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.32362524_32362624delCA913203499BRCA2c.7807_7907del (p.Ala2603CysfsTer4)
c.7438_7538del (p.Ala2480CysfsTer4)
c.274_374del (p.Ala92CysfsTer4)
c.7815_7915del (p.Leu2606AlafsTer?)
c.372_472del
n.7815_7915del
c.7711_7811del (p.Ala2571CysfsTer4)
13g.32362595_32362598dupCA10589455BRCA2c.7878_7881dup (p.Ile2628AspfsTer14)
c.7509_7512dup (p.Ile2505AspfsTer14)
c.345_348dup (p.Ile117AspfsTer14)
c.7886_7889dup (p.Tyr2631IlefsTer?)
c.443_446dup
n.7886_7889dup
c.7782_7785dup (p.Ile2596AspfsTer14)
 ClinVar dbSNP
13g.32362597T>ACA10579758BRCA2c.7880T>A (p.Ile2627Asn)
c.7511T>A (p.Ile2504Asn)
c.347T>A (p.Ile116Asn)
c.7888T>A (p.Ser2630Thr)
c.445T>A
n.7888T>A
c.7784T>A (p.Ile2595Asn)
 ClinVar dbSNP
13g.32362597T>CCA387747106BRCA2c.7880T>C (p.Ile2627Thr)
c.7511T>C (p.Ile2504Thr)
c.347T>C (p.Ile116Thr)
c.7888T>C (p.Ser2630Pro)
c.445T>C
n.7888T>C
c.7784T>C (p.Ile2595Thr)
13g.32362597T>GCA387747107BRCA2c.7880T>G (p.Ile2627Ser)
c.7511T>G (p.Ile2504Ser)
c.347T>G (p.Ile116Ser)
c.7888T>G (p.Ser2630Ala)
c.445T>G
n.7888T>G
c.7784T>G (p.Ile2595Ser)
 ClinVar dbSNP
13g.32362597T=CA2082831148BRCA2c.7880T= (p.Ile2627=)
c.7511T= (p.Ile2504=)
c.347T= (p.Ile116=)
c.7888T= (p.Ser2630=)
c.445T=
n.7888T=
c.7784T= (p.Ile2595=)
13g.32362598C>ACA483260915BRCA2c.7881C>A (p.Ile2627=)
c.7512C>A (p.Ile2504=)
c.348C>A (p.Ile116=)
c.7889C>A (p.Ser2630Ter)
c.446C>A
n.7889C>A
c.7785C>A (p.Ile2595=)
 ClinVar dbSNP gnomAD v4
13g.32362598C=CA2082831160BRCA2c.7881C= (p.Ile2627=)
c.7512C= (p.Ile2504=)
c.348C= (p.Ile116=)
c.7889C= (p.Ser2630=)
c.446C=
n.7889C=
c.7785C= (p.Ile2595=)
13g.32362598C>GCA387747108BRCA2c.7881C>G (p.Ile2627Met)
c.7512C>G (p.Ile2504Met)
c.348C>G (p.Ile116Met)
c.7889C>G (p.Ser2630Ter)
c.446C>G
n.7889C>G
c.7785C>G (p.Ile2595Met)
 dbSNP
13g.32362598C>TCA483260916BRCA2c.7881C>T (p.Ile2627=)
c.7512C>T (p.Ile2504=)
c.348C>T (p.Ile116=)
c.7889C>T (p.Ser2630Leu)
c.446C>T
n.7889C>T
c.7785C>T (p.Ile2595=)
 dbSNP
13g.32362599A=CA2082831167BRCA2c.7882A= (p.Ile2628=)
c.7513A= (p.Ile2505=)
c.349A= (p.Ile117=)
c.7890A= (p.Ser2630=)
c.447A=
n.7890A=
c.7786A= (p.Ile2596=)
13g.32362599A>CCA387747109BRCA2c.7882A>C (p.Ile2628Leu)
c.7513A>C (p.Ile2505Leu)
c.349A>C (p.Ile117Leu)
c.7890A>C (p.Ser2630=)
c.447A>C
n.7890A>C
c.7786A>C (p.Ile2596Leu)
13g.32362599A>GCA387747110BRCA2c.7882A>G (p.Ile2628Val)
c.7513A>G (p.Ile2505Val)
c.349A>G (p.Ile117Val)
c.7890A>G (p.Ser2630=)
c.447A>G
n.7890A>G
c.7786A>G (p.Ile2596Val)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32362599A>TCA387747111BRCA2c.7882A>T (p.Ile2628Leu)
c.7513A>T (p.Ile2505Leu)
c.349A>T (p.Ile117Leu)
c.7890A>T (p.Ser2630=)
c.447A>T
n.7890A>T
c.7786A>T (p.Ile2596Leu)
 ClinVar dbSNP
13g.32362600T>ACA387747112BRCA2c.7883T>A (p.Ile2628Lys)
c.7514T>A (p.Ile2505Lys)
c.350T>A (p.Ile117Lys)
c.7891T>A (p.Tyr2631Asn)
c.448T>A
n.7891T>A
c.7787T>A (p.Ile2596Lys)
 dbSNP
13g.32362600T>CCA10586080BRCA2c.7883T>C (p.Ile2628Thr)
c.7514T>C (p.Ile2505Thr)
c.350T>C (p.Ile117Thr)
c.7891T>C (p.Tyr2631His)
c.448T>C
n.7891T>C
c.7787T>C (p.Ile2596Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32362600T>GCA387747113BRCA2c.7883T>G (p.Ile2628Arg)
c.7514T>G (p.Ile2505Arg)
c.350T>G (p.Ile117Arg)
c.7891T>G (p.Tyr2631Asp)
c.448T>G
n.7891T>G
c.7787T>G (p.Ile2596Arg)
13g.32362600T=CA2082831174BRCA2c.7883T= (p.Ile2628=)
c.7514T= (p.Ile2505=)
c.350T= (p.Ile117=)
c.7891T= (p.Tyr2631=)
c.448T=
n.7891T=
c.7787T= (p.Ile2596=)
13g.32362601A=CA2082831184BRCA2c.7884A= (p.Ile2628=)
c.7515A= (p.Ile2505=)
c.351A= (p.Ile117=)
c.7892A= (p.Tyr2631=)
c.449A=
n.7892A=
c.7788A= (p.Ile2596=)
13g.32362601A>CCA483260917BRCA2c.7884A>C (p.Ile2628=)
c.7515A>C (p.Ile2505=)
c.351A>C (p.Ile117=)
c.7892A>C (p.Tyr2631Ser)
c.449A>C
n.7892A>C
c.7788A>C (p.Ile2596=)
13g.32362601A>GCA6941162BRCA2c.7884A>G (p.Ile2628Met)
c.7515A>G (p.Ile2505Met)
c.351A>G (p.Ile117Met)
c.7892A>G (p.Tyr2631Cys)
c.449A>G
n.7892A>G
c.7788A>G (p.Ile2596Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362601A>TCA483260922BRCA2c.7884A>T (p.Ile2628=)
c.7515A>T (p.Ile2505=)
c.351A>T (p.Ile117=)
c.7892A>T (p.Tyr2631Phe)
c.449A>T
n.7892A>T
c.7788A>T (p.Ile2596=)
 ClinVar dbSNP
13g.32362601dupCA025322BRCA2c.7884dup (p.Trp2629MetfsTer12)
c.7515dup (p.Trp2506MetfsTer12)
c.351dup (p.Trp118MetfsTer12)
c.7892dup (p.Tyr2631Ter)
c.449dup
n.7892dup
c.7788dup (p.Trp2597MetfsTer12)
 ClinVar dbSNP gnomAD v4
13g.32362602T>ACA387747116BRCA2c.7885T>A (p.Trp2629Arg)
c.7516T>A (p.Trp2506Arg)
c.352T>A (p.Trp118Arg)
c.7893T>A (p.Tyr2631Ter)
c.450T>A
n.7893T>A
c.7789T>A (p.Trp2597Arg)
13g.32362602T>CCA387747114BRCA2c.7885T>C (p.Trp2629Arg)
c.7516T>C (p.Trp2506Arg)
c.352T>C (p.Trp118Arg)
c.7893T>C (p.Tyr2631=)
c.450T>C
n.7893T>C
c.7789T>C (p.Trp2597Arg)
 ClinVar
13g.32362602T>GCA387747115BRCA2c.7885T>G (p.Trp2629Gly)
c.7516T>G (p.Trp2506Gly)
c.352T>G (p.Trp118Gly)
c.7893T>G (p.Tyr2631Ter)
c.450T>G
n.7893T>G
c.7789T>G (p.Trp2597Gly)
13g.32362603G>ACA025323BRCA2c.7886G>A (p.Trp2629Ter)
c.7517G>A (p.Trp2506Ter)
c.353G>A (p.Trp118Ter)
c.7894G>A (p.Gly2632Arg)
c.451G>A
n.7894G>A
c.7790G>A (p.Trp2597Ter)
 ClinVar dbSNP gnomAD v4
13g.32362603G>CCA387747117BRCA2c.7886G>C (p.Trp2629Ser)
c.7517G>C (p.Trp2506Ser)
c.353G>C (p.Trp118Ser)
c.7894G>C (p.Gly2632Arg)
c.451G>C
n.7894G>C
c.7790G>C (p.Trp2597Ser)
 dbSNP
13g.32362603G=CA2082831197BRCA2c.7886G= (p.Trp2629=)
c.7517G= (p.Trp2506=)
c.353G= (p.Trp118=)
c.7894G= (p.Gly2632=)
c.451G=
n.7894G=
c.7790G= (p.Trp2597=)
13g.32362603G>TCA387747118BRCA2c.7886G>T (p.Trp2629Leu)
c.7517G>T (p.Trp2506Leu)
c.353G>T (p.Trp118Leu)
c.7894G>T (p.Gly2632Ter)
c.451G>T
n.7894G>T
c.7790G>T (p.Trp2597Leu)
13g.32362603_32362614delCA2499222313BRCA2c.7886_7897del (p.Trp2629_Ala2633delinsSer)
c.7517_7528del (p.Trp2506_Ala2510delinsSer)
c.353_364del (p.Trp118_Ala122delinsSer)
c.7894_7905del (p.Gly2632_Gln2635del)
c.451_462del
n.7894_7905del
c.7790_7801del (p.Trp2597_Ala2601delinsSer)
 ClinVar dbSNP
13g.32362604G>ACA10589456BRCA2c.7887G>A (p.Trp2629Ter)
c.7518G>A (p.Trp2506Ter)
c.354G>A (p.Trp118Ter)
c.7895G>A (p.Gly2632Glu)
c.452G>A
n.7895G>A
c.7791G>A (p.Trp2597Ter)
 ClinVar dbSNP
13g.32362604G>CCA387747119BRCA2c.7887G>C (p.Trp2629Cys)
c.7518G>C (p.Trp2506Cys)
c.354G>C (p.Trp118Cys)
c.7895G>C (p.Gly2632Ala)
c.452G>C
n.7895G>C
c.7791G>C (p.Trp2597Cys)
 dbSNP
13g.32362604G=CA2082831212BRCA2c.7887G= (p.Trp2629=)
c.7518G= (p.Trp2506=)
c.354G= (p.Trp118=)
c.7895G= (p.Gly2632=)
c.452G=
n.7895G=
c.7791G= (p.Trp2597=)
13g.32362604G>TCA387747120BRCA2c.7887G>T (p.Trp2629Cys)
c.7518G>T (p.Trp2506Cys)
c.354G>T (p.Trp118Cys)
c.7895G>T (p.Gly2632Val)
c.452G>T
n.7895G>T
c.7791G>T (p.Trp2597Cys)
 ClinVar dbSNP
13g.32362605A=CA2082831225BRCA2c.7888A= (p.Lys2630=)
c.7519A= (p.Lys2507=)
c.355A= (p.Lys119=)
c.7896A= (p.Gly2632=)
c.453A=
n.7896A=
c.7792A= (p.Lys2598=)
13g.32362605A>CCA387747122BRCA2c.7888A>C (p.Lys2630Gln)
c.7519A>C (p.Lys2507Gln)
c.355A>C (p.Lys119Gln)
c.7896A>C (p.Gly2632=)
c.453A>C
n.7896A>C
c.7792A>C (p.Lys2598Gln)
 ClinVar dbSNP
13g.32362605A>GCA387747123BRCA2c.7888A>G (p.Lys2630Glu)
c.7519A>G (p.Lys2507Glu)
c.355A>G (p.Lys119Glu)
c.7896A>G (p.Gly2632=)
c.453A>G
n.7896A>G
c.7792A>G (p.Lys2598Glu)
 ClinVar dbSNP
13g.32362605A>TCA387747121BRCA2c.7888A>T (p.Lys2630Ter)
c.7519A>T (p.Lys2507Ter)
c.355A>T (p.Lys119Ter)
c.7896A>T (p.Gly2632=)
c.453A>T
n.7896A>T
c.7792A>T (p.Lys2598Ter)
13g.32362606_32362607dupCA025324BRCA2c.7889_7890dup (p.Leu2631AsnfsTer18)
c.7520_7521dup (p.Leu2508AsnfsTer18)
c.356_357dup (p.Leu120AsnfsTer18)
c.7897_7898dup (p.Asn2633LysfsTer11)
c.454_455dup
n.7897_7898dup
c.7793_7794dup (p.Leu2599AsnfsTer18)
 ClinVar dbSNP
13g.32362606A>CCA387747124BRCA2c.7889A>C (p.Lys2630Thr)
c.7520A>C (p.Lys2507Thr)
c.356A>C (p.Lys119Thr)
c.7897A>C (p.Asn2633His)
c.454A>C
n.7897A>C
c.7793A>C (p.Lys2598Thr)
13g.32362606A>GCA387747125BRCA2c.7889A>G (p.Lys2630Arg)
c.7520A>G (p.Lys2507Arg)
c.356A>G (p.Lys119Arg)
c.7897A>G (p.Asn2633Asp)
c.454A>G
n.7897A>G
c.7793A>G (p.Lys2598Arg)
 gnomAD v4 COSMIC COSMIC
13g.32362606A>TCA387747126BRCA2c.7889A>T (p.Lys2630Ile)
c.7520A>T (p.Lys2507Ile)
c.356A>T (p.Lys119Ile)
c.7897A>T (p.Asn2633Tyr)
c.454A>T
n.7897A>T
c.7793A>T (p.Lys2598Ile)
 dbSNP
13g.32362607A=CA2082831253BRCA2c.7890A= (p.Lys2630=)
c.7521A= (p.Lys2507=)
c.357A= (p.Lys119=)
c.7898A= (p.Asn2633=)
c.455A=
n.7898A=
c.7794A= (p.Lys2598=)
13g.32362607A>CCA387747127BRCA2c.7890A>C (p.Lys2630Asn)
c.7521A>C (p.Lys2507Asn)
c.357A>C (p.Lys119Asn)
c.7898A>C (p.Asn2633Thr)
c.455A>C
n.7898A>C
c.7794A>C (p.Lys2598Asn)
 dbSNP
13g.32362607A>GCA483260928BRCA2c.7890A>G (p.Lys2630=)
c.7521A>G (p.Lys2507=)
c.357A>G (p.Lys119=)
c.7898A>G (p.Asn2633Ser)
c.455A>G
n.7898A>G
c.7794A>G (p.Lys2598=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32362607A>TCA387747128BRCA2c.7890A>T (p.Lys2630Asn)
c.7521A>T (p.Lys2507Asn)
c.357A>T (p.Lys119Asn)
c.7898A>T (p.Asn2633Ile)
c.455A>T
n.7898A>T
c.7794A>T (p.Lys2598Asn)
 dbSNP
13g.32362608C>ACA10579759BRCA2c.7891C>A (p.Leu2631Met)
c.7522C>A (p.Leu2508Met)
c.358C>A (p.Leu120Met)
c.7899C>A (p.Asn2633Lys)
c.456C>A
n.7899C>A
c.7795C>A (p.Leu2599Met)
 ClinVar dbSNP
13g.32362608C=CA2082831278BRCA2c.7891C= (p.Leu2631=)
c.7522C= (p.Leu2508=)
c.358C= (p.Leu120=)
c.7899C= (p.Asn2633=)
c.456C=
n.7899C=
c.7795C= (p.Leu2599=)
13g.32362608C>GCA387747129BRCA2c.7891C>G (p.Leu2631Val)
c.7522C>G (p.Leu2508Val)
c.358C>G (p.Leu120Val)
c.7899C>G (p.Asn2633Lys)
c.456C>G
n.7899C>G
c.7795C>G (p.Leu2599Val)
 dbSNP
13g.32362608C>TCA483260929BRCA2c.7891C>T (p.Leu2631=)
c.7522C>T (p.Leu2508=)
c.358C>T (p.Leu120=)
c.7899C>T (p.Asn2633=)
c.456C>T
n.7899C>T
c.7795C>T (p.Leu2599=)
 ClinVar dbSNP
13g.32362609T>ACA387747132BRCA2c.7892T>A (p.Leu2631Gln)
c.7523T>A (p.Leu2508Gln)
c.359T>A (p.Leu120Gln)
c.7900T>A (p.Trp2634Arg)
c.457T>A
n.7900T>A
c.7796T>A (p.Leu2599Gln)
13g.32362609T>CCA387747130BRCA2c.7892T>C (p.Leu2631Pro)
c.7523T>C (p.Leu2508Pro)
c.359T>C (p.Leu120Pro)
c.7900T>C (p.Trp2634Arg)
c.457T>C
n.7900T>C
c.7796T>C (p.Leu2599Pro)
 ClinVar dbSNP gnomAD v4
13g.32362609T>GCA387747131BRCA2c.7892T>G (p.Leu2631Arg)
c.7523T>G (p.Leu2508Arg)
c.359T>G (p.Leu120Arg)
c.7900T>G (p.Trp2634Gly)
c.457T>G
n.7900T>G
c.7796T>G (p.Leu2599Arg)
 ClinVar dbSNP
13g.32362609T=CA2082831296BRCA2c.7892T= (p.Leu2631=)
c.7523T= (p.Leu2508=)
c.359T= (p.Leu120=)
c.7900T= (p.Trp2634=)
c.457T=
n.7900T=
c.7796T= (p.Leu2599=)
13g.32362610G>ACA483260932BRCA2c.7893G>A (p.Leu2631=)
c.7524G>A (p.Leu2508=)
c.360G>A (p.Leu120=)
c.7901G>A (p.Trp2634Ter)
c.458G>A
n.7901G>A
c.7797G>A (p.Leu2599=)
 dbSNP
13g.32362610G>CCA483260933BRCA2c.7893G>C (p.Leu2631=)
c.7524G>C (p.Leu2508=)
c.360G>C (p.Leu120=)
c.7901G>C (p.Trp2634Ser)
c.458G>C
n.7901G>C
c.7797G>C (p.Leu2599=)
 dbSNP COSMIC COSMIC
13g.32362610G>TCA483260934BRCA2c.7893G>T (p.Leu2631=)
c.7524G>T (p.Leu2508=)
c.360G>T (p.Leu120=)
c.7901G>T (p.Trp2634Leu)
c.458G>T
n.7901G>T
c.7797G>T (p.Leu2599=)
 dbSNP
13g.32362611G>ACA387747133BRCA2c.7894G>A (p.Ala2632Thr)
c.7525G>A (p.Ala2509Thr)
c.361G>A (p.Ala121Thr)
c.7902G>A (p.Trp2634Ter)
c.459G>A
n.7902G>A
c.7798G>A (p.Ala2600Thr)
 ClinVar dbSNP gnomAD v4
13g.32362611G>CCA387747134BRCA2c.7894G>C (p.Ala2632Pro)
c.7525G>C (p.Ala2509Pro)
c.361G>C (p.Ala121Pro)
c.7902G>C (p.Trp2634Cys)
c.459G>C
n.7902G>C
c.7798G>C (p.Ala2600Pro)
 dbSNP
13g.32362611G=CA2082831308BRCA2c.7894G= (p.Ala2632=)
c.7525G= (p.Ala2509=)
c.361G= (p.Ala121=)
c.7902G= (p.Trp2634=)
c.459G=
n.7902G=
c.7798G= (p.Ala2600=)
13g.32362611G>TCA387747135BRCA2c.7894G>T (p.Ala2632Ser)
c.7525G>T (p.Ala2509Ser)
c.361G>T (p.Ala121Ser)
c.7902G>T (p.Trp2634Cys)
c.459G>T
n.7902G>T
c.7798G>T (p.Ala2600Ser)
 dbSNP COSMIC COSMIC
13g.32362612delCA2695217943BRCA2c.7895del (p.Ala2632GlufsTer16)
c.7526del (p.Ala2509GlufsTer16)
c.362del (p.Ala121GlufsTer16)
c.7903del (p.Gln2635SerfsTer8)
c.460del
n.7903del
c.7799del (p.Ala2600GlufsTer16)
13g.32362612C>ACA387747136BRCA2c.7895C>A (p.Ala2632Glu)
c.7526C>A (p.Ala2509Glu)
c.362C>A (p.Ala121Glu)
c.7903C>A (p.Gln2635Lys)
c.460C>A
n.7903C>A
c.7799C>A (p.Ala2600Glu)
 dbSNP
13g.32362612C=CA2082831317BRCA2c.7895C= (p.Ala2632=)
c.7526C= (p.Ala2509=)
c.362C= (p.Ala121=)
c.7903C= (p.Gln2635=)
c.460C=
n.7903C=
c.7799C= (p.Ala2600=)
13g.32362612C>GCA247475168BRCA2c.7895C>G (p.Ala2632Gly)
c.7526C>G (p.Ala2509Gly)
c.362C>G (p.Ala121Gly)
c.7903C>G (p.Gln2635Glu)
c.460C>G
n.7903C>G
c.7799C>G (p.Ala2600Gly)
 ClinVar dbSNP
13g.32362612C>TCA387747137BRCA2c.7895C>T (p.Ala2632Val)
c.7526C>T (p.Ala2509Val)
c.362C>T (p.Ala121Val)
c.7903C>T (p.Gln2635Ter)
c.460C>T
n.7903C>T
c.7799C>T (p.Ala2600Val)
 ClinVar dbSNP gnomAD v4
13g.32362612dupCA2573149359BRCA2c.7895dup (p.Ala2633SerfsTer8)
c.7526dup (p.Ala2510SerfsTer8)
c.362dup (p.Ala122SerfsTer8)
c.7903dup (p.Gln2635ProfsTer?)
c.460dup
n.7903dup
c.7799dup (p.Ala2601SerfsTer8)
 ClinVar dbSNP
13g.32362613A>CCA483260936BRCA2c.7896A>C (p.Ala2632=)
c.7527A>C (p.Ala2509=)
c.363A>C (p.Ala121=)
c.7904A>C (p.Gln2635Pro)
c.461A>C
n.7904A>C
c.7800A>C (p.Ala2600=)
13g.32362613A>GCA483260937BRCA2c.7896A>G (p.Ala2632=)
c.7527A>G (p.Ala2509=)
c.363A>G (p.Ala121=)
c.7904A>G (p.Gln2635Arg)
c.461A>G
n.7904A>G
c.7800A>G (p.Ala2600=)
 dbSNP
13g.32362613A>TCA483260938BRCA2c.7896A>T (p.Ala2632=)
c.7527A>T (p.Ala2509=)
c.363A>T (p.Ala121=)
c.7904A>T (p.Gln2635Leu)
c.461A>T
n.7904A>T
c.7800A>T (p.Ala2600=)
 dbSNP gnomAD v4
13g.32362614G>ACA387747138BRCA2c.7897G>A (p.Ala2633Thr)
c.7528G>A (p.Ala2510Thr)
c.364G>A (p.Ala122Thr)
c.7905G>A (p.Gln2635=)
c.462G>A
n.7905G>A
c.7801G>A (p.Ala2601Thr)
 dbSNP
13g.32362614G>CCA387747139BRCA2c.7897G>C (p.Ala2633Pro)
c.7528G>C (p.Ala2510Pro)
c.364G>C (p.Ala122Pro)
c.7905G>C (p.Gln2635His)
c.462G>C
n.7905G>C
c.7801G>C (p.Ala2601Pro)
 dbSNP
13g.32362614G=CA2082831329BRCA2c.7897G= (p.Ala2633=)
c.7528G= (p.Ala2510=)
c.364G= (p.Ala122=)
c.7905G= (p.Gln2635=)
c.462G=
n.7905G=
c.7801G= (p.Ala2601=)
13g.32362614G>TCA025325BRCA2c.7897G>T (p.Ala2633Ser)
c.7528G>T (p.Ala2510Ser)
c.364G>T (p.Ala122Ser)
c.7905G>T (p.Gln2635His)
c.462G>T
n.7905G>T
c.7801G>T (p.Ala2601Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32362615C>ACA387747140BRCA2c.7898C>A (p.Ala2633Asp)
c.7529C>A (p.Ala2510Asp)
c.365C>A (p.Ala122Asp)
c.7906C>A (p.Leu2636Ile)
c.463C>A
n.7906C>A
c.7802C>A (p.Ala2601Asp)
 dbSNP
13g.32362615C=CA2082831341BRCA2c.7898C= (p.Ala2633=)
c.7529C= (p.Ala2510=)
c.365C= (p.Ala122=)
c.7906C= (p.Leu2636=)
c.463C=
n.7906C=
c.7802C= (p.Ala2601=)
13g.32362615C>GCA387747142BRCA2c.7898C>G (p.Ala2633Gly)
c.7529C>G (p.Ala2510Gly)
c.365C>G (p.Ala122Gly)
c.7906C>G (p.Leu2636Val)
c.463C>G
n.7906C>G
c.7802C>G (p.Ala2601Gly)
 ClinVar dbSNP gnomAD v4
13g.32362615C>TCA387747141BRCA2c.7898C>T (p.Ala2633Val)
c.7529C>T (p.Ala2510Val)
c.365C>T (p.Ala122Val)
c.7906C>T (p.Leu2636=)
c.463C>T
n.7906C>T
c.7802C>T (p.Ala2601Val)
 ClinVar dbSNP
13g.32362618_32362635delCA2573149360BRCA2c.7901_7918del (p.Met2634_Pro2639del)
c.7532_7549del (p.Met2511_Pro2516del)
c.368_385del (p.Met123_Pro128del)
c.7909_7926del (p.Trp2637_Leu2642del)
c.466_483del
n.7909_7926del
c.7805_7822del (p.Met2602_Pro2607del)
 ClinVar dbSNP
13g.32362616T>ACA483260940BRCA2c.7899T>A (p.Ala2633=)
c.7530T>A (p.Ala2510=)
c.366T>A (p.Ala122=)
c.7907T>A (p.Leu2636Gln)
c.464T>A
n.7907T>A
c.7803T>A (p.Ala2601=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32362616T>CCA483260941BRCA2c.7899T>C (p.Ala2633=)
c.7530T>C (p.Ala2510=)
c.366T>C (p.Ala122=)
c.7907T>C (p.Leu2636Pro)
c.464T>C
n.7907T>C
c.7803T>C (p.Ala2601=)
 dbSNP
13g.32362616T>GCA483260939BRCA2c.7899T>G (p.Ala2633=)
c.7530T>G (p.Ala2510=)
c.366T>G (p.Ala122=)
c.7907T>G (p.Leu2636Arg)
c.464T>G
n.7907T>G
c.7803T>G (p.Ala2601=)
 ClinVar dbSNP
13g.32362616T=CA2082831357BRCA2c.7899T= (p.Ala2633=)
c.7530T= (p.Ala2510=)
c.366T= (p.Ala122=)
c.7907T= (p.Leu2636=)
c.464T=
n.7907T=
c.7803T= (p.Ala2601=)
13g.32362616_32362617delinsTACA2082831360BRCA2c.7899_7900delinsTA (p.Ala2633=)
c.7530_7531delinsTA (p.Ala2510=)
c.366_367delinsTA (p.Ala122=)
c.7907_7908delinsTA (p.Leu2636=)
c.464_465delinsTA
n.7907_7908delinsTA
c.7803_7804delinsTA (p.Ala2601=)
13g.32362617delCA658761192BRCA2c.7900del (p.Met2634TrpfsTer14)
c.7531del (p.Met2511TrpfsTer14)
c.367del (p.Met123TrpfsTer14)
c.7908del (p.Trp2637GlyfsTer6)
c.465del
n.7908del
c.7804del (p.Met2602TrpfsTer14)
 ClinVar dbSNP
13g.32362617A=CA2082831368BRCA2c.7900A= (p.Met2634=)
c.7531A= (p.Met2511=)
c.367A= (p.Met123=)
c.7908A= (p.Leu2636=)
c.465A=
n.7908A=
c.7804A= (p.Met2602=)
13g.32362617A>CCA387747143BRCA2c.7900A>C (p.Met2634Leu)
c.7531A>C (p.Met2511Leu)
c.367A>C (p.Met123Leu)
c.7908A>C (p.Leu2636=)
c.465A>C
n.7908A>C
c.7804A>C (p.Met2602Leu)
13g.32362617A>GCA387747144BRCA2c.7900A>G (p.Met2634Val)
c.7531A>G (p.Met2511Val)
c.367A>G (p.Met123Val)
c.7908A>G (p.Leu2636=)
c.465A>G
n.7908A>G
c.7804A>G (p.Met2602Val)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32362617A>TCA387747145BRCA2c.7900A>T (p.Met2634Leu)
c.7531A>T (p.Met2511Leu)
c.367A>T (p.Met123Leu)
c.7908A>T (p.Leu2636=)
c.465A>T
n.7908A>T
c.7804A>T (p.Met2602Leu)
 dbSNP
13g.32362618T>ACA387747146BRCA2c.7901T>A (p.Met2634Lys)
c.7532T>A (p.Met2511Lys)
c.368T>A (p.Met123Lys)
c.7909T>A (p.Trp2637Arg)
c.466T>A
n.7909T>A
c.7805T>A (p.Met2602Lys)
 ClinVar dbSNP gnomAD v2
13g.32362618T>CCA025326BRCA2c.7901T>C (p.Met2634Thr)
c.7532T>C (p.Met2511Thr)
c.368T>C (p.Met123Thr)
c.7909T>C (p.Trp2637Arg)
c.466T>C
n.7909T>C
c.7805T>C (p.Met2602Thr)
 ClinVar dbSNP
13g.32362618T>GCA387747147BRCA2c.7901T>G (p.Met2634Arg)
c.7532T>G (p.Met2511Arg)
c.368T>G (p.Met123Arg)
c.7909T>G (p.Trp2637Gly)
c.466T>G
n.7909T>G
c.7805T>G (p.Met2602Arg)
13g.32362618T=CA2082831390BRCA2c.7901T= (p.Met2634=)
c.7532T= (p.Met2511=)
c.368T= (p.Met123=)
c.7909T= (p.Trp2637=)
c.466T=
n.7909T=
c.7805T= (p.Met2602=)
13g.32362618_32362619delCA1139770834BRCA2c.7901_7902del (p.Met2634ArgfsTer6)
c.7532_7533del (p.Met2511ArgfsTer6)
c.368_369del (p.Met123ArgfsTer6)
c.7909_7910del (p.Trp2637GlufsTer?)
c.466_467del
n.7909_7910del
c.7805_7806del (p.Met2602ArgfsTer6)
13g.32362619G>ACA387747148BRCA2c.7902G>A (p.Met2634Ile)
c.7533G>A (p.Met2511Ile)
c.369G>A (p.Met123Ile)
c.7910G>A (p.Trp2637Ter)
c.467G>A
n.7910G>A
c.7806G>A (p.Met2602Ile)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32362619G>CCA387747149BRCA2c.7902G>C (p.Met2634Ile)
c.7533G>C (p.Met2511Ile)
c.369G>C (p.Met123Ile)
c.7910G>C (p.Trp2637Ser)
c.467G>C
n.7910G>C
c.7806G>C (p.Met2602Ile)
 dbSNP
13g.32362619G=CA2082831402BRCA2c.7902G= (p.Met2634=)
c.7533G= (p.Met2511=)
c.369G= (p.Met123=)
c.7910G= (p.Trp2637=)
c.467G=
n.7910G=
c.7806G= (p.Met2602=)
13g.32362619G>TCA387747150BRCA2c.7902G>T (p.Met2634Ile)
c.7533G>T (p.Met2511Ile)
c.369G>T (p.Met123Ile)
c.7910G>T (p.Trp2637Leu)
c.467G>T
n.7910G>T
c.7806G>T (p.Met2602Ile)
13g.32362619_32362620delinsGGCA2082831407BRCA2c.7902_7903delinsGG (p.Met2634=)
c.7533_7534delinsGG (p.Met2511=)
c.369_370delinsGG (p.Met123=)
c.7910_7911delinsGG (p.Trp2637=)
c.467_468delinsGG
n.7910_7911delinsGG
c.7806_7807delinsGG (p.Met2602=)
13g.32362619_32362620delinsTTCA915946882BRCA2c.7902_7903delinsTT (p.Met2634IlefsTer2)
c.7533_7534delinsTT (p.Met2511IlefsTer2)
c.369_370delinsTT (p.Met123IlefsTer2)
c.7910_7911delinsTT (p.Trp2637Phe)
c.467_468delinsTT
n.7910_7911delinsTT
c.7806_7807delinsTT (p.Met2602IlefsTer2)
 ClinVar dbSNP
13g.32362620G>ACA387747151BRCA2c.7903G>A (p.Glu2635Lys)
c.7534G>A (p.Glu2512Lys)
c.370G>A (p.Glu124Lys)
c.7911G>A (p.Trp2637Ter)
c.468G>A
n.7911G>A
c.7807G>A (p.Glu2603Lys)
 ClinVar dbSNP
13g.32362620G>CCA387747152BRCA2c.7903G>C (p.Glu2635Gln)
c.7534G>C (p.Glu2512Gln)
c.370G>C (p.Glu124Gln)
c.7911G>C (p.Trp2637Cys)
c.468G>C
n.7911G>C
c.7807G>C (p.Glu2603Gln)
 dbSNP gnomAD v4
13g.32362620G>TCA387747153BRCA2c.7903G>T (p.Glu2635Ter)
c.7534G>T (p.Glu2512Ter)
c.370G>T (p.Glu124Ter)
c.7911G>T (p.Trp2637Cys)
c.468G>T
n.7911G>T
c.7807G>T (p.Glu2603Ter)
 ClinVar dbSNP
13g.32362621A>CCA387747156BRCA2c.7904A>C (p.Glu2635Ala)
c.7535A>C (p.Glu2512Ala)
c.371A>C (p.Glu124Ala)
c.7912A>C (p.Asn2638His)
c.469A>C
n.7912A>C
c.7808A>C (p.Glu2603Ala)
13g.32362621A>GCA387747154BRCA2c.7904A>G (p.Glu2635Gly)
c.7535A>G (p.Glu2512Gly)
c.371A>G (p.Glu124Gly)
c.7912A>G (p.Asn2638Asp)
c.469A>G
n.7912A>G
c.7808A>G (p.Glu2603Gly)
 COSMIC COSMIC
13g.32362621A>TCA387747155BRCA2c.7904A>T (p.Glu2635Val)
c.7535A>T (p.Glu2512Val)
c.371A>T (p.Glu124Val)
c.7912A>T (p.Asn2638Tyr)
c.469A>T
n.7912A>T
c.7808A>T (p.Glu2603Val)
 dbSNP
13g.32362622dupCA2695217944BRCA2c.7905dup (p.Cys2636MetfsTer5)
c.7536dup (p.Cys2513MetfsTer5)
c.372dup (p.Cys125MetfsTer5)
c.7913dup (p.Asn2638LysfsTer?)
c.470dup
n.7913dup
c.7809dup (p.Cys2604MetfsTer5)
13g.32362622A=CA2082831414BRCA2c.7905A= (p.Glu2635=)
c.7536A= (p.Glu2512=)
c.372A= (p.Glu124=)
c.7913A= (p.Asn2638=)
c.470A=
n.7913A=
c.7809A= (p.Glu2603=)
13g.32362622A>CCA387747157BRCA2c.7905A>C (p.Glu2635Asp)
c.7536A>C (p.Glu2512Asp)
c.372A>C (p.Glu124Asp)
c.7913A>C (p.Asn2638Thr)
c.470A>C
n.7913A>C
c.7809A>C (p.Glu2603Asp)
13g.32362622A>GCA483260945BRCA2c.7905A>G (p.Glu2635=)
c.7536A>G (p.Glu2512=)
c.372A>G (p.Glu124=)
c.7913A>G (p.Asn2638Ser)
c.470A>G
n.7913A>G
c.7809A>G (p.Glu2603=)
 ClinVar dbSNP
13g.32362622A>TCA10586081BRCA2c.7905A>T (p.Glu2635Asp)
c.7536A>T (p.Glu2512Asp)
c.372A>T (p.Glu124Asp)
c.7913A>T (p.Asn2638Ile)
c.470A>T
n.7913A>T
c.7809A>T (p.Glu2603Asp)
 ClinVar dbSNP
13g.32362623T>ACA387747158BRCA2c.7906T>A (p.Cys2636Ser)
c.7537T>A (p.Cys2513Ser)
c.373T>A (p.Cys125Ser)
c.7914T>A (p.Asn2638Lys)
c.471T>A
n.7914T>A
c.7810T>A (p.Cys2604Ser)
 dbSNP
13g.32362623T>CCA387747159BRCA2c.7906T>C (p.Cys2636Arg)
c.7537T>C (p.Cys2513Arg)
c.373T>C (p.Cys125Arg)
c.7914T>C (p.Asn2638=)
c.471T>C
n.7914T>C
c.7810T>C (p.Cys2604Arg)
 ClinVar dbSNP
13g.32362623T>GCA387747160BRCA2c.7906T>G (p.Cys2636Gly)
c.7537T>G (p.Cys2513Gly)
c.373T>G (p.Cys125Gly)
c.7914T>G (p.Asn2638Lys)
c.471T>G
n.7914T>G
c.7810T>G (p.Cys2604Gly)
 dbSNP
13g.32362623T=CA2082831421BRCA2c.7906T= (p.Cys2636=)
c.7537T= (p.Cys2513=)
c.373T= (p.Cys125=)
c.7914T= (p.Asn2638=)
c.471T=
n.7914T=
c.7810T= (p.Cys2604=)
13g.32362624delCA2580087412BRCA2c.7907del (p.Cys2636LeufsTer12)
c.7538del (p.Cys2513LeufsTer12)
c.374del (p.Cys125LeufsTer12)
c.7915del (p.Val2639CysfsTer4)
c.472del
n.7915del
c.7811del (p.Cys2604LeufsTer12)
 ClinVar
13g.32362624G>ACA387747161BRCA2c.7907G>A (p.Cys2636Tyr)
c.7538G>A (p.Cys2513Tyr)
c.374G>A (p.Cys125Tyr)
c.7915G>A (p.Val2639Met)
c.472G>A
n.7915G>A
c.7811G>A (p.Cys2604Tyr)
 ClinVar dbSNP gnomAD v4
13g.32362624G>CCA387747162BRCA2c.7907G>C (p.Cys2636Ser)
c.7538G>C (p.Cys2513Ser)
c.374G>C (p.Cys125Ser)
c.7915G>C (p.Val2639Leu)
c.472G>C
n.7915G>C
c.7811G>C (p.Cys2604Ser)
 dbSNP
13g.32362624G>TCA387747163BRCA2c.7907G>T (p.Cys2636Phe)
c.7538G>T (p.Cys2513Phe)
c.374G>T (p.Cys125Phe)
c.7915G>T (p.Val2639Leu)
c.472G>T
n.7915G>T
c.7811G>T (p.Cys2604Phe)
 dbSNP
13g.32362625T>ACA025327BRCA2c.7908T>A (p.Cys2636Ter)
c.7539T>A (p.Cys2513Ter)
c.375T>A (p.Cys125Ter)
c.7916T>A (p.Val2639Glu)
c.473T>A
n.7916T>A
c.7812T>A (p.Cys2604Ter)
 ClinVar dbSNP
13g.32362625T>CCA483260950BRCA2c.7908T>C (p.Cys2636=)
c.7539T>C (p.Cys2513=)
c.375T>C (p.Cys125=)
c.7916T>C (p.Val2639Ala)
c.473T>C
n.7916T>C
c.7812T>C (p.Cys2604=)
 ClinVar
13g.32362625T>GCA387747164BRCA2c.7908T>G (p.Cys2636Trp)
c.7539T>G (p.Cys2513Trp)
c.375T>G (p.Cys125Trp)
c.7916T>G (p.Val2639Gly)
c.473T>G
n.7916T>G
c.7812T>G (p.Cys2604Trp)
 dbSNP
13g.32362625T=CA2082831444BRCA2c.7908T= (p.Cys2636=)
c.7539T= (p.Cys2513=)
c.375T= (p.Cys125=)
c.7916T= (p.Val2639=)
c.473T=
n.7916T=
c.7812T= (p.Cys2604=)
13g.32362626G>ACA387747167BRCA2c.7909G>A (p.Ala2637Thr)
c.7540G>A (p.Ala2514Thr)
c.376G>A (p.Ala126Thr)
c.7917G>A (p.Val2639=)
c.474G>A
n.7917G>A
c.7813G>A (p.Ala2605Thr)
 ClinVar dbSNP gnomAD v4
13g.32362626G>CCA387747166BRCA2c.7909G>C (p.Ala2637Pro)
c.7540G>C (p.Ala2514Pro)
c.376G>C (p.Ala126Pro)
c.7917G>C (p.Val2639=)
c.474G>C
n.7917G>C
c.7813G>C (p.Ala2605Pro)
 ClinVar dbSNP
13g.32362626G=CA2082831459BRCA2c.7909G= (p.Ala2637=)
c.7540G= (p.Ala2514=)
c.376G= (p.Ala126=)
c.7917G= (p.Val2639=)
c.474G=
n.7917G=
c.7813G= (p.Ala2605=)
13g.32362626G>TCA387747165BRCA2c.7909G>T (p.Ala2637Ser)
c.7540G>T (p.Ala2514Ser)
c.376G>T (p.Ala126Ser)
c.7917G>T (p.Val2639=)
c.474G>T
n.7917G>T
c.7813G>T (p.Ala2605Ser)
13g.32362626_32362631delinsGCCTTTCA2082831455BRCA2c.7909_7914delinsGCCTTT (p.Ala2637=)
c.7540_7545delinsGCCTTT (p.Ala2514=)
c.376_381delinsGCCTTT (p.Ala126=)
c.7917_7922delinsGCCTTT (p.Val2639=)
c.474_479delinsGCCTTT
n.7917_7922delinsGCCTTT
c.7813_7818delinsGCCTTT (p.Ala2605=)
13g.32362627C>ACA387747168BRCA2c.7910C>A (p.Ala2637Asp)
c.7541C>A (p.Ala2514Asp)
c.377C>A (p.Ala126Asp)
c.7918C>A (p.Pro2640Thr)
c.475C>A
n.7918C>A
c.7814C>A (p.Ala2605Asp)
 dbSNP
13g.32362627C=CA2082831471BRCA2c.7910C= (p.Ala2637=)
c.7541C= (p.Ala2514=)
c.377C= (p.Ala126=)
c.7918C= (p.Pro2640=)
c.475C=
n.7918C=
c.7814C= (p.Ala2605=)
13g.32362627C>GCA387747169BRCA2c.7910C>G (p.Ala2637Gly)
c.7541C>G (p.Ala2514Gly)
c.377C>G (p.Ala126Gly)
c.7918C>G (p.Pro2640Ala)
c.475C>G
n.7918C>G
c.7814C>G (p.Ala2605Gly)
 dbSNP
13g.32362627C>TCA025329BRCA2c.7910C>T (p.Ala2637Val)
c.7541C>T (p.Ala2514Val)
c.377C>T (p.Ala126Val)
c.7918C>T (p.Pro2640Ser)
c.475C>T
n.7918C>T
c.7814C>T (p.Ala2605Val)
 ClinVar dbSNP
13g.32362630_32362634delCA025328BRCA2c.7913_7917del (p.Phe2638Ter)
c.7544_7548del (p.Phe2515Ter)
c.380_384del (p.Phe127Ter)
c.7921_7925del (p.Phe2641LysfsTer?)
c.478_482del
n.7921_7925del
c.7817_7821del (p.Phe2606Ter)
 ClinVar dbSNP gnomAD v4
13g.32362627_32362628insGAAACA658823757BRCA2c.7910_7911insGAAA (p.Phe2638LysfsTer4)
c.7541_7542insGAAA (p.Phe2515LysfsTer4)
c.377_378insGAAA (p.Phe127LysfsTer4)
c.7918_7919insGAAA (p.Pro2640ArgfsTer?)
c.475_476insGAAA
n.7918_7919insGAAA
c.7814_7815insGAAA (p.Phe2606LysfsTer4)
 ClinVar dbSNP
13g.32362628C>ACA483260956BRCA2c.7911C>A (p.Ala2637=)
c.7542C>A (p.Ala2514=)
c.378C>A (p.Ala126=)
c.7919C>A (p.Pro2640His)
c.476C>A
n.7919C>A
c.7815C>A (p.Ala2605=)
13g.32362628C=CA2082831481BRCA2c.7911C= (p.Ala2637=)
c.7542C= (p.Ala2514=)
c.378C= (p.Ala126=)
c.7919C= (p.Pro2640=)
c.476C=
n.7919C=
c.7815C= (p.Ala2605=)
13g.32362628C>GCA483260957BRCA2c.7911C>G (p.Ala2637=)
c.7542C>G (p.Ala2514=)
c.378C>G (p.Ala126=)
c.7919C>G (p.Pro2640Arg)
c.476C>G
n.7919C>G
c.7815C>G (p.Ala2605=)
13g.32362628C>TCA483260958BRCA2c.7911C>T (p.Ala2637=)
c.7542C>T (p.Ala2514=)
c.378C>T (p.Ala126=)
c.7919C>T (p.Pro2640Leu)
c.476C>T
n.7919C>T
c.7815C>T (p.Ala2605=)
 ClinVar
13g.32362628_32362629delinsCTCA2082831478BRCA2c.7911_7912delinsCT (p.Ala2637=)
c.7542_7543delinsCT (p.Ala2514=)
c.378_379delinsCT (p.Ala126=)
c.7919_7920delinsCT (p.Pro2640=)
c.476_477delinsCT
n.7919_7920delinsCT
c.7815_7816delinsCT (p.Ala2605=)
13g.32362628_32362629insGAAACA10589457BRCA2c.7911_7912insGAAA (p.Phe2638GlufsTer4)
c.7542_7543insGAAA (p.Phe2515GlufsTer4)
c.378_379insGAAA (p.Phe127GlufsTer4)
c.7919_7920insGAAA (p.Phe2641LysfsTer?)
c.476_477insGAAA
n.7919_7920insGAAA
c.7815_7816insGAAA (p.Phe2606GlufsTer4)
 ClinVar dbSNP
13g.32362629T>ACA387747171BRCA2c.7912T>A (p.Phe2638Ile)
c.7543T>A (p.Phe2515Ile)
c.379T>A (p.Phe127Ile)
c.7920T>A (p.Pro2640=)
c.477T>A
n.7920T>A
c.7816T>A (p.Phe2606Ile)
 dbSNP
13g.32362629T>CCA10579760BRCA2c.7912T>C (p.Phe2638Leu)
c.7543T>C (p.Phe2515Leu)
c.379T>C (p.Phe127Leu)
c.7920T>C (p.Pro2640=)
c.477T>C
n.7920T>C
c.7816T>C (p.Phe2606Leu)
 ClinVar dbSNP gnomAD v4
13g.32362629T>GCA387747170BRCA2c.7912T>G (p.Phe2638Val)
c.7543T>G (p.Phe2515Val)
c.379T>G (p.Phe127Val)
c.7920T>G (p.Pro2640=)
c.477T>G
n.7920T>G
c.7816T>G (p.Phe2606Val)
 ClinVar dbSNP
13g.32362629T=CA2082831499BRCA2c.7912T= (p.Phe2638=)
c.7543T= (p.Phe2515=)
c.379T= (p.Phe127=)
c.7920T= (p.Pro2640=)
c.477T=
n.7920T=
c.7816T= (p.Phe2606=)
13g.32362631delCA10585935BRCA2c.7914del (p.Pro2639LeufsTer9)
c.7545del (p.Pro2516LeufsTer9)
c.381del (p.Pro128LeufsTer9)
c.7922del (p.Phe2641SerfsTer2)
c.479del
n.7922del
c.7818del (p.Pro2607LeufsTer9)
 ClinVar dbSNP
13g.32362630T>ACA387747172BRCA2c.7913T>A (p.Phe2638Tyr)
c.7544T>A (p.Phe2515Tyr)
c.380T>A (p.Phe127Tyr)
c.7921T>A (p.Phe2641Ile)
c.478T>A
n.7921T>A
c.7817T>A (p.Phe2606Tyr)
 dbSNP
13g.32362630T>CCA387747173BRCA2c.7913T>C (p.Phe2638Ser)
c.7544T>C (p.Phe2515Ser)
c.380T>C (p.Phe127Ser)
c.7921T>C (p.Phe2641Leu)
c.478T>C
n.7921T>C
c.7817T>C (p.Phe2606Ser)
13g.32362630T>GCA387747174BRCA2c.7913T>G (p.Phe2638Cys)
c.7544T>G (p.Phe2515Cys)
c.380T>G (p.Phe127Cys)
c.7921T>G (p.Phe2641Val)
c.478T>G
n.7921T>G
c.7817T>G (p.Phe2606Cys)
13g.32362631T>ACA387747175BRCA2c.7914T>A (p.Phe2638Leu)
c.7545T>A (p.Phe2515Leu)
c.381T>A (p.Phe127Leu)
c.7922T>A (p.Phe2641Tyr)
c.479T>A
n.7922T>A
c.7818T>A (p.Phe2606Leu)
13g.32362631T>CCA483260961BRCA2c.7914T>C (p.Phe2638=)
c.7545T>C (p.Phe2515=)
c.381T>C (p.Phe127=)
c.7922T>C (p.Phe2641Ser)
c.479T>C
n.7922T>C
c.7818T>C (p.Phe2606=)
13g.32362631T>GCA025332BRCA2c.7914T>G (p.Phe2638Leu)
c.7545T>G (p.Phe2515Leu)
c.381T>G (p.Phe127Leu)
c.7922T>G (p.Phe2641Cys)
c.479T>G
n.7922T>G
c.7818T>G (p.Phe2606Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32362631T=CA2082831520BRCA2c.7914T= (p.Phe2638=)
c.7545T= (p.Phe2515=)
c.381T= (p.Phe127=)
c.7922T= (p.Phe2641=)
c.479T=
n.7922T=
c.7818T= (p.Phe2606=)
13g.32362632C>ACA025333BRCA2c.7915C>A (p.Pro2639Thr)
c.7546C>A (p.Pro2516Thr)
c.382C>A (p.Pro128Thr)
c.7923C>A (p.Phe2641Leu)
c.480C>A
n.7923C>A
c.7819C>A (p.Pro2607Thr)
 ClinVar dbSNP
13g.32362632C=CA2082831569BRCA2c.7915C= (p.Pro2639=)
c.7546C= (p.Pro2516=)
c.382C= (p.Pro128=)
c.7923C= (p.Phe2641=)
c.480C=
n.7923C=
c.7819C= (p.Pro2607=)
13g.32362632C>GCA025334BRCA2c.7915C>G (p.Pro2639Ala)
c.7546C>G (p.Pro2516Ala)
c.382C>G (p.Pro128Ala)
c.7923C>G (p.Phe2641Leu)
c.480C>G
n.7923C>G
c.7819C>G (p.Pro2607Ala)
 ClinVar dbSNP gnomAD v4
13g.32362632C>TCA387747176BRCA2c.7915C>T (p.Pro2639Ser)
c.7546C>T (p.Pro2516Ser)
c.382C>T (p.Pro128Ser)
c.7923C>T (p.Phe2641=)
c.480C>T
n.7923C>T
c.7819C>T (p.Pro2607Ser)
 dbSNP
13g.32362632_32362633delinsCCCA2082831577BRCA2c.7915_7916delinsCC (p.Pro2639=)
c.7546_7547delinsCC (p.Pro2516=)
c.382_383delinsCC (p.Pro128=)
c.7923_7924delinsCC (p.Phe2641=)
c.480_481delinsCC
n.7923_7924delinsCC
c.7819_7820delinsCC (p.Pro2607=)
13g.32362632_32362633delinsTTCA1139663133BRCA2c.7915_7916delinsTT (p.Pro2639Phe)
c.7546_7547delinsTT (p.Pro2516Phe)
c.382_383delinsTT (p.Pro128Phe)
c.7923_7924delinsTT (p.Phe2641=)
c.480_481delinsTT
n.7923_7924delinsTT
c.7819_7820delinsTT (p.Pro2607Phe)
 ClinVar dbSNP
13g.32362633C>ACA387747177BRCA2c.7916C>A (p.Pro2639His)
c.7547C>A (p.Pro2516His)
c.383C>A (p.Pro128His)
c.7924C>A (p.Leu2642Ile)
c.481C>A
n.7924C>A
c.7820C>A (p.Pro2607His)
 dbSNP
13g.32362633C=CA2082831597BRCA2c.7916C= (p.Pro2639=)
c.7547C= (p.Pro2516=)
c.383C= (p.Pro128=)
c.7924C= (p.Leu2642=)
c.481C=
n.7924C=
c.7820C= (p.Pro2607=)
13g.32362633C>GCA387747178BRCA2c.7916C>G (p.Pro2639Arg)
c.7547C>G (p.Pro2516Arg)
c.383C>G (p.Pro128Arg)
c.7924C>G (p.Leu2642Val)
c.481C>G
n.7924C>G
c.7820C>G (p.Pro2607Arg)
 ClinVar dbSNP
13g.32362633C>TCA338873BRCA2c.7916C>T (p.Pro2639Leu)
c.7547C>T (p.Pro2516Leu)
c.383C>T (p.Pro128Leu)
c.7924C>T (p.Leu2642=)
c.481C>T
n.7924C>T
c.7820C>T (p.Pro2607Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32362634T>ACA483260963BRCA2c.7917T>A (p.Pro2639=)
c.7548T>A (p.Pro2516=)
c.384T>A (p.Pro128=)
c.7925T>A (p.Leu2642Gln)
c.482T>A
n.7925T>A
c.7821T>A (p.Pro2607=)
 dbSNP
13g.32362634T>CCA483260964BRCA2c.7917T>C (p.Pro2639=)
c.7548T>C (p.Pro2516=)
c.384T>C (p.Pro128=)
c.7925T>C (p.Leu2642Pro)
c.482T>C
n.7925T>C
c.7821T>C (p.Pro2607=)
 dbSNP
13g.32362634T>GCA483260966BRCA2c.7917T>G (p.Pro2639=)
c.7548T>G (p.Pro2516=)
c.384T>G (p.Pro128=)
c.7925T>G (p.Leu2642Arg)
c.482T>G
n.7925T>G
c.7821T>G (p.Pro2607=)
13g.32362635A=CA2082831616BRCA2c.7918A= (p.Lys2640=)
c.7549A= (p.Lys2517=)
c.385A= (p.Lys129=)
c.7926A= (p.Leu2642=)
c.483A=
n.7926A=
c.7822A= (p.Lys2608=)
13g.32362635A>CCA387747179BRCA2c.7918A>C (p.Lys2640Gln)
c.7549A>C (p.Lys2517Gln)
c.385A>C (p.Lys129Gln)
c.7926A>C (p.Leu2642=)
c.483A>C
n.7926A>C
c.7822A>C (p.Lys2608Gln)
13g.32362635A>GCA387747180BRCA2c.7918A>G (p.Lys2640Glu)
c.7549A>G (p.Lys2517Glu)
c.385A>G (p.Lys129Glu)
c.7926A>G (p.Leu2642=)
c.483A>G
n.7926A>G
c.7822A>G (p.Lys2608Glu)
 ClinVar dbSNP
13g.32362635A>TCA387747181BRCA2c.7918A>T (p.Lys2640Ter)
c.7549A>T (p.Lys2517Ter)
c.385A>T (p.Lys129Ter)
c.7926A>T (p.Leu2642=)
c.483A>T
n.7926A>T
c.7822A>T (p.Lys2608Ter)
 dbSNP
13g.32362635_32362645delinsAAGGAATTTGCCA2082831605BRCA2c.7918_7928delinsAAGGAATTTGC (p.Lys2640=)
c.7549_7559delinsAAGGAATTTGC (p.Lys2517=)
c.385_395delinsAAGGAATTTGC (p.Lys129=)
c.7926_7936delinsAAGGAATTTGC (p.Leu2642=)
c.483_493delinsAAGGAATTTGC
n.7926_7936delinsAAGGAATTTGC
c.7822_7832delinsAAGGAATTTGC (p.Lys2608=)
13g.32362636A=CA2082831644BRCA2c.7919A= (p.Lys2640=)
c.7550A= (p.Lys2517=)
c.386A= (p.Lys129=)
c.7927A= (p.Arg2643=)
c.484A=
n.7927A=
c.7823A= (p.Lys2608=)
13g.32362636A>CCA025335BRCA2c.7919A>C (p.Lys2640Thr)
c.7550A>C (p.Lys2517Thr)
c.386A>C (p.Lys129Thr)
c.7927A>C (p.Arg2643=)
c.484A>C
n.7927A>C
c.7823A>C (p.Lys2608Thr)
 ClinVar dbSNP
13g.32362636A>GCA387747182BRCA2c.7919A>G (p.Lys2640Arg)
c.7550A>G (p.Lys2517Arg)
c.386A>G (p.Lys129Arg)
c.7927A>G (p.Arg2643Gly)
c.484A>G
n.7927A>G
c.7823A>G (p.Lys2608Arg)
 ClinVar dbSNP
13g.32362636A>TCA387747183BRCA2c.7919A>T (p.Lys2640Met)
c.7550A>T (p.Lys2517Met)
c.386A>T (p.Lys129Met)
c.7927A>T (p.Arg2643Trp)
c.484A>T
n.7927A>T
c.7823A>T (p.Lys2608Met)
 ClinVar dbSNP
13g.32362636_32362645delCA10585936BRCA2c.7919_7928del (p.Lys2640IlefsTer5)
c.7550_7559del (p.Lys2517IlefsTer5)
c.386_395del (p.Lys129IlefsTer5)
c.7927_7936del (p.Arg2643Ter)
c.484_493del
n.7927_7936del
c.7823_7832del (p.Lys2608IlefsTer5)
 ClinVar dbSNP
13g.32362637G>ACA483260973BRCA2c.7920G>A (p.Lys2640=)
c.7551G>A (p.Lys2517=)
c.387G>A (p.Lys129=)
c.7928G>A (p.Arg2643Lys)
c.485G>A
n.7928G>A
c.7824G>A (p.Lys2608=)
 ClinVar dbSNP
13g.32362637G>CCA387747184BRCA2c.7920G>C (p.Lys2640Asn)
c.7551G>C (p.Lys2517Asn)
c.387G>C (p.Lys129Asn)
c.7928G>C (p.Arg2643Thr)
c.485G>C
n.7928G>C
c.7824G>C (p.Lys2608Asn)
 ClinVar dbSNP
13g.32362637G>TCA387747185BRCA2c.7920G>T (p.Lys2640Asn)
c.7551G>T (p.Lys2517Asn)
c.387G>T (p.Lys129Asn)
c.7928G>T (p.Arg2643Met)
c.485G>T
n.7928G>T
c.7824G>T (p.Lys2608Asn)
13g.32362637_32362643delinsGGAATTTCA2082831659BRCA2c.7920_7926delinsGGAATTT (p.Lys2640=)
c.7551_7557delinsGGAATTT (p.Lys2517=)
c.387_393delinsGGAATTT (p.Lys129=)
c.7928_7934delinsGGAATTT (p.Arg2643=)
c.485_491delinsGGAATTT
n.7928_7934delinsGGAATTT
c.7824_7830delinsGGAATTT (p.Lys2608=)
13g.32362638G>ACA387747186BRCA2c.7921G>A (p.Glu2641Lys)
c.7552G>A (p.Glu2518Lys)
c.388G>A (p.Glu130Lys)
c.7929G>A (p.Arg2643=)
c.486G>A
n.7929G>A
c.7825G>A (p.Glu2609Lys)
 dbSNP
13g.32362638G>CCA387747187BRCA2c.7921G>C (p.Glu2641Gln)
c.7552G>C (p.Glu2518Gln)
c.388G>C (p.Glu130Gln)
c.7929G>C (p.Arg2643Ser)
c.486G>C
n.7929G>C
c.7825G>C (p.Glu2609Gln)
 dbSNP
13g.32362638G=CA2082831689BRCA2c.7921G= (p.Glu2641=)
c.7552G= (p.Glu2518=)
c.388G= (p.Glu130=)
c.7929G= (p.Arg2643=)
c.486G=
n.7929G=
c.7825G= (p.Glu2609=)
13g.32362638G>TCA10586582BRCA2c.7921G>T (p.Glu2641Ter)
c.7552G>T (p.Glu2518Ter)
c.388G>T (p.Glu130Ter)
c.7929G>T (p.Arg2643Ser)
c.486G>T
n.7929G>T
c.7825G>T (p.Glu2609Ter)
 ClinVar dbSNP
13g.32362638_32362643delinsAGCA025336BRCA2c.7921_7926delinsAG (p.Glu2641ArgfsTer6)
c.7552_7557delinsAG (p.Glu2518ArgfsTer6)
c.388_393delinsAG (p.Glu130ArgfsTer6)
c.7929_7934delinsAG (p.Asn2644GlyfsTer2)
c.486_491delinsAG
n.7929_7934delinsAG
c.7825_7830delinsAG (p.Glu2609ArgfsTer6)
 ClinVar dbSNP
13g.32362639A>CCA387747188BRCA2c.7922A>C (p.Glu2641Ala)
c.7553A>C (p.Glu2518Ala)
c.389A>C (p.Glu130Ala)
c.7930A>C (p.Asn2644His)
c.487A>C
n.7930A>C
c.7826A>C (p.Glu2609Ala)
13g.32362639A>GCA387747189BRCA2c.7922A>G (p.Glu2641Gly)
c.7553A>G (p.Glu2518Gly)
c.389A>G (p.Glu130Gly)
c.7930A>G (p.Asn2644Asp)
c.487A>G
n.7930A>G
c.7826A>G (p.Glu2609Gly)
 ClinVar dbSNP
13g.32362639A>TCA387747190BRCA2c.7922A>T (p.Glu2641Val)
c.7553A>T (p.Glu2518Val)
c.389A>T (p.Glu130Val)
c.7930A>T (p.Asn2644Tyr)
c.487A>T
n.7930A>T
c.7826A>T (p.Glu2609Val)
13g.32362640dupCA2573149364BRCA2c.7923dup (p.Phe2642IlefsTer3)
c.7554dup (p.Phe2519IlefsTer3)
c.390dup (p.Phe131IlefsTer3)
c.7931dup (p.Asn2644LysfsTer?)
c.488dup
n.7931dup
c.7827dup (p.Phe2610IlefsTer3)
 ClinVar dbSNP
13g.32362640A>CCA387747191BRCA2c.7923A>C (p.Glu2641Asp)
c.7554A>C (p.Glu2518Asp)
c.390A>C (p.Glu130Asp)
c.7931A>C (p.Asn2644Thr)
c.488A>C
n.7931A>C
c.7827A>C (p.Glu2609Asp)
13g.32362640A>GCA483260977BRCA2c.7923A>G (p.Glu2641=)
c.7554A>G (p.Glu2518=)
c.390A>G (p.Glu130=)
c.7931A>G (p.Asn2644Ser)
c.488A>G
n.7931A>G
c.7827A>G (p.Glu2609=)
 dbSNP gnomAD v4
13g.32362640A>TCA387747192BRCA2c.7923A>T (p.Glu2641Asp)
c.7554A>T (p.Glu2518Asp)
c.390A>T (p.Glu130Asp)
c.7931A>T (p.Asn2644Ile)
c.488A>T
n.7931A>T
c.7827A>T (p.Glu2609Asp)
 dbSNP
13g.32362640_32362641delinsATCA2082831706BRCA2c.7923_7924delinsAT (p.Glu2641=)
c.7554_7555delinsAT (p.Glu2518=)
c.390_391delinsAT (p.Glu130=)
c.7931_7932delinsAT (p.Asn2644=)
c.488_489delinsAT
n.7931_7932delinsAT
c.7827_7828delinsAT (p.Glu2609=)
13g.32362641T>ACA387747193BRCA2c.7924T>A (p.Phe2642Ile)
c.7555T>A (p.Phe2519Ile)
c.391T>A (p.Phe131Ile)
c.7932T>A (p.Asn2644Lys)
c.489T>A
n.7932T>A
c.7828T>A (p.Phe2610Ile)
 dbSNP
13g.32362641T>CCA387747194BRCA2c.7924T>C (p.Phe2642Leu)
c.7555T>C (p.Phe2519Leu)
c.391T>C (p.Phe131Leu)
c.7932T>C (p.Asn2644=)
c.489T>C
n.7932T>C
c.7828T>C (p.Phe2610Leu)
 ClinVar dbSNP gnomAD v4
13g.32362641T>GCA387747195BRCA2c.7924T>G (p.Phe2642Val)
c.7555T>G (p.Phe2519Val)
c.391T>G (p.Phe131Val)
c.7932T>G (p.Asn2644Lys)
c.489T>G
n.7932T>G
c.7828T>G (p.Phe2610Val)
13g.32362641T=CA2082831716BRCA2c.7924T= (p.Phe2642=)
c.7555T= (p.Phe2519=)
c.391T= (p.Phe131=)
c.7932T= (p.Asn2644=)
c.489T=
n.7932T=
c.7828T= (p.Phe2610=)
13g.32362643delCA025337BRCA2c.7926del (p.Phe2642LeufsTer6)
c.7557del (p.Phe2519LeufsTer6)
c.393del (p.Phe131LeufsTer6)
c.7934del (p.Leu2645CysfsTer2)
c.491del
n.7934del
c.7830del (p.Phe2610LeufsTer6)
 ClinVar dbSNP
13g.32362642T>ACA387747196BRCA2c.7925T>A (p.Phe2642Tyr)
c.7556T>A (p.Phe2519Tyr)
c.392T>A (p.Phe131Tyr)
c.7933T>A (p.Leu2645Met)
c.490T>A
n.7933T>A
c.7829T>A (p.Phe2610Tyr)
 dbSNP
13g.32362642T>CCA387747197BRCA2c.7925T>C (p.Phe2642Ser)
c.7556T>C (p.Phe2519Ser)
c.392T>C (p.Phe131Ser)
c.7933T>C (p.Leu2645=)
c.490T>C
n.7933T>C
c.7829T>C (p.Phe2610Ser)
 dbSNP gnomAD v4
13g.32362642T>GCA387747198BRCA2c.7925T>G (p.Phe2642Cys)
c.7556T>G (p.Phe2519Cys)
c.392T>G (p.Phe131Cys)
c.7933T>G (p.Leu2645Val)
c.490T>G
n.7933T>G
c.7829T>G (p.Phe2610Cys)
 ClinVar dbSNP
13g.32362642T=CA2082831721BRCA2c.7925T= (p.Phe2642=)
c.7556T= (p.Phe2519=)
c.392T= (p.Phe131=)
c.7933T= (p.Leu2645=)
c.490T=
n.7933T=
c.7829T= (p.Phe2610=)
13g.32362643T>ACA387747200BRCA2c.7926T>A (p.Phe2642Leu)
c.7557T>A (p.Phe2519Leu)
c.393T>A (p.Phe131Leu)
c.7934T>A (p.Leu2645Ter)
c.491T>A
n.7934T>A
c.7830T>A (p.Phe2610Leu)
 dbSNP
13g.32362643T>CCA483260981BRCA2c.7926T>C (p.Phe2642=)
c.7557T>C (p.Phe2519=)
c.393T>C (p.Phe131=)
c.7934T>C (p.Leu2645Ser)
c.491T>C
n.7934T>C
c.7830T>C (p.Phe2610=)
 gnomAD v4
13g.32362643T>GCA387747199BRCA2c.7926T>G (p.Phe2642Leu)
c.7557T>G (p.Phe2519Leu)
c.393T>G (p.Phe131Leu)
c.7934T>G (p.Leu2645Trp)
c.491T>G
n.7934T>G
c.7830T>G (p.Phe2610Leu)
 ClinVar dbSNP
13g.32362643T=CA2082831729BRCA2c.7926T= (p.Phe2642=)
c.7557T= (p.Phe2519=)
c.393T= (p.Phe131=)
c.7934T= (p.Leu2645=)
c.491T=
n.7934T=
c.7830T= (p.Phe2610=)
13g.32362644G>ACA387747201BRCA2c.7927G>A (p.Ala2643Thr)
c.7558G>A (p.Ala2520Thr)
c.394G>A (p.Ala132Thr)
c.7935G>A (p.Leu2645=)
c.492G>A
n.7935G>A
c.7831G>A (p.Ala2611Thr)
 ClinVar dbSNP
13g.32362644G>CCA387747202BRCA2c.7927G>C (p.Ala2643Pro)
c.7558G>C (p.Ala2520Pro)
c.394G>C (p.Ala132Pro)
c.7935G>C (p.Leu2645Phe)
c.492G>C
n.7935G>C
c.7831G>C (p.Ala2611Pro)
 dbSNP
13g.32362644G=CA2082831739BRCA2c.7927G= (p.Ala2643=)
c.7558G= (p.Ala2520=)
c.394G= (p.Ala132=)
c.7935G= (p.Leu2645=)
c.492G=
n.7935G=
c.7831G= (p.Ala2611=)
13g.32362644G>TCA387747203BRCA2c.7927G>T (p.Ala2643Ser)
c.7558G>T (p.Ala2520Ser)
c.394G>T (p.Ala132Ser)
c.7935G>T (p.Leu2645Phe)
c.492G>T
n.7935G>T
c.7831G>T (p.Ala2611Ser)
 dbSNP gnomAD v4
13g.32362645C>ACA387747204BRCA2c.7928C>A (p.Ala2643Asp)
c.7559C>A (p.Ala2520Asp)
c.395C>A (p.Ala132Asp)
c.7936C>A (p.Leu2646Ile)
c.493C>A
n.7936C>A
c.7832C>A (p.Ala2611Asp)
 dbSNP
13g.32362645C=CA2082831749BRCA2c.7928C= (p.Ala2643=)
c.7559C= (p.Ala2520=)
c.395C= (p.Ala132=)
c.7936C= (p.Leu2646=)
c.493C=
n.7936C=
c.7832C= (p.Ala2611=)
13g.32362645C>GCA025338BRCA2c.7928C>G (p.Ala2643Gly)
c.7559C>G (p.Ala2520Gly)
c.395C>G (p.Ala132Gly)
c.7936C>G (p.Leu2646Val)
c.493C>G
n.7936C>G
c.7832C>G (p.Ala2611Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362645C>TCA025339BRCA2c.7928C>T (p.Ala2643Val)
c.7559C>T (p.Ala2520Val)
c.395C>T (p.Ala132Val)
c.7936C>T (p.Leu2646=)
c.493C>T
n.7936C>T
c.7832C>T (p.Ala2611Val)
 ClinVar dbSNP gnomAD v4
13g.32362646T>ACA483260987BRCA2c.7929T>A (p.Ala2643=)
c.7560T>A (p.Ala2520=)
c.396T>A (p.Ala132=)
c.7937T>A (p.Leu2646Gln)
c.494T>A
n.7937T>A
c.7833T>A (p.Ala2611=)
13g.32362646T>CCA483260988BRCA2c.7929T>C (p.Ala2643=)
c.7560T>C (p.Ala2520=)
c.396T>C (p.Ala132=)
c.7937T>C (p.Leu2646Pro)
c.494T>C
n.7937T>C
c.7833T>C (p.Ala2611=)
 ClinVar dbSNP
13g.32362646T>GCA483260986BRCA2c.7929T>G (p.Ala2643=)
c.7560T>G (p.Ala2520=)
c.396T>G (p.Ala132=)
c.7937T>G (p.Leu2646Arg)
c.494T>G
n.7937T>G
c.7833T>G (p.Ala2611=)
13g.32362646T=CA2082831764BRCA2c.7929T= (p.Ala2643=)
c.7560T= (p.Ala2520=)
c.396T= (p.Ala132=)
c.7937T= (p.Leu2646=)
c.494T=
n.7937T=
c.7833T= (p.Ala2611=)
13g.32362647A=CA2082831776BRCA2c.7930A= (p.Asn2644=)
c.7561A= (p.Asn2521=)
c.397A= (p.Asn133=)
c.7938A= (p.Leu2646=)
c.495A=
n.7938A=
c.7834A= (p.Asn2612=)
13g.32362647A>CCA387747205BRCA2c.7930A>C (p.Asn2644His)
c.7561A>C (p.Asn2521His)
c.397A>C (p.Asn133His)
c.7938A>C (p.Leu2646=)
c.495A>C
n.7938A>C
c.7834A>C (p.Asn2612His)
13g.32362647A>GCA025340BRCA2c.7930A>G (p.Asn2644Asp)
c.7561A>G (p.Asn2521Asp)
c.397A>G (p.Asn133Asp)
c.7938A>G (p.Leu2646=)
c.495A>G
n.7938A>G
c.7834A>G (p.Asn2612Asp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362647A>TCA387747206BRCA2c.7930A>T (p.Asn2644Tyr)
c.7561A>T (p.Asn2521Tyr)
c.397A>T (p.Asn133Tyr)
c.7938A>T (p.Leu2646=)
c.495A>T
n.7938A>T
c.7834A>T (p.Asn2612Tyr)
 dbSNP
13g.32362648A=CA2082831805BRCA2c.7931A= (p.Asn2644=)
c.7562A= (p.Asn2521=)
c.398A= (p.Asn133=)
c.7939A= (p.Ile2647=)
c.496A=
n.7939A=
c.7835A= (p.Asn2612=)
13g.32362648A>CCA387747207BRCA2c.7931A>C (p.Asn2644Thr)
c.7562A>C (p.Asn2521Thr)
c.398A>C (p.Asn133Thr)
c.7939A>C (p.Ile2647Leu)
c.496A>C
n.7939A>C
c.7835A>C (p.Asn2612Thr)
 dbSNP
13g.32362648A>GCA025341BRCA2c.7931A>G (p.Asn2644Ser)
c.7562A>G (p.Asn2521Ser)
c.398A>G (p.Asn133Ser)
c.7939A>G (p.Ile2647Val)
c.496A>G
n.7939A>G
c.7835A>G (p.Asn2612Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32362648A>TCA387747208BRCA2c.7931A>T (p.Asn2644Ile)
c.7562A>T (p.Asn2521Ile)
c.398A>T (p.Asn133Ile)
c.7939A>T (p.Ile2647Leu)
c.496A>T
n.7939A>T
c.7835A>T (p.Asn2612Ile)
 dbSNP
13g.32362649T>ACA387747210BRCA2c.7932T>A (p.Asn2644Lys)
c.7563T>A (p.Asn2521Lys)
c.399T>A (p.Asn133Lys)
c.7940T>A (p.Ile2647Lys)
c.497T>A
n.7940T>A
c.7836T>A (p.Asn2612Lys)
 dbSNP
13g.32362649T>CCA16614367BRCA2c.7932T>C (p.Asn2644=)
c.7563T>C (p.Asn2521=)
c.399T>C (p.Asn133=)
c.7940T>C (p.Ile2647Thr)
c.497T>C
n.7940T>C
c.7836T>C (p.Asn2612=)
 ClinVar dbSNP
13g.32362649T>GCA387747209BRCA2c.7932T>G (p.Asn2644Lys)
c.7563T>G (p.Asn2521Lys)
c.399T>G (p.Asn133Lys)
c.7940T>G (p.Ile2647Arg)
c.497T>G
n.7940T>G
c.7836T>G (p.Asn2612Lys)
 ClinVar dbSNP
13g.32362649T=CA2082831821BRCA2c.7932T= (p.Asn2644=)
c.7563T= (p.Asn2521=)
c.399T= (p.Asn133=)
c.7940T= (p.Ile2647=)
c.497T=
n.7940T=
c.7836T= (p.Asn2612=)
13g.32362650A=CA2082831843BRCA2c.7933A= (p.Arg2645=)
c.7564A= (p.Arg2522=)
c.400A= (p.Arg134=)
c.7941A= (p.Ile2647=)
c.498A=
n.7941A=
c.7837A= (p.Arg2613=)
13g.32362650A>CCA483260991BRCA2c.7933A>C (p.Arg2645=)
c.7564A>C (p.Arg2522=)
c.400A>C (p.Arg134=)
c.7941A>C (p.Ile2647=)
c.498A>C
n.7941A>C
c.7837A>C (p.Arg2613=)
13g.32362650A>GCA10579761BRCA2c.7933A>G (p.Arg2645Gly)
c.7564A>G (p.Arg2522Gly)
c.400A>G (p.Arg134Gly)
c.7941A>G (p.Ile2647Met)
c.498A>G
n.7941A>G
c.7837A>G (p.Arg2613Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32362650A>TCA10589458BRCA2c.7933A>T (p.Arg2645Ter)
c.7564A>T (p.Arg2522Ter)
c.400A>T (p.Arg134Ter)
c.7941A>T (p.Ile2647=)
c.498A>T
n.7941A>T
c.7837A>T (p.Arg2613Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32362650_32362651delinsAGCA2082831829BRCA2c.7933_7934delinsAG (p.Arg2645=)
c.7564_7565delinsAG (p.Arg2522=)
c.400_401delinsAG (p.Arg134=)
c.7941_7942delinsAG (p.Ile2647=)
c.498_499delinsAG
n.7941_7942delinsAG
c.7837_7838delinsAG (p.Arg2613=)
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.32362651delCA025344BRCA2c.7934del (p.Arg2645AsnfsTer3)
c.7565del (p.Arg2522AsnfsTer3)
c.401del (p.Arg134AsnfsTer3)
c.7942del (p.Asp2648MetfsTer16)
c.499del
n.7942del
c.7838del (p.Arg2613AsnfsTer3)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC
13g.32362651G>ACA387747211BRCA2c.7934G>A (p.Arg2645Lys)
c.7565G>A (p.Arg2522Lys)
c.401G>A (p.Arg134Lys)
c.7942G>A (p.Asp2648Asn)
c.499G>A
n.7942G>A
c.7838G>A (p.Arg2613Lys)
 dbSNP gnomAD v4
13g.32362651G>CCA387747212BRCA2c.7934G>C (p.Arg2645Thr)
c.7565G>C (p.Arg2522Thr)
c.401G>C (p.Arg134Thr)
c.7942G>C (p.Asp2648His)
c.499G>C
n.7942G>C
c.7838G>C (p.Arg2613Thr)
 dbSNP
13g.32362651G>TCA387747213BRCA2c.7934G>T (p.Arg2645Ile)
c.7565G>T (p.Arg2522Ile)
c.401G>T (p.Arg134Ile)
c.7942G>T (p.Asp2648Tyr)
c.499G>T
n.7942G>T
c.7838G>T (p.Arg2613Ile)
13g.32362651_32362652insGCAATTTGCTAATCA2580087418BRCA2c.7934_7935insGCAATTTGCTAAT (p.Cys2646GlnfsTer20)
c.7565_7566insGCAATTTGCTAAT (p.Cys2523GlnfsTer20)
c.401_402insGCAATTTGCTAAT (p.Cys135GlnfsTer20)
c.7942_7943insGCAATTTGCTAAT (p.Asp2648GlyfsTer?)
c.499_500insGCAATTTGCTAAT
n.7942_7943insGCAATTTGCTAAT
c.7838_7839insGCAATTTGCTAAT (p.Cys2614GlnfsTer20)
 ClinVar
13g.32362652A=CA2082831873BRCA2c.7935A= (p.Arg2645=)
c.7566A= (p.Arg2522=)
c.402A= (p.Arg134=)
c.7943A= (p.Asp2648=)
c.500A=
n.7943A=
c.7839A= (p.Arg2613=)
13g.32362652A>CCA387747214BRCA2c.7935A>C (p.Arg2645Ser)
c.7566A>C (p.Arg2522Ser)
c.402A>C (p.Arg134Ser)
c.7943A>C (p.Asp2648Ala)
c.500A>C
n.7943A>C
c.7839A>C (p.Arg2613Ser)
 dbSNP
13g.32362652A>GCA483260997BRCA2c.7935A>G (p.Arg2645=)
c.7566A>G (p.Arg2522=)
c.402A>G (p.Arg134=)
c.7943A>G (p.Asp2648Gly)
c.500A>G
n.7943A>G
c.7839A>G (p.Arg2613=)
 ClinVar dbSNP
13g.32362652A>TCA387747215BRCA2c.7935A>T (p.Arg2645Ser)
c.7566A>T (p.Arg2522Ser)
c.402A>T (p.Arg134Ser)
c.7943A>T (p.Asp2648Val)
c.500A>T
n.7943A>T
c.7839A>T (p.Arg2613Ser)
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)
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_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)
 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

Number of alleles fetched