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.32356502_32356793delCA2580087468BRCA2c.7510_7617+184del
c.7141_7248+184del
c.75_182+184del
n.7510_7617+184del
c.7414_7521+184del
 ClinVar
13g.32356566_32356567delinsCACA2082815294BRCA2c.7574_7575delinsCA (p.Ala2525=)
c.7205_7206delinsCA (p.Ala2402=)
c.41_42delinsCA (p.Ala14=)
c.139_140delinsCA
n.7574_7575delinsCA
c.7478_7479delinsCA (p.Ala2493=)
13g.32356567delCA10576071BRCA2c.7575del (p.Ala2526GlnfsTer2)
c.7206del (p.Ala2403GlnfsTer2)
c.42del (p.Ala15GlnfsTer2)
c.140del
n.7575del
c.7479del (p.Ala2494GlnfsTer2)
 ClinVar dbSNP
13g.32356567A>CCA483260435BRCA2c.7575A>C (p.Ala2525=)
c.7206A>C (p.Ala2402=)
c.42A>C (p.Ala14=)
c.140A>C
n.7575A>C
c.7479A>C (p.Ala2493=)
13g.32356567A>GCA483260434BRCA2c.7575A>G (p.Ala2525=)
c.7206A>G (p.Ala2402=)
c.42A>G (p.Ala14=)
c.140A>G
n.7575A>G
c.7479A>G (p.Ala2493=)
13g.32356567A>TCA483260433BRCA2c.7575A>T (p.Ala2525=)
c.7206A>T (p.Ala2402=)
c.42A>T (p.Ala14=)
c.140A>T
n.7575A>T
c.7479A>T (p.Ala2493=)
 ClinVar dbSNP gnomAD v4
13g.32356568G>ACA387743810BRCA2c.7576G>A (p.Ala2526Thr)
c.7207G>A (p.Ala2403Thr)
c.43G>A (p.Ala15Thr)
c.141G>A
n.7576G>A
c.7480G>A (p.Ala2494Thr)
 ClinVar dbSNP
13g.32356568G>CCA387743812BRCA2c.7576G>C (p.Ala2526Pro)
c.7207G>C (p.Ala2403Pro)
c.43G>C (p.Ala15Pro)
c.141G>C
n.7576G>C
c.7480G>C (p.Ala2494Pro)
 dbSNP
13g.32356568G=CA2082815304BRCA2c.7576G= (p.Ala2526=)
c.7207G= (p.Ala2403=)
c.43G= (p.Ala15=)
c.141G=
n.7576G=
c.7480G= (p.Ala2494=)
13g.32356568G>TCA387743814BRCA2c.7576G>T (p.Ala2526Ser)
c.7207G>T (p.Ala2403Ser)
c.43G>T (p.Ala15Ser)
c.141G>T
n.7576G>T
c.7480G>T (p.Ala2494Ser)
13g.32356569C>ACA387743815BRCA2c.7577C>A (p.Ala2526Glu)
c.7208C>A (p.Ala2403Glu)
c.44C>A (p.Ala15Glu)
c.142C>A
n.7577C>A
c.7481C>A (p.Ala2494Glu)
 dbSNP
13g.32356569C=CA2082815312BRCA2c.7577C= (p.Ala2526=)
c.7208C= (p.Ala2403=)
c.44C= (p.Ala15=)
c.142C=
n.7577C=
c.7481C= (p.Ala2494=)
13g.32356569C>GCA387743818BRCA2c.7577C>G (p.Ala2526Gly)
c.7208C>G (p.Ala2403Gly)
c.44C>G (p.Ala15Gly)
c.142C>G
n.7577C>G
c.7481C>G (p.Ala2494Gly)
 ClinVar dbSNP
13g.32356569C>TCA387743820BRCA2c.7577C>T (p.Ala2526Val)
c.7208C>T (p.Ala2403Val)
c.44C>T (p.Ala15Val)
c.142C>T
n.7577C>T
c.7481C>T (p.Ala2494Val)
 ClinVar dbSNP
13g.32356569_32356571delinsCAGCA2082815314BRCA2c.7577_7579delinsCAG (p.Ala2526=)
c.7208_7210delinsCAG (p.Ala2403=)
c.44_46delinsCAG (p.Ala15=)
c.142_144delinsCAG
n.7577_7579delinsCAG
c.7481_7483delinsCAG (p.Ala2494=)
13g.32356569_32356572delCA2622571688BRCA2c.7577_7580del (p.Ala2526GlufsTer24)
c.7208_7211del (p.Ala2403GlufsTer24)
c.44_47del (p.Ala15GlufsTer24)
c.142_145del
n.7577_7580del
c.7481_7484del (p.Ala2494GlufsTer24)
 ClinVar gnomAD v4
13g.32356569_32356575delinsAGGACA2695217911BRCA2c.7577_7583delinsAGGA (p.Ala2526_Gly2528delinsGluGlu)
c.7208_7214delinsAGGA (p.Ala2403_Gly2405delinsGluGlu)
c.44_50delinsAGGA (p.Ala15_Gly17delinsGluGlu)
c.142_148delinsAGGA
n.7577_7583delinsAGGA
c.7481_7487delinsAGGA (p.Ala2494_Gly2496delinsGluGlu)
13g.32356570A=CA2082815321BRCA2c.7578A= (p.Ala2526=)
c.7209A= (p.Ala2403=)
c.45A= (p.Ala15=)
c.143A=
n.7578A=
c.7482A= (p.Ala2494=)
13g.32356570A>CCA483260438BRCA2c.7578A>C (p.Ala2526=)
c.7209A>C (p.Ala2403=)
c.45A>C (p.Ala15=)
c.143A>C
n.7578A>C
c.7482A>C (p.Ala2494=)
13g.32356570A>GCA483260437BRCA2c.7578A>G (p.Ala2526=)
c.7209A>G (p.Ala2403=)
c.45A>G (p.Ala15=)
c.143A>G
n.7578A>G
c.7482A>G (p.Ala2494=)
 ClinVar gnomAD v4
13g.32356570A>TCA483260436BRCA2c.7578A>T (p.Ala2526=)
c.7209A>T (p.Ala2403=)
c.45A>T (p.Ala15=)
c.143A>T
n.7578A>T
c.7482A>T (p.Ala2494=)
13g.32356570_32356571delCA1139663193BRCA2c.7578_7579del (p.Val2527ArgfsTer11)
c.7209_7210del (p.Val2404ArgfsTer11)
c.45_46del (p.Val16ArgfsTer11)
c.143_144del
n.7578_7579del
c.7482_7483del (p.Val2495ArgfsTer11)
 ClinVar dbSNP
13g.32356570_32356571delinsAGCA2082815318BRCA2c.7578_7579delinsAG (p.Ala2526=)
c.7209_7210delinsAG (p.Ala2403=)
c.45_46delinsAG (p.Ala15=)
c.143_144delinsAG
n.7578_7579delinsAG
c.7482_7483delinsAG (p.Ala2494=)
13g.32356572_32356574delCA2573149395BRCA2c.7580_7582del (p.Val2527del)
c.7211_7213del (p.Val2404del)
c.47_49del (p.Val16del)
c.145_147del
n.7580_7582del
c.7484_7486del (p.Val2495del)
 ClinVar dbSNP
13g.32356571delCA658683852BRCA2c.7579del (p.Val2527Ter)
c.7210del (p.Val2404Ter)
c.46del (p.Val16Ter)
c.144del
n.7579del
c.7483del (p.Val2495Ter)
 ClinVar dbSNP
13g.32356571G>ACA387743822BRCA2c.7579G>A (p.Val2527Ile)
c.7210G>A (p.Val2404Ile)
c.46G>A (p.Val16Ile)
c.144G>A
n.7579G>A
c.7483G>A (p.Val2495Ile)
 ClinVar dbSNP
13g.32356571G>CCA387743827BRCA2c.7579G>C (p.Val2527Leu)
c.7210G>C (p.Val2404Leu)
c.46G>C (p.Val16Leu)
c.144G>C
n.7579G>C
c.7483G>C (p.Val2495Leu)
 dbSNP
13g.32356571G=CA2082815340BRCA2c.7579G= (p.Val2527=)
c.7210G= (p.Val2404=)
c.46G= (p.Val16=)
c.144G=
n.7579G=
c.7483G= (p.Val2495=)
13g.32356571G>TCA387743824BRCA2c.7579G>T (p.Val2527Leu)
c.7210G>T (p.Val2404Leu)
c.46G>T (p.Val16Leu)
c.144G>T
n.7579G>T
c.7483G>T (p.Val2495Leu)
 ClinVar dbSNP gnomAD v4
13g.32356572_32356575dupCA658656436BRCA2c.7580_7583dup (p.Gly2529ArgfsTer11)
c.7211_7214dup (p.Gly2406ArgfsTer11)
c.47_50dup (p.Gly18ArgfsTer11)
c.145_148dup
n.7580_7583dup
c.7484_7487dup (p.Gly2497ArgfsTer11)
 ClinVar dbSNP
13g.32356572T>ACA387743828BRCA2c.7580T>A (p.Val2527Glu)
c.7211T>A (p.Val2404Glu)
c.47T>A (p.Val16Glu)
c.145T>A
n.7580T>A
c.7484T>A (p.Val2495Glu)
 dbSNP
13g.32356572T>CCA025161BRCA2c.7580T>C (p.Val2527Ala)
c.7211T>C (p.Val2404Ala)
c.47T>C (p.Val16Ala)
c.145T>C
n.7580T>C
c.7484T>C (p.Val2495Ala)
 ClinVar dbSNP gnomAD v4
13g.32356572T>GCA387743833BRCA2c.7580T>G (p.Val2527Gly)
c.7211T>G (p.Val2404Gly)
c.47T>G (p.Val16Gly)
c.145T>G
n.7580T>G
c.7484T>G (p.Val2495Gly)
13g.32356572T=CA2082815355BRCA2c.7580T= (p.Val2527=)
c.7211T= (p.Val2404=)
c.47T= (p.Val16=)
c.145T=
n.7580T=
c.7484T= (p.Val2495=)
13g.32356572dupCA645372940BRCA2c.7580dup (p.Gly2528ArgfsTer11)
c.7211dup (p.Gly2405ArgfsTer11)
c.47dup (p.Gly17ArgfsTer11)
c.145dup
n.7580dup
c.7484dup (p.Gly2496ArgfsTer11)
 ClinVar dbSNP gnomAD v4
13g.32356573A=CA2082815365BRCA2c.7581A= (p.Val2527=)
c.7212A= (p.Val2404=)
c.48A= (p.Val16=)
c.146A=
n.7581A=
c.7485A= (p.Val2495=)
13g.32356573A>CCA483260441BRCA2c.7581A>C (p.Val2527=)
c.7212A>C (p.Val2404=)
c.48A>C (p.Val16=)
c.146A>C
n.7581A>C
c.7485A>C (p.Val2495=)
13g.32356573A>GCA483260440BRCA2c.7581A>G (p.Val2527=)
c.7212A>G (p.Val2404=)
c.48A>G (p.Val16=)
c.146A>G
n.7581A>G
c.7485A>G (p.Val2495=)
 ClinVar dbSNP gnomAD v2
13g.32356573A>TCA483260439BRCA2c.7581A>T (p.Val2527=)
c.7212A>T (p.Val2404=)
c.48A>T (p.Val16=)
c.146A>T
n.7581A>T
c.7485A>T (p.Val2495=)
13g.32356576_32356578delCA2573130315BRCA2c.7584_7586del (p.Gly2529del)
c.7215_7217del (p.Gly2406del)
c.51_53del (p.Gly18del)
c.149_151del
n.7584_7586del
c.7488_7490del (p.Gly2497del)
 ClinVar dbSNP
13g.32356574G>ACA387743837BRCA2c.7582G>A (p.Gly2528Arg)
c.7213G>A (p.Gly2405Arg)
c.49G>A (p.Gly17Arg)
c.147G>A
n.7582G>A
c.7486G>A (p.Gly2496Arg)
 ClinVar dbSNP
13g.32356574G>CCA387743839BRCA2c.7582G>C (p.Gly2528Arg)
c.7213G>C (p.Gly2405Arg)
c.49G>C (p.Gly17Arg)
c.147G>C
n.7582G>C
c.7486G>C (p.Gly2496Arg)
 dbSNP
13g.32356574G=CA2082815368BRCA2c.7582G= (p.Gly2528=)
c.7213G= (p.Gly2405=)
c.49G= (p.Gly17=)
c.147G=
n.7582G=
c.7486G= (p.Gly2496=)
13g.32356574G>TCA387743842BRCA2c.7582G>T (p.Gly2528Ter)
c.7213G>T (p.Gly2405Ter)
c.49G>T (p.Gly17Ter)
c.147G>T
n.7582G>T
c.7486G>T (p.Gly2496Ter)
13g.32356574_32356575insACA2622571701BRCA2c.7582_7583insA (p.Gly2528GlufsTer11)
c.7213_7214insA (p.Gly2405GlufsTer11)
c.49_50insA (p.Gly17GlufsTer11)
c.147_148insA
n.7582_7583insA
c.7486_7487insA (p.Gly2496GlufsTer11)
 ClinVar gnomAD v4
13g.32356575G>ACA025162BRCA2c.7583G>A (p.Gly2528Glu)
c.7214G>A (p.Gly2405Glu)
c.50G>A (p.Gly17Glu)
c.148G>A
n.7583G>A
c.7487G>A (p.Gly2496Glu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32356575G>CCA387743846BRCA2c.7583G>C (p.Gly2528Ala)
c.7214G>C (p.Gly2405Ala)
c.50G>C (p.Gly17Ala)
c.148G>C
n.7583G>C
c.7487G>C (p.Gly2496Ala)
 dbSNP
13g.32356575G=CA2082815372BRCA2c.7583G= (p.Gly2528=)
c.7214G= (p.Gly2405=)
c.50G= (p.Gly17=)
c.148G=
n.7583G=
c.7487G= (p.Gly2496=)
13g.32356575G>TCA387743848BRCA2c.7583G>T (p.Gly2528Val)
c.7214G>T (p.Gly2405Val)
c.50G>T (p.Gly17Val)
c.148G>T
n.7583G>T
c.7487G>T (p.Gly2496Val)
13g.32356576A>CCA483260444BRCA2c.7584A>C (p.Gly2528=)
c.7215A>C (p.Gly2405=)
c.51A>C (p.Gly17=)
c.149A>C
n.7584A>C
c.7488A>C (p.Gly2496=)
13g.32356576A>GCA483260442BRCA2c.7584A>G (p.Gly2528=)
c.7215A>G (p.Gly2405=)
c.51A>G (p.Gly17=)
c.149A>G
n.7584A>G
c.7488A>G (p.Gly2496=)
13g.32356576A>TCA483260443BRCA2c.7584A>T (p.Gly2528=)
c.7215A>T (p.Gly2405=)
c.51A>T (p.Gly17=)
c.149A>T
n.7584A>T
c.7488A>T (p.Gly2496=)
 dbSNP
13g.32356576_32356577delinsAGCA2082815376BRCA2c.7584_7585delinsAG (p.Gly2528=)
c.7215_7216delinsAG (p.Gly2405=)
c.51_52delinsAG (p.Gly17=)
c.149_150delinsAG
n.7584_7585delinsAG
c.7488_7489delinsAG (p.Gly2496=)
13g.32356577G>ACA025163BRCA2c.7585G>A (p.Gly2529Ser)
c.7216G>A (p.Gly2406Ser)
c.52G>A (p.Gly18Ser)
c.150G>A
n.7585G>A
c.7489G>A (p.Gly2497Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32356577G>CCA387743854BRCA2c.7585G>C (p.Gly2529Arg)
c.7216G>C (p.Gly2406Arg)
c.52G>C (p.Gly18Arg)
c.150G>C
n.7585G>C
c.7489G>C (p.Gly2497Arg)
 ClinVar dbSNP
13g.32356577G=CA2082815382BRCA2c.7585G= (p.Gly2529=)
c.7216G= (p.Gly2406=)
c.52G= (p.Gly18=)
c.150G=
n.7585G=
c.7489G= (p.Gly2497=)
13g.32356577G>TCA387743857BRCA2c.7585G>T (p.Gly2529Cys)
c.7216G>T (p.Gly2406Cys)
c.52G>T (p.Gly18Cys)
c.150G>T
n.7585G>T
c.7489G>T (p.Gly2497Cys)
 dbSNP
13g.32356578delCA1139663194BRCA2c.7586del (p.Gly2529AlafsTer22)
c.7217del (p.Gly2406AlafsTer22)
c.53del (p.Gly18AlafsTer22)
c.151del
n.7586del
c.7490del (p.Gly2497AlafsTer22)
 ClinVar dbSNP
13g.32356578G>ACA387743860BRCA2c.7586G>A (p.Gly2529Asp)
c.7217G>A (p.Gly2406Asp)
c.53G>A (p.Gly18Asp)
c.151G>A
n.7586G>A
c.7490G>A (p.Gly2497Asp)
13g.32356578G>CCA387743863BRCA2c.7586G>C (p.Gly2529Ala)
c.7217G>C (p.Gly2406Ala)
c.53G>C (p.Gly18Ala)
c.151G>C
n.7586G>C
c.7490G>C (p.Gly2497Ala)
13g.32356578G>TCA387743862BRCA2c.7586G>T (p.Gly2529Val)
c.7217G>T (p.Gly2406Val)
c.53G>T (p.Gly18Val)
c.151G>T
n.7586G>T
c.7490G>T (p.Gly2497Val)
13g.32356578_32356579delinsGCCA2082815387BRCA2c.7586_7587delinsGC (p.Gly2529=)
c.7217_7218delinsGC (p.Gly2406=)
c.53_54delinsGC (p.Gly18=)
c.151_152delinsGC
n.7586_7587delinsGC
c.7490_7491delinsGC (p.Gly2497=)
13g.32356579C>ACA483260447BRCA2c.7587C>A (p.Gly2529=)
c.7218C>A (p.Gly2406=)
c.54C>A (p.Gly18=)
c.152C>A
n.7587C>A
c.7491C>A (p.Gly2497=)
 dbSNP
13g.32356579C>GCA483260448BRCA2c.7587C>G (p.Gly2529=)
c.7218C>G (p.Gly2406=)
c.54C>G (p.Gly18=)
c.152C>G
n.7587C>G
c.7491C>G (p.Gly2497=)
 dbSNP
13g.32356579C>TCA483260449BRCA2c.7587C>T (p.Gly2529=)
c.7218C>T (p.Gly2406=)
c.54C>T (p.Gly18=)
c.152C>T
n.7587C>T
c.7491C>T (p.Gly2497=)
 ClinVar dbSNP
13g.32356580delCA025164BRCA2c.7588del (p.Gln2530LysfsTer21)
c.7219del (p.Gln2407LysfsTer21)
c.55del (p.Gln19LysfsTer21)
c.153del
n.7588del
c.7492del (p.Gln2498LysfsTer21)
 ClinVar dbSNP
13g.32356580C>ACA387743867BRCA2c.7588C>A (p.Gln2530Lys)
c.7219C>A (p.Gln2407Lys)
c.55C>A (p.Gln19Lys)
c.153C>A
n.7588C>A
c.7492C>A (p.Gln2498Lys)
13g.32356580C>GCA387743870BRCA2c.7588C>G (p.Gln2530Glu)
c.7219C>G (p.Gln2407Glu)
c.55C>G (p.Gln19Glu)
c.153C>G
n.7588C>G
c.7492C>G (p.Gln2498Glu)
13g.32356580C>TCA387743872BRCA2c.7588C>T (p.Gln2530Ter)
c.7219C>T (p.Gln2407Ter)
c.55C>T (p.Gln19Ter)
c.153C>T
n.7588C>T
c.7492C>T (p.Gln2498Ter)
 ClinVar gnomAD v4
13g.32356581A=CA2082815395BRCA2c.7589A= (p.Gln2530=)
c.7220A= (p.Gln2407=)
c.56A= (p.Gln19=)
c.154A=
n.7589A=
c.7493A= (p.Gln2498=)
13g.32356581A>CCA387743874BRCA2c.7589A>C (p.Gln2530Pro)
c.7220A>C (p.Gln2407Pro)
c.56A>C (p.Gln19Pro)
c.154A>C
n.7589A>C
c.7493A>C (p.Gln2498Pro)
 dbSNP gnomAD v3 gnomAD v4
13g.32356581A>GCA387743876BRCA2c.7589A>G (p.Gln2530Arg)
c.7220A>G (p.Gln2407Arg)
c.56A>G (p.Gln19Arg)
c.154A>G
n.7589A>G
c.7493A>G (p.Gln2498Arg)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32356581A>TCA387743878BRCA2c.7589A>T (p.Gln2530Leu)
c.7220A>T (p.Gln2407Leu)
c.56A>T (p.Gln19Leu)
c.154A>T
n.7589A>T
c.7493A>T (p.Gln2498Leu)
13g.32356582A=CA2082815408BRCA2c.7590A= (p.Gln2530=)
c.7221A= (p.Gln2407=)
c.57A= (p.Gln19=)
c.155A=
n.7590A=
c.7494A= (p.Gln2498=)
13g.32356582A>CCA025165BRCA2c.7590A>C (p.Gln2530His)
c.7221A>C (p.Gln2407His)
c.57A>C (p.Gln19His)
c.155A>C
n.7590A>C
c.7494A>C (p.Gln2498His)
 ClinVar dbSNP
13g.32356582A>GCA483260450BRCA2c.7590A>G (p.Gln2530=)
c.7221A>G (p.Gln2407=)
c.57A>G (p.Gln19=)
c.155A>G
n.7590A>G
c.7494A>G (p.Gln2498=)
 ClinVar dbSNP gnomAD v4
13g.32356582A>TCA387743883BRCA2c.7590A>T (p.Gln2530His)
c.7221A>T (p.Gln2407His)
c.57A>T (p.Gln19His)
c.155A>T
n.7590A>T
c.7494A>T (p.Gln2498His)
 ClinVar dbSNP
13g.32356583G>ACA387743888BRCA2c.7591G>A (p.Val2531Ile)
c.7222G>A (p.Val2408Ile)
c.58G>A (p.Val20Ile)
c.156G>A
n.7591G>A
c.7495G>A (p.Val2499Ile)
 ClinVar dbSNP
13g.32356583G>CCA387743891BRCA2c.7591G>C (p.Val2531Leu)
c.7222G>C (p.Val2408Leu)
c.58G>C (p.Val20Leu)
c.156G>C
n.7591G>C
c.7495G>C (p.Val2499Leu)
 dbSNP
13g.32356583G>TCA387743886BRCA2c.7591G>T (p.Val2531Phe)
c.7222G>T (p.Val2408Phe)
c.58G>T (p.Val20Phe)
c.156G>T
n.7591G>T
c.7495G>T (p.Val2499Phe)
13g.32356583_32356584delinsGTCA2082815416BRCA2c.7591_7592delinsGT (p.Val2531=)
c.7222_7223delinsGT (p.Val2408=)
c.58_59delinsGT (p.Val20=)
c.156_157delinsGT
n.7591_7592delinsGT
c.7495_7496delinsGT (p.Val2499=)
13g.32356583_32356587delinsGTTCCCA2082815418BRCA2c.7591_7595delinsGTTCC (p.Val2531=)
c.7222_7226delinsGTTCC (p.Val2408=)
c.58_62delinsGTTCC (p.Val20=)
c.156_160delinsGTTCC
n.7591_7595delinsGTTCC
c.7495_7499delinsGTTCC (p.Val2499=)
13g.32356584T>ACA387743899BRCA2c.7592T>A (p.Val2531Asp)
c.7223T>A (p.Val2408Asp)
c.59T>A (p.Val20Asp)
c.157T>A
n.7592T>A
c.7496T>A (p.Val2499Asp)
 dbSNP
13g.32356584T>CCA387743892BRCA2c.7592T>C (p.Val2531Ala)
c.7223T>C (p.Val2408Ala)
c.59T>C (p.Val20Ala)
c.157T>C
n.7592T>C
c.7496T>C (p.Val2499Ala)
13g.32356584T>GCA387743895BRCA2c.7592T>G (p.Val2531Gly)
c.7223T>G (p.Val2408Gly)
c.59T>G (p.Val20Gly)
c.157T>G
n.7592T>G
c.7496T>G (p.Val2499Gly)
13g.32356585delCA025166BRCA2c.7593del (p.Ser2533LeufsTer18)
c.7224del (p.Ser2410LeufsTer18)
c.60del (p.Ser22LeufsTer18)
c.158del
n.7593del
c.7497del (p.Ser2501LeufsTer18)
 ClinVar dbSNP
13g.32356584_32356587delinsCAGTAGGAGGCA915946872BRCA2c.7592_7595delinsCAGTAGGAGG (p.Val2531_Pro2532delinsAlaValGlyGly)
c.7223_7226delinsCAGTAGGAGG (p.Val2408_Pro2409delinsAlaValGlyGly)
c.59_62delinsCAGTAGGAGG (p.Val20_Pro21delinsAlaValGlyGly)
c.157_160delinsCAGTAGGAGG
n.7592_7595delinsCAGTAGGAGG
c.7496_7499delinsCAGTAGGAGG (p.Val2499_Pro2500delinsAlaValGlyGly)
 ClinVar dbSNP
13g.32356585T>ACA483260452BRCA2c.7593T>A (p.Val2531=)
c.7224T>A (p.Val2408=)
c.60T>A (p.Val20=)
c.158T>A
n.7593T>A
c.7497T>A (p.Val2499=)
 ClinVar dbSNP gnomAD v4
13g.32356585T>CCA247470129BRCA2c.7593T>C (p.Val2531=)
c.7224T>C (p.Val2408=)
c.60T>C (p.Val20=)
c.158T>C
n.7593T>C
c.7497T>C (p.Val2499=)
 dbSNP
13g.32356585T>GCA483260453BRCA2c.7593T>G (p.Val2531=)
c.7224T>G (p.Val2408=)
c.60T>G (p.Val20=)
c.158T>G
n.7593T>G
c.7497T>G (p.Val2499=)
13g.32356585T=CA2018069962BRCA2c.7593T= (p.Val2531=)
c.7224T= (p.Val2408=)
c.60T= (p.Val20=)
c.158T=
n.7593T=
c.7497T= (p.Val2499=)
13g.32356586C>ACA387743902BRCA2c.7594C>A (p.Pro2532Thr)
c.7225C>A (p.Pro2409Thr)
c.61C>A (p.Pro21Thr)
c.159C>A
n.7594C>A
c.7498C>A (p.Pro2500Thr)
 ClinVar dbSNP
13g.32356586C=CA2082815439BRCA2c.7594C= (p.Pro2532=)
c.7225C= (p.Pro2409=)
c.61C= (p.Pro21=)
c.159C=
n.7594C=
c.7498C= (p.Pro2500=)
13g.32356586C>GCA387743906BRCA2c.7594C>G (p.Pro2532Ala)
c.7225C>G (p.Pro2409Ala)
c.61C>G (p.Pro21Ala)
c.159C>G
n.7594C>G
c.7498C>G (p.Pro2500Ala)
 ClinVar dbSNP
13g.32356586C>TCA025167BRCA2c.7594C>T (p.Pro2532Ser)
c.7225C>T (p.Pro2409Ser)
c.61C>T (p.Pro21Ser)
c.159C>T
n.7594C>T
c.7498C>T (p.Pro2500Ser)
 ClinVar dbSNP gnomAD v4
13g.32356586_32356600delinsCCCTCTGCGTGTTCTCA2082815459BRCA2c.7594_7608delinsCCCTCTGCGTGTTCT (p.Pro2532=)
c.7225_7239delinsCCCTCTGCGTGTTCT (p.Pro2409=)
c.61_75delinsCCCTCTGCGTGTTCT (p.Pro21=)
c.159_173delinsCCCTCTGCGTGTTCT
n.7594_7608delinsCCCTCTGCGTGTTCT
c.7498_7512delinsCCCTCTGCGTGTTCT (p.Pro2500=)
13g.32356586_32356587insTTCA658823748BRCA2c.7594_7595insTT (p.Pro2532LeufsTer20)
c.7225_7226insTT (p.Pro2409LeufsTer20)
c.61_62insTT (p.Pro21LeufsTer20)
c.159_160insTT
n.7594_7595insTT
c.7498_7499insTT (p.Pro2500LeufsTer20)
 ClinVar dbSNP
13g.32356587C>ACA247470136BRCA2c.7595C>A (p.Pro2532His)
c.7226C>A (p.Pro2409His)
c.62C>A (p.Pro21His)
c.160C>A
n.7595C>A
c.7499C>A (p.Pro2500His)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32356587C=CA2082815481BRCA2c.7595C= (p.Pro2532=)
c.7226C= (p.Pro2409=)
c.62C= (p.Pro21=)
c.160C=
n.7595C=
c.7499C= (p.Pro2500=)
13g.32356587C>GCA387743927BRCA2c.7595C>G (p.Pro2532Arg)
c.7226C>G (p.Pro2409Arg)
c.62C>G (p.Pro21Arg)
c.160C>G
n.7595C>G
c.7499C>G (p.Pro2500Arg)
 dbSNP
13g.32356587C>TCA387743924BRCA2c.7595C>T (p.Pro2532Leu)
c.7226C>T (p.Pro2409Leu)
c.62C>T (p.Pro21Leu)
c.160C>T
n.7595C>T
c.7499C>T (p.Pro2500Leu)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC
13g.32356588_32356601delCA025169BRCA2c.7596_7609del (p.Ser2533Ter)
c.7227_7240del (p.Ser2410Ter)
c.63_76del (p.Ser22Ter)
c.161_174del
n.7596_7609del
c.7500_7513del (p.Ser2501Ter)
 ClinVar dbSNP
13g.32356587_32356588insTTCA025168BRCA2c.7595_7596insTT (p.Ala2534LeufsTer18)
c.7226_7227insTT (p.Ala2411LeufsTer18)
c.62_63insTT (p.Ala23LeufsTer18)
c.160_161insTT
n.7595_7596insTT
c.7499_7500insTT (p.Ala2502LeufsTer18)
 ClinVar dbSNP
13g.32356587_32356588insAGTAGGAGGCA2573149397BRCA2c.7595_7596insAGTAGGAGG (p.Pro2532_Ser2533insValGlyGly)
c.7226_7227insAGTAGGAGG (p.Pro2409_Ser2410insValGlyGly)
c.62_63insAGTAGGAGG (p.Pro21_Ser22insValGlyGly)
c.160_161insAGTAGGAGG
n.7595_7596insAGTAGGAGG
c.7499_7500insAGTAGGAGG (p.Pro2500_Ser2501insValGlyGly)
 dbSNP
13g.32356588C>ACA483260454BRCA2c.7596C>A (p.Pro2532=)
c.7227C>A (p.Pro2409=)
c.63C>A (p.Pro21=)
c.161C>A
n.7596C>A
c.7500C>A (p.Pro2500=)
 ClinVar dbSNP
13g.32356588C=CA2082815550BRCA2c.7596C= (p.Pro2532=)
c.7227C= (p.Pro2409=)
c.63C= (p.Pro21=)
c.161C=
n.7596C=
c.7500C= (p.Pro2500=)
13g.32356588C>GCA025170BRCA2c.7596C>G (p.Pro2532=)
c.7227C>G (p.Pro2409=)
c.63C>G (p.Pro21=)
c.161C>G
n.7596C>G
c.7500C>G (p.Pro2500=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32356588C>TCA025171BRCA2c.7596C>T (p.Pro2532=)
c.7227C>T (p.Pro2409=)
c.63C>T (p.Pro21=)
c.161C>T
n.7596C>T
c.7500C>T (p.Pro2500=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32356588_32356871delinsCTCTGCGTGTTCTCATAAACAGGTATGTGTTTGTCTACAATACTGATGGCTTTTATGACAGAGTGTAATTTTATTTCATTAACTAGTATCTACAAATGGCTTTGTTTAAAGAATGAACACATTAGTGCAGGAATGGATGAATGAAATCATCATATTTTCTAATTAGCCTGCAGTGGCAGCCTCTGGCCCCTTGCTAGGCCTGCCTCATCCTGCTAAAGTGATCTGTGCTTCCAAATTACTACTTCTTTTCCCCCTTCAAATCTTTCTTATTTTGTCATTGTAAACA2082815558BRCA2c.7596_7617+262delinsCTCTGCGTGTTCTCATAAACAGGTATGTGTTTGTCTACAATACTGATGGCTTTTATGACAGAGTGTAATTTTATTTCATTAACTAGTATCTACAAATGGCTTTGTTTAAAGAATGAACACATTAGTGCAGGAATGGATGAATGAAATCATCATATTTTCTAATTAGCCTGCAGTGGCAGCCTCTGGCCCCTTGCTAGGCCTGCCTCATCCTGCTAAAGTGATCTGTGCTTCCAAATTACTACTTCTTTTCCCCCTTCAAATCTTTCTTATTTTGTCATTGTAAA
c.7227_7248+262delinsCTCTGCGTGTTCTCATAAACAGGTATGTGTTTGTCTACAATACTGATGGCTTTTATGACAGAGTGTAATTTTATTTCATTAACTAGTATCTACAAATGGCTTTGTTTAAAGAATGAACACATTAGTGCAGGAATGGATGAATGAAATCATCATATTTTCTAATTAGCCTGCAGTGGCAGCCTCTGGCCCCTTGCTAGGCCTGCCTCATCCTGCTAAAGTGATCTGTGCTTCCAAATTACTACTTCTTTTCCCCCTTCAAATCTTTCTTATTTTGTCATTGTAAA
c.63_84+262delinsCTCTGCGTGTTCTCATAAACAGGTATGTGTTTGTCTACAATACTGATGGCTTTTATGACAGAGTGTAATTTTATTTCATTAACTAGTATCTACAAATGGCTTTGTTTAAAGAATGAACACATTAGTGCAGGAATGGATGAATGAAATCATCATATTTTCTAATTAGCCTGCAGTGGCAGCCTCTGGCCCCTTGCTAGGCCTGCCTCATCCTGCTAAAGTGATCTGTGCTTCCAAATTACTACTTCTTTTCCCCCTTCAAATCTTTCTTATTTTGTCATTGTAAA
c.161_182+262delinsCTCTGCGTGTTCTCATAAACAGGTATGTGTTTGTCTACAATACTGATGGCTTTTATGACAGAGTGTAATTTTATTTCATTAACTAGTATCTACAAATGGCTTTGTTTAAAGAATGAACACATTAGTGCAGGAATGGATGAATGAAATCATCATATTTTCTAATTAGCCTGCAGTGGCAGCCTCTGGCCCCTTGCTAGGCCTGCCTCATCCTGCTAAAGTGATCTGTGCTTCCAAATTACTACTTCTTTTCCCCCTTCAAATCTTTCTTATTTTGTCATTGTAAA
n.7596_7617+262delinsCTCTGCGTGTTCTCATAAACAGGTATGTGTTTGTCTACAATACTGATGGCTTTTATGACAGAGTGTAATTTTATTTCATTAACTAGTATCTACAAATGGCTTTGTTTAAAGAATGAACACATTAGTGCAGGAATGGATGAATGAAATCATCATATTTTCTAATTAGCCTGCAGTGGCAGCCTCTGGCCCCTTGCTAGGCCTGCCTCATCCTGCTAAAGTGATCTGTGCTTCCAAATTACTACTTCTTTTCCCCCTTCAAATCTTTCTTATTTTGTCATTGTAAA
c.7500_7521+262delinsCTCTGCGTGTTCTCATAAACAGGTATGTGTTTGTCTACAATACTGATGGCTTTTATGACAGAGTGTAATTTTATTTCATTAACTAGTATCTACAAATGGCTTTGTTTAAAGAATGAACACATTAGTGCAGGAATGGATGAATGAAATCATCATATTTTCTAATTAGCCTGCAGTGGCAGCCTCTGGCCCCTTGCTAGGCCTGCCTCATCCTGCTAAAGTGATCTGTGCTTCCAAATTACTACTTCTTTTCCCCCTTCAAATCTTTCTTATTTTGTCATTGTAAA
13g.32356589T>ACA387743933BRCA2c.7597T>A (p.Ser2533Thr)
c.7228T>A (p.Ser2410Thr)
c.64T>A (p.Ser22Thr)
c.162T>A
n.7597T>A
c.7501T>A (p.Ser2501Thr)
 ClinVar dbSNP
13g.32356589T>CCA387743938BRCA2c.7597T>C (p.Ser2533Pro)
c.7228T>C (p.Ser2410Pro)
c.64T>C (p.Ser22Pro)
c.162T>C
n.7597T>C
c.7501T>C (p.Ser2501Pro)
 ClinVar dbSNP
13g.32356589T>GCA025172BRCA2c.7597T>G (p.Ser2533Ala)
c.7228T>G (p.Ser2410Ala)
c.64T>G (p.Ser22Ala)
c.162T>G
n.7597T>G
c.7501T>G (p.Ser2501Ala)
 ClinVar dbSNP
13g.32356589T=CA2082815567BRCA2c.7597T= (p.Ser2533=)
c.7228T= (p.Ser2410=)
c.64T= (p.Ser22=)
c.162T=
n.7597T=
c.7501T= (p.Ser2501=)
13g.32356590_32356872delCA10586327BRCA2c.7598_7617+263del
c.7229_7248+263del
c.65_84+263del
c.163_182+263del
n.7598_7617+263del
c.7502_7521+263del
 ClinVar dbSNP
13g.32356590C>ACA387743941BRCA2c.7598C>A (p.Ser2533Tyr)
c.7229C>A (p.Ser2410Tyr)
c.65C>A (p.Ser22Tyr)
c.163C>A
n.7598C>A
c.7502C>A (p.Ser2501Tyr)
 dbSNP
13g.32356590C=CA2082815574BRCA2c.7598C= (p.Ser2533=)
c.7229C= (p.Ser2410=)
c.65C= (p.Ser22=)
c.163C=
n.7598C=
c.7502C= (p.Ser2501=)
13g.32356590C>GCA025173BRCA2c.7598C>G (p.Ser2533Cys)
c.7229C>G (p.Ser2410Cys)
c.65C>G (p.Ser22Cys)
c.163C>G
n.7598C>G
c.7502C>G (p.Ser2501Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32356590C>TCA387743945BRCA2c.7598C>T (p.Ser2533Phe)
c.7229C>T (p.Ser2410Phe)
c.65C>T (p.Ser22Phe)
c.163C>T
n.7598C>T
c.7502C>T (p.Ser2501Phe)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32356591T>ACA483260462BRCA2c.7599T>A (p.Ser2533=)
c.7230T>A (p.Ser2410=)
c.66T>A (p.Ser22=)
c.164T>A
n.7599T>A
c.7503T>A (p.Ser2501=)
 dbSNP
13g.32356591T>CCA483260455BRCA2c.7599T>C (p.Ser2533=)
c.7230T>C (p.Ser2410=)
c.66T>C (p.Ser22=)
c.164T>C
n.7599T>C
c.7503T>C (p.Ser2501=)
 ClinVar dbSNP
13g.32356591T>GCA483260456BRCA2c.7599T>G (p.Ser2533=)
c.7230T>G (p.Ser2410=)
c.66T>G (p.Ser22=)
c.164T>G
n.7599T>G
c.7503T>G (p.Ser2501=)
13g.32356591T=CA2082815581BRCA2c.7599T= (p.Ser2533=)
c.7230T= (p.Ser2410=)
c.66T= (p.Ser22=)
c.164T=
n.7599T=
c.7503T= (p.Ser2501=)
13g.32356592G>ACA387743948BRCA2c.7600G>A (p.Ala2534Thr)
c.7231G>A (p.Ala2411Thr)
c.67G>A (p.Ala23Thr)
c.165G>A
n.7600G>A
c.7504G>A (p.Ala2502Thr)
 ClinVar dbSNP gnomAD v4
13g.32356592G>CCA387743949BRCA2c.7600G>C (p.Ala2534Pro)
c.7231G>C (p.Ala2411Pro)
c.67G>C (p.Ala23Pro)
c.165G>C
n.7600G>C
c.7504G>C (p.Ala2502Pro)
 dbSNP
13g.32356592G=CA2082815587BRCA2c.7600G= (p.Ala2534=)
c.7231G= (p.Ala2411=)
c.67G= (p.Ala23=)
c.165G=
n.7600G=
c.7504G= (p.Ala2502=)
13g.32356592G>TCA387743951BRCA2c.7600G>T (p.Ala2534Ser)
c.7231G>T (p.Ala2411Ser)
c.67G>T (p.Ala23Ser)
c.165G>T
n.7600G>T
c.7504G>T (p.Ala2502Ser)
13g.32356593C>ACA387743953BRCA2c.7601C>A (p.Ala2534Glu)
c.7232C>A (p.Ala2411Glu)
c.68C>A (p.Ala23Glu)
c.166C>A
n.7601C>A
c.7505C>A (p.Ala2502Glu)
 ClinVar dbSNP
13g.32356593C=CA2082815604BRCA2c.7601C= (p.Ala2534=)
c.7232C= (p.Ala2411=)
c.68C= (p.Ala23=)
c.166C=
n.7601C=
c.7505C= (p.Ala2502=)
13g.32356593C>GCA387743956BRCA2c.7601C>G (p.Ala2534Gly)
c.7232C>G (p.Ala2411Gly)
c.68C>G (p.Ala23Gly)
c.166C>G
n.7601C>G
c.7505C>G (p.Ala2502Gly)
 ClinVar dbSNP
13g.32356593C>TCA025174BRCA2c.7601C>T (p.Ala2534Val)
c.7232C>T (p.Ala2411Val)
c.68C>T (p.Ala23Val)
c.166C>T
n.7601C>T
c.7505C>T (p.Ala2502Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
13g.32356593_32356594delinsCGCA2082815595BRCA2c.7601_7602delinsCG (p.Ala2534=)
c.7232_7233delinsCG (p.Ala2411=)
c.68_69delinsCG (p.Ala23=)
c.166_167delinsCG
n.7601_7602delinsCG
c.7505_7506delinsCG (p.Ala2502=)
13g.32356593_32356594insTTGCTATTGAGCAAGGTTGCTTGATCAGTAAGGATGCCGATATCACGCA2549432224BRCA2c.7601_7602insTTGCTATTGAGCAAGGTTGCTTGATCAGTAAGGATGCCGATATCACG (p.Ser2536TyrfsTer2)
c.7232_7233insTTGCTATTGAGCAAGGTTGCTTGATCAGTAAGGATGCCGATATCACG (p.Ser2413TyrfsTer2)
c.68_69insTTGCTATTGAGCAAGGTTGCTTGATCAGTAAGGATGCCGATATCACG (p.Ser25TyrfsTer2)
c.166_167insTTGCTATTGAGCAAGGTTGCTTGATCAGTAAGGATGCCGATATCACG
n.7601_7602insTTGCTATTGAGCAAGGTTGCTTGATCAGTAAGGATGCCGATATCACG
c.7505_7506insTTGCTATTGAGCAAGGTTGCTTGATCAGTAAGGATGCCGATATCACG (p.Ser2504TyrfsTer2)
13g.32356594delCA10579745BRCA2c.7602del (p.Cys2535ValfsTer16)
c.7233del (p.Cys2412ValfsTer16)
c.69del (p.Cys24ValfsTer16)
c.167del
n.7602del
c.7506del (p.Cys2503ValfsTer16)
 ClinVar dbSNP
13g.32356594G>ACA025175BRCA2c.7602G>A (p.Ala2534=)
c.7233G>A (p.Ala2411=)
c.69G>A (p.Ala23=)
c.167G>A
n.7602G>A
c.7506G>A (p.Ala2502=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32356594G>CCA025176BRCA2c.7602G>C (p.Ala2534=)
c.7233G>C (p.Ala2411=)
c.69G>C (p.Ala23=)
c.167G>C
n.7602G>C
c.7506G>C (p.Ala2502=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32356594G=CA2082815619BRCA2c.7602G= (p.Ala2534=)
c.7233G= (p.Ala2411=)
c.69G= (p.Ala23=)
c.167G=
n.7602G=
c.7506G= (p.Ala2502=)
13g.32356594G>TCA247470176BRCA2c.7602G>T (p.Ala2534=)
c.7233G>T (p.Ala2411=)
c.69G>T (p.Ala23=)
c.167G>T
n.7602G>T
c.7506G>T (p.Ala2502=)
 ClinVar dbSNP gnomAD v4
13g.32356595T>ACA387743964BRCA2c.7603T>A (p.Cys2535Ser)
c.7234T>A (p.Cys2412Ser)
c.70T>A (p.Cys24Ser)
c.168T>A
n.7603T>A
c.7507T>A (p.Cys2503Ser)
 ClinVar dbSNP
13g.32356595T>CCA387743967BRCA2c.7603T>C (p.Cys2535Arg)
c.7234T>C (p.Cys2412Arg)
c.70T>C (p.Cys24Arg)
c.168T>C
n.7603T>C
c.7507T>C (p.Cys2503Arg)
 ClinVar dbSNP
13g.32356595T>GCA387743968BRCA2c.7603T>G (p.Cys2535Gly)
c.7234T>G (p.Cys2412Gly)
c.70T>G (p.Cys24Gly)
c.168T>G
n.7603T>G
c.7507T>G (p.Cys2503Gly)
13g.32356595T=CA2082815629BRCA2c.7603T= (p.Cys2535=)
c.7234T= (p.Cys2412=)
c.70T= (p.Cys24=)
c.168T=
n.7603T=
c.7507T= (p.Cys2503=)
13g.32356596G>ACA025177BRCA2c.7604G>A (p.Cys2535Tyr)
c.7235G>A (p.Cys2412Tyr)
c.71G>A (p.Cys24Tyr)
c.169G>A
n.7604G>A
c.7508G>A (p.Cys2503Tyr)
 ClinVar dbSNP gnomAD v4
13g.32356596G>CCA387743971BRCA2c.7604G>C (p.Cys2535Ser)
c.7235G>C (p.Cys2412Ser)
c.71G>C (p.Cys24Ser)
c.169G>C
n.7604G>C
c.7508G>C (p.Cys2503Ser)
 dbSNP
13g.32356596G=CA2082815636BRCA2c.7604G= (p.Cys2535=)
c.7235G= (p.Cys2412=)
c.71G= (p.Cys24=)
c.169G=
n.7604G=
c.7508G= (p.Cys2503=)
13g.32356596G>TCA387743974BRCA2c.7604G>T (p.Cys2535Phe)
c.7235G>T (p.Cys2412Phe)
c.71G>T (p.Cys24Phe)
c.169G>T
n.7604G>T
c.7508G>T (p.Cys2503Phe)
13g.32356596_32356597delinsAGCA2695217912BRCA2c.7604_7605delinsAG (p.Cys2535Ter)
c.7235_7236delinsAG (p.Cys2412Ter)
c.71_72delinsAG (p.Cys24Ter)
c.169_170delinsAG
n.7604_7605delinsAG
c.7508_7509delinsAG (p.Cys2503Ter)
13g.32356596_32356597insGCCTCA2535514322BRCA2c.7604_7605insGCCT (p.Cys2535TrpfsTer5)
c.7235_7236insGCCT (p.Cys2412TrpfsTer5)
c.71_72insGCCT (p.Cys24TrpfsTer5)
c.169_170insGCCT
n.7604_7605insGCCT
c.7508_7509insGCCT (p.Cys2503TrpfsTer5)
13g.32356597T>ACA387743975BRCA2c.7605T>A (p.Cys2535Ter)
c.7236T>A (p.Cys2412Ter)
c.72T>A (p.Cys24Ter)
c.170T>A
n.7605T>A
c.7509T>A (p.Cys2503Ter)
 dbSNP
13g.32356597T>CCA483260465BRCA2c.7605T>C (p.Cys2535=)
c.7236T>C (p.Cys2412=)
c.72T>C (p.Cys24=)
c.170T>C
n.7605T>C
c.7509T>C (p.Cys2503=)
 ClinVar dbSNP
13g.32356597T>GCA16614351BRCA2c.7605T>G (p.Cys2535Trp)
c.7236T>G (p.Cys2412Trp)
c.72T>G (p.Cys24Trp)
c.170T>G
n.7605T>G
c.7509T>G (p.Cys2503Trp)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32356597T=CA2082815642BRCA2c.7605T= (p.Cys2535=)
c.7236T= (p.Cys2412=)
c.72T= (p.Cys24=)
c.170T=
n.7605T=
c.7509T= (p.Cys2503=)
13g.32356597_32356598insGGAGCCA2082815645BRCA2c.7605_7606insGGAGC (p.Ser2536GlyfsTer17)
c.7236_7237insGGAGC (p.Ser2413GlyfsTer17)
c.72_73insGGAGC (p.Ser25GlyfsTer17)
c.170_171insGGAGC
n.7605_7606insGGAGC
c.7509_7510insGGAGC (p.Ser2504GlyfsTer17)
 dbSNP
13g.32356598T>ACA387743977BRCA2c.7606T>A (p.Ser2536Thr)
c.7237T>A (p.Ser2413Thr)
c.73T>A (p.Ser25Thr)
c.171T>A
n.7606T>A
c.7510T>A (p.Ser2504Thr)
 dbSNP
13g.32356598T>CCA10579746BRCA2c.7606T>C (p.Ser2536Pro)
c.7237T>C (p.Ser2413Pro)
c.73T>C (p.Ser25Pro)
c.171T>C
n.7606T>C
c.7510T>C (p.Ser2504Pro)
 ClinVar dbSNP
13g.32356598T>GCA387743985BRCA2c.7606T>G (p.Ser2536Ala)
c.7237T>G (p.Ser2413Ala)
c.73T>G (p.Ser25Ala)
c.171T>G
n.7606T>G
c.7510T>G (p.Ser2504Ala)
13g.32356598T=CA2018008790BRCA2c.7606T= (p.Ser2536=)
c.7237T= (p.Ser2413=)
c.73T= (p.Ser25=)
c.171T=
n.7606T=
c.7510T= (p.Ser2504=)
13g.32356598_32356599insACCCGAGCTCTTCACCGTGACCTCGGCGGAGTATGAAGCGATGCACA2082815649BRCA2c.7606_7607insACCCGAGCTCTTCACCGTGACCTCGGCGGAGTATGAAGCGATGCA (p.Ser2536TyrfsTer7)
c.7237_7238insACCCGAGCTCTTCACCGTGACCTCGGCGGAGTATGAAGCGATGCA (p.Ser2413TyrfsTer7)
c.73_74insACCCGAGCTCTTCACCGTGACCTCGGCGGAGTATGAAGCGATGCA (p.Ser25TyrfsTer7)
c.171_172insACCCGAGCTCTTCACCGTGACCTCGGCGGAGTATGAAGCGATGCA
n.7606_7607insACCCGAGCTCTTCACCGTGACCTCGGCGGAGTATGAAGCGATGCA
c.7510_7511insACCCGAGCTCTTCACCGTGACCTCGGCGGAGTATGAAGCGATGCA (p.Ser2504TyrfsTer7)
 dbSNP
13g.32356599C>ACA387743993BRCA2c.7607C>A (p.Ser2536Tyr)
c.7238C>A (p.Ser2413Tyr)
c.74C>A (p.Ser25Tyr)
c.172C>A
n.7607C>A
c.7511C>A (p.Ser2504Tyr)
13g.32356599C>GCA387743995BRCA2c.7607C>G (p.Ser2536Cys)
c.7238C>G (p.Ser2413Cys)
c.74C>G (p.Ser25Cys)
c.172C>G
n.7607C>G
c.7511C>G (p.Ser2504Cys)
13g.32356599C>TCA387743989BRCA2c.7607C>T (p.Ser2536Phe)
c.7238C>T (p.Ser2413Phe)
c.74C>T (p.Ser25Phe)
c.172C>T
n.7607C>T
c.7511C>T (p.Ser2504Phe)
13g.32356599_32356600insGGGTGGAGCTACCCGAGCTCTCA2507401192BRCA2c.7607_7608insGGGTGGAGCTACCCGAGCTCT (p.Ser2536_His2537insGlyGlyAlaThrArgAlaLeu)
c.7238_7239insGGGTGGAGCTACCCGAGCTCT (p.Ser2413_His2414insGlyGlyAlaThrArgAlaLeu)
c.74_75insGGGTGGAGCTACCCGAGCTCT (p.Ser25_His26insGlyGlyAlaThrArgAlaLeu)
c.172_173insGGGTGGAGCTACCCGAGCTCT
n.7607_7608insGGGTGGAGCTACCCGAGCTCT
c.7511_7512insGGGTGGAGCTACCCGAGCTCT (p.Ser2504_His2505insGlyGlyAlaThrArgAlaLeu)
13g.32356600T>ACA483260469BRCA2c.7608T>A (p.Ser2536=)
c.7239T>A (p.Ser2413=)
c.75T>A (p.Ser25=)
c.173T>A
n.7608T>A
c.7512T>A (p.Ser2504=)
 dbSNP
13g.32356600T>CCA483260467BRCA2c.7608T>C (p.Ser2536=)
c.7239T>C (p.Ser2413=)
c.75T>C (p.Ser25=)
c.173T>C
n.7608T>C
c.7512T>C (p.Ser2504=)
 dbSNP
13g.32356600T>GCA483260466BRCA2c.7608T>G (p.Ser2536=)
c.7239T>G (p.Ser2413=)
c.75T>G (p.Ser25=)
c.173T>G
n.7608T>G
c.7512T>G (p.Ser2504=)
13g.32356601C>ACA387743997BRCA2c.7609C>A (p.His2537Asn)
c.7240C>A (p.His2414Asn)
c.76C>A (p.His26Asn)
c.174C>A
n.7609C>A
c.7513C>A (p.His2505Asn)
13g.32356601C=CA2082815652BRCA2c.7609C= (p.His2537=)
c.7240C= (p.His2414=)
c.76C= (p.His26=)
c.174C=
n.7609C=
c.7513C= (p.His2505=)
13g.32356601C>GCA387744004BRCA2c.7609C>G (p.His2537Asp)
c.7240C>G (p.His2414Asp)
c.76C>G (p.His26Asp)
c.174C>G
n.7609C>G
c.7513C>G (p.His2505Asp)
 dbSNP
13g.32356601C>TCA387744005BRCA2c.7609C>T (p.His2537Tyr)
c.7240C>T (p.His2414Tyr)
c.76C>T (p.His26Tyr)
c.174C>T
n.7609C>T
c.7513C>T (p.His2505Tyr)
 ClinVar dbSNP
13g.32356602A=CA2082815668BRCA2c.7610A= (p.His2537=)
c.7241A= (p.His2414=)
c.77A= (p.His26=)
c.175A=
n.7610A=
c.7514A= (p.His2505=)
13g.32356602A>CCA387744006BRCA2c.7610A>C (p.His2537Pro)
c.7241A>C (p.His2414Pro)
c.77A>C (p.His26Pro)
c.175A>C
n.7610A>C
c.7514A>C (p.His2505Pro)
 gnomAD v4
13g.32356602A>GCA025178BRCA2c.7610A>G (p.His2537Arg)
c.7241A>G (p.His2414Arg)
c.77A>G (p.His26Arg)
c.175A>G
n.7610A>G
c.7514A>G (p.His2505Arg)
 ClinVar dbSNP gnomAD v4
13g.32356602A>TCA387744008BRCA2c.7610A>T (p.His2537Leu)
c.7241A>T (p.His2414Leu)
c.77A>T (p.His26Leu)
c.175A>T
n.7610A>T
c.7514A>T (p.His2505Leu)
 dbSNP
13g.32356602_32356603insCCGTGACCTCGGCAGAGCA2571358683BRCA2c.7610_7611insCCGTGACCTCGGCAGAG (p.Lys2538ArgfsTer19)
c.7241_7242insCCGTGACCTCGGCAGAG (p.Lys2415ArgfsTer19)
c.77_78insCCGTGACCTCGGCAGAG (p.Lys27ArgfsTer19)
c.175_176insCCGTGACCTCGGCAGAG
n.7610_7611insCCGTGACCTCGGCAGAG
c.7514_7515insCCGTGACCTCGGCAGAG (p.Lys2506ArgfsTer19)
13g.32356603T>ACA387744009BRCA2c.7611T>A (p.His2537Gln)
c.7242T>A (p.His2414Gln)
c.78T>A (p.His26Gln)
c.176T>A
n.7611T>A
c.7515T>A (p.His2505Gln)
13g.32356603T>CCA483260472BRCA2c.7611T>C (p.His2537=)
c.7242T>C (p.His2414=)
c.78T>C (p.His26=)
c.176T>C
n.7611T>C
c.7515T>C (p.His2505=)
 ClinVar dbSNP
13g.32356603T>GCA387744011BRCA2c.7611T>G (p.His2537Gln)
c.7242T>G (p.His2414Gln)
c.78T>G (p.His26Gln)
c.176T>G
n.7611T>G
c.7515T>G (p.His2505Gln)
 gnomAD v4
13g.32356603T=CA2082815679BRCA2c.7611T= (p.His2537=)
c.7242T= (p.His2414=)
c.78T= (p.His26=)
c.176T=
n.7611T=
c.7515T= (p.His2505=)
13g.32356604A=CA2082815690BRCA2c.7612A= (p.Lys2538=)
c.7243A= (p.Lys2415=)
c.79A= (p.Lys27=)
c.177A=
n.7612A=
c.7516A= (p.Lys2506=)
13g.32356604A>CCA387744012BRCA2c.7612A>C (p.Lys2538Gln)
c.7243A>C (p.Lys2415Gln)
c.79A>C (p.Lys27Gln)
c.177A>C
n.7612A>C
c.7516A>C (p.Lys2506Gln)
13g.32356604A>GCA025179BRCA2c.7612A>G (p.Lys2538Glu)
c.7243A>G (p.Lys2415Glu)
c.79A>G (p.Lys27Glu)
c.177A>G
n.7612A>G
c.7516A>G (p.Lys2506Glu)
 ClinVar dbSNP
13g.32356604A>TCA025180BRCA2c.7612A>T (p.Lys2538Ter)
c.7243A>T (p.Lys2415Ter)
c.79A>T (p.Lys27Ter)
c.177A>T
n.7612A>T
c.7516A>T (p.Lys2506Ter)
 ClinVar dbSNP
13g.32356605_32356606dupCA913188531BRCA2c.7613_7614dup (p.Gln2539AsnfsTer13)
c.7244_7245dup (p.Gln2416AsnfsTer13)
c.80_81dup (p.Gln28AsnfsTer13)
c.178_179dup
n.7613_7614dup
c.7517_7518dup (p.Gln2507AsnfsTer13)
 ClinVar dbSNP
13g.32356604_32356605insTGCA2520953627BRCA2c.7612_7613insTG (p.Lys2538MetfsTer14)
c.7243_7244insTG (p.Lys2415MetfsTer14)
c.79_80insTG (p.Lys27MetfsTer14)
c.177_178insTG
n.7612_7613insTG
c.7516_7517insTG (p.Lys2506MetfsTer14)
13g.32356605A>CCA387744018BRCA2c.7613A>C (p.Lys2538Thr)
c.7244A>C (p.Lys2415Thr)
c.80A>C (p.Lys27Thr)
c.178A>C
n.7613A>C
c.7517A>C (p.Lys2506Thr)
13g.32356605A>GCA387744020BRCA2c.7613A>G (p.Lys2538Arg)
c.7244A>G (p.Lys2415Arg)
c.80A>G (p.Lys27Arg)
c.178A>G
n.7613A>G
c.7517A>G (p.Lys2506Arg)
 dbSNP
13g.32356605A>TCA387744023BRCA2c.7613A>T (p.Lys2538Ile)
c.7244A>T (p.Lys2415Ile)
c.80A>T (p.Lys27Ile)
c.178A>T
n.7613A>T
c.7517A>T (p.Lys2506Ile)
13g.32356606A>CCA387744028BRCA2c.7614A>C (p.Lys2538Asn)
c.7245A>C (p.Lys2415Asn)
c.81A>C (p.Lys27Asn)
c.179A>C
n.7614A>C
c.7518A>C (p.Lys2506Asn)
13g.32356606A>GCA483260476BRCA2c.7614A>G (p.Lys2538=)
c.7245A>G (p.Lys2415=)
c.81A>G (p.Lys27=)
c.179A>G
n.7614A>G
c.7518A>G (p.Lys2506=)
13g.32356606A>TCA387744025BRCA2c.7614A>T (p.Lys2538Asn)
c.7245A>T (p.Lys2415Asn)
c.81A>T (p.Lys27Asn)
c.179A>T
n.7614A>T
c.7518A>T (p.Lys2506Asn)
 dbSNP
13g.32356606_32356607insGCGATGCA2506417875BRCA2c.7614_7615insGCGATG (p.Lys2538_Gln2539insAlaMet)
c.7245_7246insGCGATG (p.Lys2415_Gln2416insAlaMet)
c.81_82insGCGATG (p.Lys27_Gln28insAlaMet)
c.179_180insGCGATG
n.7614_7615insGCGATG
c.7518_7519insGCGATG (p.Lys2506_Gln2507insAlaMet)
13g.32356607C>ACA387744031BRCA2c.7615C>A (p.Gln2539Lys)
c.7246C>A (p.Gln2416Lys)
c.82C>A (p.Gln28Lys)
c.180C>A
n.7615C>A
c.7519C>A (p.Gln2507Lys)
13g.32356607C=CA2082815697BRCA2c.7615C= (p.Gln2539=)
c.7246C= (p.Gln2416=)
c.82C= (p.Gln28=)
c.180C=
n.7615C=
c.7519C= (p.Gln2507=)
13g.32356607C>GCA387744035BRCA2c.7615C>G (p.Gln2539Glu)
c.7246C>G (p.Gln2416Glu)
c.82C>G (p.Gln28Glu)
c.180C>G
n.7615C>G
c.7519C>G (p.Gln2507Glu)
 dbSNP
13g.32356607C>TCA10589440BRCA2c.7615C>T (p.Gln2539Ter)
c.7246C>T (p.Gln2416Ter)
c.82C>T (p.Gln28Ter)
c.180C>T
n.7615C>T
c.7519C>T (p.Gln2507Ter)
 ClinVar dbSNP gnomAD v4
13g.32356608A=CA2082815703BRCA2c.7616A= (p.Gln2539=)
c.7247A= (p.Gln2416=)
c.83A= (p.Gln28=)
c.181A=
n.7616A=
c.7520A= (p.Gln2507=)
13g.32356608A>CCA387744037BRCA2c.7616A>C (p.Gln2539Pro)
c.7247A>C (p.Gln2416Pro)
c.83A>C (p.Gln28Pro)
c.181A>C
n.7616A>C
c.7520A>C (p.Gln2507Pro)
13g.32356608A>GCA025181BRCA2c.7616A>G (p.Gln2539Arg)
c.7247A>G (p.Gln2416Arg)
c.83A>G (p.Gln28Arg)
c.181A>G
n.7616A>G
c.7520A>G (p.Gln2507Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32356608A>TCA387744038BRCA2c.7616A>T (p.Gln2539Leu)
c.7247A>T (p.Gln2416Leu)
c.83A>T (p.Gln28Leu)
c.181A>T
n.7616A>T
c.7520A>T (p.Gln2507Leu)
13g.32356608_32356609delinsAGCA2082815705BRCA2c.7616_7617delinsAG (p.Gln2539=)
c.7247_7248delinsAG (p.Gln2416=)
c.83_84delinsAG (p.Gln28=)
c.181_182delinsAG
n.7616_7617delinsAG
c.7520_7521delinsAG (p.Gln2507=)
13g.32356608_32356609insCTCGGCATGGCATAAGGCCA2531307307BRCA2c.7616_7617insCTCGGCATGGCATAAGGC (p.Gln2539delinsHisSerAlaTrpHisLysAla)
c.7247_7248insCTCGGCATGGCATAAGGC (p.Gln2416delinsHisSerAlaTrpHisLysAla)
c.83_84insCTCGGCATGGCATAAGGC (p.Gln28delinsHisSerAlaTrpHisLysAla)
c.181_182insCTCGGCATGGCATAAGGC
n.7616_7617insCTCGGCATGGCATAAGGC
c.7520_7521insCTCGGCATGGCATAAGGC (p.Gln2507delinsHisSerAlaTrpHisLysAla)
13g.32356609G>ACA483260480BRCA2c.7617G>A (p.Gln2539=)
c.7248G>A (p.Gln2416=)
c.84G>A (p.Gln28=)
c.182G>A
n.7617G>A
c.7521G>A (p.Gln2507=)
 ClinVar dbSNP
13g.32356609G>CCA387744043BRCA2c.7617G>C (p.Gln2539His)
c.7248G>C (p.Gln2416His)
c.84G>C (p.Gln28His)
c.182G>C
n.7617G>C
c.7521G>C (p.Gln2507His)
 ClinVar dbSNP
13g.32356609G=CA2082815712BRCA2c.7617G= (p.Gln2539=)
c.7248G= (p.Gln2416=)
c.84G= (p.Gln28=)
c.182G=
n.7617G=
c.7521G= (p.Gln2507=)
13g.32356609G>TCA387744048BRCA2c.7617G>T (p.Gln2539His)
c.7248G>T (p.Gln2416His)
c.84G>T (p.Gln28His)
c.182G>T
n.7617G>T
c.7521G>T (p.Gln2507His)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
13g.32356610delCA915946873BRCA2c.7617+1del
c.7248+1del
c.84+1del
c.182+1del
n.7617+1del
c.7521+1del
 ClinVar dbSNP
13g.32356610G>ACA025182BRCA2c.7617+1G>A (n.7617+1G>A)
c.7248+1G>A (n.7248+1G>A)
c.84+1G>A (n.84+1G>A)
c.182+1G>A
n.7617+1G>A
c.7521+1G>A (n.7521+1G>A)
 ClinVar dbSNP gnomAD v4
13g.32356610G>CCA10584451BRCA2c.7617+1G>C (n.7617+1G>C)
c.7248+1G>C (n.7248+1G>C)
c.84+1G>C (n.84+1G>C)
c.182+1G>C
n.7617+1G>C
c.7521+1G>C (n.7521+1G>C)
 ClinVar dbSNP
13g.32356610G=CA2082815725BRCA2c.7617+1G= (n.7617+1G=)
c.7248+1G= (n.7248+1G=)
c.84+1G= (n.84+1G=)
c.182+1G=
n.7617+1G=
c.7521+1G= (n.7521+1G=)
13g.32356610G>TCA025183BRCA2c.7617+1G>T (n.7617+1G>T)
c.7248+1G>T (n.7248+1G>T)
c.84+1G>T (n.84+1G>T)
c.182+1G>T
n.7617+1G>T
c.7521+1G>T (n.7521+1G>T)
 ClinVar dbSNP
13g.32356610_32356627delinsGTATGTGTTTGTCTACAACA2082815722BRCA2c.7617+1_7617+18delinsGTATGTGTTTGTCTACAA (n.7617+1_7617+18delinsGTATGTGTTTGTCTACAA)
c.7248+1_7248+18delinsGTATGTGTTTGTCTACAA (n.7248+1_7248+18delinsGTATGTGTTTGTCTACAA)
c.84+1_84+18delinsGTATGTGTTTGTCTACAA (n.84+1_84+18delinsGTATGTGTTTGTCTACAA)
c.182+1_182+18delinsGTATGTGTTTGTCTACAA
n.7617+1_7617+18delinsGTATGTGTTTGTCTACAA
c.7521+1_7521+18delinsGTATGTGTTTGTCTACAA (n.7521+1_7521+18delinsGTATGTGTTTGTCTACAA)
13g.32356611T>ACA387744059BRCA2c.7617+2T>A (n.7617+2T>A)
c.7248+2T>A (n.7248+2T>A)
c.84+2T>A (n.84+2T>A)
c.182+2T>A
n.7617+2T>A
c.7521+2T>A (n.7521+2T>A)
 dbSNP
13g.32356611T>CCA387744060BRCA2c.7617+2T>C (n.7617+2T>C)
c.7248+2T>C (n.7248+2T>C)
c.84+2T>C (n.84+2T>C)
c.182+2T>C
n.7617+2T>C
c.7521+2T>C (n.7521+2T>C)
 dbSNP
13g.32356611T>GCA025184BRCA2c.7617+2T>G (n.7617+2T>G)
c.7248+2T>G (n.7248+2T>G)
c.84+2T>G (n.84+2T>G)
c.182+2T>G
n.7617+2T>G
c.7521+2T>G (n.7521+2T>G)
 ClinVar dbSNP gnomAD v4
13g.32356611T=CA2082815733BRCA2c.7617+2T= (n.7617+2T=)
c.7248+2T= (n.7248+2T=)
c.84+2T= (n.84+2T=)
c.182+2T=
n.7617+2T=
c.7521+2T= (n.7521+2T=)
13g.32356611dupCA2622571725BRCA2c.7617+2dup (n.7617+2dup)
c.7248+2dup (n.7248+2dup)
c.84+2dup (n.84+2dup)
c.182+2dup
n.7617+2dup
c.7521+2dup (n.7521+2dup)
 ClinVar gnomAD v4
13g.32356613_32356629delCA697350952BRCA2c.7617+4_7617+20del (n.7617+4_7617+20del)
c.7248+4_7248+20del (n.7248+4_7248+20del)
c.84+4_84+20del (n.84+4_84+20del)
c.182+4_182+20del
n.7617+4_7617+20del
c.7521+4_7521+20del (n.7521+4_7521+20del)
 ClinVar dbSNP
13g.32356612A=CA2082815742BRCA2c.7617+3A= (n.7617+3A=)
c.7248+3A= (n.7248+3A=)
c.84+3A= (n.84+3A=)
c.182+3A=
n.7617+3A=
c.7521+3A= (n.7521+3A=)
13g.32356612A>GCA609453974BRCA2c.7617+3A>G (n.7617+3A>G)
c.7248+3A>G (n.7248+3A>G)
c.84+3A>G (n.84+3A>G)
c.182+3A>G
n.7617+3A>G
c.7521+3A>G (n.7521+3A>G)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32356612A>TCA2727856590BRCA2c.7617+3A>T (n.7617+3A>T)
c.7248+3A>T (n.7248+3A>T)
c.84+3A>T (n.84+3A>T)
c.182+3A>T
n.7617+3A>T
c.7521+3A>T (n.7521+3A>T)
 dbSNP
13g.32356613T>ACA2727836588BRCA2c.7617+4T>A (n.7617+4T>A)
c.7248+4T>A (n.7248+4T>A)
c.84+4T>A (n.84+4T>A)
c.182+4T>A
n.7617+4T>A
c.7521+4T>A (n.7521+4T>A)
 dbSNP
13g.32356613T>CCA025185BRCA2c.7617+4T>C (n.7617+4T>C)
c.7248+4T>C (n.7248+4T>C)
c.84+4T>C (n.84+4T>C)
c.182+4T>C
n.7617+4T>C
c.7521+4T>C (n.7521+4T>C)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32356613T>GCA609453975BRCA2c.7617+4T>G (n.7617+4T>G)
c.7248+4T>G (n.7248+4T>G)
c.84+4T>G (n.84+4T>G)
c.182+4T>G
n.7617+4T>G
c.7521+4T>G (n.7521+4T>G)
 dbSNP gnomAD v2 gnomAD v4
13g.32356613T=CA2082815745BRCA2c.7617+4T= (n.7617+4T=)
c.7248+4T= (n.7248+4T=)
c.84+4T= (n.84+4T=)
c.182+4T=
n.7617+4T=
c.7521+4T= (n.7521+4T=)
13g.32356614G>ACA2697551782BRCA2c.7617+5G>A (n.7617+5G>A)
c.7248+5G>A (n.7248+5G>A)
c.84+5G>A (n.84+5G>A)
c.182+5G>A
n.7617+5G>A
c.7521+5G>A (n.7521+5G>A)
 ClinVar dbSNP
13g.32356614G>CCA2622571728BRCA2c.7617+5G>C (n.7617+5G>C)
c.7248+5G>C (n.7248+5G>C)
c.84+5G>C (n.84+5G>C)
c.182+5G>C
n.7617+5G>C
c.7521+5G>C (n.7521+5G>C)
 dbSNP gnomAD v4
13g.32356615T>ACA2622571729BRCA2c.7617+6T>A (n.7617+6T>A)
c.7248+6T>A (n.7248+6T>A)
c.84+6T>A (n.84+6T>A)
c.182+6T>A
n.7617+6T>A
c.7521+6T>A (n.7521+6T>A)
 dbSNP gnomAD v4
13g.32356615T>CCA2575388055BRCA2c.7617+6T>C (n.7617+6T>C)
c.7248+6T>C (n.7248+6T>C)
c.84+6T>C (n.84+6T>C)
c.182+6T>C
n.7617+6T>C
c.7521+6T>C (n.7521+6T>C)
 ClinVar
13g.32356618_32356621delCA2499222297BRCA2c.7617+9_7617+12del (n.7617+9_7617+12del)
c.7248+9_7248+12del (n.7248+9_7248+12del)
c.84+9_84+12del (n.84+9_84+12del)
c.182+9_182+12del
n.7617+9_7617+12del
c.7521+9_7521+12del (n.7521+9_7521+12del)
 ClinVar dbSNP
13g.32356616G>ACA2622571730BRCA2c.7617+7G>A (n.7617+7G>A)
c.7248+7G>A (n.7248+7G>A)
c.84+7G>A (n.84+7G>A)
c.182+7G>A
n.7617+7G>A
c.7521+7G>A (n.7521+7G>A)
 ClinVar dbSNP gnomAD v4
13g.32356616G>CCA2727924732BRCA2c.7617+7G>C (n.7617+7G>C)
c.7248+7G>C (n.7248+7G>C)
c.84+7G>C (n.84+7G>C)
c.182+7G>C
n.7617+7G>C
c.7521+7G>C (n.7521+7G>C)
 dbSNP
13g.32356617T>ACA2727924749BRCA2c.7617+8T>A (n.7617+8T>A)
c.7248+8T>A (n.7248+8T>A)
c.84+8T>A (n.84+8T>A)
c.182+8T>A
n.7617+8T>A
c.7521+8T>A (n.7521+8T>A)
 dbSNP
13g.32356619delCA645593676BRCA2c.7617+10del (n.7617+10del)
c.7248+10del (n.7248+10del)
c.84+10del (n.84+10del)
c.182+10del
n.7617+10del
c.7521+10del (n.7521+10del)
 COSMIC COSMIC
13g.32356618T>ACA2727924753BRCA2c.7617+9T>A (n.7617+9T>A)
c.7248+9T>A (n.7248+9T>A)
c.84+9T>A (n.84+9T>A)
c.182+9T>A
n.7617+9T>A
c.7521+9T>A (n.7521+9T>A)
 dbSNP
13g.32356618T>CCA2727924752BRCA2c.7617+9T>C (n.7617+9T>C)
c.7248+9T>C (n.7248+9T>C)
c.84+9T>C (n.84+9T>C)
c.182+9T>C
n.7617+9T>C
c.7521+9T>C (n.7521+9T>C)
 dbSNP
13g.32356619T>ACA2727924754BRCA2c.7617+10T>A (n.7617+10T>A)
c.7248+10T>A (n.7248+10T>A)
c.84+10T>A (n.84+10T>A)
c.182+10T>A
n.7617+10T>A
c.7521+10T>A (n.7521+10T>A)
 dbSNP
13g.32356619_32356620delinsTGCA2082815751BRCA2c.7617+10_7617+11delinsTG (n.7617+10_7617+11delinsTG)
c.7248+10_7248+11delinsTG (n.7248+10_7248+11delinsTG)
c.84+10_84+11delinsTG (n.84+10_84+11delinsTG)
c.182+10_182+11delinsTG
n.7617+10_7617+11delinsTG
c.7521+10_7521+11delinsTG (n.7521+10_7521+11delinsTG)
13g.32356620delCA6941109BRCA2c.7617+11del (n.7617+11del)
c.7248+11del (n.7248+11del)
c.84+11del (n.84+11del)
c.182+11del
n.7617+11del
c.7521+11del (n.7521+11del)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.32356620G>ACA658656445BRCA2c.7617+11G>A (n.7617+11G>A)
c.7248+11G>A (n.7248+11G>A)
c.84+11G>A (n.84+11G>A)
c.182+11G>A
n.7617+11G>A
c.7521+11G>A (n.7521+11G>A)
 ClinVar dbSNP gnomAD v4
13g.32356620G>CCA609453976BRCA2c.7617+11G>C (n.7617+11G>C)
c.7248+11G>C (n.7248+11G>C)
c.84+11G>C (n.84+11G>C)
c.182+11G>C
n.7617+11G>C
c.7521+11G>C (n.7521+11G>C)
 dbSNP gnomAD v2 gnomAD v4
13g.32356620G=CA2082815756BRCA2c.7617+11G= (n.7617+11G=)
c.7248+11G= (n.7248+11G=)
c.84+11G= (n.84+11G=)
c.182+11G=
n.7617+11G=
c.7521+11G= (n.7521+11G=)
13g.32356620G>TCA2580087491BRCA2c.7617+11G>T (n.7617+11G>T)
c.7248+11G>T (n.7248+11G>T)
c.84+11G>T (n.84+11G>T)
c.182+11G>T
n.7617+11G>T
c.7521+11G>T (n.7521+11G>T)
 ClinVar
13g.32356621T>ACA915946874BRCA2c.7617+12T>A (n.7617+12T>A)
c.7248+12T>A (n.7248+12T>A)
c.84+12T>A (n.84+12T>A)
c.182+12T>A
n.7617+12T>A
c.7521+12T>A (n.7521+12T>A)
 ClinVar dbSNP
13g.32356621T=CA2082815763BRCA2c.7617+12T= (n.7617+12T=)
c.7248+12T= (n.7248+12T=)
c.84+12T= (n.84+12T=)
c.182+12T=
n.7617+12T=
c.7521+12T= (n.7521+12T=)
13g.32356622C>ACA2727840721BRCA2c.7617+13C>A (n.7617+13C>A)
c.7248+13C>A (n.7248+13C>A)
c.84+13C>A (n.84+13C>A)
c.182+13C>A
n.7617+13C>A
c.7521+13C>A (n.7521+13C>A)
 dbSNP
13g.32356622C=CA2082815775BRCA2c.7617+13C= (n.7617+13C=)
c.7248+13C= (n.7248+13C=)
c.84+13C= (n.84+13C=)
c.182+13C=
n.7617+13C=
c.7521+13C= (n.7521+13C=)
13g.32356622C>GCA2727840720BRCA2c.7617+13C>G (n.7617+13C>G)
c.7248+13C>G (n.7248+13C>G)
c.84+13C>G (n.84+13C>G)
c.182+13C>G
n.7617+13C>G
c.7521+13C>G (n.7521+13C>G)
 dbSNP
13g.32356622C>TCA6941110BRCA2c.7617+13C>T (n.7617+13C>T)
c.7248+13C>T (n.7248+13C>T)
c.84+13C>T (n.84+13C>T)
c.182+13C>T
n.7617+13C>T
c.7521+13C>T (n.7521+13C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32356623T>ACA2727924769BRCA2c.7617+14T>A (n.7617+14T>A)
c.7248+14T>A (n.7248+14T>A)
c.84+14T>A (n.84+14T>A)
c.182+14T>A
n.7617+14T>A
c.7521+14T>A (n.7521+14T>A)
 dbSNP
13g.32356623T>CCA2727924756BRCA2c.7617+14T>C (n.7617+14T>C)
c.7248+14T>C (n.7248+14T>C)
c.84+14T>C (n.84+14T>C)
c.182+14T>C
n.7617+14T>C
c.7521+14T>C (n.7521+14T>C)
 dbSNP
13g.32356623T>GCA2573149400BRCA2c.7617+14T>G (n.7617+14T>G)
c.7248+14T>G (n.7248+14T>G)
c.84+14T>G (n.84+14T>G)
c.182+14T>G
n.7617+14T>G
c.7521+14T>G (n.7521+14T>G)
 ClinVar dbSNP
13g.32356623_32356624delCA2739277514BRCA2c.7617+14_7617+15del (n.7617+14_7617+15del)
c.7248+14_7248+15del (n.7248+14_7248+15del)
c.84+14_84+15del (n.84+14_84+15del)
c.182+14_182+15del
n.7617+14_7617+15del
c.7521+14_7521+15del (n.7521+14_7521+15del)
 ClinVar
13g.32356624A>GCA2499222298BRCA2c.7617+15A>G (n.7617+15A>G)
c.7248+15A>G (n.7248+15A>G)
c.84+15A>G (n.84+15A>G)
c.182+15A>G
n.7617+15A>G
c.7521+15A>G (n.7521+15A>G)
 ClinVar dbSNP
13g.32356624A>TCA2727924786BRCA2c.7617+15A>T (n.7617+15A>T)
c.7248+15A>T (n.7248+15A>T)
c.84+15A>T (n.84+15A>T)
c.182+15A>T
n.7617+15A>T
c.7521+15A>T (n.7521+15A>T)
 dbSNP
13g.32356625C=CA2082815780BRCA2c.7617+16C= (n.7617+16C=)
c.7248+16C= (n.7248+16C=)
c.84+16C= (n.84+16C=)
c.182+16C=
n.7617+16C=
c.7521+16C= (n.7521+16C=)
13g.32356625C>GCA2727873216BRCA2c.7617+16C>G (n.7617+16C>G)
c.7248+16C>G (n.7248+16C>G)
c.84+16C>G (n.84+16C>G)
c.182+16C>G
n.7617+16C>G
c.7521+16C>G (n.7521+16C>G)
 dbSNP
13g.32356625C>TCA658798117BRCA2c.7617+16C>T (n.7617+16C>T)
c.7248+16C>T (n.7248+16C>T)
c.84+16C>T (n.84+16C>T)
c.182+16C>T
n.7617+16C>T
c.7521+16C>T (n.7521+16C>T)
 ClinVar dbSNP gnomAD v4
13g.32356626A=CA2082815784BRCA2c.7617+17A= (n.7617+17A=)
c.7248+17A= (n.7248+17A=)
c.84+17A= (n.84+17A=)
c.182+17A=
n.7617+17A=
c.7521+17A= (n.7521+17A=)
13g.32356626A>CCA2573149401BRCA2c.7617+17A>C (n.7617+17A>C)
c.7248+17A>C (n.7248+17A>C)
c.84+17A>C (n.84+17A>C)
c.182+17A>C
n.7617+17A>C
c.7521+17A>C (n.7521+17A>C)
 ClinVar dbSNP
13g.32356626A>GCA658798118BRCA2c.7617+17A>G (n.7617+17A>G)
c.7248+17A>G (n.7248+17A>G)
c.84+17A>G (n.84+17A>G)
c.182+17A>G
n.7617+17A>G
c.7521+17A>G (n.7521+17A>G)
 ClinVar dbSNP
13g.32356627A>GCA2573053823BRCA2c.7617+18A>G (n.7617+18A>G)
c.7248+18A>G (n.7248+18A>G)
c.84+18A>G (n.84+18A>G)
c.182+18A>G
n.7617+18A>G
c.7521+18A>G (n.7521+18A>G)
 ClinVar dbSNP gnomAD v4
13g.32356628T>CCA2622571732BRCA2c.7617+19T>C (n.7617+19T>C)
c.7248+19T>C (n.7248+19T>C)
c.84+19T>C (n.84+19T>C)
c.182+19T>C
n.7617+19T>C
c.7521+19T>C (n.7521+19T>C)
 gnomAD v4
13g.32356629A=CA2082815793BRCA2c.7617+20A= (n.7617+20A=)
c.7248+20A= (n.7248+20A=)
c.84+20A= (n.84+20A=)
c.182+20A=
n.7617+20A=
c.7521+20A= (n.7521+20A=)
13g.32356629A>GCA954697042BRCA2c.7617+20A>G (n.7617+20A>G)
c.7248+20A>G (n.7248+20A>G)
c.84+20A>G (n.84+20A>G)
c.182+20A>G
n.7617+20A>G
c.7521+20A>G (n.7521+20A>G)
 dbSNP gnomAD v4
13g.32356629A>TCA2727912911BRCA2c.7617+20A>T (n.7617+20A>T)
c.7248+20A>T (n.7248+20A>T)
c.84+20A>T (n.84+20A>T)
c.182+20A>T
n.7617+20A>T
c.7521+20A>T (n.7521+20A>T)
 dbSNP
13g.32356630C>ACA2727924836BRCA2c.7617+21C>A (n.7617+21C>A)
c.7248+21C>A (n.7248+21C>A)
c.84+21C>A (n.84+21C>A)
c.182+21C>A
n.7617+21C>A
c.7521+21C>A (n.7521+21C>A)
 dbSNP
13g.32356630C>GCA2727924834BRCA2c.7617+21C>G (n.7617+21C>G)
c.7248+21C>G (n.7248+21C>G)
c.84+21C>G (n.84+21C>G)
c.182+21C>G
n.7617+21C>G
c.7521+21C>G (n.7521+21C>G)
 dbSNP
13g.32356631T>ACA2727858015BRCA2c.7617+22T>A (n.7617+22T>A)
c.7248+22T>A (n.7248+22T>A)
c.84+22T>A (n.84+22T>A)
c.182+22T>A
n.7617+22T>A
c.7521+22T>A (n.7521+22T>A)
 dbSNP
13g.32356631T>GCA697350972BRCA2c.7617+22T>G (n.7617+22T>G)
c.7248+22T>G (n.7248+22T>G)
c.84+22T>G (n.84+22T>G)
c.182+22T>G
n.7617+22T>G
c.7521+22T>G (n.7521+22T>G)
 dbSNP gnomAD v3 gnomAD v4
13g.32356631T=CA2082815798BRCA2c.7617+22T= (n.7617+22T=)
c.7248+22T= (n.7248+22T=)
c.84+22T= (n.84+22T=)
c.182+22T=
n.7617+22T=
c.7521+22T= (n.7521+22T=)
13g.32356632G>ACA2727924858BRCA2c.7617+23G>A (n.7617+23G>A)
c.7248+23G>A (n.7248+23G>A)
c.84+23G>A (n.84+23G>A)
c.182+23G>A
n.7617+23G>A
c.7521+23G>A (n.7521+23G>A)
 dbSNP
13g.32356632G>CCA2727924857BRCA2c.7617+23G>C (n.7617+23G>C)
c.7248+23G>C (n.7248+23G>C)
c.84+23G>C (n.84+23G>C)
c.182+23G>C
n.7617+23G>C
c.7521+23G>C (n.7521+23G>C)
 dbSNP
13g.32356632G>TCA2727924860BRCA2c.7617+23G>T (n.7617+23G>T)
c.7248+23G>T (n.7248+23G>T)
c.84+23G>T (n.84+23G>T)
c.182+23G>T
n.7617+23G>T
c.7521+23G>T (n.7521+23G>T)
 dbSNP
13g.32356633A>TCA2727924891BRCA2c.7617+24A>T (n.7617+24A>T)
c.7248+24A>T (n.7248+24A>T)
c.84+24A>T (n.84+24A>T)
c.182+24A>T
n.7617+24A>T
c.7521+24A>T (n.7521+24A>T)
 dbSNP
13g.32356634T>ACA2727924914BRCA2c.7617+25T>A (n.7617+25T>A)
c.7248+25T>A (n.7248+25T>A)
c.84+25T>A (n.84+25T>A)
c.182+25T>A
n.7617+25T>A
c.7521+25T>A (n.7521+25T>A)
 dbSNP
13g.32356634T>CCA2622571733BRCA2c.7617+25T>C (n.7617+25T>C)
c.7248+25T>C (n.7248+25T>C)
c.84+25T>C (n.84+25T>C)
c.182+25T>C
n.7617+25T>C
c.7521+25T>C (n.7521+25T>C)
 gnomAD v4
13g.32356635G>ACA2727924949BRCA2c.7617+26G>A (n.7617+26G>A)
c.7248+26G>A (n.7248+26G>A)
c.84+26G>A (n.84+26G>A)
c.182+26G>A
n.7617+26G>A
c.7521+26G>A (n.7521+26G>A)
 dbSNP
13g.32356635G>CCA2727924935BRCA2c.7617+26G>C (n.7617+26G>C)
c.7248+26G>C (n.7248+26G>C)
c.84+26G>C (n.84+26G>C)
c.182+26G>C
n.7617+26G>C
c.7521+26G>C (n.7521+26G>C)
 dbSNP
13g.32356635G>TCA2727925016BRCA2c.7617+26G>T (n.7617+26G>T)
c.7248+26G>T (n.7248+26G>T)
c.84+26G>T (n.84+26G>T)
c.182+26G>T
n.7617+26G>T
c.7521+26G>T (n.7521+26G>T)
 dbSNP
13g.32356636G>ACA2727925040BRCA2c.7617+27G>A (n.7617+27G>A)
c.7248+27G>A (n.7248+27G>A)
c.84+27G>A (n.84+27G>A)
c.182+27G>A
n.7617+27G>A
c.7521+27G>A (n.7521+27G>A)
 dbSNP
13g.32356636G>CCA2727925039BRCA2c.7617+27G>C (n.7617+27G>C)
c.7248+27G>C (n.7248+27G>C)
c.84+27G>C (n.84+27G>C)
c.182+27G>C
n.7617+27G>C
c.7521+27G>C (n.7521+27G>C)
 dbSNP
13g.32356636G>TCA2622571734BRCA2c.7617+27G>T (n.7617+27G>T)
c.7248+27G>T (n.7248+27G>T)
c.84+27G>T (n.84+27G>T)
c.182+27G>T
n.7617+27G>T
c.7521+27G>T (n.7521+27G>T)
 dbSNP gnomAD v4
13g.32356637C>ACA2622571735BRCA2c.7617+28C>A (n.7617+28C>A)
c.7248+28C>A (n.7248+28C>A)
c.84+28C>A (n.84+28C>A)
c.182+28C>A
n.7617+28C>A
c.7521+28C>A (n.7521+28C>A)
 gnomAD v4
13g.32356637C>TCA2622571736BRCA2c.7617+28C>T (n.7617+28C>T)
c.7248+28C>T (n.7248+28C>T)
c.84+28C>T (n.84+28C>T)
c.182+28C>T
n.7617+28C>T
c.7521+28C>T (n.7521+28C>T)
 dbSNP gnomAD v4
13g.32356639T>CCA2622571737BRCA2c.7617+30T>C (n.7617+30T>C)
c.7248+30T>C (n.7248+30T>C)
c.84+30T>C (n.84+30T>C)
c.182+30T>C
n.7617+30T>C
c.7521+30T>C (n.7521+30T>C)
 gnomAD v4
13g.32356639T>GCA2622571738BRCA2c.7617+30T>G (n.7617+30T>G)
c.7248+30T>G (n.7248+30T>G)
c.84+30T>G (n.84+30T>G)
c.182+30T>G
n.7617+30T>G
c.7521+30T>G (n.7521+30T>G)
 gnomAD v4
13g.32356640T>CCA609453977BRCA2c.7617+31T>C (n.7617+31T>C)
c.7248+31T>C (n.7248+31T>C)
c.84+31T>C (n.84+31T>C)
c.182+31T>C
n.7617+31T>C
c.7521+31T>C (n.7521+31T>C)
 dbSNP gnomAD v2 gnomAD v4
13g.32356640T=CA2082815804BRCA2c.7617+31T= (n.7617+31T=)
c.7248+31T= (n.7248+31T=)
c.84+31T= (n.84+31T=)
c.182+31T=
n.7617+31T=
c.7521+31T= (n.7521+31T=)
13g.32356642A>GCA2727925130BRCA2c.7617+33A>G (n.7617+33A>G)
c.7248+33A>G (n.7248+33A>G)
c.84+33A>G (n.84+33A>G)
c.182+33A>G
n.7617+33A>G
c.7521+33A>G (n.7521+33A>G)
 dbSNP
13g.32356644G>ACA2622571739BRCA2c.7617+35G>A (n.7617+35G>A)
c.7248+35G>A (n.7248+35G>A)
c.84+35G>A (n.84+35G>A)
c.182+35G>A
n.7617+35G>A
c.7521+35G>A (n.7521+35G>A)
 dbSNP gnomAD v4
13g.32356644G>CCA2727925153BRCA2c.7617+35G>C (n.7617+35G>C)
c.7248+35G>C (n.7248+35G>C)
c.84+35G>C (n.84+35G>C)
c.182+35G>C
n.7617+35G>C
c.7521+35G>C (n.7521+35G>C)
 dbSNP
13g.32356645A>GCA2727925188BRCA2c.7617+36A>G (n.7617+36A>G)
c.7248+36A>G (n.7248+36A>G)
c.84+36A>G (n.84+36A>G)
c.182+36A>G
n.7617+36A>G
c.7521+36A>G (n.7521+36A>G)
 dbSNP
13g.32356645A>TCA2622571740BRCA2c.7617+36A>T (n.7617+36A>T)
c.7248+36A>T (n.7248+36A>T)
c.84+36A>T (n.84+36A>T)
c.182+36A>T
n.7617+36A>T
c.7521+36A>T (n.7521+36A>T)
 dbSNP gnomAD v4
13g.32356646C>ACA2727839907BRCA2c.7617+37C>A (n.7617+37C>A)
c.7248+37C>A (n.7248+37C>A)
c.84+37C>A (n.84+37C>A)
c.182+37C>A
n.7617+37C>A
c.7521+37C>A (n.7521+37C>A)
 dbSNP
13g.32356646C=CA2082815808BRCA2c.7617+37C= (n.7617+37C=)
c.7248+37C= (n.7248+37C=)
c.84+37C= (n.84+37C=)
c.182+37C=
n.7617+37C=
c.7521+37C= (n.7521+37C=)
13g.32356646C>GCA2727839906BRCA2c.7617+37C>G (n.7617+37C>G)
c.7248+37C>G (n.7248+37C>G)
c.84+37C>G (n.84+37C>G)
c.182+37C>G
n.7617+37C>G
c.7521+37C>G (n.7521+37C>G)
 dbSNP
13g.32356646C>TCA6941111BRCA2c.7617+37C>T (n.7617+37C>T)
c.7248+37C>T (n.7248+37C>T)
c.84+37C>T (n.84+37C>T)
c.182+37C>T
n.7617+37C>T
c.7521+37C>T (n.7521+37C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.32356646_32356648delinsCAGCA2082815810BRCA2c.7617+37_7617+39delinsCAG (n.7617+37_7617+39delinsCAG)
c.7248+37_7248+39delinsCAG (n.7248+37_7248+39delinsCAG)
c.84+37_84+39delinsCAG (n.84+37_84+39delinsCAG)
c.182+37_182+39delinsCAG
n.7617+37_7617+39delinsCAG
c.7521+37_7521+39delinsCAG (n.7521+37_7521+39delinsCAG)
13g.32356647A=CA2082815817BRCA2c.7617+38A= (n.7617+38A=)
c.7248+38A= (n.7248+38A=)
c.84+38A= (n.84+38A=)
c.182+38A=
n.7617+38A=
c.7521+38A= (n.7521+38A=)
13g.32356647A>GCA645509329BRCA2c.7617+38A>G (n.7617+38A>G)
c.7248+38A>G (n.7248+38A>G)
c.84+38A>G (n.84+38A>G)
c.182+38A>G
n.7617+38A>G
c.7521+38A>G (n.7521+38A>G)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32356649_32356650delCA2082815815BRCA2c.7617+40_7617+41del (n.7617+40_7617+41del)
c.7248+40_7248+41del (n.7248+40_7248+41del)
c.84+40_84+41del (n.84+40_84+41del)
c.182+40_182+41del
n.7617+40_7617+41del
c.7521+40_7521+41del (n.7521+40_7521+41del)
 dbSNP gnomAD v4
13g.32356648G>ACA6941112BRCA2c.7617+39G>A (n.7617+39G>A)
c.7248+39G>A (n.7248+39G>A)
c.84+39G>A (n.84+39G>A)
c.182+39G>A
n.7617+39G>A
c.7521+39G>A (n.7521+39G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32356648G>CCA609453978BRCA2c.7617+39G>C (n.7617+39G>C)
c.7248+39G>C (n.7248+39G>C)
c.84+39G>C (n.84+39G>C)
c.182+39G>C
n.7617+39G>C
c.7521+39G>C (n.7521+39G>C)
 dbSNP gnomAD v2 gnomAD v4
13g.32356648G=CA2082815826BRCA2c.7617+39G= (n.7617+39G=)
c.7248+39G= (n.7248+39G=)
c.84+39G= (n.84+39G=)
c.182+39G=
n.7617+39G=
c.7521+39G= (n.7521+39G=)
13g.32356649A>GCA2575388056BRCA2c.7617+40A>G (n.7617+40A>G)
c.7248+40A>G (n.7248+40A>G)
c.84+40A>G (n.84+40A>G)
c.182+40A>G
n.7617+40A>G
c.7521+40A>G (n.7521+40A>G)
13g.32356650G>ACA247470253BRCA2c.7617+41G>A (n.7617+41G>A)
c.7248+41G>A (n.7248+41G>A)
c.84+41G>A (n.84+41G>A)
c.182+41G>A
n.7617+41G>A
c.7521+41G>A (n.7521+41G>A)
 dbSNP gnomAD v4
13g.32356650G>CCA2727851108BRCA2c.7617+41G>C (n.7617+41G>C)
c.7248+41G>C (n.7248+41G>C)
c.84+41G>C (n.84+41G>C)
c.182+41G>C
n.7617+41G>C
c.7521+41G>C (n.7521+41G>C)
 dbSNP
13g.32356650G=CA2082815832BRCA2c.7617+41G= (n.7617+41G=)
c.7248+41G= (n.7248+41G=)
c.84+41G= (n.84+41G=)
c.182+41G=
n.7617+41G=
c.7521+41G= (n.7521+41G=)
13g.32356651T>ACA6941113BRCA2c.7617+42T>A (n.7617+42T>A)
c.7248+42T>A (n.7248+42T>A)
c.84+42T>A (n.84+42T>A)
c.182+42T>A
n.7617+42T>A
c.7521+42T>A (n.7521+42T>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32356651T=CA2082815835BRCA2c.7617+42T= (n.7617+42T=)
c.7248+42T= (n.7248+42T=)
c.84+42T= (n.84+42T=)
c.182+42T=
n.7617+42T=
c.7521+42T= (n.7521+42T=)
13g.32356651_32356652insCACA919242776BRCA2c.7617+42_7617+43insCA (n.7617+42_7617+43insCA)
c.7248+42_7248+43insCA (n.7248+42_7248+43insCA)
c.84+42_84+43insCA (n.84+42_84+43insCA)
c.182+42_182+43insCA
n.7617+42_7617+43insCA
c.7521+42_7521+43insCA (n.7521+42_7521+43insCA)
 dbSNP
13g.32356652G>ACA2575388057BRCA2c.7617+43G>A (n.7617+43G>A)
c.7248+43G>A (n.7248+43G>A)
c.84+43G>A (n.84+43G>A)
c.182+43G>A
n.7617+43G>A
c.7521+43G>A (n.7521+43G>A)
 dbSNP gnomAD v4
13g.32356652G>CCA2727925204BRCA2c.7617+43G>C (n.7617+43G>C)
c.7248+43G>C (n.7248+43G>C)
c.84+43G>C (n.84+43G>C)
c.182+43G>C
n.7617+43G>C
c.7521+43G>C (n.7521+43G>C)
 dbSNP
13g.32356653T>ACA2727925258BRCA2c.7617+44T>A (n.7617+44T>A)
c.7248+44T>A (n.7248+44T>A)
c.84+44T>A (n.84+44T>A)
c.182+44T>A
n.7617+44T>A
c.7521+44T>A (n.7521+44T>A)
 dbSNP
13g.32356653T>CCA2727925234BRCA2c.7617+44T>C (n.7617+44T>C)
c.7248+44T>C (n.7248+44T>C)
c.84+44T>C (n.84+44T>C)
c.182+44T>C
n.7617+44T>C
c.7521+44T>C (n.7521+44T>C)
 dbSNP
13g.32356659dupCA2622571742BRCA2c.7617+50dup (n.7617+50dup)
c.7248+50dup (n.7248+50dup)
c.84+50dup (n.84+50dup)
c.182+50dup
n.7617+50dup
c.7521+50dup (n.7521+50dup)
 gnomAD v4
13g.32356657T>ACA2727925305BRCA2c.7617+48T>A (n.7617+48T>A)
c.7248+48T>A (n.7248+48T>A)
c.84+48T>A (n.84+48T>A)
c.182+48T>A
n.7617+48T>A
c.7521+48T>A (n.7521+48T>A)
 dbSNP
13g.32356658T>ACA2622571743BRCA2c.7617+49T>A (n.7617+49T>A)
c.7248+49T>A (n.7248+49T>A)
c.84+49T>A (n.84+49T>A)
c.182+49T>A
n.7617+49T>A
c.7521+49T>A (n.7521+49T>A)
 gnomAD v4
13g.32356659T>CCA2622571744BRCA2c.7617+50T>C (n.7617+50T>C)
c.7248+50T>C (n.7248+50T>C)
c.84+50T>C (n.84+50T>C)
c.182+50T>C
n.7617+50T>C
c.7521+50T>C (n.7521+50T>C)
 gnomAD v4
13g.32356660A>TCA2727925340BRCA2c.7617+51A>T (n.7617+51A>T)
c.7248+51A>T (n.7248+51A>T)
c.84+51A>T (n.84+51A>T)
c.182+51A>T
n.7617+51A>T
c.7521+51A>T (n.7521+51A>T)
 dbSNP
13g.32356662T>GCA697350987BRCA2c.7617+53T>G (n.7617+53T>G)
c.7248+53T>G (n.7248+53T>G)
c.84+53T>G (n.84+53T>G)
c.182+53T>G
n.7617+53T>G
c.7521+53T>G (n.7521+53T>G)
 dbSNP gnomAD v3 gnomAD v4
13g.32356662T=CA2082815840BRCA2c.7617+53T= (n.7617+53T=)
c.7248+53T= (n.7248+53T=)
c.84+53T= (n.84+53T=)
c.182+53T=
n.7617+53T=
c.7521+53T= (n.7521+53T=)
13g.32356664C>ACA2082815842BRCA2c.7617+55C>A (n.7617+55C>A)
c.7248+55C>A (n.7248+55C>A)
c.84+55C>A (n.84+55C>A)
c.182+55C>A
n.7617+55C>A
c.7521+55C>A (n.7521+55C>A)
 dbSNP gnomAD v4
13g.32356664C=CA2082815843BRCA2c.7617+55C= (n.7617+55C=)
c.7248+55C= (n.7248+55C=)
c.84+55C= (n.84+55C=)
c.182+55C=
n.7617+55C=
c.7521+55C= (n.7521+55C=)
13g.32356665A>TCA2727925421BRCA2c.7617+56A>T (n.7617+56A>T)
c.7248+56A>T (n.7248+56A>T)
c.84+56A>T (n.84+56A>T)
c.182+56A>T
n.7617+56A>T
c.7521+56A>T (n.7521+56A>T)
 dbSNP
13g.32356666T>ACA2727925423BRCA2c.7617+57T>A (n.7617+57T>A)
c.7248+57T>A (n.7248+57T>A)
c.84+57T>A (n.84+57T>A)
c.182+57T>A
n.7617+57T>A
c.7521+57T>A (n.7521+57T>A)
 dbSNP
13g.32356667T>ACA2727925475BRCA2c.7617+58T>A (n.7617+58T>A)
c.7248+58T>A (n.7248+58T>A)
c.84+58T>A (n.84+58T>A)
c.182+58T>A
n.7617+58T>A
c.7521+58T>A (n.7521+58T>A)
 dbSNP

Number of alleles fetched