7610G>C (p.Gly2537Ala)
 dbSNP
13g.32357830G=CA2082818386BRCA2c.7706G= (p.Gly2569=)
c.7337G= (p.Gly2446=)
c.173G= (p.Gly58=)
c.271G=
n.7706G=
c.7610G= (p.Gly2537=)
13g.32357830G>TCA387745313BRCA2c.7706G>T (p.Gly2569Val)
c.7337G>T (p.Gly2446Val)
c.173G>T (p.Gly58Val)
c.271G>T
n.7706G>T
c.7610G>T (p.Gly2537Val)
 dbSNP
13g.32357830_32357831delinsGTCA2082818385BRCA2c.7706_7707delinsGT (p.Gly2569=)
c.7337_7338delinsGT (p.Gly2446=)
c.173_174delinsGT (p.Gly58=)
c.271_272delinsGT
n.7706_7707delinsGT
c.7610_7611delinsGT (p.Gly2537=)
13g.32357832_32357840delCA6941134BRCA2c.7708_7716del (p.Lys2570_Ser2572del)
c.7339_7347del (p.Lys2447_Ser2449del)
c.175_183del (p.Lys59_Ser61del)
c.273_281del
n.7708_7716del
c.7612_7620del (p.Lys2538_Ser2540del)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357831delCA025239BRCA2c.7707del (p.Lys2570ArgfsTer?)
c.7338del (p.Lys2447ArgfsTer?)
c.174del (p.Lys59ArgfsTer?)
c.272del
n.7707del
c.7611del (p.Lys2538ArgfsTer?)
 ClinVar dbSNP
13g.32357831T>ACA483439196BRCA2c.7707T>A (p.Gly2569=)
c.7338T>A (p.Gly2446=)
c.174T>A (p.Gly58=)
c.272T>A
n.7707T>A
c.7611T>A (p.Gly2537=)
13g.32357831T>CCA483439194BRCA2c.7707T>C (p.Gly2569=)
c.7338T>C (p.Gly2446=)
c.174T>C (p.Gly58=)
c.272T>C
n.7707T>C
c.7611T>C (p.Gly2537=)
13g.32357831T>GCA483439195BRCA2c.7707T>G (p.Gly2569=)
c.7338T>G (p.Gly2446=)
c.174T>G (p.Gly58=)
c.272T>G
n.7707T>G
c.7611T>G (p.Gly2537=)
13g.32357832A=CA2082818402BRCA2c.7708A= (p.Lys2570=)
c.7339A= (p.Lys2447=)
c.175A= (p.Lys59=)
c.273A=
n.7708A=
c.7612A= (p.Lys2538=)
13g.32357832A>CCA387745321BRCA2c.7708A>C (p.Lys2570Gln)
c.7339A>C (p.Lys2447Gln)
c.175A>C (p.Lys59Gln)
c.273A>C
n.7708A>C
c.7612A>C (p.Lys2538Gln)
13g.32357832A>GCA10579749BRCA2c.7708A>G (p.Lys2570Glu)
c.7339A>G (p.Lys2447Glu)
c.175A>G (p.Lys59Glu)
c.273A>G
n.7708A>G
c.7612A>G (p.Lys2538Glu)
 ClinVar dbSNP
13g.32357832A>TCA10589447BRCA2c.7708A>T (p.Lys2570Ter)
c.7339A>T (p.Lys2447Ter)
c.175A>T (p.Lys59Ter)
c.273A>T
n.7708A>T
c.7612A>T (p.Lys2538Ter)
 ClinVar dbSNP COSMIC COSMIC
13g.32357833A=CA2082818413BRCA2c.7709A= (p.Lys2570=)
c.7340A= (p.Lys2447=)
c.176A= (p.Lys59=)
c.274A=
n.7709A=
c.7613A= (p.Lys2538=)
13g.32357833A>CCA387745328BRCA2c.7709A>C (p.Lys2570Thr)
c.7340A>C (p.Lys2447Thr)
c.176A>C (p.Lys59Thr)
c.274A>C
n.7709A>C
c.7613A>C (p.Lys2538Thr)
 gnomAD v4
13g.32357833A>GCA025240BRCA2c.7709A>G (p.Lys2570Arg)
c.7340A>G (p.Lys2447Arg)
c.176A>G (p.Lys59Arg)
c.274A>G
n.7709A>G
c.7613A>G (p.Lys2538Arg)
 ClinVar dbSNP
13g.32357833A>TCA387745334BRCA2c.7709A>T (p.Lys2570Met)
c.7340A>T (p.Lys2447Met)
c.176A>T (p.Lys59Met)
c.274A>T
n.7709A>T
c.7613A>T (p.Lys2538Met)
 dbSNP
13g.32357834G>ACA483439198BRCA2c.7710G>A (p.Lys2570=)
c.7341G>A (p.Lys2447=)
c.177G>A (p.Lys59=)
c.275G>A
n.7710G>A
c.7614G>A (p.Lys2538=)
 ClinVar dbSNP gnomAD v4
13g.32357834G>CCA387745335BRCA2c.7710G>C (p.Lys2570Asn)
c.7341G>C (p.Lys2447Asn)
c.177G>C (p.Lys59Asn)
c.275G>C
n.7710G>C
c.7614G>C (p.Lys2538Asn)
 ClinVar dbSNP
13g.32357834G>TCA387745336BRCA2c.7710G>T (p.Lys2570Asn)
c.7341G>T (p.Lys2447Asn)
c.177G>T (p.Lys59Asn)
c.275G>T
n.7710G>T
c.7614G>T (p.Lys2538Asn)
13g.32357835dupCA2695199706BRCA2c.7711dup (p.Glu2571GlyfsTer13)
c.7342dup (p.Glu2448GlyfsTer13)
c.178dup (p.Glu60GlyfsTer13)
c.276dup
n.7711dup
c.7615dup (p.Glu2539GlyfsTer13)
 ClinVar
13g.32357835G>ACA10579750BRCA2c.7711G>A (p.Glu2571Lys)
c.7342G>A (p.Glu2448Lys)
c.178G>A (p.Glu60Lys)
c.276G>A
n.7711G>A
c.7615G>A (p.Glu2539Lys)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357835G>CCA387745347BRCA2c.7711G>C (p.Glu2571Gln)
c.7342G>C (p.Glu2448Gln)
c.178G>C (p.Glu60Gln)
c.276G>C
n.7711G>C
c.7615G>C (p.Glu2539Gln)
 dbSNP
13g.32357835G=CA2082818420BRCA2c.7711G= (p.Glu2571=)
c.7342G= (p.Glu2448=)
c.178G= (p.Glu60=)
c.276G=
n.7711G=
c.7615G= (p.Glu2539=)
13g.32357835G>TCA387745341BRCA2c.7711G>T (p.Glu2571Ter)
c.7342G>T (p.Glu2448Ter)
c.178G>T (p.Glu60Ter)
c.276G>T
n.7711G>T
c.7615G>T (p.Glu2539Ter)
 dbSNP
13g.32357836A=CA2082818428BRCA2c.7712A= (p.Glu2571=)
c.7343A= (p.Glu2448=)
c.179A= (p.Glu60=)
c.277A=
n.7712A=
c.7616A= (p.Glu2539=)
13g.32357836A>CCA387745363BRCA2c.7712A>C (p.Glu2571Ala)
c.7343A>C (p.Glu2448Ala)
c.179A>C (p.Glu60Ala)
c.277A>C
n.7712A>C
c.7616A>C (p.Glu2539Ala)
 dbSNP
13g.32357836A>GCA025242BRCA2c.7712A>G (p.Glu2571Gly)
c.7343A>G (p.Glu2448Gly)
c.179A>G (p.Glu60Gly)
c.277A>G
n.7712A>G
c.7616A>G (p.Glu2539Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32357836A>TCA387745364BRCA2c.7712A>T (p.Glu2571Val)
c.7343A>T (p.Glu2448Val)
c.179A>T (p.Glu60Val)
c.277A>T
n.7712A>T
c.7616A>T (p.Glu2539Val)
 ClinVar dbSNP
13g.32357837A>CCA387745365BRCA2c.7713A>C (p.Glu2571Asp)
c.7344A>C (p.Glu2448Asp)
c.180A>C (p.Glu60Asp)
c.278A>C
n.7713A>C
c.7617A>C (p.Glu2539Asp)
13g.32357837A>GCA483439202BRCA2c.7713A>G (p.Glu2571=)
c.7344A>G (p.Glu2448=)
c.180A>G (p.Glu60=)
c.278A>G
n.7713A>G
c.7617A>G (p.Glu2539=)
 ClinVar
13g.32357837A>TCA387745366BRCA2c.7713A>T (p.Glu2571Asp)
c.7344A>T (p.Glu2448Asp)
c.180A>T (p.Glu60Asp)
c.278A>T
n.7713A>T
c.7617A>T (p.Glu2539Asp)
13g.32357838A=CA2082818439BRCA2c.7714A= (p.Ser2572=)
c.7345A= (p.Ser2449=)
c.181A= (p.Ser61=)
c.279A=
n.7714A=
c.7618A= (p.Ser2540=)
13g.32357838A>CCA16614353BRCA2c.7714A>C (p.Ser2572Arg)
c.7345A>C (p.Ser2449Arg)
c.181A>C (p.Ser61Arg)
c.279A>C
n.7714A>C
c.7618A>C (p.Ser2540Arg)
 ClinVar dbSNP
13g.32357838A>GCA387745375BRCA2c.7714A>G (p.Ser2572Gly)
c.7345A>G (p.Ser2449Gly)
c.181A>G (p.Ser61Gly)
c.279A>G
n.7714A>G
c.7618A>G (p.Ser2540Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32357838A>TCA387745377BRCA2c.7714A>T (p.Ser2572Cys)
c.7345A>T (p.Ser2449Cys)
c.181A>T (p.Ser61Cys)
c.279A>T
n.7714A>T
c.7618A>T (p.Ser2540Cys)
13g.32357839G>ACA387745382BRCA2c.7715G>A (p.Ser2572Asn)
c.7346G>A (p.Ser2449Asn)
c.182G>A (p.Ser61Asn)
c.280G>A
n.7715G>A
c.7619G>A (p.Ser2540Asn)
 ClinVar dbSNP
13g.32357839G>CCA387745395BRCA2c.7715G>C (p.Ser2572Thr)
c.7346G>C (p.Ser2449Thr)
c.182G>C (p.Ser61Thr)
c.280G>C
n.7715G>C
c.7619G>C (p.Ser2540Thr)
13g.32357839G=CA2082818445BRCA2c.7715G= (p.Ser2572=)
c.7346G= (p.Ser2449=)
c.182G= (p.Ser61=)
c.280G=
n.7715G=
c.7619G= (p.Ser2540=)
13g.32357839G>TCA387745396BRCA2c.7715G>T (p.Ser2572Ile)
c.7346G>T (p.Ser2449Ile)
c.182G>T (p.Ser61Ile)
c.280G>T
n.7715G>T
c.7619G>T (p.Ser2540Ile)
13g.32357840T>ACA387745406BRCA2c.7716T>A (p.Ser2572Arg)
c.7347T>A (p.Ser2449Arg)
c.183T>A (p.Ser61Arg)
c.281T>A
n.7716T>A
c.7620T>A (p.Ser2540Arg)
 dbSNP
13g.32357840T>CCA483439203BRCA2c.7716T>C (p.Ser2572=)
c.7347T>C (p.Ser2449=)
c.183T>C (p.Ser61=)
c.281T>C
n.7716T>C
c.7620T>C (p.Ser2540=)
 ClinVar dbSNP
13g.32357840T>GCA387745401BRCA2c.7716T>G (p.Ser2572Arg)
c.7347T>G (p.Ser2449Arg)
c.183T>G (p.Ser61Arg)
c.281T>G
n.7716T>G
c.7620T>G (p.Ser2540Arg)
 dbSNP
13g.32357840T=CA2082818449BRCA2c.7716T= (p.Ser2572=)
c.7347T= (p.Ser2449=)
c.183T= (p.Ser61=)
c.281T=
n.7716T=
c.7620T= (p.Ser2540=)
13g.32357842delCA2580087353BRCA2c.7718del (p.Leu2573TyrfsTer?)
c.7349del (p.Leu2450TyrfsTer?)
c.185del (p.Leu62TyrfsTer?)
c.283del
n.7718del
c.7622del (p.Leu2541TyrfsTer?)
 ClinVar
13g.32357841_32357842delCA2573149410BRCA2c.7717_7718del (p.Leu2573MetfsTer10)
c.7348_7349del (p.Leu2450MetfsTer10)
c.184_185del (p.Leu62MetfsTer10)
c.282_283del
n.7717_7718del
c.7621_7622del (p.Leu2541MetfsTer10)
 ClinVar dbSNP
13g.32357841T>ACA387745410BRCA2c.7717T>A (p.Leu2573Ile)
c.7348T>A (p.Leu2450Ile)
c.184T>A (p.Leu62Ile)
c.282T>A
n.7717T>A
c.7621T>A (p.Leu2541Ile)
13g.32357841T>CCA483439204BRCA2c.7717T>C (p.Leu2573=)
c.7348T>C (p.Leu2450=)
c.184T>C (p.Leu62=)
c.282T>C
n.7717T>C
c.7621T>C (p.Leu2541=)
13g.32357841T>GCA387745412BRCA2c.7717T>G (p.Leu2573Val)
c.7348T>G (p.Leu2450Val)
c.184T>G (p.Leu62Val)
c.282T>G
n.7717T>G
c.7621T>G (p.Leu2541Val)
 dbSNP
13g.32357842T>ACA387745427BRCA2c.7718T>A (p.Leu2573Ter)
c.7349T>A (p.Leu2450Ter)
c.185T>A (p.Leu62Ter)
c.283T>A
n.7718T>A
c.7622T>A (p.Leu2541Ter)
 dbSNP
13g.32357842T>CCA387745430BRCA2c.7718T>C (p.Leu2573Ser)
c.7349T>C (p.Leu2450Ser)
c.185T>C (p.Leu62Ser)
c.283T>C
n.7718T>C
c.7622T>C (p.Leu2541Ser)
13g.32357842T>GCA025244BRCA2c.7718T>G (p.Leu2573Ter)
c.7349T>G (p.Leu2450Ter)
c.185T>G (p.Leu62Ter)
c.283T>G
n.7718T>G
c.7622T>G (p.Leu2541Ter)
 ClinVar dbSNP
13g.32357842T=CA2082818458BRCA2c.7718T= (p.Leu2573=)
c.7349T= (p.Leu2450=)
c.185T= (p.Leu62=)
c.283T=
n.7718T=
c.7622T= (p.Leu2541=)
13g.32357843A>CCA387745438BRCA2c.7719A>C (p.Leu2573Phe)
c.7350A>C (p.Leu2450Phe)
c.186A>C (p.Leu62Phe)
c.284A>C
n.7719A>C
c.7623A>C (p.Leu2541Phe)
13g.32357843A>GCA483439206BRCA2c.7719A>G (p.Leu2573=)
c.7350A>G (p.Leu2450=)
c.186A>G (p.Leu62=)
c.284A>G
n.7719A>G
c.7623A>G (p.Leu2541=)
 ClinVar
13g.32357843A>TCA387745439BRCA2c.7719A>T (p.Leu2573Phe)
c.7350A>T (p.Leu2450Phe)
c.186A>T (p.Leu62Phe)
c.284A>T
n.7719A>T
c.7623A>T (p.Leu2541Phe)
 dbSNP
13g.32357843dupCA025245BRCA2c.7719dup (p.Trp2574MetfsTer10)
c.7350dup (p.Trp2451MetfsTer10)
c.186dup (p.Trp63MetfsTer10)
c.284dup
n.7719dup
c.7623dup (p.Trp2542MetfsTer10)
 ClinVar dbSNP
13g.32357844T>ACA387745446BRCA2c.7720T>A (p.Trp2574Arg)
c.7351T>A (p.Trp2451Arg)
c.187T>A (p.Trp63Arg)
c.285T>A
n.7720T>A
c.7624T>A (p.Trp2542Arg)
13g.32357844T>CCA025246BRCA2c.7720T>C (p.Trp2574Arg)
c.7351T>C (p.Trp2451Arg)
c.187T>C (p.Trp63Arg)
c.285T>C
n.7720T>C
c.7624T>C (p.Trp2542Arg)
 ClinVar dbSNP
13g.32357844T>GCA387745449BRCA2c.7720T>G (p.Trp2574Gly)
c.7351T>G (p.Trp2451Gly)
c.187T>G (p.Trp63Gly)
c.285T>G
n.7720T>G
c.7624T>G (p.Trp2542Gly)
13g.32357844T=CA2082818472BRCA2c.7720T= (p.Trp2574=)
c.7351T= (p.Trp2451=)
c.187T= (p.Trp63=)
c.285T=
n.7720T=
c.7624T= (p.Trp2542=)
13g.32357845G>ACA025247BRCA2c.7721G>A (p.Trp2574Ter)
c.7352G>A (p.Trp2451Ter)
c.188G>A (p.Trp63Ter)
c.286G>A
n.7721G>A
c.7625G>A (p.Trp2542Ter)
 ClinVar dbSNP
13g.32357845G>CCA387745450BRCA2c.7721G>C (p.Trp2574Ser)
c.7352G>C (p.Trp2451Ser)
c.188G>C (p.Trp63Ser)
c.286G>C
n.7721G>C
c.7625G>C (p.Trp2542Ser)
 dbSNP
13g.32357845G=CA2082818479BRCA2c.7721G= (p.Trp2574=)
c.7352G= (p.Trp2451=)
c.188G= (p.Trp63=)
c.286G=
n.7721G=
c.7625G= (p.Trp2542=)
13g.32357845G>TCA387745451BRCA2c.7721G>T (p.Trp2574Leu)
c.7352G>T (p.Trp2451Leu)
c.188G>T (p.Trp63Leu)
c.286G>T
n.7721G>T
c.7625G>T (p.Trp2542Leu)
13g.32357846G>ACA16614212BRCA2c.7722G>A (p.Trp2574Ter)
c.7353G>A (p.Trp2451Ter)
c.189G>A (p.Trp63Ter)
c.287G>A
n.7722G>A
c.7626G>A (p.Trp2542Ter)
 ClinVar dbSNP
13g.32357846G>CCA387745454BRCA2c.7722G>C (p.Trp2574Cys)
c.7353G>C (p.Trp2451Cys)
c.189G>C (p.Trp63Cys)
c.287G>C
n.7722G>C
c.7626G>C (p.Trp2542Cys)
 dbSNP
13g.32357846G=CA2082818489BRCA2c.7722G= (p.Trp2574=)
c.7353G= (p.Trp2451=)
c.189G= (p.Trp63=)
c.287G=
n.7722G=
c.7626G= (p.Trp2542=)
13g.32357846G>TCA387745455BRCA2c.7722G>T (p.Trp2574Cys)
c.7353G>T (p.Trp2451Cys)
c.189G>T (p.Trp63Cys)
c.287G>T
n.7722G>T
c.7626G>T (p.Trp2542Cys)
 ClinVar dbSNP
13g.32357847_32357906dupCA2580614662BRCA2c.7723_7782dup (p.Lys2594_Ala2595insThrGlyLysGlyIleGlnLeuAlaAspGlyGlyTrpLeuIleProSerAsnAspGlyLys)
c.7354_7413dup (p.Lys2471_Ala2472insThrGlyLysGlyIleGlnLeuAlaAspGlyGlyTrpLeuIleProSerAsnAspGlyLys)
c.190_249dup (p.Lys83_Ala84insThrGlyLysGlyIleGlnLeuAlaAspGlyGlyTrpLeuIleProSerAsnAspGlyLys)
c.288_347dup
n.7723_7782dup
c.7627_7686dup (p.Lys2562_Ala2563insThrGlyLysGlyIleGlnLeuAlaAspGlyGlyTrpLeuIleProSerAsnAspGlyLys)
 ClinVar
13g.32357847A=CA2082818510BRCA2c.7723A= (p.Thr2575=)
c.7354A= (p.Thr2452=)
c.190A= (p.Thr64=)
c.288A=
n.7723A=
c.7627A= (p.Thr2543=)
13g.32357847A>CCA387745463BRCA2c.7723A>C (p.Thr2575Pro)
c.7354A>C (p.Thr2452Pro)
c.190A>C (p.Thr64Pro)
c.288A>C
n.7723A>C
c.7627A>C (p.Thr2543Pro)
13g.32357847A>GCA16619767BRCA2c.7723A>G (p.Thr2575Ala)
c.7354A>G (p.Thr2452Ala)
c.190A>G (p.Thr64Ala)
c.288A>G
n.7723A>G
c.7627A>G (p.Thr2543Ala)
 ClinVar dbSNP
13g.32357847A>TCA387745467BRCA2c.7723A>T (p.Thr2575Ser)
c.7354A>T (p.Thr2452Ser)
c.190A>T (p.Thr64Ser)
c.288A>T
n.7723A>T
c.7627A>T (p.Thr2543Ser)
 dbSNP
13g.32357848C>ACA387745471BRCA2c.7724C>A (p.Thr2575Asn)
c.7355C>A (p.Thr2452Asn)
c.191C>A (p.Thr64Asn)
c.289C>A
n.7724C>A
c.7628C>A (p.Thr2543Asn)
 dbSNP
13g.32357848C>GCA387745474BRCA2c.7724C>G (p.Thr2575Ser)
c.7355C>G (p.Thr2452Ser)
c.191C>G (p.Thr64Ser)
c.289C>G
n.7724C>G
c.7628C>G (p.Thr2543Ser)
 dbSNP
13g.32357848C>TCA387745482BRCA2c.7724C>T (p.Thr2575Ile)
c.7355C>T (p.Thr2452Ile)
c.191C>T (p.Thr64Ile)
c.289C>T
n.7724C>T
c.7628C>T (p.Thr2543Ile)
13g.32357849T>ACA483439208BRCA2c.7725T>A (p.Thr2575=)
c.7356T>A (p.Thr2452=)
c.192T>A (p.Thr64=)
c.290T>A
n.7725T>A
c.7629T>A (p.Thr2543=)
13g.32357849T>CCA483439209BRCA2c.7725T>C (p.Thr2575=)
c.7356T>C (p.Thr2452=)
c.192T>C (p.Thr64=)
c.290T>C
n.7725T>C
c.7629T>C (p.Thr2543=)
 ClinVar dbSNP gnomAD v4
13g.32357849T>GCA483439210BRCA2c.7725T>G (p.Thr2575=)
c.7356T>G (p.Thr2452=)
c.192T>G (p.Thr64=)
c.290T>G
n.7725T>G
c.7629T>G (p.Thr2543=)
 ClinVar
13g.32357850G>ACA387745484BRCA2c.7726G>A (p.Gly2576Arg)
c.7357G>A (p.Gly2453Arg)
c.193G>A (p.Gly65Arg)
c.291G>A
n.7726G>A
c.7630G>A (p.Gly2544Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32357850G>CCA387745486BRCA2c.7726G>C (p.Gly2576Arg)
c.7357G>C (p.Gly2453Arg)
c.193G>C (p.Gly65Arg)
c.291G>C
n.7726G>C
c.7630G>C (p.Gly2544Arg)
 ClinVar dbSNP
13g.32357850G=CA2082818523BRCA2c.7726G= (p.Gly2576=)
c.7357G= (p.Gly2453=)
c.193G= (p.Gly65=)
c.291G=
n.7726G=
c.7630G= (p.Gly2544=)
13g.32357850G>TCA387745496BRCA2c.7726G>T (p.Gly2576Ter)
c.7357G>T (p.Gly2453Ter)
c.193G>T (p.Gly65Ter)
c.291G>T
n.7726G>T
c.7630G>T (p.Gly2544Ter)
 ClinVar dbSNP
13g.32357851G>ACA387745500BRCA2c.7727G>A (p.Gly2576Glu)
c.7358G>A (p.Gly2453Glu)
c.194G>A (p.Gly65Glu)
c.292G>A
n.7727G>A
c.7631G>A (p.Gly2544Glu)
13g.32357851G>CCA387745504BRCA2c.7727G>C (p.Gly2576Ala)
c.7358G>C (p.Gly2453Ala)
c.194G>C (p.Gly65Ala)
c.292G>C
n.7727G>C
c.7631G>C (p.Gly2544Ala)
 ClinVar COSMIC COSMIC
13g.32357851G>TCA387745506BRCA2c.7727G>T (p.Gly2576Val)
c.7358G>T (p.Gly2453Val)
c.194G>T (p.Gly65Val)
c.292G>T
n.7727G>T
c.7631G>T (p.Gly2544Val)
13g.32357851_32357852delinsGACA2082818534BRCA2c.7727_7728delinsGA (p.Gly2576=)
c.7358_7359delinsGA (p.Gly2453=)
c.194_195delinsGA (p.Gly65=)
c.292_293delinsGA
n.7727_7728delinsGA
c.7631_7632delinsGA (p.Gly2544=)
13g.32357852_32357856delCA2499222304BRCA2c.7728_7732del (p.Lys2577AsnfsTer5)
c.7359_7363del (p.Lys2454AsnfsTer5)
c.195_199del (p.Lys66AsnfsTer5)
c.293_297del
n.7728_7732del
c.7632_7636del (p.Lys2545AsnfsTer5)
 ClinVar dbSNP
13g.32357852A>CCA483439213BRCA2c.7728A>C (p.Gly2576=)
c.7359A>C (p.Gly2453=)
c.195A>C (p.Gly65=)
c.293A>C
n.7728A>C
c.7632A>C (p.Gly2544=)
13g.32357852A>GCA483439214BRCA2c.7728A>G (p.Gly2576=)
c.7359A>G (p.Gly2453=)
c.195A>G (p.Gly65=)
c.293A>G
n.7728A>G
c.7632A>G (p.Gly2544=)
 ClinVar dbSNP
13g.32357852A>TCA483439215BRCA2c.7728A>T (p.Gly2576=)
c.7359A>T (p.Gly2453=)
c.195A>T (p.Gly65=)
c.293A>T
n.7728A>T
c.7632A>T (p.Gly2544=)
 dbSNP
13g.32357855delCA1139663203BRCA2c.7731del (p.Gly2578GlufsTer?)
c.7362del (p.Gly2455GlufsTer?)
c.198del (p.Gly67GlufsTer?)
c.296del
n.7731del
c.7635del (p.Gly2546GlufsTer?)
 ClinVar dbSNP
13g.32357853A>CCA387745509BRCA2c.7729A>C (p.Lys2577Gln)
c.7360A>C (p.Lys2454Gln)
c.196A>C (p.Lys66Gln)
c.294A>C
n.7729A>C
c.7633A>C (p.Lys2545Gln)
13g.32357853A>GCA387745515BRCA2c.7729A>G (p.Lys2577Glu)
c.7360A>G (p.Lys2454Glu)
c.196A>G (p.Lys66Glu)
c.294A>G
n.7729A>G
c.7633A>G (p.Lys2545Glu)
13g.32357853A>TCA387745513BRCA2c.7729A>T (p.Lys2577Ter)
c.7360A>T (p.Lys2454Ter)
c.196A>T (p.Lys66Ter)
c.294A>T
n.7729A>T
c.7633A>T (p.Lys2545Ter)
 ClinVar dbSNP
13g.32357853_32357856delCA2580087354BRCA2c.7729_7732del (p.Lys2577GlufsTer?)
c.7360_7363del (p.Lys2454GlufsTer?)
c.196_199del (p.Lys66GlufsTer?)
c.294_297del
n.7729_7732del
c.7633_7636del (p.Lys2545GlufsTer?)
 ClinVar
13g.32357854A=CA2082818552BRCA2c.7730A= (p.Lys2577=)
c.7361A= (p.Lys2454=)
c.197A= (p.Lys66=)
c.295A=
n.7730A=
c.7634A= (p.Lys2545=)
13g.32357854A>CCA387745520BRCA2c.7730A>C (p.Lys2577Thr)
c.7361A>C (p.Lys2454Thr)
c.197A>C (p.Lys66Thr)
c.295A>C
n.7730A>C
c.7634A>C (p.Lys2545Thr)
13g.32357854A>GCA387745536BRCA2c.7730A>G (p.Lys2577Arg)
c.7361A>G (p.Lys2454Arg)
c.197A>G (p.Lys66Arg)
c.295A>G
n.7730A>G
c.7634A>G (p.Lys2545Arg)
 ClinVar dbSNP
13g.32357854A>TCA387745526BRCA2c.7730A>T (p.Lys2577Ile)
c.7361A>T (p.Lys2454Ile)
c.197A>T (p.Lys66Ile)
c.295A>T
n.7730A>T
c.7634A>T (p.Lys2545Ile)
13g.32357855A>CCA387745541BRCA2c.7731A>C (p.Lys2577Asn)
c.7362A>C (p.Lys2454Asn)
c.198A>C (p.Lys66Asn)
c.296A>C
n.7731A>C
c.7635A>C (p.Lys2545Asn)
 ClinVar dbSNP
13g.32357855A>GCA483439216BRCA2c.7731A>G (p.Lys2577=)
c.7362A>G (p.Lys2454=)
c.198A>G (p.Lys66=)
c.296A>G
n.7731A>G
c.7635A>G (p.Lys2545=)
 ClinVar dbSNP
13g.32357855A>TCA387745543BRCA2c.7731A>T (p.Lys2577Asn)
c.7362A>T (p.Lys2454Asn)
c.198A>T (p.Lys66Asn)
c.296A>T
n.7731A>T
c.7635A>T (p.Lys2545Asn)
 ClinVar dbSNP
13g.32357856G>ACA387745549BRCA2c.7732G>A (p.Gly2578Arg)
c.7363G>A (p.Gly2455Arg)
c.199G>A (p.Gly67Arg)
c.297G>A
n.7732G>A
c.7636G>A (p.Gly2546Arg)
 dbSNP
13g.32357856G>CCA387745552BRCA2c.7732G>C (p.Gly2578Arg)
c.7363G>C (p.Gly2455Arg)
c.199G>C (p.Gly67Arg)
c.297G>C
n.7732G>C
c.7636G>C (p.Gly2546Arg)
 dbSNP
13g.32357856G=CA2082818561BRCA2c.7732G= (p.Gly2578=)
c.7363G= (p.Gly2455=)
c.199G= (p.Gly67=)
c.297G=
n.7732G=
c.7636G= (p.Gly2546=)
13g.32357856G>TCA387745555BRCA2c.7732G>T (p.Gly2578Ter)
c.7363G>T (p.Gly2455Ter)
c.199G>T (p.Gly67Ter)
c.297G>T
n.7732G>T
c.7636G>T (p.Gly2546Ter)
 ClinVar dbSNP
13g.32357858_32357868delCA2580087355BRCA2c.7734_7744del (p.Ile2579Ter)
c.7365_7375del (p.Ile2456Ter)
c.201_211del (p.Ile68Ter)
c.299_309del
n.7734_7744del
c.7638_7648del (p.Ile2547Ter)
 ClinVar
13g.32357857G>ACA025249BRCA2c.7733G>A (p.Gly2578Glu)
c.7364G>A (p.Gly2455Glu)
c.200G>A (p.Gly67Glu)
c.298G>A
n.7733G>A
c.7637G>A (p.Gly2546Glu)
 ClinVar dbSNP
13g.32357857G>CCA387745571BRCA2c.7733G>C (p.Gly2578Ala)
c.7364G>C (p.Gly2455Ala)
c.200G>C (p.Gly67Ala)
c.298G>C
n.7733G>C
c.7637G>C (p.Gly2546Ala)
13g.32357857G=CA2082818577BRCA2c.7733G= (p.Gly2578=)
c.7364G= (p.Gly2455=)
c.200G= (p.Gly67=)
c.298G=
n.7733G=
c.7637G= (p.Gly2546=)
13g.32357857G>TCA387745575BRCA2c.7733G>T (p.Gly2578Val)
c.7364G>T (p.Gly2455Val)
c.200G>T (p.Gly67Val)
c.298G>T
n.7733G>T
c.7637G>T (p.Gly2546Val)
 ClinVar dbSNP
13g.32357857_32357863delinsGAATACACA2082818572BRCA2c.7733_7739delinsGAATACA (p.Gly2578=)
c.7364_7370delinsGAATACA (p.Gly2455=)
c.200_206delinsGAATACA (p.Gly67=)
c.298_304delinsGAATACA
n.7733_7739delinsGAATACA
c.7637_7643delinsGAATACA (p.Gly2546=)
13g.32357858A>CCA483439220BRCA2c.7734A>C (p.Gly2578=)
c.7365A>C (p.Gly2455=)
c.201A>C (p.Gly67=)
c.299A>C
n.7734A>C
c.7638A>C (p.Gly2546=)
13g.32357858A>GCA483439219BRCA2c.7734A>G (p.Gly2578=)
c.7365A>G (p.Gly2455=)
c.201A>G (p.Gly67=)
c.299A>G
n.7734A>G
c.7638A>G (p.Gly2546=)
 ClinVar
13g.32357858A>TCA483439218BRCA2c.7734A>T (p.Gly2578=)
c.7365A>T (p.Gly2455=)
c.201A>T (p.Gly67=)
c.299A>T
n.7734A>T
c.7638A>T (p.Gly2546=)
13g.32357858_32357863delinsCTGATGGTGCA658823755BRCA2c.7734_7739delinsCTGATGGTG (p.Gly2579Ter)
c.7365_7370delinsCTGATGGTG (p.Gly2456Ter)
c.201_206delinsCTGATGGTG (p.Gly68Ter)
c.299_304delinsCTGATGGTG
n.7734_7739delinsCTGATGGTG
c.7638_7643delinsCTGATGGTG (p.Gly2547Ter)
 ClinVar dbSNP
13g.32357859A>CCA387745577BRCA2c.7735A>C (p.Ile2579Leu)
c.7366A>C (p.Ile2456Leu)
c.202A>C (p.Ile68Leu)
c.300A>C
n.7735A>C
c.7639A>C (p.Ile2547Leu)
13g.32357859A>GCA387745580BRCA2c.7735A>G (p.Ile2579Val)
c.7366A>G (p.Ile2456Val)
c.202A>G (p.Ile68Val)
c.300A>G
n.7735A>G
c.7639A>G (p.Ile2547Val)
 ClinVar dbSNP
13g.32357859A>TCA387745592BRCA2c.7735A>T (p.Ile2579Leu)
c.7366A>T (p.Ile2456Leu)
c.202A>T (p.Ile68Leu)
c.300A>T
n.7735A>T
c.7639A>T (p.Ile2547Leu)
13g.32357860T>ACA387745595BRCA2c.7736T>A (p.Ile2579Lys)
c.7367T>A (p.Ile2456Lys)
c.203T>A (p.Ile68Lys)
c.301T>A
n.7736T>A
c.7640T>A (p.Ile2547Lys)
 dbSNP
13g.32357860T>CCA387745598BRCA2c.7736T>C (p.Ile2579Thr)
c.7367T>C (p.Ile2456Thr)
c.203T>C (p.Ile68Thr)
c.301T>C
n.7736T>C
c.7640T>C (p.Ile2547Thr)
 ClinVar dbSNP
13g.32357860T>GCA387745602BRCA2c.7736T>G (p.Ile2579Arg)
c.7367T>G (p.Ile2456Arg)
c.203T>G (p.Ile68Arg)
c.301T>G
n.7736T>G
c.7640T>G (p.Ile2547Arg)
 dbSNP
13g.32357860T=CA2082818590BRCA2c.7736T= (p.Ile2579=)
c.7367T= (p.Ile2456=)
c.203T= (p.Ile68=)
c.301T=
n.7736T=
c.7640T= (p.Ile2547=)
13g.32357861A>CCA483439221BRCA2c.7737A>C (p.Ile2579=)
c.7368A>C (p.Ile2456=)
c.204A>C (p.Ile68=)
c.302A>C
n.7737A>C
c.7641A>C (p.Ile2547=)
 dbSNP
13g.32357861A>GCA387745607BRCA2c.7737A>G (p.Ile2579Met)
c.7368A>G (p.Ile2456Met)
c.204A>G (p.Ile68Met)
c.302A>G
n.7737A>G
c.7641A>G (p.Ile2547Met)
13g.32357861A>TCA483439223BRCA2c.7737A>T (p.Ile2579=)
c.7368A>T (p.Ile2456=)
c.204A>T (p.Ile68=)
c.302A>T
n.7737A>T
c.7641A>T (p.Ile2547=)
 dbSNP
13g.32357862C>ACA387745610BRCA2c.7738C>A (p.Gln2580Lys)
c.7369C>A (p.Gln2457Lys)
c.205C>A (p.Gln69Lys)
c.303C>A
n.7738C>A
c.7642C>A (p.Gln2548Lys)
 ClinVar COSMIC COSMIC
13g.32357862C=CA2082818595BRCA2c.7738C= (p.Gln2580=)
c.7369C= (p.Gln2457=)
c.205C= (p.Gln69=)
c.303C=
n.7738C=
c.7642C= (p.Gln2548=)
13g.32357862C>GCA387745614BRCA2c.7738C>G (p.Gln2580Glu)
c.7369C>G (p.Gln2457Glu)
c.205C>G (p.Gln69Glu)
c.303C>G
n.7738C>G
c.7642C>G (p.Gln2548Glu)
13g.32357862C>TCA025250BRCA2c.7738C>T (p.Gln2580Ter)
c.7369C>T (p.Gln2457Ter)
c.205C>T (p.Gln69Ter)
c.303C>T
n.7738C>T
c.7642C>T (p.Gln2548Ter)
 ClinVar dbSNP
13g.32357863A=CA2082818609BRCA2c.7739A= (p.Gln2580=)
c.7370A= (p.Gln2457=)
c.206A= (p.Gln69=)
c.304A=
n.7739A=
c.7643A= (p.Gln2548=)
13g.32357863A>CCA387745617BRCA2c.7739A>C (p.Gln2580Pro)
c.7370A>C (p.Gln2457Pro)
c.206A>C (p.Gln69Pro)
c.304A>C
n.7739A>C
c.7643A>C (p.Gln2548Pro)
13g.32357863A>GCA16619768BRCA2c.7739A>G (p.Gln2580Arg)
c.7370A>G (p.Gln2457Arg)
c.206A>G (p.Gln69Arg)
c.304A>G
n.7739A>G
c.7643A>G (p.Gln2548Arg)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357863A>TCA387745619BRCA2c.7739A>T (p.Gln2580Leu)
c.7370A>T (p.Gln2457Leu)
c.206A>T (p.Gln69Leu)
c.304A>T
n.7739A>T
c.7643A>T (p.Gln2548Leu)
 dbSNP
13g.32357863dupCA915946876BRCA2c.7739dup (p.Leu2581ValfsTer3)
c.7370dup (p.Leu2458ValfsTer3)
c.206dup (p.Leu70ValfsTer3)
c.304dup
n.7739dup
c.7643dup (p.Leu2549ValfsTer3)
 ClinVar dbSNP
13g.32357864G>ACA483439226BRCA2c.7740G>A (p.Gln2580=)
c.7371G>A (p.Gln2457=)
c.207G>A (p.Gln69=)
c.305G>A
n.7740G>A
c.7644G>A (p.Gln2548=)
 ClinVar dbSNP
13g.32357864G>CCA387745621BRCA2c.7740G>C (p.Gln2580His)
c.7371G>C (p.Gln2457His)
c.207G>C (p.Gln69His)
c.305G>C
n.7740G>C
c.7644G>C (p.Gln2548His)
 dbSNP
13g.32357864G=CA2082818622BRCA2c.7740G= (p.Gln2580=)
c.7371G= (p.Gln2457=)
c.207G= (p.Gln69=)
c.305G=
n.7740G=
c.7644G= (p.Gln2548=)
13g.32357864G>TCA387745623BRCA2c.7740G>T (p.Gln2580His)
c.7371G>T (p.Gln2457His)
c.207G>T (p.Gln69His)
c.305G>T
n.7740G>T
c.7644G>T (p.Gln2548His)
 ClinVar dbSNP
13g.32357865T>ACA387745626BRCA2c.7741T>A (p.Leu2581Met)
c.7372T>A (p.Leu2458Met)
c.208T>A (p.Leu70Met)
c.306T>A
n.7741T>A
c.7645T>A (p.Leu2549Met)
 dbSNP
13g.32357865T>CCA483439227BRCA2c.7741T>C (p.Leu2581=)
c.7372T>C (p.Leu2458=)
c.208T>C (p.Leu70=)
c.306T>C
n.7741T>C
c.7645T>C (p.Leu2549=)
 gnomAD v4
13g.32357865T>GCA387745636BRCA2c.7741T>G (p.Leu2581Val)
c.7372T>G (p.Leu2458Val)
c.208T>G (p.Leu70Val)
c.306T>G
n.7741T>G
c.7645T>G (p.Leu2549Val)
 ClinVar
13g.32357865_32357872delinsTTGGCTGACA2082818626BRCA2c.7741_7748delinsTTGGCTGA (p.Leu2581=)
c.7372_7379delinsTTGGCTGA (p.Leu2458=)
c.208_215delinsTTGGCTGA (p.Leu70=)
c.306_313delinsTTGGCTGA
n.7741_7748delinsTTGGCTGA
c.7645_7652delinsTTGGCTGA (p.Leu2549=)
13g.32357866T>ACA387745641BRCA2c.7742T>A (p.Leu2581Ter)
c.7373T>A (p.Leu2458Ter)
c.209T>A (p.Leu70Ter)
c.307T>A
n.7742T>A
c.7646T>A (p.Leu2549Ter)
13g.32357866T>CCA387745650BRCA2c.7742T>C (p.Leu2581Ser)
c.7373T>C (p.Leu2458Ser)
c.209T>C (p.Leu70Ser)
c.307T>C
n.7742T>C
c.7646T>C (p.Leu2549Ser)
 dbSNP
13g.32357866T>GCA025251BRCA2c.7742T>G (p.Leu2581Trp)
c.7373T>G (p.Leu2458Trp)
c.209T>G (p.Leu70Trp)
c.307T>G
n.7742T>G
c.7646T>G (p.Leu2549Trp)
 ClinVar dbSNP
13g.32357866T=CA2082818635BRCA2c.7742T= (p.Leu2581=)
c.7373T= (p.Leu2458=)
c.209T= (p.Leu70=)
c.307T=
n.7742T=
c.7646T= (p.Leu2549=)
13g.32357866_32357867delinsTGCA2082818658BRCA2c.7742_7743delinsTG (p.Leu2581=)
c.7373_7374delinsTG (p.Leu2458=)
c.209_210delinsTG (p.Leu70=)
c.307_308delinsTG
n.7742_7743delinsTG
c.7646_7647delinsTG (p.Leu2549=)
13g.32357869_32357875dupCA2499222305BRCA2c.7745_7751dup (p.Gly2585Ter)
c.7376_7382dup (p.Gly2462Ter)
c.212_218dup (p.Gly74Ter)
c.310_316dup
n.7745_7751dup
c.7649_7655dup (p.Gly2553Ter)
 ClinVar dbSNP
13g.32357869_32357875delCA915946877BRCA2c.7745_7751del (p.Ala2582ValfsTer?)
c.7376_7382del (p.Ala2459ValfsTer?)
c.212_218del (p.Ala71ValfsTer?)
c.7745_7751del (p.Ala2582ValfsTer25)
c.310_316del
n.7745_7751del
c.7649_7655del (p.Ala2550ValfsTer?)
 ClinVar dbSNP

Number of alleles fetched