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.32362650_32362660delinsCTATTAGCACA2573053824BRCA2c.7933_7943delinsCTATTAGCA (p.Arg2645LeufsTer16)
c.7564_7574delinsCTATTAGCA (p.Arg2522LeufsTer16)
c.400_410delinsCTATTAGCA (p.Arg134LeufsTer16)
c.7941_7951delinsCTATTAGCA (n.[c.7941_7951delinsCTATTAGCA;Asp2648TyrfsTer2])
c.498_508delinsCTATTAGCA
c.7837_7847delinsCTATTAGCA (p.Arg2613LeufsTer16)
 ClinVar dbSNP
13g.32362653T>ACA387747216BRCA2c.7936T>A (p.Cys2646Ser)
c.7567T>A (p.Cys2523Ser)
c.403T>A (p.Cys135Ser)
c.7944T>A (p.Asp2648Glu)
c.501T>A
n.7944T>A
c.7840T>A (p.Cys2614Ser)
 dbSNP
13g.32362653T>CCA387747217BRCA2c.7936T>C (p.Cys2646Arg)
c.7567T>C (p.Cys2523Arg)
c.403T>C (p.Cys135Arg)
c.7944T>C (p.Asp2648=)
c.501T>C
n.7944T>C
c.7840T>C (p.Cys2614Arg)
13g.32362653T>GCA387747218BRCA2c.7936T>G (p.Cys2646Gly)
c.7567T>G (p.Cys2523Gly)
c.403T>G (p.Cys135Gly)
c.7944T>G (p.Asp2648Glu)
c.501T>G
n.7944T>G
c.7840T>G (p.Cys2614Gly)
13g.32362656_32362674delCA2580087419BRCA2c.7939_7957del (p.Leu2647PhefsTer4)
c.7570_7588del (p.Leu2524PhefsTer4)
c.406_424del (p.Leu136PhefsTer4)
c.7947_7965del (n.[c.7947_7965del;Ter2650SerextTer8])
c.504_522del
c.7843_7861del (p.Leu2615PhefsTer4)
 ClinVar
13g.32362654G>ACA247475247BRCA2c.7937G>A (p.Cys2646Tyr)
c.7568G>A (p.Cys2523Tyr)
c.404G>A (p.Cys135Tyr)
c.7945G>A (p.Ala2649Thr)
c.502G>A
n.7945G>A
c.7841G>A (p.Cys2614Tyr)
 ClinVar dbSNP
13g.32362654G>CCA247475250BRCA2c.7937G>C (p.Cys2646Ser)
c.7568G>C (p.Cys2523Ser)
c.404G>C (p.Cys135Ser)
c.7945G>C (p.Ala2649Pro)
c.502G>C
n.7945G>C
c.7841G>C (p.Cys2614Ser)
 dbSNP
13g.32362654G=CA2082831885BRCA2c.7937G= (p.Cys2646=)
c.7568G= (p.Cys2523=)
c.404G= (p.Cys135=)
c.7945G= (p.Ala2649=)
c.502G=
n.7945G=
c.7841G= (p.Cys2614=)
13g.32362654G>TCA387747219BRCA2c.7937G>T (p.Cys2646Phe)
c.7568G>T (p.Cys2523Phe)
c.404G>T (p.Cys135Phe)
c.7945G>T (p.Ala2649Ser)
c.502G>T
n.7945G>T
c.7841G>T (p.Cys2614Phe)
 dbSNP
13g.32362655C>ACA387747220BRCA2c.7938C>A (p.Cys2646Ter)
c.7569C>A (p.Cys2523Ter)
c.405C>A (p.Cys135Ter)
c.7946C>A (p.Ala2649Asp)
c.503C>A
n.7946C>A
c.7842C>A (p.Cys2614Ter)
 dbSNP
13g.32362655C=CA2082831922BRCA2c.7938C= (p.Cys2646=)
c.7569C= (p.Cys2523=)
c.405C= (p.Cys135=)
c.7946C= (p.Ala2649=)
c.503C=
n.7946C=
c.7842C= (p.Cys2614=)
13g.32362655C>GCA16619773BRCA2c.7938C>G (p.Cys2646Trp)
c.7569C>G (p.Cys2523Trp)
c.405C>G (p.Cys135Trp)
c.7946C>G (p.Ala2649Gly)
c.503C>G
n.7946C>G
c.7842C>G (p.Cys2614Trp)
 ClinVar dbSNP
13g.32362655C>TCA483261000BRCA2c.7938C>T (p.Cys2646=)
c.7569C>T (p.Cys2523=)
c.405C>T (p.Cys135=)
c.7946C>T (p.Ala2649Val)
c.503C>T
n.7946C>T
c.7842C>T (p.Cys2614=)
 ClinVar dbSNP gnomAD v4
13g.32362656dupCA658823758BRCA2c.7939dup (p.Leu2647ProfsTer15)
c.7570dup (p.Leu2524ProfsTer15)
c.406dup (p.Leu136ProfsTer15)
c.7947dup (p.Ter2650LeuextTer?)
c.504dup
n.7947dup
c.7843dup (p.Leu2615ProfsTer15)
 ClinVar dbSNP
13g.32362656C>ACA387747221BRCA2c.7939C>A (p.Leu2647Ile)
c.7570C>A (p.Leu2524Ile)
c.406C>A (p.Leu136Ile)
c.7947C>A (p.Ala2649=)
c.504C>A
n.7947C>A
c.7843C>A (p.Leu2615Ile)
 dbSNP
13g.32362656C=CA2082831933BRCA2c.7939C= (p.Leu2647=)
c.7570C= (p.Leu2524=)
c.406C= (p.Leu136=)
c.7947C= (p.Ala2649=)
c.504C=
n.7947C=
c.7843C= (p.Leu2615=)
13g.32362656C>GCA025345BRCA2c.7939C>G (p.Leu2647Val)
c.7570C>G (p.Leu2524Val)
c.406C>G (p.Leu136Val)
c.7947C>G (p.Ala2649=)
c.504C>G
n.7947C>G
c.7843C>G (p.Leu2615Val)
 ClinVar dbSNP gnomAD v4
13g.32362656C>TCA247475257BRCA2c.7939C>T (p.Leu2647=)
c.7570C>T (p.Leu2524=)
c.406C>T (p.Leu136=)
c.7947C>T (p.Ala2649=)
c.504C>T
n.7947C>T
c.7843C>T (p.Leu2615=)
 ClinVar dbSNP gnomAD v4
13g.32362657T>ACA387747222BRCA2c.7940T>A (p.Leu2647Gln)
c.7571T>A (p.Leu2524Gln)
c.407T>A (p.Leu136Gln)
c.7948T>A (p.Ter2650Lys)
c.505T>A
n.7948T>A
c.7844T>A (p.Leu2615Gln)
13g.32362657T>CCA025346BRCA2c.7940T>C (p.Leu2647Pro)
c.7571T>C (p.Leu2524Pro)
c.407T>C (p.Leu136Pro)
c.7948T>C (p.Ter2650Gln)
c.505T>C
n.7948T>C
c.7844T>C (p.Leu2615Pro)
 ClinVar dbSNP
13g.32362657T>GCA387747223BRCA2c.7940T>G (p.Leu2647Arg)
c.7571T>G (p.Leu2524Arg)
c.407T>G (p.Leu136Arg)
c.7948T>G (p.Ter2650Glu)
c.505T>G
n.7948T>G
c.7844T>G (p.Leu2615Arg)
13g.32362657T=CA2082831982BRCA2c.7940T= (p.Leu2647=)
c.7571T= (p.Leu2524=)
c.407T= (p.Leu136=)
c.7948T= (p.Ter2650=)
c.505T=
n.7948T=
c.7844T= (p.Leu2615=)
13g.32362657_32362658insCCA10581593BRCA2c.7940_7941insC (p.Ser2648LysfsTer14)
c.7571_7572insC (p.Ser2525LysfsTer14)
c.407_408insC (p.Ser137LysfsTer14)
c.7948_7949insC (p.Ter2650SerextTer?)
c.505_506insC
n.7948_7949insC
c.7844_7845insC (p.Ser2616LysfsTer14)
 ClinVar dbSNP
13g.32362658A=CA2082831993BRCA2c.7941A= (p.Leu2647=)
c.7572A= (p.Leu2524=)
c.408A= (p.Leu136=)
c.7949A= (p.Ter2650=)
c.506A=
n.7949A=
c.7845A= (p.Leu2615=)
13g.32362658A>CCA025348BRCA2c.7941A>C (p.Leu2647=)
c.7572A>C (p.Leu2524=)
c.408A>C (p.Leu136=)
c.7949A>C (p.Ter2650Ser)
c.506A>C
n.7949A>C
c.7845A>C (p.Leu2615=)
 ClinVar dbSNP
13g.32362658A>GCA247475268BRCA2c.7941A>G (p.Leu2647=)
c.7572A>G (p.Leu2524=)
c.408A>G (p.Leu136=)
c.7949A>G (p.Ter2650=)
c.506A>G
n.7949A>G
c.7845A>G (p.Leu2615=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32362658A>TCA483261005BRCA2c.7941A>T (p.Leu2647=)
c.7572A>T (p.Leu2524=)
c.408A>T (p.Leu136=)
c.7949A>T (p.Ter2650Leu)
c.506A>T
n.7949A>T
c.7845A>T (p.Leu2615=)
 dbSNP
13g.32362659A>CCA387747224BRCA2c.7942A>C (p.Ser2648Arg)
c.7573A>C (p.Ser2525Arg)
c.409A>C (p.Ser137Arg)
c.7950A>C (p.Ter2650Tyr)
c.507A>C
n.7950A>C
c.7846A>C (p.Ser2616Arg)
 ClinVar
13g.32362659A>GCA387747225BRCA2c.7942A>G (p.Ser2648Gly)
c.7573A>G (p.Ser2525Gly)
c.409A>G (p.Ser137Gly)
c.7950A>G (p.Ter2650=)
c.507A>G
n.7950A>G
c.7846A>G (p.Ser2616Gly)
13g.32362659A>TCA387747226BRCA2c.7942A>T (p.Ser2648Cys)
c.7573A>T (p.Ser2525Cys)
c.409A>T (p.Ser137Cys)
c.7950A>T (p.Ter2650Tyr)
c.507A>T
n.7950A>T
c.7846A>T (p.Ser2616Cys)
 dbSNP COSMIC COSMIC
13g.32362660G>ACA387747227BRCA2c.7943G>A (p.Ser2648Asn)
c.7574G>A (p.Ser2525Asn)
c.410G>A (p.Ser137Asn)
c.7951G>A (n.7951G>A)
c.508G>A
c.7847G>A (p.Ser2616Asn)
13g.32362660G>CCA387747228BRCA2c.7943G>C (p.Ser2648Thr)
c.7574G>C (p.Ser2525Thr)
c.410G>C (p.Ser137Thr)
c.7951G>C (n.7951G>C)
c.508G>C
c.7847G>C (p.Ser2616Thr)
13g.32362660G=CA2082832003BRCA2c.7943G= (p.Ser2648=)
c.7574G= (p.Ser2525=)
c.410G= (p.Ser137=)
c.7951G= (n.7951G=)
c.508G=
c.7847G= (p.Ser2616=)
13g.32362660G>TCA16614218BRCA2c.7943G>T (p.Ser2648Ile)
c.7574G>T (p.Ser2525Ile)
c.410G>T (p.Ser137Ile)
c.7951G>T (n.7951G>T)
c.508G>T
c.7847G>T (p.Ser2616Ile)
 ClinVar dbSNP
13g.32362660_32362661delinsGCCA2082832002BRCA2c.7943_7944delinsGC (p.Ser2648=)
c.7574_7575delinsGC (p.Ser2525=)
c.410_411delinsGC (p.Ser137=)
c.7951_7952delinsGC (n.7951_7952delinsGC)
c.508_509delinsGC
c.7847_7848delinsGC (p.Ser2616=)
13g.32362661C>ACA387747229BRCA2c.7944C>A (p.Ser2648Arg)
c.7575C>A (p.Ser2525Arg)
c.411C>A (p.Ser137Arg)
c.7952C>A (n.7952C>A)
c.509C>A
c.7848C>A (p.Ser2616Arg)
 dbSNP
13g.32362661C=CA2082832015BRCA2c.7944C= (p.Ser2648=)
c.7575C= (p.Ser2525=)
c.411C= (p.Ser137=)
c.7952C= (n.7952C=)
c.509C=
c.7848C= (p.Ser2616=)
13g.32362661C>GCA387747230BRCA2c.7944C>G (p.Ser2648Arg)
c.7575C>G (p.Ser2525Arg)
c.411C>G (p.Ser137Arg)
c.7952C>G (n.7952C>G)
c.509C>G
c.7848C>G (p.Ser2616Arg)
 dbSNP
13g.32362661C>TCA483261009BRCA2c.7944C>T (p.Ser2648=)
c.7575C>T (p.Ser2525=)
c.411C>T (p.Ser137=)
c.7952C>T (n.7952C>T)
c.509C>T
c.7848C>T (p.Ser2616=)
 ClinVar dbSNP
13g.32362663delCA336502BRCA2c.7946del (p.Pro2649GlnfsTer8)
c.7577del (p.Pro2526GlnfsTer8)
c.413del (p.Pro138GlnfsTer8)
c.7954del (n.7954del)
c.511del
c.7850del (p.Pro2617GlnfsTer8)
 ClinVar dbSNP
13g.32362662C>ACA387747232BRCA2c.7945C>A (p.Pro2649Thr)
c.7576C>A (p.Pro2526Thr)
c.412C>A (p.Pro138Thr)
c.7953C>A (n.7953C>A)
c.510C>A
c.7849C>A (p.Pro2617Thr)
 dbSNP
13g.32362662C>GCA387747231BRCA2c.7945C>G (p.Pro2649Ala)
c.7576C>G (p.Pro2526Ala)
c.412C>G (p.Pro138Ala)
c.7953C>G (n.7953C>G)
c.510C>G
c.7849C>G (p.Pro2617Ala)
 dbSNP gnomAD v4
13g.32362662C>TCA387747233BRCA2c.7945C>T (p.Pro2649Ser)
c.7576C>T (p.Pro2526Ser)
c.412C>T (p.Pro138Ser)
c.7953C>T (n.7953C>T)
c.510C>T
c.7849C>T (p.Pro2617Ser)
 ClinVar dbSNP
13g.32362663C>ACA387747236BRCA2c.7946C>A (p.Pro2649Gln)
c.7577C>A (p.Pro2526Gln)
c.413C>A (p.Pro138Gln)
c.7954C>A (n.7954C>A)
c.511C>A
c.7850C>A (p.Pro2617Gln)
 dbSNP
13g.32362663C=CA2082832021BRCA2c.7946C= (p.Pro2649=)
c.7577C= (p.Pro2526=)
c.413C= (p.Pro138=)
c.7954C= (n.7954C=)
c.511C=
c.7850C= (p.Pro2617=)
13g.32362663C>GCA387747234BRCA2c.7946C>G (p.Pro2649Arg)
c.7577C>G (p.Pro2526Arg)
c.413C>G (p.Pro138Arg)
c.7954C>G (n.7954C>G)
c.511C>G
c.7850C>G (p.Pro2617Arg)
 dbSNP
13g.32362663C>TCA387747235BRCA2c.7946C>T (p.Pro2649Leu)
c.7577C>T (p.Pro2526Leu)
c.413C>T (p.Pro138Leu)
c.7954C>T (n.7954C>T)
c.511C>T
c.7850C>T (p.Pro2617Leu)
13g.32362664A=CA2082832027BRCA2c.7947A= (p.Pro2649=)
c.7578A= (p.Pro2526=)
c.414A= (p.Pro138=)
c.7955A= (n.7955A=)
c.512A=
c.7851A= (p.Pro2617=)
13g.32362664A>CCA483261012BRCA2c.7947A>C (p.Pro2649=)
c.7578A>C (p.Pro2526=)
c.414A>C (p.Pro138=)
c.7955A>C (n.7955A>C)
c.512A>C
c.7851A>C (p.Pro2617=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32362664A>GCA025349BRCA2c.7947A>G (p.Pro2649=)
c.7578A>G (p.Pro2526=)
c.414A>G (p.Pro138=)
c.7955A>G (n.7955A>G)
c.512A>G
c.7851A>G (p.Pro2617=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362664A>TCA483261013BRCA2c.7947A>T (p.Pro2649=)
c.7578A>T (p.Pro2526=)
c.414A>T (p.Pro138=)
c.7955A>T (n.7955A>T)
c.512A>T
c.7851A>T (p.Pro2617=)
 dbSNP
13g.32362664dupCA10589459BRCA2c.7947dup (p.Glu2650ArgfsTer12)
c.7578dup (p.Glu2527ArgfsTer12)
c.414dup (p.Glu139ArgfsTer12)
c.7955dup (n.7955dup)
c.512dup
c.7851dup (p.Glu2618ArgfsTer12)
 ClinVar dbSNP gnomAD v4
13g.32362665G>ACA387747237BRCA2c.7948G>A (p.Glu2650Lys)
c.7579G>A (p.Glu2527Lys)
c.415G>A (p.Glu139Lys)
c.7956G>A (n.7956G>A)
c.513G>A
c.7852G>A (p.Glu2618Lys)
 ClinVar dbSNP gnomAD v4
13g.32362665G>CCA387747238BRCA2c.7948G>C (p.Glu2650Gln)
c.7579G>C (p.Glu2527Gln)
c.415G>C (p.Glu139Gln)
c.7956G>C (n.7956G>C)
c.513G>C
c.7852G>C (p.Glu2618Gln)
 ClinVar dbSNP COSMIC COSMIC
13g.32362665G=CA2082832033BRCA2c.7948G= (p.Glu2650=)
c.7579G= (p.Glu2527=)
c.415G= (p.Glu139=)
c.7956G= (n.7956G=)
c.513G=
c.7852G= (p.Glu2618=)
13g.32362665G>TCA387747239BRCA2c.7948G>T (p.Glu2650Ter)
c.7579G>T (p.Glu2527Ter)
c.415G>T (p.Glu139Ter)
c.7956G>T (n.7956G>T)
c.513G>T
c.7852G>T (p.Glu2618Ter)
13g.32362665_32362666delinsGACA2082832032BRCA2c.7948_7949delinsGA (p.Glu2650=)
c.7579_7580delinsGA (p.Glu2527=)
c.415_416delinsGA (p.Glu139=)
c.7956_7957delinsGA (n.7956_7957delinsGA)
c.513_514delinsGA
c.7852_7853delinsGA (p.Glu2618=)
13g.32362666A>CCA387747240BRCA2c.7949A>C (p.Glu2650Ala)
c.7580A>C (p.Glu2527Ala)
c.416A>C (p.Glu139Ala)
c.7957A>C (n.7957A>C)
c.514A>C
c.7853A>C (p.Glu2618Ala)
13g.32362666A>GCA387747241BRCA2c.7949A>G (p.Glu2650Gly)
c.7580A>G (p.Glu2527Gly)
c.416A>G (p.Glu139Gly)
c.7957A>G (n.7957A>G)
c.514A>G
c.7853A>G (p.Glu2618Gly)
 ClinVar gnomAD v4
13g.32362666A>TCA387747242BRCA2c.7949A>T (p.Glu2650Val)
c.7580A>T (p.Glu2527Val)
c.416A>T (p.Glu139Val)
c.7957A>T (n.7957A>T)
c.514A>T
c.7853A>T (p.Glu2618Val)
 dbSNP
13g.32362668delCA10586583BRCA2c.7951del (p.Arg2651GlyfsTer6)
c.7582del (p.Arg2528GlyfsTer6)
c.418del (p.Arg140GlyfsTer6)
c.7959del (n.7959del)
c.516del
c.7855del (p.Arg2619GlyfsTer6)
 ClinVar dbSNP
13g.32362667A>CCA387747243BRCA2c.7950A>C (p.Glu2650Asp)
c.7581A>C (p.Glu2527Asp)
c.417A>C (p.Glu139Asp)
c.7958A>C (n.7958A>C)
c.515A>C
c.7854A>C (p.Glu2618Asp)
13g.32362667A>GCA483261016BRCA2c.7950A>G (p.Glu2650=)
c.7581A>G (p.Glu2527=)
c.417A>G (p.Glu139=)
c.7958A>G (n.7958A>G)
c.515A>G
c.7854A>G (p.Glu2618=)
13g.32362667A>TCA387747244BRCA2c.7950A>T (p.Glu2650Asp)
c.7581A>T (p.Glu2527Asp)
c.417A>T (p.Glu139Asp)
c.7958A>T (n.7958A>T)
c.515A>T
c.7854A>T (p.Glu2618Asp)
13g.32362668A=CA2082832040BRCA2c.7951A= (p.Arg2651=)
c.7582A= (p.Arg2528=)
c.418A= (p.Arg140=)
c.7959A= (n.7959A=)
c.516A=
c.7855A= (p.Arg2619=)
13g.32362668A>CCA483261017BRCA2c.7951A>C (p.Arg2651=)
c.7582A>C (p.Arg2528=)
c.418A>C (p.Arg140=)
c.7959A>C (n.7959A>C)
c.516A>C
c.7855A>C (p.Arg2619=)
13g.32362668A>GCA387747245BRCA2c.7951A>G (p.Arg2651Gly)
c.7582A>G (p.Arg2528Gly)
c.418A>G (p.Arg140Gly)
c.7959A>G (n.7959A>G)
c.516A>G
c.7855A>G (p.Arg2619Gly)
 ClinVar dbSNP
13g.32362668A>TCA387747246BRCA2c.7951A>T (p.Arg2651Trp)
c.7582A>T (p.Arg2528Trp)
c.418A>T (p.Arg140Trp)
c.7959A>T (n.7959A>T)
c.516A>T
c.7855A>T (p.Arg2619Trp)
 dbSNP
13g.32362668_32362669delinsAGCA2082832039BRCA2c.7951_7952delinsAG (p.Arg2651=)
c.7582_7583delinsAG (p.Arg2528=)
c.418_419delinsAG (p.Arg140=)
c.7959_7960delinsAG (n.7959_7960delinsAG)
c.516_517delinsAG
c.7855_7856delinsAG (p.Arg2619=)
13g.32362669G>ACA387747247BRCA2c.7952G>A (p.Arg2651Lys)
c.7583G>A (p.Arg2528Lys)
c.419G>A (p.Arg140Lys)
c.7960G>A (n.7960G>A)
c.517G>A
c.7856G>A (p.Arg2619Lys)
 dbSNP
13g.32362669G>CCA387747248BRCA2c.7952G>C (p.Arg2651Thr)
c.7583G>C (p.Arg2528Thr)
c.419G>C (p.Arg140Thr)
c.7960G>C (n.7960G>C)
c.517G>C
c.7856G>C (p.Arg2619Thr)
 ClinVar dbSNP gnomAD v4
13g.32362669G=CA2082832045BRCA2c.7952G= (p.Arg2651=)
c.7583G= (p.Arg2528=)
c.419G= (p.Arg140=)
c.7960G= (n.7960G=)
c.517G=
c.7856G= (p.Arg2619=)
13g.32362669G>TCA387747249BRCA2c.7952G>T (p.Arg2651Met)
c.7583G>T (p.Arg2528Met)
c.419G>T (p.Arg140Met)
c.7960G>T (n.7960G>T)
c.517G>T
c.7856G>T (p.Arg2619Met)
13g.32362671dupCA2499222314BRCA2c.7954dup (p.Val2652GlyfsTer10)
c.7585dup (p.Val2529GlyfsTer10)
c.421dup (p.Val141GlyfsTer10)
c.7962dup (n.7962dup)
c.519dup
c.7858dup (p.Val2620GlyfsTer10)
13g.32362671delCA025353BRCA2c.7954del (p.Val2652CysfsTer5)
c.7585del (p.Val2529CysfsTer5)
c.421del (p.Val141CysfsTer5)
c.7962del (n.7962del)
c.519del
c.7858del (p.Val2620CysfsTer5)
 ClinVar dbSNP
13g.32362670G>ACA483261023BRCA2c.7953G>A (p.Arg2651=)
c.7584G>A (p.Arg2528=)
c.420G>A (p.Arg140=)
c.7961G>A (n.7961G>A)
c.518G>A
c.7857G>A (p.Arg2619=)
 dbSNP
13g.32362670G>CCA387747251BRCA2c.7953G>C (p.Arg2651Ser)
c.7584G>C (p.Arg2528Ser)
c.420G>C (p.Arg140Ser)
c.7961G>C (n.7961G>C)
c.518G>C
c.7857G>C (p.Arg2619Ser)
 ClinVar dbSNP
13g.32362670G=CA2082832056BRCA2c.7953G= (p.Arg2651=)
c.7584G= (p.Arg2528=)
c.420G= (p.Arg140=)
c.7961G= (n.7961G=)
c.518G=
c.7857G= (p.Arg2619=)
13g.32362670G>TCA025352BRCA2c.7953G>T (p.Arg2651Ser)
c.7584G>T (p.Arg2528Ser)
c.420G>T (p.Arg140Ser)
c.7961G>T (n.7961G>T)
c.518G>T
c.7857G>T (p.Arg2619Ser)
 ClinVar dbSNP gnomAD v4
13g.32362671G>ACA387747253BRCA2c.7954G>A (p.Val2652Met)
c.7585G>A (p.Val2529Met)
c.421G>A (p.Val141Met)
c.7962G>A (n.7962G>A)
c.519G>A
c.7858G>A (p.Val2620Met)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32362671G>CCA387747256BRCA2c.7954G>C (p.Val2652Leu)
c.7585G>C (p.Val2529Leu)
c.421G>C (p.Val141Leu)
c.7962G>C (n.7962G>C)
c.519G>C
c.7858G>C (p.Val2620Leu)
 dbSNP
13g.32362671G=CA2082832097BRCA2c.7954G= (p.Val2652=)
c.7585G= (p.Val2529=)
c.421G= (p.Val141=)
c.7962G= (n.7962G=)
c.519G=
c.7858G= (p.Val2620=)
13g.32362671G>TCA387747258BRCA2c.7954G>T (p.Val2652Leu)
c.7585G>T (p.Val2529Leu)
c.421G>T (p.Val141Leu)
c.7962G>T (n.7962G>T)
c.519G>T
c.7858G>T (p.Val2620Leu)
 gnomAD v4
13g.32362672T>ACA387747264BRCA2c.7955T>A (p.Val2652Glu)
c.7586T>A (p.Val2529Glu)
c.422T>A (p.Val141Glu)
c.7963T>A (n.7963T>A)
c.520T>A
c.7859T>A (p.Val2620Glu)
 ClinVar dbSNP
13g.32362672T>CCA387747266BRCA2c.7955T>C (p.Val2652Ala)
c.7586T>C (p.Val2529Ala)
c.422T>C (p.Val141Ala)
c.7963T>C (n.7963T>C)
c.520T>C
c.7859T>C (p.Val2620Ala)
13g.32362672T>GCA387747262BRCA2c.7955T>G (p.Val2652Gly)
c.7586T>G (p.Val2529Gly)
c.422T>G (p.Val141Gly)
c.7963T>G (n.7963T>G)
c.520T>G
c.7859T>G (p.Val2620Gly)
 ClinVar dbSNP gnomAD v4
13g.32362672T=CA2082832112BRCA2c.7955T= (p.Val2652=)
c.7586T= (p.Val2529=)
c.422T= (p.Val141=)
c.7963T= (n.7963T=)
c.520T=
c.7859T= (p.Val2620=)
13g.32362673_32362676dupCA2499222315BRCA2c.7956_7959dup (p.Leu2654AlafsTer9)
c.7587_7590dup (p.Leu2531AlafsTer9)
c.423_426dup (p.Leu143AlafsTer9)
c.7964_7967dup (n.7964_7967dup)
c.521_524dup
c.7860_7863dup (p.Leu2622AlafsTer9)
 ClinVar dbSNP
13g.32362673G>ACA483261027BRCA2c.7956G>A (p.Val2652=)
c.7587G>A (p.Val2529=)
c.423G>A (p.Val141=)
c.7964G>A (n.7964G>A)
c.521G>A
c.7860G>A (p.Val2620=)
 ClinVar dbSNP
13g.32362673G>CCA483261028BRCA2c.7956G>C (p.Val2652=)
c.7587G>C (p.Val2529=)
c.423G>C (p.Val141=)
c.7964G>C (n.7964G>C)
c.521G>C
c.7860G>C (p.Val2620=)
 dbSNP
13g.32362673G>TCA483261029BRCA2c.7956G>T (p.Val2652=)
c.7587G>T (p.Val2529=)
c.423G>T (p.Val141=)
c.7964G>T (n.7964G>T)
c.521G>T
c.7860G>T (p.Val2620=)
13g.32362673_32362674delCA2825002146BRCA2c.7956_7957del (p.Leu2653SerfsTer8)
c.7587_7588del (p.Leu2530SerfsTer8)
c.423_424del (p.Leu142SerfsTer8)
c.7964_7965del (n.7964_7965del)
c.521_522del
c.7860_7861del (p.Leu2621SerfsTer8)
 ClinVar
13g.32362673_32362676delinsGCTTCA2082832117BRCA2c.7956_7959delinsGCTT (p.Val2652=)
c.7587_7590delinsGCTT (p.Val2529=)
c.423_426delinsGCTT (p.Val141=)
c.7964_7967delinsGCTT (n.7964_7967delinsGCTT)
c.521_524delinsGCTT
c.7860_7863delinsGCTT (p.Val2620=)
13g.32362674C>ACA387747269BRCA2c.7957C>A (p.Leu2653Ile)
c.7588C>A (p.Leu2530Ile)
c.424C>A (p.Leu142Ile)
c.7965C>A (n.7965C>A)
c.522C>A
c.7861C>A (p.Leu2621Ile)
 dbSNP
13g.32362674C=CA2082832124BRCA2c.7957C= (p.Leu2653=)
c.7588C= (p.Leu2530=)
c.424C= (p.Leu142=)
c.7965C= (n.7965C=)
c.522C=
c.7861C= (p.Leu2621=)
13g.32362674C>GCA387747272BRCA2c.7957C>G (p.Leu2653Val)
c.7588C>G (p.Leu2530Val)
c.424C>G (p.Leu142Val)
c.7965C>G (n.7965C>G)
c.522C>G
c.7861C>G (p.Leu2621Val)
 ClinVar dbSNP
13g.32362674C>TCA6941163BRCA2c.7957C>T (p.Leu2653Phe)
c.7588C>T (p.Leu2530Phe)
c.424C>T (p.Leu142Phe)
c.7965C>T (n.7965C>T)
c.522C>T
c.7861C>T (p.Leu2621Phe)
 dbSNP ExAC gnomAD v2
13g.32362674_32362675delinsCTCA2082832119BRCA2c.7957_7958delinsCT (p.Leu2653=)
c.7588_7589delinsCT (p.Leu2530=)
c.424_425delinsCT (p.Leu142=)
c.7965_7966delinsCT (n.7965_7966delinsCT)
c.522_523delinsCT
c.7861_7862delinsCT (p.Leu2621=)
13g.32362678_32362680delCA915946883BRCA2c.7961_7963del (p.Leu2654del)
c.7592_7594del (p.Leu2531del)
c.428_430del (p.Leu143del)
c.7969_7971del (n.7969_7971del)
c.526_528del
c.7865_7867del (p.Leu2622del)
 ClinVar dbSNP
13g.32362675T>ACA387747275BRCA2c.7958T>A (p.Leu2653His)
c.7589T>A (p.Leu2530His)
c.425T>A (p.Leu142His)
c.7966T>A (n.7966T>A)
c.523T>A
c.7862T>A (p.Leu2621His)
 dbSNP
13g.32362675T>CCA025354BRCA2c.7958T>C (p.Leu2653Pro)
c.7589T>C (p.Leu2530Pro)
c.425T>C (p.Leu142Pro)
c.7966T>C (n.7966T>C)
c.523T>C
c.7862T>C (p.Leu2621Pro)
 ClinVar dbSNP gnomAD v4
13g.32362675T>GCA16614368BRCA2c.7958T>G (p.Leu2653Arg)
c.7589T>G (p.Leu2530Arg)
c.425T>G (p.Leu142Arg)
c.7966T>G (n.7966T>G)
c.523T>G
c.7862T>G (p.Leu2621Arg)
 ClinVar dbSNP
13g.32362675T=CA2082832137BRCA2c.7958T= (p.Leu2653=)
c.7589T= (p.Leu2530=)
c.425T= (p.Leu142=)
c.7966T= (n.7966T=)
c.523T=
c.7862T= (p.Leu2621=)
13g.32362675_32362676dupCA891843893BRCA2c.7958_7959dup (p.Leu2654PhefsTer4)
c.7589_7590dup (p.Leu2531PhefsTer4)
c.425_426dup (p.Leu143PhefsTer4)
c.7966_7967dup (n.7966_7967dup)
c.523_524dup
c.7862_7863dup (p.Leu2622PhefsTer4)
 ClinVar dbSNP
13g.32362676delCA1139663136BRCA2c.7959del (p.Leu2654PhefsTer3)
c.7590del (p.Leu2531PhefsTer3)
c.426del (p.Leu143PhefsTer3)
c.7967del (n.7967del)
c.524del
c.7863del (p.Leu2622PhefsTer3)
 ClinVar dbSNP
13g.32362676T>ACA483261031BRCA2c.7959T>A (p.Leu2653=)
c.7590T>A (p.Leu2530=)
c.426T>A (p.Leu142=)
c.7967T>A (n.7967T>A)
c.524T>A
c.7863T>A (p.Leu2621=)
 dbSNP
13g.32362676T>CCA483261034BRCA2c.7959T>C (p.Leu2653=)
c.7590T>C (p.Leu2530=)
c.426T>C (p.Leu142=)
c.7967T>C (n.7967T>C)
c.524T>C
c.7863T>C (p.Leu2621=)
 ClinVar
13g.32362676T>GCA483261032BRCA2c.7959T>G (p.Leu2653=)
c.7590T>G (p.Leu2530=)
c.426T>G (p.Leu142=)
c.7967T>G (n.7967T>G)
c.524T>G
c.7863T>G (p.Leu2621=)
 ClinVar dbSNP
13g.32362676T=CA2082832157BRCA2c.7959T= (p.Leu2653=)
c.7590T= (p.Leu2530=)
c.426T= (p.Leu142=)
c.7967T= (n.7967T=)
c.524T=
c.7863T= (p.Leu2621=)
13g.32362677C>ACA387747280BRCA2c.7960C>A (p.Leu2654Ile)
c.7591C>A (p.Leu2531Ile)
c.427C>A (p.Leu143Ile)
c.7968C>A (n.7968C>A)
c.525C>A
c.7864C>A (p.Leu2622Ile)
13g.32362677C>GCA387747282BRCA2c.7960C>G (p.Leu2654Val)
c.7591C>G (p.Leu2531Val)
c.427C>G (p.Leu143Val)
c.7968C>G (n.7968C>G)
c.525C>G
c.7864C>G (p.Leu2622Val)
 dbSNP
13g.32362677C>TCA387747284BRCA2c.7960C>T (p.Leu2654Phe)
c.7591C>T (p.Leu2531Phe)
c.427C>T (p.Leu143Phe)
c.7968C>T (n.7968C>T)
c.525C>T
c.7864C>T (p.Leu2622Phe)
 dbSNP COSMIC COSMIC
13g.32362678T>ACA387747286BRCA2c.7961T>A (p.Leu2654His)
c.7592T>A (p.Leu2531His)
c.428T>A (p.Leu143His)
c.7969T>A (n.7969T>A)
c.526T>A
c.7865T>A (p.Leu2622His)
13g.32362678T>CCA025355BRCA2c.7961T>C (p.Leu2654Pro)
c.7592T>C (p.Leu2531Pro)
c.428T>C (p.Leu143Pro)
c.7969T>C (n.7969T>C)
c.526T>C
c.7865T>C (p.Leu2622Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32362678T>GCA387747289BRCA2c.7961T>G (p.Leu2654Arg)
c.7592T>G (p.Leu2531Arg)
c.428T>G (p.Leu143Arg)
c.7969T>G (n.7969T>G)
c.526T>G
c.7865T>G (p.Leu2622Arg)
13g.32362678T=CA2082832164BRCA2c.7961T= (p.Leu2654=)
c.7592T= (p.Leu2531=)
c.428T= (p.Leu143=)
c.7969T= (n.7969T=)
c.526T=
c.7865T= (p.Leu2622=)
13g.32362679T>ACA483261039BRCA2c.7962T>A (p.Leu2654=)
c.7593T>A (p.Leu2531=)
c.429T>A (p.Leu143=)
c.7970T>A (n.7970T>A)
c.527T>A
c.7866T>A (p.Leu2622=)
 dbSNP
13g.32362679T>CCA483261041BRCA2c.7962T>C (p.Leu2654=)
c.7593T>C (p.Leu2531=)
c.429T>C (p.Leu143=)
c.7970T>C (n.7970T>C)
c.527T>C
c.7866T>C (p.Leu2622=)
13g.32362679T>GCA483261043BRCA2c.7962T>G (p.Leu2654=)
c.7593T>G (p.Leu2531=)
c.429T>G (p.Leu143=)
c.7970T>G (n.7970T>G)
c.527T>G
c.7866T>G (p.Leu2622=)
13g.32362679_32362680delinsTCCA2082832166BRCA2c.7962_7963delinsTC (p.Leu2654=)
c.7593_7594delinsTC (p.Leu2531=)
c.429_430delinsTC (p.Leu143=)
c.7970_7971delinsTC (n.7970_7971delinsTC)
c.527_528delinsTC
c.7866_7867delinsTC (p.Leu2622=)
13g.32362680delCA025357BRCA2c.7963del (p.Gln2655AsnfsTer2)
c.7594del (p.Gln2532AsnfsTer2)
c.430del (p.Gln144AsnfsTer2)
c.7971del (n.7971del)
c.528del
c.7867del (p.Gln2623AsnfsTer2)
 ClinVar dbSNP
13g.32362680C>ACA387747299BRCA2c.7963C>A (p.Gln2655Lys)
c.7594C>A (p.Gln2532Lys)
c.430C>A (p.Gln144Lys)
c.7971C>A (n.7971C>A)
c.528C>A
c.7867C>A (p.Gln2623Lys)
13g.32362680C=CA2082832173BRCA2c.7963C= (p.Gln2655=)
c.7594C= (p.Gln2532=)
c.430C= (p.Gln144=)
c.7971C= (n.7971C=)
c.528C=
c.7867C= (p.Gln2623=)
13g.32362680C>GCA387747297BRCA2c.7963C>G (p.Gln2655Glu)
c.7594C>G (p.Gln2532Glu)
c.430C>G (p.Gln144Glu)
c.7971C>G (n.7971C>G)
c.528C>G
c.7867C>G (p.Gln2623Glu)
13g.32362680C>TCA025356BRCA2c.7963C>T (p.Gln2655Ter)
c.7594C>T (p.Gln2532Ter)
c.430C>T (p.Gln144Ter)
c.7971C>T (n.7971C>T)
c.528C>T
c.7867C>T (p.Gln2623Ter)
 ClinVar dbSNP COSMIC COSMIC
13g.32362680_32362681delinsCACA2082832178BRCA2c.7963_7964delinsCA (p.Gln2655=)
c.7594_7595delinsCA (p.Gln2532=)
c.430_431delinsCA (p.Gln144=)
c.7971_7972delinsCA (n.7971_7972delinsCA)
c.528_529delinsCA
c.7867_7868delinsCA (p.Gln2623=)
13g.32362680_32362691delCA1139771309BRCA2c.7963_7974del (p.Gln2655_Tyr2658del)
c.7594_7605del (p.Gln2532_Tyr2535del)
c.430_441del (p.Gln144_Tyr147del)
c.7971_7982del (n.7971_7982del)
c.528_539del
c.7867_7878del (p.Gln2623_Tyr2626del)
13g.32362681A=CA2082832187BRCA2c.7964A= (p.Gln2655=)
c.7595A= (p.Gln2532=)
c.431A= (p.Gln144=)
c.7972A= (n.7972A=)
c.529A=
c.7868A= (p.Gln2623=)
13g.32362681A>CCA387747301BRCA2c.7964A>C (p.Gln2655Pro)
c.7595A>C (p.Gln2532Pro)
c.431A>C (p.Gln144Pro)
c.7972A>C (n.7972A>C)
c.529A>C
c.7868A>C (p.Gln2623Pro)
13g.32362681A>GCA025358BRCA2c.7964A>G (p.Gln2655Arg)
c.7595A>G (p.Gln2532Arg)
c.431A>G (p.Gln144Arg)
c.7972A>G (n.7972A>G)
c.529A>G
c.7868A>G (p.Gln2623Arg)
 ClinVar dbSNP gnomAD v4
13g.32362681A>TCA387747306BRCA2c.7964A>T (p.Gln2655Leu)
c.7595A>T (p.Gln2532Leu)
c.431A>T (p.Gln144Leu)
c.7972A>T (n.7972A>T)
c.529A>T
c.7868A>T (p.Gln2623Leu)
 ClinVar dbSNP
13g.32362681_32362682delCA2582341813BRCA2c.7964_7965del (p.Gln2655ProfsTer6)
c.7595_7596del (p.Gln2532ProfsTer6)
c.431_432del (p.Gln144ProfsTer6)
c.7972_7973del (n.7972_7973del)
c.529_530del
c.7868_7869del (p.Gln2623ProfsTer6)
 ClinVar
13g.32362682delCA913190910BRCA2c.7965del (p.Gln2655HisfsTer2)
c.7596del (p.Gln2532HisfsTer2)
c.432del (p.Gln144HisfsTer2)
c.7973del (n.7973del)
c.530del
c.7869del (p.Gln2623HisfsTer2)
 ClinVar dbSNP
13g.32362682A=CA2082832192BRCA2c.7965A= (p.Gln2655=)
c.7596A= (p.Gln2532=)
c.432A= (p.Gln144=)
c.7973A= (n.7973A=)
c.530A=
c.7869A= (p.Gln2623=)
13g.32362682A>CCA387747309BRCA2c.7965A>C (p.Gln2655His)
c.7596A>C (p.Gln2532His)
c.432A>C (p.Gln144His)
c.7973A>C (n.7973A>C)
c.530A>C
c.7869A>C (p.Gln2623His)
13g.32362682A>GCA247475304BRCA2c.7965A>G (p.Gln2655=)
c.7596A>G (p.Gln2532=)
c.432A>G (p.Gln144=)
c.7973A>G (n.7973A>G)
c.530A>G
c.7869A>G (p.Gln2623=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32362682A>TCA387747311BRCA2c.7965A>T (p.Gln2655His)
c.7596A>T (p.Gln2532His)
c.432A>T (p.Gln144His)
c.7973A>T (n.7973A>T)
c.530A>T
c.7869A>T (p.Gln2623His)
 ClinVar dbSNP
13g.32362683C>ACA387747314BRCA2c.7966C>A (p.Leu2656Ile)
c.7597C>A (p.Leu2533Ile)
c.433C>A (p.Leu145Ile)
c.7974C>A (n.7974C>A)
c.531C>A
c.7870C>A (p.Leu2624Ile)
 dbSNP COSMIC COSMIC
13g.32362683C=CA2082832202BRCA2c.7966C= (p.Leu2656=)
c.7597C= (p.Leu2533=)
c.433C= (p.Leu145=)
c.7974C= (n.7974C=)
c.531C=
c.7870C= (p.Leu2624=)
13g.32362683C>GCA387747316BRCA2c.7966C>G (p.Leu2656Val)
c.7597C>G (p.Leu2533Val)
c.433C>G (p.Leu145Val)
c.7974C>G (n.7974C>G)
c.531C>G
c.7870C>G (p.Leu2624Val)
 ClinVar dbSNP
13g.32362683C>TCA483261053BRCA2c.7966C>T (p.Leu2656=)
c.7597C>T (p.Leu2533=)
c.433C>T (p.Leu145=)
c.7974C>T (n.7974C>T)
c.531C>T
c.7870C>T (p.Leu2624=)
 ClinVar dbSNP gnomAD v4
13g.32362684T>ACA16613950BRCA2c.7967T>A (p.Leu2656Gln)
c.7598T>A (p.Leu2533Gln)
c.434T>A (p.Leu145Gln)
c.7975T>A (n.7975T>A)
c.532T>A
c.7871T>A (p.Leu2624Gln)
 ClinVar dbSNP
13g.32362684T>CCA10575929BRCA2c.7967T>C (p.Leu2656Pro)
c.7598T>C (p.Leu2533Pro)
c.434T>C (p.Leu145Pro)
c.7975T>C (n.7975T>C)
c.532T>C
c.7871T>C (p.Leu2624Pro)
 ClinVar dbSNP
13g.32362684T>GCA387747320BRCA2c.7967T>G (p.Leu2656Arg)
c.7598T>G (p.Leu2533Arg)
c.434T>G (p.Leu145Arg)
c.7975T>G (n.7975T>G)
c.532T>G
c.7871T>G (p.Leu2624Arg)
13g.32362684T=CA2082832208BRCA2c.7967T= (p.Leu2656=)
c.7598T= (p.Leu2533=)
c.434T= (p.Leu145=)
c.7975T= (n.7975T=)
c.532T=
c.7871T= (p.Leu2624=)
13g.32362688_32362704delCA2580612214BRCA2c.7971_7976+11del
c.7602_7607+11del
c.438_443+11del
c.7979_7984+11del
c.536_541+11del
c.7875_7880+11del
13g.32362685A=CA2082832235BRCA2c.7968A= (p.Leu2656=)
c.7599A= (p.Leu2533=)
c.435A= (p.Leu145=)
c.7976A= (n.7976A=)
c.533A=
c.7872A= (p.Leu2624=)
13g.32362685A>CCA483261054BRCA2c.7968A>C (p.Leu2656=)
c.7599A>C (p.Leu2533=)
c.435A>C (p.Leu145=)
c.7976A>C (n.7976A>C)
c.533A>C
c.7872A>C (p.Leu2624=)
13g.32362685A>GCA483261055BRCA2c.7968A>G (p.Leu2656=)
c.7599A>G (p.Leu2533=)
c.435A>G (p.Leu145=)
c.7976A>G (n.7976A>G)
c.533A>G
c.7872A>G (p.Leu2624=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32362685A>TCA483261056BRCA2c.7968A>T (p.Leu2656=)
c.7599A>T (p.Leu2533=)
c.435A>T (p.Leu145=)
c.7976A>T (n.7976A>T)
c.533A>T
c.7872A>T (p.Leu2624=)
13g.32362688dupCA2727917416BRCA2c.7971dup (p.Tyr2658IlefsTer4)
c.7602dup (p.Tyr2535IlefsTer4)
c.438dup (p.Tyr147IlefsTer4)
c.7979dup (n.7979dup)
c.536dup
c.7875dup (p.Tyr2626IlefsTer4)
 dbSNP
13g.32362686A>CCA387747323BRCA2c.7969A>C (p.Lys2657Gln)
c.7600A>C (p.Lys2534Gln)
c.436A>C (p.Lys146Gln)
c.7977A>C (n.7977A>C)
c.534A>C
c.7873A>C (p.Lys2625Gln)
13g.32362686A>GCA387747324BRCA2c.7969A>G (p.Lys2657Glu)
c.7600A>G (p.Lys2534Glu)
c.436A>G (p.Lys146Glu)
c.7977A>G (n.7977A>G)
c.534A>G
c.7873A>G (p.Lys2625Glu)
 ClinVar dbSNP
13g.32362686A>TCA387747327BRCA2c.7969A>T (p.Lys2657Ter)
c.7600A>T (p.Lys2534Ter)
c.436A>T (p.Lys146Ter)
c.7977A>T (n.7977A>T)
c.534A>T
c.7873A>T (p.Lys2625Ter)
 ClinVar gnomAD v4
13g.32362688_32362697delCA2580087432BRCA2c.7971_7976+4del
c.7602_7607+4del
c.438_443+4del
c.7979_7984+4del
c.536_541+4del
c.7875_7880+4del
 ClinVar
13g.32362687A=CA2082832254BRCA2c.7970A= (p.Lys2657=)
c.7601A= (p.Lys2534=)
c.437A= (p.Lys146=)
c.7978A= (n.7978A=)
c.535A=
c.7874A= (p.Lys2625=)
13g.32362687A>CCA387747333BRCA2c.7970A>C (p.Lys2657Thr)
c.7601A>C (p.Lys2534Thr)
c.437A>C (p.Lys146Thr)
c.7978A>C (n.7978A>C)
c.535A>C
c.7874A>C (p.Lys2625Thr)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32362687A>GCA387747335BRCA2c.7970A>G (p.Lys2657Arg)
c.7601A>G (p.Lys2534Arg)
c.437A>G (p.Lys146Arg)
c.7978A>G (n.7978A>G)
c.535A>G
c.7874A>G (p.Lys2625Arg)
13g.32362687A>TCA387747331BRCA2c.7970A>T (p.Lys2657Ile)
c.7601A>T (p.Lys2534Ile)
c.437A>T (p.Lys146Ile)
c.7978A>T (n.7978A>T)
c.535A>T
c.7874A>T (p.Lys2625Ile)
13g.32362688A=CA2082832265BRCA2c.7971A= (p.Lys2657=)
c.7602A= (p.Lys2534=)
c.438A= (p.Lys146=)
c.7979A= (n.7979A=)
c.536A=
c.7875A= (p.Lys2625=)
13g.32362688A>CCA387747340BRCA2c.7971A>C (p.Lys2657Asn)
c.7602A>C (p.Lys2534Asn)
c.438A>C (p.Lys146Asn)
c.7979A>C (n.7979A>C)
c.536A>C
c.7875A>C (p.Lys2625Asn)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32362688A>GCA338244BRCA2c.7971A>G (p.Lys2657=)
c.7602A>G (p.Lys2534=)
c.438A>G (p.Lys146=)
c.7979A>G (n.7979A>G)
c.536A>G
c.7875A>G (p.Lys2625=)
 ClinVar dbSNP
13g.32362688A>TCA387747341BRCA2c.7971A>T (p.Lys2657Asn)
c.7602A>T (p.Lys2534Asn)
c.438A>T (p.Lys146Asn)
c.7979A>T (n.7979A>T)
c.536A>T
c.7875A>T (p.Lys2625Asn)
 dbSNP
13g.32362689T>ACA387747344BRCA2c.7972T>A (p.Tyr2658Asn)
c.7603T>A (p.Tyr2535Asn)
c.439T>A (p.Tyr147Asn)
c.7980T>A (n.7980T>A)
c.537T>A
c.7876T>A (p.Tyr2626Asn)
 dbSNP
13g.32362689T>CCA025360BRCA2c.7972T>C (p.Tyr2658His)
c.7603T>C (p.Tyr2535His)
c.439T>C (p.Tyr147His)
c.7980T>C (n.7980T>C)
c.537T>C
c.7876T>C (p.Tyr2626His)
 ClinVar dbSNP
13g.32362689T>GCA387747347BRCA2c.7972T>G (p.Tyr2658Asp)
c.7603T>G (p.Tyr2535Asp)
c.439T>G (p.Tyr147Asp)
c.7980T>G (n.7980T>G)
c.537T>G
c.7876T>G (p.Tyr2626Asp)
13g.32362689T=CA2082832272BRCA2c.7972T= (p.Tyr2658=)
c.7603T= (p.Tyr2535=)
c.439T= (p.Tyr147=)
c.7980T= (n.7980T=)
c.537T=
c.7876T= (p.Tyr2626=)
13g.32362690A=CA2082832288BRCA2c.7973A= (p.Tyr2658=)
c.7604A= (p.Tyr2535=)
c.440A= (p.Tyr147=)
c.7981A= (n.7981A=)
c.538A=
c.7877A= (p.Tyr2626=)
13g.32362690A>CCA387747351BRCA2c.7973A>C (p.Tyr2658Ser)
c.7604A>C (p.Tyr2535Ser)
c.440A>C (p.Tyr147Ser)
c.7981A>C (n.7981A>C)
c.538A>C
c.7877A>C (p.Tyr2626Ser)
 dbSNP
13g.32362690A>GCA387747356BRCA2c.7973A>G (p.Tyr2658Cys)
c.7604A>G (p.Tyr2535Cys)
c.440A>G (p.Tyr147Cys)
c.7981A>G (n.7981A>G)
c.538A>G
c.7877A>G (p.Tyr2626Cys)
 ClinVar dbSNP
13g.32362690A>TCA387747353BRCA2c.7973A>T (p.Tyr2658Phe)
c.7604A>T (p.Tyr2535Phe)
c.440A>T (p.Tyr147Phe)
c.7981A>T (n.7981A>T)
c.538A>T
c.7877A>T (p.Tyr2626Phe)
 dbSNP
13g.32362691C>ACA10589460BRCA2c.7974C>A (p.Tyr2658Ter)
c.7605C>A (p.Tyr2535Ter)
c.441C>A (p.Tyr147Ter)
c.7982C>A (n.7982C>A)
c.539C>A
c.7878C>A (p.Tyr2626Ter)
 ClinVar dbSNP
13g.32362691C=CA2082832305BRCA2c.7974C= (p.Tyr2658=)
c.7605C= (p.Tyr2535=)
c.441C= (p.Tyr147=)
c.7982C= (n.7982C=)
c.539C=
c.7878C= (p.Tyr2626=)
13g.32362691C>GCA025361BRCA2c.7974C>G (p.Tyr2658Ter)
c.7605C>G (p.Tyr2535Ter)
c.441C>G (p.Tyr147Ter)
c.7982C>G (n.7982C>G)
c.539C>G
c.7878C>G (p.Tyr2626Ter)
 ClinVar dbSNP
13g.32362691C>TCA483261063BRCA2c.7974C>T (p.Tyr2658=)
c.7605C>T (p.Tyr2535=)
c.441C>T (p.Tyr147=)
c.7982C>T (n.7982C>T)
c.539C>T
c.7878C>T (p.Tyr2626=)
 ClinVar dbSNP
13g.32362692A=CA2082832327BRCA2c.7975A= (p.Arg2659=)
c.7606A= (p.Arg2536=)
c.442A= (p.Arg148=)
c.7983A= (n.7983A=)
c.540A=
c.7879A= (p.Arg2627=)
13g.32362692A>CCA483261064BRCA2c.7975A>C (p.Arg2659=)
c.7606A>C (p.Arg2536=)
c.442A>C (p.Arg148=)
c.7983A>C (n.7983A>C)
c.540A>C
c.7879A>C (p.Arg2627=)
 dbSNP
13g.32362692A>GCA025362BRCA2c.7975A>G (p.Arg2659Gly)
c.7606A>G (p.Arg2536Gly)
c.442A>G (p.Arg148Gly)
c.7983A>G (n.7983A>G)
c.540A>G
c.7879A>G (p.Arg2627Gly)
 ClinVar dbSNP gnomAD v4
13g.32362692A>TCA387747363BRCA2c.7975A>T (p.Arg2659Ter)
c.7606A>T (p.Arg2536Ter)
c.442A>T (p.Arg148Ter)
c.7983A>T (n.7983A>T)
c.540A>T
c.7879A>T (p.Arg2627Ter)
13g.32362693G>ACA025368BRCA2c.7976G>A (p.Arg2659Lys)
c.7607G>A (p.Arg2536Lys)
c.443G>A (p.Arg148Lys)
c.7984G>A (n.7984G>A)
c.541G>A
c.7880G>A (p.Arg2627Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32362693G>CCA025369BRCA2c.7976G>C (p.Arg2659Thr)
c.7607G>C (p.Arg2536Thr)
c.443G>C (p.Arg148Thr)
c.7984G>C (n.7984G>C)
c.541G>C
c.7880G>C (p.Arg2627Thr)
 ClinVar dbSNP
13g.32362693G=CA2082832336BRCA2c.7976G= (p.Arg2659=)
c.7607G= (p.Arg2536=)
c.443G= (p.Arg148=)
c.7984G= (n.7984G=)
c.541G=
c.7880G= (p.Arg2627=)
13g.32362693G>TCA387747368BRCA2c.7976G>T (p.Arg2659Ile)
c.7607G>T (p.Arg2536Ile)
c.443G>T (p.Arg148Ile)
c.7984G>T (n.7984G>T)
c.541G>T
c.7880G>T (p.Arg2627Ile)
 ClinVar dbSNP
13g.32362694G>ACA025364BRCA2c.7976+1G>A (n.7976+1G>A)
c.7607+1G>A (n.7607+1G>A)
c.443+1G>A (n.443+1G>A)
c.7984+1G>A (n.7984+1G>A)
c.541+1G>A
c.7880+1G>A (n.7880+1G>A)
 ClinVar dbSNP
13g.32362694G>CCA387747372BRCA2c.7976+1G>C (n.7976+1G>C)
c.7607+1G>C (n.7607+1G>C)
c.443+1G>C (n.443+1G>C)
c.7984+1G>C (n.7984+1G>C)
c.541+1G>C
c.7880+1G>C (n.7880+1G>C)
 dbSNP
13g.32362694G=CA2082832350BRCA2c.7976+1G= (n.7976+1G=)
c.7607+1G= (n.7607+1G=)
c.443+1G= (n.443+1G=)
c.7984+1G= (n.7984+1G=)
c.541+1G=
c.7880+1G= (n.7880+1G=)
13g.32362694G>TCA387747374BRCA2c.7976+1G>T (n.7976+1G>T)
c.7607+1G>T (n.7607+1G>T)
c.443+1G>T (n.443+1G>T)
c.7984+1G>T (n.7984+1G>T)
c.541+1G>T
c.7880+1G>T (n.7880+1G>T)
 ClinVar dbSNP
13g.32362695C>ACA10602543BRCA2c.7976+2C>A (n.7976+2C>A)
c.7607+2C>A (n.7607+2C>A)
c.443+2C>A (n.443+2C>A)
c.7984+2C>A (n.7984+2C>A)
c.541+2C>A
c.7880+2C>A (n.7880+2C>A)
 ClinVar dbSNP
13g.32362695C=CA2082832361BRCA2c.7976+2C= (n.7976+2C=)
c.7607+2C= (n.7607+2C=)
c.443+2C= (n.443+2C=)
c.7984+2C= (n.7984+2C=)
c.541+2C=
c.7880+2C= (n.7880+2C=)
13g.32362695C>GCA16619774BRCA2c.7976+2C>G (n.7976+2C>G)
c.7607+2C>G (n.7607+2C>G)
c.443+2C>G (n.443+2C>G)
c.7984+2C>G (n.7984+2C>G)
c.541+2C>G
c.7880+2C>G (n.7880+2C>G)
 ClinVar dbSNP
13g.32362695C>TCA387747377BRCA2c.7976+2C>T (n.7976+2C>T)
c.7607+2C>T (n.7607+2C>T)
c.443+2C>T (n.443+2C>T)
c.7984+2C>T (n.7984+2C>T)
c.541+2C>T
c.7880+2C>T (n.7880+2C>T)
 dbSNP gnomAD v4
13g.32362695_32362697delinsCAACA2082832359BRCA2c.7976+2_7976+4delinsCAA (n.7976+2_7976+4delinsCAA)
c.7607+2_7607+4delinsCAA (n.7607+2_7607+4delinsCAA)
c.443+2_443+4delinsCAA (n.443+2_443+4delinsCAA)
c.7984+2_7984+4delinsCAA (n.7984+2_7984+4delinsCAA)
c.541+2_541+4delinsCAA
c.7880+2_7880+4delinsCAA (n.7880+2_7880+4delinsCAA)
13g.32362696A=CA2082832370BRCA2c.7976+3A= (n.7976+3A=)
c.7607+3A= (n.7607+3A=)
c.443+3A= (n.443+3A=)
c.7984+3A= (n.7984+3A=)
c.541+3A=
c.7880+3A= (n.7880+3A=)
13g.32362696A>CCA658653813BRCA2c.7976+3A>C (n.7976+3A>C)
c.7607+3A>C (n.7607+3A>C)
c.443+3A>C (n.443+3A>C)
c.7984+3A>C (n.7984+3A>C)
c.541+3A>C
c.7880+3A>C (n.7880+3A>C)
 ClinVar dbSNP
13g.32362696A>GCA2727873208BRCA2c.7976+3A>G (n.7976+3A>G)
c.7607+3A>G (n.7607+3A>G)
c.443+3A>G (n.443+3A>G)
c.7984+3A>G (n.7984+3A>G)
c.541+3A>G
c.7880+3A>G (n.7880+3A>G)
 dbSNP
13g.32362696A>TCA2727873209BRCA2c.7976+3A>T (n.7976+3A>T)
c.7607+3A>T (n.7607+3A>T)
c.443+3A>T (n.443+3A>T)
c.7984+3A>T (n.7984+3A>T)
c.541+3A>T
c.7880+3A>T (n.7880+3A>T)
 dbSNP
13g.32362696_32362697delCA025366BRCA2c.7976+3_7976+4del (n.7976+3_7976+4del)
c.7607+3_7607+4del (n.7607+3_7607+4del)
c.443+3_443+4del (n.443+3_443+4del)
c.7984+3_7984+4del (n.7984+3_7984+4del)
c.541+3_541+4del
c.7880+3_7880+4del (n.7880+3_7880+4del)
 ClinVar dbSNP
13g.32362697A=CA2082832375BRCA2c.7976+4A= (n.7976+4A=)
c.7607+4A= (n.7607+4A=)
c.443+4A= (n.443+4A=)
c.7984+4A= (n.7984+4A=)
c.541+4A=
c.7880+4A= (n.7880+4A=)
13g.32362697A>CCA658656487BRCA2c.7976+4A>C (n.7976+4A>C)
c.7607+4A>C (n.7607+4A>C)
c.443+4A>C (n.443+4A>C)
c.7984+4A>C (n.7984+4A>C)
c.541+4A>C
c.7880+4A>C (n.7880+4A>C)
 ClinVar dbSNP
13g.32362697A>GCA10579762BRCA2c.7976+4A>G (n.7976+4A>G)
c.7607+4A>G (n.7607+4A>G)
c.443+4A>G (n.443+4A>G)
c.7984+4A>G (n.7984+4A>G)
c.541+4A>G
c.7880+4A>G (n.7880+4A>G)
 ClinVar dbSNP gnomAD v4
13g.32362697A>TCA2727841632BRCA2c.7976+4A>T (n.7976+4A>T)
c.7607+4A>T (n.7607+4A>T)
c.443+4A>T (n.443+4A>T)
c.7984+4A>T (n.7984+4A>T)
c.541+4A>T
c.7880+4A>T (n.7880+4A>T)
 dbSNP
13g.32362698G>ACA025367BRCA2c.7976+5G>A (n.7976+5G>A)
c.7607+5G>A (n.7607+5G>A)
c.443+5G>A (n.443+5G>A)
c.7984+5G>A (n.7984+5G>A)
c.541+5G>A
c.7880+5G>A (n.7880+5G>A)
 ClinVar dbSNP gnomAD v4
13g.32362698G>CCA609091813BRCA2c.7976+5G>C (n.7976+5G>C)
c.7607+5G>C (n.7607+5G>C)
c.443+5G>C (n.443+5G>C)
c.7984+5G>C (n.7984+5G>C)
c.541+5G>C
c.7880+5G>C (n.7880+5G>C)
 dbSNP gnomAD v2 gnomAD v4
13g.32362698G=CA2082832392BRCA2c.7976+5G= (n.7976+5G=)
c.7607+5G= (n.7607+5G=)
c.443+5G= (n.443+5G=)
c.7984+5G= (n.7984+5G=)
c.541+5G=
c.7880+5G= (n.7880+5G=)
13g.32362698G>TCA658656488BRCA2c.7976+5G>T (n.7976+5G>T)
c.7607+5G>T (n.7607+5G>T)
c.443+5G>T (n.443+5G>T)
c.7984+5G>T (n.7984+5G>T)
c.541+5G>T
c.7880+5G>T (n.7880+5G>T)
 ClinVar dbSNP
13g.32362699T>ACA2727917464BRCA2c.7976+6T>A (n.7976+6T>A)
c.7607+6T>A (n.7607+6T>A)
c.443+6T>A (n.443+6T>A)
c.7984+6T>A (n.7984+6T>A)
c.541+6T>A
c.7880+6T>A (n.7880+6T>A)
 dbSNP
13g.32362700T>ACA2499222316BRCA2c.7976+7T>A (n.7976+7T>A)
c.7607+7T>A (n.7607+7T>A)
c.443+7T>A (n.443+7T>A)
c.7984+7T>A (n.7984+7T>A)
c.541+7T>A
c.7880+7T>A (n.7880+7T>A)
 ClinVar dbSNP
13g.32362700T>CCA915946884BRCA2c.7976+7T>C (n.7976+7T>C)
c.7607+7T>C (n.7607+7T>C)
c.443+7T>C (n.443+7T>C)
c.7984+7T>C (n.7984+7T>C)
c.541+7T>C
c.7880+7T>C (n.7880+7T>C)
 ClinVar dbSNP
13g.32362700T=CA2082832406BRCA2c.7976+7T= (n.7976+7T=)
c.7607+7T= (n.7607+7T=)
c.443+7T= (n.443+7T=)
c.7984+7T= (n.7984+7T=)
c.541+7T=
c.7880+7T= (n.7880+7T=)
13g.32362701T>ACA2727917468BRCA2c.7976+8T>A (n.7976+8T>A)
c.7607+8T>A (n.7607+8T>A)
c.443+8T>A (n.443+8T>A)
c.7984+8T>A (n.7984+8T>A)
c.541+8T>A
c.7880+8T>A (n.7880+8T>A)
 dbSNP
13g.32362701_32362702delinsTACA2082832408BRCA2c.7976+8_7976+9delinsTA (n.7976+8_7976+9delinsTA)
c.7607+8_7607+9delinsTA (n.7607+8_7607+9delinsTA)
c.443+8_443+9delinsTA (n.443+8_443+9delinsTA)
c.7984+8_7984+9delinsTA (n.7984+8_7984+9delinsTA)
c.541+8_541+9delinsTA
c.7880+8_7880+9delinsTA (n.7880+8_7880+9delinsTA)
13g.32362702A=CA2082832413BRCA2c.7976+9A= (n.7976+9A=)
c.7607+9A= (n.7607+9A=)
c.443+9A= (n.443+9A=)
c.7984+9A= (n.7984+9A=)
c.541+9A=
c.7880+9A= (n.7880+9A=)
13g.32362702A>CCA2580087439BRCA2c.7976+9A>C (n.7976+9A>C)
c.7607+9A>C (n.7607+9A>C)
c.443+9A>C (n.443+9A>C)
c.7984+9A>C (n.7984+9A>C)
c.541+9A>C
c.7880+9A>C (n.7880+9A>C)
 ClinVar
13g.32362702A>GCA2082832412BRCA2c.7976+9A>G (n.7976+9A>G)
c.7607+9A>G (n.7607+9A>G)
c.443+9A>G (n.443+9A>G)
c.7984+9A>G (n.7984+9A>G)
c.541+9A>G
c.7880+9A>G (n.7880+9A>G)
 dbSNP
13g.32362704delCA6941164BRCA2c.7976+11del (n.7976+11del)
c.7607+11del (n.7607+11del)
c.443+11del (n.443+11del)
c.7984+11del (n.7984+11del)
c.541+11del
c.7880+11del (n.7880+11del)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.32362703A=CA2082832432BRCA2c.7976+10A= (n.7976+10A=)
c.7607+10A= (n.7607+10A=)
c.443+10A= (n.443+10A=)
c.7984+10A= (n.7984+10A=)
c.541+10A=
c.7880+10A= (n.7880+10A=)
13g.32362703A>GCA2727874192BRCA2c.7976+10A>G (n.7976+10A>G)
c.7607+10A>G (n.7607+10A>G)
c.443+10A>G (n.443+10A>G)
c.7984+10A>G (n.7984+10A>G)
c.541+10A>G
c.7880+10A>G (n.7880+10A>G)
 dbSNP
13g.32362703A>TCA913188565BRCA2c.7976+10A>T (n.7976+10A>T)
c.7607+10A>T (n.7607+10A>T)
c.443+10A>T (n.443+10A>T)
c.7984+10A>T (n.7984+10A>T)
c.541+10A>T
c.7880+10A>T (n.7880+10A>T)
 ClinVar dbSNP
13g.32362704A=CA2082832436BRCA2c.7976+11A= (n.7976+11A=)
c.7607+11A= (n.7607+11A=)
c.443+11A= (n.443+11A=)
c.7984+11A= (n.7984+11A=)
c.541+11A=
c.7880+11A= (n.7880+11A=)
13g.32362704A>CCA658798127BRCA2c.7976+11A>C (n.7976+11A>C)
c.7607+11A>C (n.7607+11A>C)
c.443+11A>C (n.443+11A>C)
c.7984+11A>C (n.7984+11A>C)
c.541+11A>C
c.7880+11A>C (n.7880+11A>C)
 ClinVar dbSNP
13g.32362705G>ACA025363BRCA2c.7976+12G>A (n.7976+12G>A)
c.7607+12G>A (n.7607+12G>A)
c.443+12G>A (n.443+12G>A)
c.7984+12G>A (n.7984+12G>A)
c.541+12G>A
c.7880+12G>A (n.7880+12G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362705G=CA2082832444BRCA2c.7976+12G= (n.7976+12G=)
c.7607+12G= (n.7607+12G=)
c.443+12G= (n.443+12G=)
c.7984+12G= (n.7984+12G=)
c.541+12G=
c.7880+12G= (n.7880+12G=)
13g.32362706C>GCA2727917474BRCA2c.7976+13C>G (n.7976+13C>G)
c.7607+13C>G (n.7607+13C>G)
c.443+13C>G (n.443+13C>G)
c.7984+13C>G (n.7984+13C>G)
c.541+13C>G
c.7880+13C>G (n.7880+13C>G)
 dbSNP
13g.32362706C>TCA2697551755BRCA2c.7976+13C>T (n.7976+13C>T)
c.7607+13C>T (n.7607+13C>T)
c.443+13C>T (n.443+13C>T)
c.7984+13C>T (n.7984+13C>T)
c.541+13C>T
c.7880+13C>T (n.7880+13C>T)
 ClinVar dbSNP
13g.32362707A=CA2082832448BRCA2c.7976+14A= (n.7976+14A=)
c.7607+14A= (n.7607+14A=)
c.443+14A= (n.443+14A=)
c.7984+14A= (n.7984+14A=)
c.541+14A=
c.7880+14A= (n.7880+14A=)
13g.32362707A>GCA6941165BRCA2c.7976+14A>G (n.7976+14A>G)
c.7607+14A>G (n.7607+14A>G)
c.443+14A>G (n.443+14A>G)
c.7984+14A>G (n.7984+14A>G)
c.541+14A>G
c.7880+14A>G (n.7880+14A>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362708T>ACA2727917495BRCA2c.7976+15T>A (n.7976+15T>A)
c.7607+15T>A (n.7607+15T>A)
c.443+15T>A (n.443+15T>A)
c.7984+15T>A (n.7984+15T>A)
c.541+15T>A
c.7880+15T>A (n.7880+15T>A)
 dbSNP
13g.32362709T>ACA2727917516BRCA2c.7976+16T>A (n.7976+16T>A)
c.7607+16T>A (n.7607+16T>A)
c.443+16T>A (n.443+16T>A)
c.7984+16T>A (n.7984+16T>A)
c.541+16T>A
c.7880+16T>A (n.7880+16T>A)
 dbSNP
13g.32362709T>CCA2727917510BRCA2c.7976+16T>C (n.7976+16T>C)
c.7607+16T>C (n.7607+16T>C)
c.443+16T>C (n.443+16T>C)
c.7984+16T>C (n.7984+16T>C)
c.541+16T>C
c.7880+16T>C (n.7880+16T>C)
 dbSNP
13g.32362710A=CA2082832455BRCA2c.7976+17A= (n.7976+17A=)
c.7607+17A= (n.7607+17A=)
c.443+17A= (n.443+17A=)
c.7984+17A= (n.7984+17A=)
c.541+17A=
c.7880+17A= (n.7880+17A=)
13g.32362710A>GCA6941166BRCA2c.7976+17A>G (n.7976+17A>G)
c.7607+17A>G (n.7607+17A>G)
c.443+17A>G (n.443+17A>G)
c.7984+17A>G (n.7984+17A>G)
c.541+17A>G
c.7880+17A>G (n.7880+17A>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362710A>TCA2727839134BRCA2c.7976+17A>T (n.7976+17A>T)
c.7607+17A>T (n.7607+17A>T)
c.443+17A>T (n.443+17A>T)
c.7984+17A>T (n.7984+17A>T)
c.541+17A>T
c.7880+17A>T (n.7880+17A>T)
 dbSNP
13g.32362711C>ACA609091814BRCA2c.7976+18C>A (n.7976+18C>A)
c.7607+18C>A (n.7607+18C>A)
c.443+18C>A (n.443+18C>A)
c.7984+18C>A (n.7984+18C>A)
c.541+18C>A
c.7880+18C>A (n.7880+18C>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32362711C=CA2082832466BRCA2c.7976+18C= (n.7976+18C=)
c.7607+18C= (n.7607+18C=)
c.443+18C= (n.443+18C=)
c.7984+18C= (n.7984+18C=)
c.541+18C=
c.7880+18C= (n.7880+18C=)
13g.32362711C>GCA2727853389BRCA2c.7976+18C>G (n.7976+18C>G)
c.7607+18C>G (n.7607+18C>G)
c.443+18C>G (n.443+18C>G)
c.7984+18C>G (n.7984+18C>G)
c.541+18C>G
c.7880+18C>G (n.7880+18C>G)
 dbSNP
13g.32362711C>TCA16606819BRCA2c.7976+18C>T (n.7976+18C>T)
c.7607+18C>T (n.7607+18C>T)
c.443+18C>T (n.443+18C>T)
c.7984+18C>T (n.7984+18C>T)
c.541+18C>T
c.7880+18C>T (n.7880+18C>T)
 ClinVar dbSNP
13g.32362712A=CA2082832482BRCA2c.7976+19A= (n.7976+19A=)
c.7607+19A= (n.7607+19A=)
c.443+19A= (n.443+19A=)
c.7984+19A= (n.7984+19A=)
c.541+19A=
c.7880+19A= (n.7880+19A=)
13g.32362712A>GCA658798128BRCA2c.7976+19A>G (n.7976+19A>G)
c.7607+19A>G (n.7607+19A>G)
c.443+19A>G (n.443+19A>G)
c.7984+19A>G (n.7984+19A>G)
c.541+19A>G
c.7880+19A>G (n.7880+19A>G)
 ClinVar dbSNP gnomAD v4
13g.32362712A>TCA2082832493BRCA2c.7976+19A>T (n.7976+19A>T)
c.7607+19A>T (n.7607+19A>T)
c.443+19A>T (n.443+19A>T)
c.7984+19A>T (n.7984+19A>T)
c.541+19A>T
c.7880+19A>T (n.7880+19A>T)
 dbSNP
13g.32362713T>ACA2727917577BRCA2c.7976+20T>A (n.7976+20T>A)
c.7607+20T>A (n.7607+20T>A)
c.443+20T>A (n.443+20T>A)
c.7984+20T>A (n.7984+20T>A)
c.541+20T>A
c.7880+20T>A (n.7880+20T>A)
 dbSNP
13g.32362713T>CCA2727917579BRCA2c.7976+20T>C (n.7976+20T>C)
c.7607+20T>C (n.7607+20T>C)
c.443+20T>C (n.443+20T>C)
c.7984+20T>C (n.7984+20T>C)
c.541+20T>C
c.7880+20T>C (n.7880+20T>C)
 dbSNP
13g.32362714T>ACA2727839874BRCA2c.7976+21T>A (n.7976+21T>A)
c.7607+21T>A (n.7607+21T>A)
c.443+21T>A (n.443+21T>A)
c.7984+21T>A (n.7984+21T>A)
c.541+21T>A
c.7880+21T>A (n.7880+21T>A)
 dbSNP
13g.32362714T>GCA6941167BRCA2c.7976+21T>G (n.7976+21T>G)
c.7607+21T>G (n.7607+21T>G)
c.443+21T>G (n.443+21T>G)
c.7984+21T>G (n.7984+21T>G)
c.541+21T>G
c.7880+21T>G (n.7880+21T>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.32362714T=CA2082832499BRCA2c.7976+21T= (n.7976+21T=)
c.7607+21T= (n.7607+21T=)
c.443+21T= (n.443+21T=)
c.7984+21T= (n.7984+21T=)
c.541+21T=
c.7880+21T= (n.7880+21T=)
13g.32362715A>TCA2727917697BRCA2c.7976+22A>T (n.7976+22A>T)
c.7607+22A>T (n.7607+22A>T)
c.443+22A>T (n.443+22A>T)
c.7984+22A>T (n.7984+22A>T)
c.541+22A>T
c.7880+22A>T (n.7880+22A>T)
 dbSNP
13g.32362716C>ACA6941168BRCA2c.7976+23C>A (n.7976+23C>A)
c.7607+23C>A (n.7607+23C>A)
c.443+23C>A (n.443+23C>A)
c.7984+23C>A (n.7984+23C>A)
c.541+23C>A
c.7880+23C>A (n.7880+23C>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362716C=CA2082832507BRCA2c.7976+23C= (n.7976+23C=)
c.7607+23C= (n.7607+23C=)
c.443+23C= (n.443+23C=)
c.7984+23C= (n.7984+23C=)
c.541+23C=
c.7880+23C= (n.7880+23C=)
13g.32362716C>GCA10576073BRCA2c.7976+23C>G (n.7976+23C>G)
c.7607+23C>G (n.7607+23C>G)
c.443+23C>G (n.443+23C>G)
c.7984+23C>G (n.7984+23C>G)
c.541+23C>G
c.7880+23C>G (n.7880+23C>G)
 ClinVar dbSNP
13g.32362716C>TCA025365BRCA2c.7976+23C>T (n.7976+23C>T)
c.7607+23C>T (n.7607+23C>T)
c.443+23C>T (n.443+23C>T)
c.7984+23C>T (n.7984+23C>T)
c.541+23C>T
c.7880+23C>T (n.7880+23C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362717G>ACA6941169BRCA2c.7976+24G>A (n.7976+24G>A)
c.7607+24G>A (n.7607+24G>A)
c.443+24G>A (n.443+24G>A)
c.7984+24G>A (n.7984+24G>A)
c.541+24G>A
c.7880+24G>A (n.7880+24G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362717G>CCA2727835703BRCA2c.7976+24G>C (n.7976+24G>C)
c.7607+24G>C (n.7607+24G>C)
c.443+24G>C (n.443+24G>C)
c.7984+24G>C (n.7984+24G>C)
c.541+24G>C
c.7880+24G>C (n.7880+24G>C)
 dbSNP
13g.32362717G=CA2082832513BRCA2c.7976+24G= (n.7976+24G=)
c.7607+24G= (n.7607+24G=)
c.443+24G= (n.443+24G=)
c.7984+24G= (n.7984+24G=)
c.541+24G=
c.7880+24G= (n.7880+24G=)
13g.32362718T>ACA2622572913BRCA2c.7976+25T>A (n.7976+25T>A)
c.7607+25T>A (n.7607+25T>A)
c.443+25T>A (n.443+25T>A)
c.7984+25T>A (n.7984+25T>A)
c.541+25T>A
c.7880+25T>A (n.7880+25T>A)
 gnomAD v4
13g.32362719A=CA2082832519BRCA2c.7976+26A= (n.7976+26A=)
c.7607+26A= (n.7607+26A=)
c.443+26A= (n.443+26A=)
c.7984+26A= (n.7984+26A=)
c.541+26A=
c.7880+26A= (n.7880+26A=)
13g.32362719A>CCA2082832520BRCA2c.7976+26A>C (n.7976+26A>C)
c.7607+26A>C (n.7607+26A>C)
c.443+26A>C (n.443+26A>C)
c.7984+26A>C (n.7984+26A>C)
c.541+26A>C
c.7880+26A>C (n.7880+26A>C)
 dbSNP
13g.32362720A>GCA2622572914BRCA2c.7976+27A>G (n.7976+27A>G)
c.7607+27A>G (n.7607+27A>G)
c.443+27A>G (n.443+27A>G)
c.7984+27A>G (n.7984+27A>G)
c.541+27A>G
c.7880+27A>G (n.7880+27A>G)
 gnomAD v4
13g.32362720A>TCA2727917698BRCA2c.7976+27A>T (n.7976+27A>T)
c.7607+27A>T (n.7607+27A>T)
c.443+27A>T (n.443+27A>T)
c.7984+27A>T (n.7984+27A>T)
c.541+27A>T
c.7880+27A>T (n.7880+27A>T)
 dbSNP
13g.32362722C>ACA2727917737BRCA2c.7976+29C>A (n.7976+29C>A)
c.7607+29C>A (n.7607+29C>A)
c.443+29C>A (n.443+29C>A)
c.7984+29C>A (n.7984+29C>A)
c.541+29C>A
c.7880+29C>A (n.7880+29C>A)
 dbSNP
13g.32362722C>GCA2727917736BRCA2c.7976+29C>G (n.7976+29C>G)
c.7607+29C>G (n.7607+29C>G)
c.443+29C>G (n.443+29C>G)
c.7984+29C>G (n.7984+29C>G)
c.541+29C>G
c.7880+29C>G (n.7880+29C>G)
 dbSNP
13g.32362722C>TCA2727917715BRCA2c.7976+29C>T (n.7976+29C>T)
c.7607+29C>T (n.7607+29C>T)
c.443+29C>T (n.443+29C>T)
c.7984+29C>T (n.7984+29C>T)
c.541+29C>T
c.7880+29C>T (n.7880+29C>T)
 dbSNP
13g.32362723A=CA2082832521BRCA2c.7976+30A= (n.7976+30A=)
c.7607+30A= (n.7607+30A=)
c.443+30A= (n.443+30A=)
c.7984+30A= (n.7984+30A=)
c.541+30A=
c.7880+30A= (n.7880+30A=)
13g.32362723A>GCA697355342BRCA2c.7976+30A>G (n.7976+30A>G)
c.7607+30A>G (n.7607+30A>G)
c.443+30A>G (n.443+30A>G)
c.7984+30A>G (n.7984+30A>G)
c.541+30A>G
c.7880+30A>G (n.7880+30A>G)
 dbSNP gnomAD v3 gnomAD v4
13g.32362724T>ACA2727917774BRCA2c.7976+31T>A (n.7976+31T>A)
c.7607+31T>A (n.7607+31T>A)
c.443+31T>A (n.443+31T>A)
c.7984+31T>A (n.7984+31T>A)
c.541+31T>A
c.7880+31T>A (n.7880+31T>A)
 dbSNP
13g.32362724T>CCA2727917752BRCA2c.7976+31T>C (n.7976+31T>C)
c.7607+31T>C (n.7607+31T>C)
c.443+31T>C (n.443+31T>C)
c.7984+31T>C (n.7984+31T>C)
c.541+31T>C
c.7880+31T>C (n.7880+31T>C)
 dbSNP
13g.32362726T>ACA2727874193BRCA2c.7976+33T>A (n.7976+33T>A)
c.7607+33T>A (n.7607+33T>A)
c.443+33T>A (n.443+33T>A)
c.7984+33T>A (n.7984+33T>A)
c.541+33T>A
c.7880+33T>A (n.7880+33T>A)
 dbSNP
13g.32362726T>CCA2082832525BRCA2c.7976+33T>C (n.7976+33T>C)
c.7607+33T>C (n.7607+33T>C)
c.443+33T>C (n.443+33T>C)
c.7984+33T>C (n.7984+33T>C)
c.541+33T>C
c.7880+33T>C (n.7880+33T>C)
 dbSNP
13g.32362726T>GCA2622572915BRCA2c.7976+33T>G (n.7976+33T>G)
c.7607+33T>G (n.7607+33T>G)
c.443+33T>G (n.443+33T>G)
c.7984+33T>G (n.7984+33T>G)
c.541+33T>G
c.7880+33T>G (n.7880+33T>G)
 gnomAD v4
13g.32362726T=CA2082832524BRCA2c.7976+33T= (n.7976+33T=)
c.7607+33T= (n.7607+33T=)
c.443+33T= (n.443+33T=)
c.7984+33T= (n.7984+33T=)
c.541+33T=
c.7880+33T= (n.7880+33T=)
13g.32362727A>TCA2727917777BRCA2c.7976+34A>T (n.7976+34A>T)
c.7607+34A>T (n.7607+34A>T)
c.443+34A>T (n.443+34A>T)
c.7984+34A>T (n.7984+34A>T)
c.541+34A>T
c.7880+34A>T (n.7880+34A>T)
 dbSNP
13g.32362728C>ACA6941170BRCA2c.7976+35C>A (n.7976+35C>A)
c.7607+35C>A (n.7607+35C>A)
c.443+35C>A (n.443+35C>A)
c.7984+35C>A (n.7984+35C>A)
c.541+35C>A
c.7880+35C>A (n.7880+35C>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362728C=CA2082832536BRCA2c.7976+35C= (n.7976+35C=)
c.7607+35C= (n.7607+35C=)
c.443+35C= (n.443+35C=)
c.7984+35C= (n.7984+35C=)
c.541+35C=
c.7880+35C= (n.7880+35C=)
13g.32362728C>GCA2727834943BRCA2c.7976+35C>G (n.7976+35C>G)
c.7607+35C>G (n.7607+35C>G)
c.443+35C>G (n.443+35C>G)
c.7984+35C>G (n.7984+35C>G)
c.541+35C>G
c.7880+35C>G (n.7880+35C>G)
 dbSNP
13g.32362728C>TCA6941171BRCA2c.7976+35C>T (n.7976+35C>T)
c.7607+35C>T (n.7607+35C>T)
c.443+35C>T (n.443+35C>T)
c.7984+35C>T (n.7984+35C>T)
c.541+35C>T
c.7880+35C>T (n.7880+35C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362729G>ACA247475401BRCA2c.7976+36G>A (n.7976+36G>A)
c.7607+36G>A (n.7607+36G>A)
c.443+36G>A (n.443+36G>A)
c.7984+36G>A (n.7984+36G>A)
c.541+36G>A
c.7880+36G>A (n.7880+36G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32362729G>CCA2727836145BRCA2c.7976+36G>C (n.7976+36G>C)
c.7607+36G>C (n.7607+36G>C)
c.443+36G>C (n.443+36G>C)
c.7984+36G>C (n.7984+36G>C)
c.541+36G>C
c.7880+36G>C (n.7880+36G>C)
 dbSNP
13g.32362729G=CA2082832545BRCA2c.7976+36G= (n.7976+36G=)
c.7607+36G= (n.7607+36G=)
c.443+36G= (n.443+36G=)
c.7984+36G= (n.7984+36G=)
c.541+36G=
c.7880+36G= (n.7880+36G=)
13g.32362730G>ACA609091815BRCA2c.7976+37G>A (n.7976+37G>A)
c.7607+37G>A (n.7607+37G>A)
c.443+37G>A (n.443+37G>A)
c.7984+37G>A (n.7984+37G>A)
c.541+37G>A
c.7880+37G>A (n.7880+37G>A)
 dbSNP gnomAD v2 gnomAD v4
13g.32362730G=CA2082832556BRCA2c.7976+37G= (n.7976+37G=)
c.7607+37G= (n.7607+37G=)
c.443+37G= (n.443+37G=)
c.7984+37G= (n.7984+37G=)
c.541+37G=
c.7880+37G= (n.7880+37G=)
13g.32362730G>TCA2622572916BRCA2c.7976+37G>T (n.7976+37G>T)
c.7607+37G>T (n.7607+37G>T)
c.443+37G>T (n.443+37G>T)
c.7984+37G>T (n.7984+37G>T)
c.541+37G>T
c.7880+37G>T (n.7880+37G>T)
 gnomAD v4
13g.32362730_32362734delCA2575388234BRCA2c.7976+37_7976+41del (n.7976+37_7976+41del)
c.7607+37_7607+41del (n.7607+37_7607+41del)
c.443+37_443+41del (n.443+37_443+41del)
c.7984+37_7984+41del (n.7984+37_7984+41del)
c.541+37_541+41del
c.7880+37_7880+41del (n.7880+37_7880+41del)
13g.32362731C>ACA2622572917BRCA2c.7976+38C>A (n.7976+38C>A)
c.7607+38C>A (n.7607+38C>A)
c.443+38C>A (n.443+38C>A)
c.7984+38C>A (n.7984+38C>A)
c.541+38C>A
c.7880+38C>A (n.7880+38C>A)
 dbSNP gnomAD v4
13g.32362731C>GCA2727917828BRCA2c.7976+38C>G (n.7976+38C>G)
c.7607+38C>G (n.7607+38C>G)
c.443+38C>G (n.443+38C>G)
c.7984+38C>G (n.7984+38C>G)
c.541+38C>G
c.7880+38C>G (n.7880+38C>G)
 dbSNP
13g.32362731C>TCA2727917839BRCA2c.7976+38C>T (n.7976+38C>T)
c.7607+38C>T (n.7607+38C>T)
c.443+38C>T (n.443+38C>T)
c.7984+38C>T (n.7984+38C>T)
c.541+38C>T
c.7880+38C>T (n.7880+38C>T)
 dbSNP
13g.32362732A>GCA2727917863BRCA2c.7976+39A>G (n.7976+39A>G)
c.7607+39A>G (n.7607+39A>G)
c.443+39A>G (n.443+39A>G)
c.7984+39A>G (n.7984+39A>G)
c.541+39A>G
c.7880+39A>G (n.7880+39A>G)
 dbSNP
13g.32362732A>TCA2727917840BRCA2c.7976+39A>T (n.7976+39A>T)
c.7607+39A>T (n.7607+39A>T)
c.443+39A>T (n.443+39A>T)
c.7984+39A>T (n.7984+39A>T)
c.541+39A>T
c.7880+39A>T (n.7880+39A>T)
 dbSNP
13g.32362733G>ACA2082832558BRCA2c.7976+40G>A (n.7976+40G>A)
c.7607+40G>A (n.7607+40G>A)
c.443+40G>A (n.443+40G>A)
c.7984+40G>A (n.7984+40G>A)
c.541+40G>A
c.7880+40G>A (n.7880+40G>A)
 dbSNP
13g.32362733G=CA2082832557BRCA2c.7976+40G= (n.7976+40G=)
c.7607+40G= (n.7607+40G=)
c.443+40G= (n.443+40G=)
c.7984+40G= (n.7984+40G=)
c.541+40G=
c.7880+40G= (n.7880+40G=)
13g.32362734T>ACA2727864197BRCA2c.7976+41T>A (n.7976+41T>A)
c.7607+41T>A (n.7607+41T>A)
c.443+41T>A (n.443+41T>A)
c.7984+41T>A (n.7984+41T>A)
c.541+41T>A
c.7880+41T>A (n.7880+41T>A)
 dbSNP
13g.32362734T>CCA609091816BRCA2c.7976+41T>C (n.7976+41T>C)
c.7607+41T>C (n.7607+41T>C)
c.443+41T>C (n.443+41T>C)
c.7984+41T>C (n.7984+41T>C)
c.541+41T>C
c.7880+41T>C (n.7880+41T>C)
 dbSNP gnomAD v2 gnomAD v4
13g.32362734T=CA2082832562BRCA2c.7976+41T= (n.7976+41T=)
c.7607+41T= (n.7607+41T=)
c.443+41T= (n.443+41T=)
c.7984+41T= (n.7984+41T=)
c.541+41T=
c.7880+41T= (n.7880+41T=)
13g.32362735A=CA2082832570BRCA2c.7976+42A= (n.7976+42A=)
c.7607+42A= (n.7607+42A=)
c.443+42A= (n.443+42A=)
c.7984+42A= (n.7984+42A=)
c.541+42A=
c.7880+42A= (n.7880+42A=)
13g.32362735A>GCA609091817BRCA2c.7976+42A>G (n.7976+42A>G)
c.7607+42A>G (n.7607+42A>G)
c.443+42A>G (n.443+42A>G)
c.7984+42A>G (n.7984+42A>G)
c.541+42A>G
c.7880+42A>G (n.7880+42A>G)
 dbSNP gnomAD v2 gnomAD v4
13g.32362735A>TCA2727855207BRCA2c.7976+42A>T (n.7976+42A>T)
c.7607+42A>T (n.7607+42A>T)
c.443+42A>T (n.443+42A>T)
c.7984+42A>T (n.7984+42A>T)
c.541+42A>T
c.7880+42A>T (n.7880+42A>T)
 dbSNP
13g.32362736T>ACA2558562514BRCA2c.7976+43T>A (n.7976+43T>A)
c.7607+43T>A (n.7607+43T>A)
c.443+43T>A (n.443+43T>A)
c.7984+43T>A (n.7984+43T>A)
c.541+43T>A
c.7880+43T>A (n.7880+43T>A)
13g.32362737G>ACA2622572918BRCA2c.7976+44G>A (n.7976+44G>A)
c.7607+44G>A (n.7607+44G>A)
c.443+44G>A (n.443+44G>A)
c.7984+44G>A (n.7984+44G>A)
c.541+44G>A
c.7880+44G>A (n.7880+44G>A)
 dbSNP gnomAD v4
13g.32362738G>CCA277582BRCA2c.7976+45G>C (n.7976+45G>C)
c.7607+45G>C (n.7607+45G>C)
c.443+45G>C (n.443+45G>C)
c.7984+45G>C (n.7984+45G>C)
c.541+45G>C
c.7880+45G>C (n.7880+45G>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362738G=CA2082832574BRCA2c.7976+45G= (n.7976+45G=)
c.7607+45G= (n.7607+45G=)
c.443+45G= (n.443+45G=)
c.7984+45G= (n.7984+45G=)
c.541+45G=
c.7880+45G= (n.7880+45G=)
13g.32362738G>TCA2798720276BRCA2c.7976+45G>T (n.7976+45G>T)
c.7607+45G>T (n.7607+45G>T)
c.443+45G>T (n.443+45G>T)
c.7984+45G>T (n.7984+45G>T)
c.541+45G>T
c.7880+45G>T (n.7880+45G>T)
13g.32362739T>ACA2727917893BRCA2c.7976+46T>A (n.7976+46T>A)
c.7607+46T>A (n.7607+46T>A)
c.443+46T>A (n.443+46T>A)
c.7984+46T>A (n.7984+46T>A)
c.541+46T>A
c.7880+46T>A (n.7880+46T>A)
 dbSNP
13g.32362740T>ACA2727917895BRCA2c.7976+47T>A (n.7976+47T>A)
c.7607+47T>A (n.7607+47T>A)
c.443+47T>A (n.443+47T>A)
c.7984+47T>A (n.7984+47T>A)
c.541+47T>A
c.7880+47T>A (n.7880+47T>A)
 dbSNP
13g.32362741A>TCA2529692393BRCA2c.7976+48A>T (n.7976+48A>T)
c.7607+48A>T (n.7607+48A>T)
c.443+48A>T (n.443+48A>T)
c.7984+48A>T (n.7984+48A>T)
c.541+48A>T
c.7880+48A>T (n.7880+48A>T)
13g.32362742A>GCA2622572919BRCA2c.7976+49A>G (n.7976+49A>G)
c.7607+49A>G (n.7607+49A>G)
c.443+49A>G (n.443+49A>G)
c.7984+49A>G (n.7984+49A>G)
c.541+49A>G
c.7880+49A>G (n.7880+49A>G)
 gnomAD v4
13g.32362743G>ACA609091821BRCA2c.7976+50G>A (n.7976+50G>A)
c.7607+50G>A (n.7607+50G>A)
c.443+50G>A (n.443+50G>A)
c.7984+50G>A (n.7984+50G>A)
c.541+50G>A
c.7880+50G>A (n.7880+50G>A)
 dbSNP gnomAD v2
13g.32362743G>CCA609091823BRCA2c.7976+50G>C (n.7976+50G>C)
c.7607+50G>C (n.7607+50G>C)
c.443+50G>C (n.443+50G>C)
c.7984+50G>C (n.7984+50G>C)
c.541+50G>C
c.7880+50G>C (n.7880+50G>C)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32362743G=CA2082832584BRCA2c.7976+50G= (n.7976+50G=)
c.7607+50G= (n.7607+50G=)
c.443+50G= (n.443+50G=)
c.7984+50G= (n.7984+50G=)
c.541+50G=
c.7880+50G= (n.7880+50G=)
13g.32362743G>TCA2727870104BRCA2c.7976+50G>T (n.7976+50G>T)
c.7607+50G>T (n.7607+50G>T)
c.443+50G>T (n.443+50G>T)
c.7984+50G>T (n.7984+50G>T)
c.541+50G>T
c.7880+50G>T (n.7880+50G>T)
 dbSNP
13g.32362744G>ACA2082832615BRCA2c.7976+51G>A (n.7976+51G>A)
c.7607+51G>A (n.7607+51G>A)
c.443+51G>A (n.443+51G>A)
c.7984+51G>A (n.7984+51G>A)
c.541+51G>A
c.7880+51G>A (n.7880+51G>A)
 dbSNP
13g.32362744G>CCA609091825BRCA2c.7976+51G>C (n.7976+51G>C)
c.7607+51G>C (n.7607+51G>C)
c.443+51G>C (n.443+51G>C)
c.7984+51G>C (n.7984+51G>C)
c.541+51G>C
c.7880+51G>C (n.7880+51G>C)
 dbSNP gnomAD v2 gnomAD v4
13g.32362744G=CA2082832611BRCA2c.7976+51G= (n.7976+51G=)
c.7607+51G= (n.7607+51G=)
c.443+51G= (n.443+51G=)
c.7984+51G= (n.7984+51G=)
c.541+51G=
c.7880+51G= (n.7880+51G=)
13g.32362744G>TCA6941172BRCA2c.7976+51G>T (n.7976+51G>T)
c.7607+51G>T (n.7607+51G>T)
c.443+51G>T (n.443+51G>T)
c.7984+51G>T (n.7984+51G>T)
c.541+51G>T
c.7880+51G>T (n.7880+51G>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.32362745T>CCA2526148053BRCA2c.7976+52T>C (n.7976+52T>C)
c.7607+52T>C (n.7607+52T>C)
c.443+52T>C (n.443+52T>C)
c.7984+52T>C (n.7984+52T>C)
c.541+52T>C
c.7880+52T>C (n.7880+52T>C)
13g.32362746T>ACA247475409BRCA2c.7976+53T>A (n.7976+53T>A)
c.7607+53T>A (n.7607+53T>A)
c.443+53T>A (n.443+53T>A)
c.7984+53T>A (n.7984+53T>A)
c.541+53T>A
c.7880+53T>A (n.7880+53T>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32362746T=CA2082832621BRCA2c.7976+53T= (n.7976+53T=)
c.7607+53T= (n.7607+53T=)
c.443+53T= (n.443+53T=)
c.7984+53T= (n.7984+53T=)
c.541+53T=
c.7880+53T= (n.7880+53T=)
13g.32362748C>GCA2727917913BRCA2c.7976+55C>G (n.7976+55C>G)
c.7607+55C>G (n.7607+55C>G)
c.443+55C>G (n.443+55C>G)
c.7984+55C>G (n.7984+55C>G)
c.541+55C>G
c.7880+55C>G (n.7880+55C>G)
 dbSNP
13g.32362748C>TCA2522096018BRCA2c.7976+55C>T (n.7976+55C>T)
c.7607+55C>T (n.7607+55C>T)
c.443+55C>T (n.443+55C>T)
c.7984+55C>T (n.7984+55C>T)
c.541+55C>T
c.7880+55C>T (n.7880+55C>T)
13g.32362750G>ACA2622572920BRCA2c.7976+57G>A (n.7976+57G>A)
c.7607+57G>A (n.7607+57G>A)
c.443+57G>A (n.443+57G>A)
c.7984+57G>A (n.7984+57G>A)
c.541+57G>A
c.7880+57G>A (n.7880+57G>A)
 dbSNP gnomAD v4
13g.32362750G>CCA247475411BRCA2c.7976+57G>C (n.7976+57G>C)
c.7607+57G>C (n.7607+57G>C)
c.443+57G>C (n.443+57G>C)
c.7984+57G>C (n.7984+57G>C)
c.541+57G>C
c.7880+57G>C (n.7880+57G>C)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32362750G=CA2082832624BRCA2c.7976+57G= (n.7976+57G=)
c.7607+57G= (n.7607+57G=)
c.443+57G= (n.443+57G=)
c.7984+57G= (n.7984+57G=)
c.541+57G=
c.7880+57G= (n.7880+57G=)
13g.32362751T>ACA2727917935BRCA2c.7976+58T>A (n.7976+58T>A)
c.7607+58T>A (n.7607+58T>A)
c.443+58T>A (n.443+58T>A)
c.7984+58T>A (n.7984+58T>A)
c.541+58T>A
c.7880+58T>A (n.7880+58T>A)
 dbSNP
13g.32362752G>ACA2082832637BRCA2c.7976+59G>A (n.7976+59G>A)
c.7607+59G>A (n.7607+59G>A)
c.443+59G>A (n.443+59G>A)
c.7984+59G>A (n.7984+59G>A)
c.541+59G>A
c.7880+59G>A (n.7880+59G>A)
 dbSNP gnomAD v4
13g.32362752G>CCA2727912856BRCA2c.7976+59G>C (n.7976+59G>C)
c.7607+59G>C (n.7607+59G>C)
c.443+59G>C (n.443+59G>C)
c.7984+59G>C (n.7984+59G>C)
c.541+59G>C
c.7880+59G>C (n.7880+59G>C)
 dbSNP
13g.32362752G=CA2082832630BRCA2c.7976+59G= (n.7976+59G=)
c.7607+59G= (n.7607+59G=)
c.443+59G= (n.443+59G=)
c.7984+59G= (n.7984+59G=)
c.541+59G=
c.7880+59G= (n.7880+59G=)
13g.32362753T>ACA2727917939BRCA2c.7976+60T>A (n.7976+60T>A)
c.7607+60T>A (n.7607+60T>A)
c.443+60T>A (n.443+60T>A)
c.7984+60T>A (n.7984+60T>A)
c.541+60T>A
c.7880+60T>A (n.7880+60T>A)
 dbSNP
13g.32362753T>CCA2508967095BRCA2c.7976+60T>C (n.7976+60T>C)
c.7607+60T>C (n.7607+60T>C)
c.443+60T>C (n.443+60T>C)
c.7984+60T>C (n.7984+60T>C)
c.541+60T>C
c.7880+60T>C (n.7880+60T>C)

Number of alleles fetched