Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32356426_32356798delCA2499222288BRCA2c.7436-2_7617+189del
c.7067-2_7248+189del
n.7436-2_7617+189del
c.7340-2_7521+189del
 ClinVar dbSNP
13g.32356446_32356472delinsAGAATGCCAGAGATATACAGGATATGCCA2082814115BRCA2c.7454_7480delinsAGAATGCCAGAGATATACAGGATATGC (p.Gln2485=)
c.7085_7111delinsAGAATGCCAGAGATATACAGGATATGC (p.Gln2362=)
c.19_45delinsAGAATGCCAGAGATATACAGGATATGC
n.7454_7480delinsAGAATGCCAGAGATATACAGGATATGC
c.7358_7384delinsAGAATGCCAGAGATATACAGGATATGC (p.Gln2453=)
13g.32356451_32356476delCA16619762BRCA2c.7459_7484del (p.Ala2487Ter)
c.7090_7115del (p.Ala2364Ter)
c.24_49del
n.7459_7484del
c.7363_7388del (p.Ala2455Ter)
 ClinVar dbSNP
13g.32356455G>ACA025097BRCA2c.7463G>A (p.Arg2488Lys)
c.7094G>A (p.Arg2365Lys)
c.28G>A
n.7463G>A
c.7367G>A (p.Arg2456Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32356455G>CCA387743142BRCA2c.7463G>C (p.Arg2488Thr)
c.7094G>C (p.Arg2365Thr)
c.28G>C
n.7463G>C
c.7367G>C (p.Arg2456Thr)
 ClinVar dbSNP COSMIC COSMIC
13g.32356455G=CA2082814150BRCA2c.7463G= (p.Arg2488=)
c.7094G= (p.Arg2365=)
c.28G=
n.7463G=
c.7367G= (p.Arg2456=)
13g.32356455G>TCA387743145BRCA2c.7463G>T (p.Arg2488Ile)
c.7094G>T (p.Arg2365Ile)
c.28G>T
n.7463G>T
c.7367G>T (p.Arg2456Ile)
13g.32356455_32356456insTACA658823745BRCA2c.7463_7464insTA (p.Arg2488SerfsTer?)
c.7094_7095insTA (p.Arg2365SerfsTer?)
c.28_29insTA
n.7463_7464insTA
c.7367_7368insTA (p.Arg2456SerfsTer?)
 ClinVar dbSNP
13g.32356456A=CA2082814166BRCA2c.7464A= (p.Arg2488=)
c.7095A= (p.Arg2365=)
c.29A=
n.7464A=
c.7368A= (p.Arg2456=)
13g.32356456A>CCA025098BRCA2c.7464A>C (p.Arg2488Ser)
c.7095A>C (p.Arg2365Ser)
c.29A>C
n.7464A>C
c.7368A>C (p.Arg2456Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32356456A>GCA483260366BRCA2c.7464A>G (p.Arg2488=)
c.7095A>G (p.Arg2365=)
c.29A>G
n.7464A>G
c.7368A>G (p.Arg2456=)
 dbSNP gnomAD v3 gnomAD v4
13g.32356456A>TCA387743165BRCA2c.7464A>T (p.Arg2488Ser)
c.7095A>T (p.Arg2365Ser)
c.29A>T
n.7464A>T
c.7368A>T (p.Arg2456Ser)
13g.32356456_32356457insTACA10586575BRCA2c.7464_7465insTA (p.Asp2489Ter)
c.7095_7096insTA (p.Asp2366Ter)
c.29_30insTA
n.7464_7465insTA
c.7368_7369insTA (p.Asp2457Ter)
 ClinVar dbSNP
13g.32356457G>ACA387743173BRCA2c.7465G>A (p.Asp2489Asn)
c.7096G>A (p.Asp2366Asn)
c.30G>A
n.7465G>A
c.7369G>A (p.Asp2457Asn)
 ClinVar dbSNP
13g.32356457G>CCA387743172BRCA2c.7465G>C (p.Asp2489His)
c.7096G>C (p.Asp2366His)
c.30G>C
n.7465G>C
c.7369G>C (p.Asp2457His)
 dbSNP
13g.32356457G=CA2082814181BRCA2c.7465G= (p.Asp2489=)
c.7096G= (p.Asp2366=)
c.30G=
n.7465G=
c.7369G= (p.Asp2457=)
13g.32356457G>TCA387743174BRCA2c.7465G>T (p.Asp2489Tyr)
c.7096G>T (p.Asp2366Tyr)
c.30G>T
n.7465G>T
c.7369G>T (p.Asp2457Tyr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32356462_32356470delCA2580614679BRCA2c.7470_7478del (p.Ile2490_Asp2492del)
c.7101_7109del (p.Ile2367_Asp2369del)
c.35_43del
n.7470_7478del
c.7374_7382del (p.Ile2458_Asp2460del)
 ClinVar
13g.32356458A=CA2082814190BRCA2c.7466A= (p.Asp2489=)
c.7097A= (p.Asp2366=)
c.31A=
n.7466A=
c.7370A= (p.Asp2457=)
13g.32356458A>CCA387743177BRCA2c.7466A>C (p.Asp2489Ala)
c.7097A>C (p.Asp2366Ala)
c.31A>C
n.7466A>C
c.7370A>C (p.Asp2457Ala)
13g.32356458A>GCA025100BRCA2c.7466A>G (p.Asp2489Gly)
c.7097A>G (p.Asp2366Gly)
c.31A>G
n.7466A>G
c.7370A>G (p.Asp2457Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32356458A>TCA387743183BRCA2c.7466A>T (p.Asp2489Val)
c.7097A>T (p.Asp2366Val)
c.31A>T
n.7466A>T
c.7370A>T (p.Asp2457Val)
 dbSNP
13g.32356459T>ACA387743188BRCA2c.7467T>A (p.Asp2489Glu)
c.7098T>A (p.Asp2366Glu)
c.32T>A
n.7467T>A
c.7371T>A (p.Asp2457Glu)
 dbSNP
13g.32356459T>CCA483260367BRCA2c.7467T>C (p.Asp2489=)
c.7098T>C (p.Asp2366=)
c.32T>C
n.7467T>C
c.7371T>C (p.Asp2457=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32356459T>GCA387743191BRCA2c.7467T>G (p.Asp2489Glu)
c.7098T>G (p.Asp2366Glu)
c.32T>G
n.7467T>G
c.7371T>G (p.Asp2457Glu)
 ClinVar dbSNP
13g.32356459T=CA2082814204BRCA2c.7467T= (p.Asp2489=)
c.7098T= (p.Asp2366=)
c.32T=
n.7467T=
c.7371T= (p.Asp2457=)
13g.32356459dupCA025102BRCA2c.7467dup (p.Ile2490TyrfsTer7)
c.7098dup (p.Ile2367TyrfsTer7)
c.32dup
n.7467dup
c.7371dup (p.Ile2458TyrfsTer7)
 ClinVar dbSNP
13g.32356460A=CA2082814213BRCA2c.7468A= (p.Ile2490=)
c.7099A= (p.Ile2367=)
c.33A=
n.7468A=
c.7372A= (p.Ile2458=)
13g.32356460A>CCA387743196BRCA2c.7468A>C (p.Ile2490Leu)
c.7099A>C (p.Ile2367Leu)
c.33A>C
n.7468A>C
c.7372A>C (p.Ile2458Leu)
13g.32356460A>GCA387743199BRCA2c.7468A>G (p.Ile2490Val)
c.7099A>G (p.Ile2367Val)
c.33A>G
n.7468A>G
c.7372A>G (p.Ile2458Val)
 ClinVar dbSNP
13g.32356460A>TCA387743200BRCA2c.7468A>T (p.Ile2490Leu)
c.7099A>T (p.Ile2367Leu)
c.33A>T
n.7468A>T
c.7372A>T (p.Ile2458Leu)
 dbSNP
13g.32356460_32356461delinsATCA2082814212BRCA2c.7468_7469delinsAT (p.Ile2490=)
c.7099_7100delinsAT (p.Ile2367=)
c.33_34delinsAT
n.7468_7469delinsAT
c.7372_7373delinsAT (p.Ile2458=)
13g.32356461delCA10589429BRCA2c.7469del (p.Ile2490AsnfsTer?)
c.7100del (p.Ile2367AsnfsTer?)
c.34del
n.7469del
c.7373del (p.Ile2458AsnfsTer?)
 ClinVar dbSNP
13g.32356461T>ACA387743202BRCA2c.7469T>A (p.Ile2490Lys)
c.7100T>A (p.Ile2367Lys)
c.34T>A
n.7469T>A
c.7373T>A (p.Ile2458Lys)
 dbSNP
13g.32356461T>CCA025105BRCA2c.7469T>C (p.Ile2490Thr)
c.7100T>C (p.Ile2367Thr)
c.34T>C
n.7469T>C
c.7373T>C (p.Ile2458Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32356461T>GCA387743205BRCA2c.7469T>G (p.Ile2490Arg)
c.7100T>G (p.Ile2367Arg)
c.34T>G
n.7469T>G
c.7373T>G (p.Ile2458Arg)
13g.32356461T=CA2082814227BRCA2c.7469T= (p.Ile2490=)
c.7100T= (p.Ile2367=)
c.34T=
n.7469T=
c.7373T= (p.Ile2458=)
13g.32356461dupCA025104BRCA2c.7469dup (p.Gln2491ThrfsTer6)
c.7100dup (p.Gln2368ThrfsTer6)
c.34dup
n.7469dup
c.7373dup (p.Gln2459ThrfsTer6)
 ClinVar dbSNP
13g.32356462A=CA2082814239BRCA2c.7470A= (p.Ile2490=)
c.7101A= (p.Ile2367=)
c.35A=
n.7470A=
c.7374A= (p.Ile2458=)
13g.32356462A>CCA483260368BRCA2c.7470A>C (p.Ile2490=)
c.7101A>C (p.Ile2367=)
c.35A>C
n.7470A>C
c.7374A>C (p.Ile2458=)
13g.32356462A>GCA16606809BRCA2c.7470A>G (p.Ile2490Met)
c.7101A>G (p.Ile2367Met)
c.35A>G
n.7470A>G
c.7374A>G (p.Ile2458Met)
 ClinVar dbSNP gnomAD v4
13g.32356462A>TCA483260369BRCA2c.7470A>T (p.Ile2490=)
c.7101A>T (p.Ile2367=)
c.35A>T
n.7470A>T
c.7374A>T (p.Ile2458=)
 dbSNP
13g.32356462_32356463delinsACCA2082814238BRCA2c.7470_7471delinsAC (p.Ile2490=)
c.7101_7102delinsAC (p.Ile2367=)
c.35_36delinsAC
n.7470_7471delinsAC
c.7374_7375delinsAC (p.Ile2458=)
13g.32356463delCA10586576BRCA2c.7471del (p.Gln2491ArgfsTer?)
c.7102del (p.Gln2368ArgfsTer?)
c.36del
n.7471del
c.7375del (p.Gln2459ArgfsTer?)
 ClinVar dbSNP
13g.32356463C>ACA387743221BRCA2c.7471C>A (p.Gln2491Lys)
c.7102C>A (p.Gln2368Lys)
c.36C>A
n.7471C>A
c.7375C>A (p.Gln2459Lys)
 dbSNP
13g.32356463C=CA2082814252BRCA2c.7471C= (p.Gln2491=)
c.7102C= (p.Gln2368=)
c.36C=
n.7471C=
c.7375C= (p.Gln2459=)
13g.32356463C>GCA387743224BRCA2c.7471C>G (p.Gln2491Glu)
c.7102C>G (p.Gln2368Glu)
c.36C>G
n.7471C>G
c.7375C>G (p.Gln2459Glu)
 dbSNP
13g.32356463C>TCA025106BRCA2c.7471C>T (p.Gln2491Ter)
c.7102C>T (p.Gln2368Ter)
c.36C>T
n.7471C>T
c.7375C>T (p.Gln2459Ter)
 ClinVar dbSNP gnomAD v4
13g.32356464A=CA2082814263BRCA2c.7472A= (p.Gln2491=)
c.7103A= (p.Gln2368=)
c.37A=
n.7472A=
c.7376A= (p.Gln2459=)
13g.32356464A>CCA387743228BRCA2c.7472A>C (p.Gln2491Pro)
c.7103A>C (p.Gln2368Pro)
c.37A>C
n.7472A>C
c.7376A>C (p.Gln2459Pro)

Number of alleles fetched