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.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.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)
13g.32356464A>GCA247469683BRCA2c.7472A>G (p.Gln2491Arg)
c.7103A>G (p.Gln2368Arg)
c.37A>G
n.7472A>G
c.7376A>G (p.Gln2459Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32356464A>TCA387743232BRCA2c.7472A>T (p.Gln2491Leu)
c.7103A>T (p.Gln2368Leu)
c.37A>T
n.7472A>T
c.7376A>T (p.Gln2459Leu)
ClinVar dbSNP
13g.32356465G>ACA483260370BRCA2c.7473G>A (p.Gln2491=)
c.7104G>A (p.Gln2368=)
c.38G>A
n.7473G>A
c.7377G>A (p.Gln2459=)
ClinVar dbSNP gnomAD v4
13g.32356465G>CCA387743234BRCA2c.7473G>C (p.Gln2491His)
c.7104G>C (p.Gln2368His)
c.38G>C
n.7473G>C
c.7377G>C (p.Gln2459His)
ClinVar dbSNP
13g.32356465G>TCA387743236BRCA2c.7473G>T (p.Gln2491His)
c.7104G>T (p.Gln2368His)
c.38G>T
n.7473G>T
c.7377G>T (p.Gln2459His)
dbSNP
13g.32356465_32356467delinsGGACA2082814270BRCA2c.7473_7475delinsGGA (p.Gln2491=)
c.7104_7106delinsGGA (p.Gln2368=)
c.38_40delinsGGA
n.7473_7475delinsGGA
c.7377_7379delinsGGA (p.Gln2459=)
13g.32356466G>ACA387743238BRCA2c.7474G>A (p.Asp2492Asn)
c.7105G>A (p.Asp2369Asn)
c.39G>A
n.7474G>A
c.7378G>A (p.Asp2460Asn)
dbSNP
13g.32356466G>CCA387743240BRCA2c.7474G>C (p.Asp2492His)
c.7105G>C (p.Asp2369His)
c.39G>C
n.7474G>C
c.7378G>C (p.Asp2460His)
dbSNP
13g.32356466G>TCA387743245BRCA2c.7474G>T (p.Asp2492Tyr)
c.7105G>T (p.Asp2369Tyr)
c.39G>T
n.7474G>T
c.7378G>T (p.Asp2460Tyr)
13g.32356466_32356467delCA025107BRCA2c.7474_7475del (p.Asp2492TyrfsTer4)
c.7105_7106del (p.Asp2369TyrfsTer4)
c.39_40del
n.7474_7475del
c.7378_7379del (p.Asp2460TyrfsTer4)
ClinVar dbSNP
13g.32356467A>CCA387743249BRCA2c.7475A>C (p.Asp2492Ala)
c.7106A>C (p.Asp2369Ala)
c.40A>C
n.7475A>C
c.7379A>C (p.Asp2460Ala)
13g.32356467A>GCA387743250BRCA2c.7475A>G (p.Asp2492Gly)
c.7106A>G (p.Asp2369Gly)
c.40A>G
n.7475A>G
c.7379A>G (p.Asp2460Gly)
13g.32356467A>TCA387743248BRCA2c.7475A>T (p.Asp2492Val)
c.7106A>T (p.Asp2369Val)
c.40A>T
n.7475A>T
c.7379A>T (p.Asp2460Val)
13g.32356468T>ACA387743251BRCA2c.7476T>A (p.Asp2492Glu)
c.7107T>A (p.Asp2369Glu)
c.41T>A
n.7476T>A
c.7380T>A (p.Asp2460Glu)
dbSNP
13g.32356468T>CCA483260371BRCA2c.7476T>C (p.Asp2492=)
c.7107T>C (p.Asp2369=)
c.41T>C
n.7476T>C
c.7380T>C (p.Asp2460=)
ClinVar gnomAD v4
13g.32356468T>GCA387743253BRCA2c.7476T>G (p.Asp2492Glu)
c.7107T>G (p.Asp2369Glu)
c.41T>G
n.7476T>G
c.7380T>G (p.Asp2460Glu)
dbSNP
13g.32356469A=CA2082814287BRCA2c.7477A= (p.Met2493=)
c.7108A= (p.Met2370=)
c.42A=
n.7477A=
c.7381A= (p.Met2461=)
13g.32356469A>CCA387743256BRCA2c.7477A>C (p.Met2493Leu)
c.7108A>C (p.Met2370Leu)
c.42A>C
n.7477A>C
c.7381A>C (p.Met2461Leu)
13g.32356469A>GCA16619763BRCA2c.7477A>G (p.Met2493Val)
c.7108A>G (p.Met2370Val)
c.42A>G
n.7477A>G
c.7381A>G (p.Met2461Val)
ClinVar dbSNP
13g.32356469A>TCA387743260BRCA2c.7477A>T (p.Met2493Leu)
c.7108A>T (p.Met2370Leu)
c.42A>T
n.7477A>T
c.7381A>T (p.Met2461Leu)
ClinVar dbSNP gnomAD v4
13g.32356470T>ACA387743264BRCA2c.7478T>A (p.Met2493Lys)
c.7109T>A (p.Met2370Lys)
c.43T>A
n.7478T>A
c.7382T>A (p.Met2461Lys)
dbSNP
13g.32356470T>CCA336705BRCA2c.7478T>C (p.Met2493Thr)
c.7109T>C (p.Met2370Thr)
c.43T>C
n.7478T>C
c.7382T>C (p.Met2461Thr)
ClinVar dbSNP gnomAD v4
13g.32356470T>GCA10583131BRCA2c.7478T>G (p.Met2493Arg)
c.7109T>G (p.Met2370Arg)
c.43T>G
n.7478T>G
c.7382T>G (p.Met2461Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched