Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32354860_32355660delCA2499222270BRCA2c.7008-1_7435+372del
c.6639-1_7066+372del
n.7008-1_7435+372del
c.6912-1_7339+372del
ClinVar dbSNP
13g.32355016_32355021delinsCAAGAACA2082809360BRCA2c.7163_7168delinsCAAGAA (p.Thr2388=)
c.6794_6799delinsCAAGAA (p.Thr2265=)
n.7163_7168delinsCAAGAA
c.7067_7072delinsCAAGAA (p.Thr2356=)
13g.32355018_32355022delCA16619758BRCA2c.7165_7169del (p.Arg2389Ter)
c.6796_6800del (p.Arg2266Ter)
n.7165_7169del
c.7069_7073del (p.Arg2357Ter)
ClinVar dbSNP
13g.32355021A=CA2082809405BRCA2c.7168A= (p.Asn2390=)
c.6799A= (p.Asn2267=)
n.7168A=
c.7072A= (p.Asn2358=)
13g.32355021A>CCA387739427BRCA2c.7168A>C (p.Asn2390His)
c.6799A>C (p.Asn2267His)
n.7168A>C
c.7072A>C (p.Asn2358His)
13g.32355021A>GCA10579725BRCA2c.7168A>G (p.Asn2390Asp)
c.6799A>G (p.Asn2267Asp)
n.7168A>G
c.7072A>G (p.Asn2358Asp)
ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32355021A>TCA387739452BRCA2c.7168A>T (p.Asn2390Tyr)
c.6799A>T (p.Asn2267Tyr)
n.7168A>T
c.7072A>T (p.Asn2358Tyr)
dbSNP
13g.32355022A>CCA387739458BRCA2c.7169A>C (p.Asn2390Thr)
c.6800A>C (p.Asn2267Thr)
n.7169A>C
c.7073A>C (p.Asn2358Thr)
13g.32355022A>GCA387739460BRCA2c.7169A>G (p.Asn2390Ser)
c.6800A>G (p.Asn2267Ser)
n.7169A>G
c.7073A>G (p.Asn2358Ser)
13g.32355022A>TCA387739464BRCA2c.7169A>T (p.Asn2390Ile)
c.6800A>T (p.Asn2267Ile)
n.7169A>T
c.7073A>T (p.Asn2358Ile)
dbSNP
13g.32355023T>ACA387739495BRCA2c.7170T>A (p.Asn2390Lys)
c.6801T>A (p.Asn2267Lys)
n.7170T>A
c.7074T>A (p.Asn2358Lys)
ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32355023T>CCA483439645BRCA2c.7170T>C (p.Asn2390=)
c.6801T>C (p.Asn2267=)
n.7170T>C
c.7074T>C (p.Asn2358=)
ClinVar dbSNP
13g.32355023T>GCA387739499BRCA2c.7170T>G (p.Asn2390Lys)
c.6801T>G (p.Asn2267Lys)
n.7170T>G
c.7074T>G (p.Asn2358Lys)
dbSNP gnomAD v4
13g.32355023T=CA2082809416BRCA2c.7170T= (p.Asn2390=)
c.6801T= (p.Asn2267=)
n.7170T=
c.7074T= (p.Asn2358=)
13g.32355024G>ACA387739509BRCA2c.7171G>A (p.Glu2391Lys)
c.6802G>A (p.Glu2268Lys)
n.7171G>A
c.7075G>A (p.Glu2359Lys)
dbSNP gnomAD v3 gnomAD v4 COSMIC
13g.32355024G>CCA387739507BRCA2c.7171G>C (p.Glu2391Gln)
c.6802G>C (p.Glu2268Gln)
n.7171G>C
c.7075G>C (p.Glu2359Gln)
dbSNP
13g.32355024G>TCA387739504BRCA2c.7171G>T (p.Glu2391Ter)
c.6802G>T (p.Glu2268Ter)
n.7171G>T
c.7075G>T (p.Glu2359Ter)
ClinVar
13g.32355024_32355025delinsGACA2082809423BRCA2c.7171_7172delinsGA (p.Glu2391=)
c.6802_6803delinsGA (p.Glu2268=)
n.7171_7172delinsGA
c.7075_7076delinsGA (p.Glu2359=)
13g.32355025A=CA2082809427BRCA2c.7172A= (p.Glu2391=)
c.6803A= (p.Glu2268=)
n.7172A=
c.7076A= (p.Glu2359=)
13g.32355025A>CCA387739510BRCA2c.7172A>C (p.Glu2391Ala)
c.6803A>C (p.Glu2268Ala)
n.7172A>C
c.7076A>C (p.Glu2359Ala)
13g.32355025A>GCA387739512BRCA2c.7172A>G (p.Glu2391Gly)
c.6803A>G (p.Glu2268Gly)
n.7172A>G
c.7076A>G (p.Glu2359Gly)
dbSNP gnomAD v2 gnomAD v4
13g.32355025A>TCA387739517BRCA2c.7172A>T (p.Glu2391Val)
c.6803A>T (p.Glu2268Val)
n.7172A>T
c.7076A>T (p.Glu2359Val)
13g.32355030dupCA024922BRCA2c.7177dup (p.Met2393AsnfsTer19)
c.6808dup (p.Met2270AsnfsTer19)
n.7177dup
c.7081dup (p.Met2361AsnfsTer19)
ClinVar dbSNP gnomAD v4
13g.32355030delCA1139770422BRCA2c.7177del (p.Met2393Ter)
c.6808del (p.Met2270Ter)
n.7177del
c.7081del (p.Met2361Ter)
ClinVar dbSNP
13g.32355026A=CA2082809428BRCA2c.7173A= (p.Glu2391=)
c.6804A= (p.Glu2268=)
n.7173A=
c.7077A= (p.Glu2359=)
13g.32355026A>CCA387739522BRCA2c.7173A>C (p.Glu2391Asp)
c.6804A>C (p.Glu2268Asp)
n.7173A>C
c.7077A>C (p.Glu2359Asp)
ClinVar dbSNP
13g.32355026A>GCA483439654BRCA2c.7173A>G (p.Glu2391=)
c.6804A>G (p.Glu2268=)
n.7173A>G
c.7077A>G (p.Glu2359=)
ClinVar dbSNP
13g.32355026A>TCA387739525BRCA2c.7173A>T (p.Glu2391Asp)
c.6804A>T (p.Glu2268Asp)
n.7173A>T
c.7077A>T (p.Glu2359Asp)
dbSNP
13g.32355027A=CA2082809432BRCA2c.7174A= (p.Lys2392=)
c.6805A= (p.Lys2269=)
n.7174A=
c.7078A= (p.Lys2360=)
13g.32355027A>CCA387739532BRCA2c.7174A>C (p.Lys2392Gln)
c.6805A>C (p.Lys2269Gln)
n.7174A>C
c.7078A>C (p.Lys2360Gln)
13g.32355027A>GCA6941066BRCA2c.7174A>G (p.Lys2392Glu)
c.6805A>G (p.Lys2269Glu)
n.7174A>G
c.7078A>G (p.Lys2360Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32355027A>TCA387739533BRCA2c.7174A>T (p.Lys2392Ter)
c.6805A>T (p.Lys2269Ter)
n.7174A>T
c.7078A>T (p.Lys2360Ter)
13g.32355028A=CA2082809433BRCA2c.7175A= (p.Lys2392=)
c.6806A= (p.Lys2269=)
n.7175A=
c.7079A= (p.Lys2360=)
13g.32355028A>CCA387739534BRCA2c.7175A>C (p.Lys2392Thr)
c.6806A>C (p.Lys2269Thr)
n.7175A>C
c.7079A>C (p.Lys2360Thr)
ClinVar dbSNP
13g.32355028A>GCA387739535BRCA2c.7175A>G (p.Lys2392Arg)
c.6806A>G (p.Lys2269Arg)
n.7175A>G
c.7079A>G (p.Lys2360Arg)
dbSNP
13g.32355028A>TCA387739536BRCA2c.7175A>T (p.Lys2392Ile)
c.6806A>T (p.Lys2269Ile)
n.7175A>T
c.7079A>T (p.Lys2360Ile)
13g.32355029A>CCA387739538BRCA2c.7176A>C (p.Lys2392Asn)
c.6807A>C (p.Lys2269Asn)
n.7176A>C
c.7080A>C (p.Lys2360Asn)
13g.32355029A>GCA483439658BRCA2c.7176A>G (p.Lys2392=)
c.6807A>G (p.Lys2269=)
n.7176A>G
c.7080A>G (p.Lys2360=)
13g.32355029A>TCA387739542BRCA2c.7176A>T (p.Lys2392Asn)
c.6807A>T (p.Lys2269Asn)
n.7176A>T
c.7080A>T (p.Lys2360Asn)
dbSNP
13g.32355030A=CA2082809434BRCA2c.7177A= (p.Met2393=)
c.6808A= (p.Met2270=)
n.7177A=
c.7081A= (p.Met2361=)
13g.32355030A>CCA387739547BRCA2c.7177A>C (p.Met2393Leu)
c.6808A>C (p.Met2270Leu)
n.7177A>C
c.7081A>C (p.Met2361Leu)
13g.32355030A>GCA024924BRCA2c.7177A>G (p.Met2393Val)
c.6808A>G (p.Met2270Val)
n.7177A>G
c.7081A>G (p.Met2361Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32355030A>TCA387739546BRCA2c.7177A>T (p.Met2393Leu)
c.6808A>T (p.Met2270Leu)
n.7177A>T
c.7081A>T (p.Met2361Leu)
dbSNP
13g.32355030_32355032delinsATGCA2082809435BRCA2c.7177_7179delinsATG (p.Met2393=)
c.6808_6810delinsATG (p.Met2270=)
n.7177_7179delinsATG
c.7081_7083delinsATG (p.Met2361=)
13g.32355031T>ACA387739551BRCA2c.7178T>A (p.Met2393Lys)
c.6809T>A (p.Met2270Lys)
n.7178T>A
c.7082T>A (p.Met2361Lys)
dbSNP
13g.32355031T>CCA024926BRCA2c.7178T>C (p.Met2393Thr)
c.6809T>C (p.Met2270Thr)
n.7178T>C
c.7082T>C (p.Met2361Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32355031T>GCA387739554BRCA2c.7178T>G (p.Met2393Arg)
c.6809T>G (p.Met2270Arg)
n.7178T>G
c.7082T>G (p.Met2361Arg)
13g.32355031T=CA2082809438BRCA2c.7178T= (p.Met2393=)
c.6809T= (p.Met2270=)
n.7178T=
c.7082T= (p.Met2361=)
13g.32355031_32355032delCA919242705BRCA2c.7178_7179del (p.Met2393LysfsTer18)
c.6809_6810del (p.Met2270LysfsTer18)
n.7178_7179del
c.7082_7083del (p.Met2361LysfsTer18)
dbSNP
13g.32355032G>ACA387739556BRCA2c.7179G>A (p.Met2393Ile)
c.6810G>A (p.Met2270Ile)
n.7179G>A
c.7083G>A (p.Met2361Ile)
ClinVar dbSNP

Number of alleles fetched