Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32357847_32357906dupCA2580614662BRCA2c.7723_7782dup (p.Lys2594_Ala2595insThrGlyLysGlyIleGlnLeuAlaAspGlyGlyTrpLeuIleProSerAsnAspGlyLys)
c.7354_7413dup (p.Lys2471_Ala2472insThrGlyLysGlyIleGlnLeuAlaAspGlyGlyTrpLeuIleProSerAsnAspGlyLys)
c.190_249dup (p.Lys83_Ala84insThrGlyLysGlyIleGlnLeuAlaAspGlyGlyTrpLeuIleProSerAsnAspGlyLys)
c.288_347dup
n.7723_7782dup
c.7627_7686dup (p.Lys2562_Ala2563insThrGlyLysGlyIleGlnLeuAlaAspGlyGlyTrpLeuIleProSerAsnAspGlyLys)
 ClinVar
13g.32357858_32357868delCA2580087355BRCA2c.7734_7744del (p.Ile2579Ter)
c.7365_7375del (p.Ile2456Ter)
c.201_211del (p.Ile68Ter)
c.299_309del
n.7734_7744del
c.7638_7648del (p.Ile2547Ter)
 ClinVar
13g.32357865_32357872delinsTTGGCTGACA2082818626BRCA2c.7741_7748delinsTTGGCTGA (p.Leu2581=)
c.7372_7379delinsTTGGCTGA (p.Leu2458=)
c.208_215delinsTTGGCTGA (p.Leu70=)
c.306_313delinsTTGGCTGA
n.7741_7748delinsTTGGCTGA
c.7645_7652delinsTTGGCTGA (p.Leu2549=)
13g.32357866T>ACA387745641BRCA2c.7742T>A (p.Leu2581Ter)
c.7373T>A (p.Leu2458Ter)
c.209T>A (p.Leu70Ter)
c.307T>A
n.7742T>A
c.7646T>A (p.Leu2549Ter)
13g.32357866T>CCA387745650BRCA2c.7742T>C (p.Leu2581Ser)
c.7373T>C (p.Leu2458Ser)
c.209T>C (p.Leu70Ser)
c.307T>C
n.7742T>C
c.7646T>C (p.Leu2549Ser)
 dbSNP
13g.32357866T>GCA025251BRCA2c.7742T>G (p.Leu2581Trp)
c.7373T>G (p.Leu2458Trp)
c.209T>G (p.Leu70Trp)
c.307T>G
n.7742T>G
c.7646T>G (p.Leu2549Trp)
 ClinVar dbSNP
13g.32357866T=CA2082818635BRCA2c.7742T= (p.Leu2581=)
c.7373T= (p.Leu2458=)
c.209T= (p.Leu70=)
c.307T=
n.7742T=
c.7646T= (p.Leu2549=)
13g.32357866_32357867delinsTGCA2082818658BRCA2c.7742_7743delinsTG (p.Leu2581=)
c.7373_7374delinsTG (p.Leu2458=)
c.209_210delinsTG (p.Leu70=)
c.307_308delinsTG
n.7742_7743delinsTG
c.7646_7647delinsTG (p.Leu2549=)
13g.32357869_32357875dupCA2499222305BRCA2c.7745_7751dup (p.Gly2585Ter)
c.7376_7382dup (p.Gly2462Ter)
c.212_218dup (p.Gly74Ter)
c.310_316dup
n.7745_7751dup
c.7649_7655dup (p.Gly2553Ter)
 ClinVar dbSNP
13g.32357869_32357875delCA915946877BRCA2c.7745_7751del (p.Ala2582ValfsTer?)
c.7376_7382del (p.Ala2459ValfsTer?)
c.212_218del (p.Ala71ValfsTer?)
c.7745_7751del (p.Ala2582ValfsTer25)
c.310_316del
n.7745_7751del
c.7649_7655del (p.Ala2550ValfsTer?)
 ClinVar dbSNP
13g.32357867G>ACA483439230BRCA2c.7743G>A (p.Leu2581=)
c.7374G>A (p.Leu2458=)
c.210G>A (p.Leu70=)
c.308G>A
n.7743G>A
c.7647G>A (p.Leu2549=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32357867G>CCA387745658BRCA2c.7743G>C (p.Leu2581Phe)
c.7374G>C (p.Leu2458Phe)
c.210G>C (p.Leu70Phe)
c.308G>C
n.7743G>C
c.7647G>C (p.Leu2549Phe)
13g.32357867G=CA2082818669BRCA2c.7743G= (p.Leu2581=)
c.7374G= (p.Leu2458=)
c.210G= (p.Leu70=)
c.308G=
n.7743G=
c.7647G= (p.Leu2549=)
13g.32357867G>TCA387745660BRCA2c.7743G>T (p.Leu2581Phe)
c.7374G>T (p.Leu2458Phe)
c.210G>T (p.Leu70Phe)
c.308G>T
n.7743G>T
c.7647G>T (p.Leu2549Phe)
 dbSNP
13g.32357868delCA10589448BRCA2c.7744del (p.Ala2582LeufsTer?)
c.7375del (p.Ala2459LeufsTer?)
c.211del (p.Ala71LeufsTer?)
c.7744del (p.Ala2582LeufsTer27)
c.309del
n.7744del
c.7648del (p.Ala2550LeufsTer?)
 ClinVar dbSNP
13g.32357868G>ACA10579751BRCA2c.7744G>A (p.Ala2582Thr)
c.7375G>A (p.Ala2459Thr)
c.211G>A (p.Ala71Thr)
c.309G>A
n.7744G>A
c.7648G>A (p.Ala2550Thr)
 ClinVar dbSNP gnomAD v4
13g.32357868G>CCA387745661BRCA2c.7744G>C (p.Ala2582Pro)
c.7375G>C (p.Ala2459Pro)
c.211G>C (p.Ala71Pro)
c.309G>C
n.7744G>C
c.7648G>C (p.Ala2550Pro)
 dbSNP gnomAD v4
13g.32357868G=CA2082818677BRCA2c.7744G= (p.Ala2582=)
c.7375G= (p.Ala2459=)
c.211G= (p.Ala71=)
c.309G=
n.7744G=
c.7648G= (p.Ala2550=)
13g.32357868G>TCA387745664BRCA2c.7744G>T (p.Ala2582Ser)
c.7375G>T (p.Ala2459Ser)
c.211G>T (p.Ala71Ser)
c.309G>T
n.7744G>T
c.7648G>T (p.Ala2550Ser)
 dbSNP
13g.32357869delCA2697551788BRCA2c.7745del (p.Ala2582ValfsTer?)
c.7376del (p.Ala2459ValfsTer?)
c.212del (p.Ala71ValfsTer?)
c.7745del (p.Ala2582ValfsTer27)
c.310del
n.7745del
c.7649del (p.Ala2550ValfsTer?)
 ClinVar
13g.32357869C>ACA387745676BRCA2c.7745C>A (p.Ala2582Asp)
c.7376C>A (p.Ala2459Asp)
c.212C>A (p.Ala71Asp)
c.310C>A
n.7745C>A
c.7649C>A (p.Ala2550Asp)
 dbSNP
13g.32357869C>GCA387745679BRCA2c.7745C>G (p.Ala2582Gly)
c.7376C>G (p.Ala2459Gly)
c.212C>G (p.Ala71Gly)
c.310C>G
n.7745C>G
c.7649C>G (p.Ala2550Gly)
 dbSNP
13g.32357869C>TCA387745686BRCA2c.7745C>T (p.Ala2582Val)
c.7376C>T (p.Ala2459Val)
c.212C>T (p.Ala71Val)
c.310C>T
n.7745C>T
c.7649C>T (p.Ala2550Val)
 dbSNP
13g.32357870T>ACA483439233BRCA2c.7746T>A (p.Ala2582=)
c.7377T>A (p.Ala2459=)
c.213T>A (p.Ala71=)
c.311T>A
n.7746T>A
c.7650T>A (p.Ala2550=)
13g.32357870T>CCA483439234BRCA2c.7746T>C (p.Ala2582=)
c.7377T>C (p.Ala2459=)
c.213T>C (p.Ala71=)
c.311T>C
n.7746T>C
c.7650T>C (p.Ala2550=)
 COSMIC COSMIC
13g.32357870T>GCA483439235BRCA2c.7746T>G (p.Ala2582=)
c.7377T>G (p.Ala2459=)
c.213T>G (p.Ala71=)
c.311T>G
n.7746T>G
c.7650T>G (p.Ala2550=)
13g.32357871G>ACA387745690BRCA2c.7747G>A (p.Asp2583Asn)
c.7378G>A (p.Asp2460Asn)
c.214G>A (p.Asp72Asn)
c.312G>A
n.7747G>A
c.7651G>A (p.Asp2551Asn)
 dbSNP gnomAD v4
13g.32357871G>CCA387745693BRCA2c.7747G>C (p.Asp2583His)
c.7378G>C (p.Asp2460His)
c.214G>C (p.Asp72His)
c.312G>C
n.7747G>C
c.7651G>C (p.Asp2551His)
 ClinVar dbSNP
13g.32357871G=CA2082818681BRCA2c.7747G= (p.Asp2583=)
c.7378G= (p.Asp2460=)
c.214G= (p.Asp72=)
c.312G=
n.7747G=
c.7651G= (p.Asp2551=)
13g.32357871G>TCA387745698BRCA2c.7747G>T (p.Asp2583Tyr)
c.7378G>T (p.Asp2460Tyr)
c.214G>T (p.Asp72Tyr)
c.312G>T
n.7747G>T
c.7651G>T (p.Asp2551Tyr)
13g.32357876_32357882delCA2727929030BRCA2c.7752_7758del (p.Gly2585SerfsTer?)
c.7383_7389del (p.Gly2462SerfsTer?)
c.219_225del (p.Gly74SerfsTer?)
c.7752_7758del (p.Gly2585SerfsTer22)
c.317_323del
n.7752_7758del
c.7656_7662del (p.Gly2553SerfsTer?)
 dbSNP
13g.32357872A=CA2082818686BRCA2c.7748A= (p.Asp2583=)
c.7379A= (p.Asp2460=)
c.215A= (p.Asp72=)
c.313A=
n.7748A=
c.7652A= (p.Asp2551=)
13g.32357872A>CCA387745712BRCA2c.7748A>C (p.Asp2583Ala)
c.7379A>C (p.Asp2460Ala)
c.215A>C (p.Asp72Ala)
c.313A>C
n.7748A>C
c.7652A>C (p.Asp2551Ala)
13g.32357872A>GCA387745715BRCA2c.7748A>G (p.Asp2583Gly)
c.7379A>G (p.Asp2460Gly)
c.215A>G (p.Asp72Gly)
c.313A>G
n.7748A>G
c.7652A>G (p.Asp2551Gly)
 dbSNP
13g.32357872A>TCA387745727BRCA2c.7748A>T (p.Asp2583Val)
c.7379A>T (p.Asp2460Val)
c.215A>T (p.Asp72Val)
c.313A>T
n.7748A>T
c.7652A>T (p.Asp2551Val)
 ClinVar dbSNP
13g.32357873T>ACA387745743BRCA2c.7749T>A (p.Asp2583Glu)
c.7380T>A (p.Asp2460Glu)
c.216T>A (p.Asp72Glu)
c.314T>A
n.7749T>A
c.7653T>A (p.Asp2551Glu)
13g.32357873T>CCA025254BRCA2c.7749T>C (p.Asp2583=)
c.7380T>C (p.Asp2460=)
c.216T>C (p.Asp72=)
c.314T>C
n.7749T>C
c.7653T>C (p.Asp2551=)
 ClinVar dbSNP gnomAD v4
13g.32357873T>GCA387745739BRCA2c.7749T>G (p.Asp2583Glu)
c.7380T>G (p.Asp2460Glu)
c.216T>G (p.Asp72Glu)
c.314T>G
n.7749T>G
c.7653T>G (p.Asp2551Glu)
13g.32357873T=CA2082818697BRCA2c.7749T= (p.Asp2583=)
c.7380T= (p.Asp2460=)
c.216T= (p.Asp72=)
c.314T=
n.7749T=
c.7653T= (p.Asp2551=)
13g.32357873_32357874delinsTGCA2082818694BRCA2c.7749_7750delinsTG (p.Asp2583=)
c.7380_7381delinsTG (p.Asp2460=)
c.216_217delinsTG (p.Asp72=)
c.314_315delinsTG
n.7749_7750delinsTG
c.7653_7654delinsTG (p.Asp2551=)
13g.32357874G>ACA387745746BRCA2c.7750G>A (p.Gly2584Ser)
c.7381G>A (p.Gly2461Ser)
c.217G>A (p.Gly73Ser)
c.315G>A
n.7750G>A
c.7654G>A (p.Gly2552Ser)
 dbSNP
13g.32357874G>CCA387745748BRCA2c.7750G>C (p.Gly2584Arg)
c.7381G>C (p.Gly2461Arg)
c.217G>C (p.Gly73Arg)
c.315G>C
n.7750G>C
c.7654G>C (p.Gly2552Arg)
13g.32357874G=CA2082818708BRCA2c.7750G= (p.Gly2584=)
c.7381G= (p.Gly2461=)
c.217G= (p.Gly73=)
c.315G=
n.7750G=
c.7654G= (p.Gly2552=)
13g.32357874G>TCA387745750BRCA2c.7750G>T (p.Gly2584Cys)
c.7381G>T (p.Gly2461Cys)
c.217G>T (p.Gly73Cys)
c.315G>T
n.7750G>T
c.7654G>T (p.Gly2552Cys)
 ClinVar dbSNP COSMIC COSMIC
13g.32357875delCA025255BRCA2c.7751del (p.Gly2584ValfsTer?)
c.7382del (p.Gly2461ValfsTer?)
c.218del (p.Gly73ValfsTer?)
c.7751del (p.Gly2584ValfsTer25)
c.316del
n.7751del
c.7655del (p.Gly2552ValfsTer?)
 ClinVar dbSNP
13g.32357875G>ACA025256BRCA2c.7751G>A (p.Gly2584Asp)
c.7382G>A (p.Gly2461Asp)
c.218G>A (p.Gly73Asp)
c.316G>A
n.7751G>A
c.7655G>A (p.Gly2552Asp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357875G>CCA387745756BRCA2c.7751G>C (p.Gly2584Ala)
c.7382G>C (p.Gly2461Ala)
c.218G>C (p.Gly73Ala)
c.316G>C
n.7751G>C
c.7655G>C (p.Gly2552Ala)
 dbSNP
13g.32357875G=CA2082818713BRCA2c.7751G= (p.Gly2584=)
c.7382G= (p.Gly2461=)
c.218G= (p.Gly73=)
c.316G=
n.7751G=
c.7655G= (p.Gly2552=)
13g.32357875G>TCA387745757BRCA2c.7751G>T (p.Gly2584Val)
c.7382G>T (p.Gly2461Val)
c.218G>T (p.Gly73Val)
c.316G>T
n.7751G>T
c.7655G>T (p.Gly2552Val)
13g.32357876T>ACA483439241BRCA2c.7752T>A (p.Gly2584=)
c.7383T>A (p.Gly2461=)
c.219T>A (p.Gly73=)
c.317T>A
n.7752T>A
c.7656T>A (p.Gly2552=)
13g.32357876T>CCA483439243BRCA2c.7752T>C (p.Gly2584=)
c.7383T>C (p.Gly2461=)
c.219T>C (p.Gly73=)
c.317T>C
n.7752T>C
c.7656T>C (p.Gly2552=)
13g.32357876T>GCA483439245BRCA2c.7752T>G (p.Gly2584=)
c.7383T>G (p.Gly2461=)
c.219T>G (p.Gly73=)
c.317T>G
n.7752T>G
c.7656T>G (p.Gly2552=)
 ClinVar
13g.32357877G>ACA025257BRCA2c.7753G>A (p.Gly2585Arg)
c.7384G>A (p.Gly2462Arg)
c.220G>A (p.Gly74Arg)
c.318G>A
n.7753G>A
c.7657G>A (p.Gly2553Arg)
 ClinVar dbSNP gnomAD v4
13g.32357877G>CCA387745760BRCA2c.7753G>C (p.Gly2585Arg)
c.7384G>C (p.Gly2462Arg)
c.220G>C (p.Gly74Arg)
c.318G>C
n.7753G>C
c.7657G>C (p.Gly2553Arg)
13g.32357877G=CA2082818720BRCA2c.7753G= (p.Gly2585=)
c.7384G= (p.Gly2462=)
c.220G= (p.Gly74=)
c.318G=
n.7753G=
c.7657G= (p.Gly2553=)
13g.32357877G>TCA387745764BRCA2c.7753G>T (p.Gly2585Ter)
c.7384G>T (p.Gly2462Ter)
c.220G>T (p.Gly74Ter)
c.318G>T
n.7753G>T
c.7657G>T (p.Gly2553Ter)
13g.32357878G>ACA387745772BRCA2c.7754G>A (p.Gly2585Glu)
c.7385G>A (p.Gly2462Glu)
c.221G>A (p.Gly74Glu)
c.319G>A
n.7754G>A
c.7658G>A (p.Gly2553Glu)
 dbSNP
13g.32357878G>CCA6941135BRCA2c.7754G>C (p.Gly2585Ala)
c.7385G>C (p.Gly2462Ala)
c.221G>C (p.Gly74Ala)
c.319G>C
n.7754G>C
c.7658G>C (p.Gly2553Ala)
 dbSNP ExAC gnomAD v2
13g.32357878G=CA2082818723BRCA2c.7754G= (p.Gly2585=)
c.7385G= (p.Gly2462=)
c.221G= (p.Gly74=)
c.319G=
n.7754G=
c.7658G= (p.Gly2553=)
13g.32357878G>TCA387745768BRCA2c.7754G>T (p.Gly2585Val)
c.7385G>T (p.Gly2462Val)
c.221G>T (p.Gly74Val)
c.319G>T
n.7754G>T
c.7658G>T (p.Gly2553Val)
 dbSNP
13g.32357879A=CA2082818728BRCA2c.7755A= (p.Gly2585=)
c.7386A= (p.Gly2462=)
c.222A= (p.Gly74=)
c.320A=
n.7755A=
c.7659A= (p.Gly2553=)
13g.32357879A>CCA483439248BRCA2c.7755A>C (p.Gly2585=)
c.7386A>C (p.Gly2462=)
c.222A>C (p.Gly74=)
c.320A>C
n.7755A>C
c.7659A>C (p.Gly2553=)
 ClinVar
13g.32357879A>GCA483439247BRCA2c.7755A>G (p.Gly2585=)
c.7386A>G (p.Gly2462=)
c.222A>G (p.Gly74=)
c.320A>G
n.7755A>G
c.7659A>G (p.Gly2553=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32357879A>TCA6941136BRCA2c.7755A>T (p.Gly2585=)
c.7386A>T (p.Gly2462=)
c.222A>T (p.Gly74=)
c.320A>T
n.7755A>T
c.7659A>T (p.Gly2553=)
 ClinVar dbSNP ExAC gnomAD v2
13g.32357880T>ACA387745801BRCA2c.7756T>A (p.Trp2586Arg)
c.7387T>A (p.Trp2463Arg)
c.223T>A (p.Trp75Arg)
c.321T>A
n.7756T>A
c.7660T>A (p.Trp2554Arg)
13g.32357880T>CCA387745788BRCA2c.7756T>C (p.Trp2586Arg)
c.7387T>C (p.Trp2463Arg)
c.223T>C (p.Trp75Arg)
c.321T>C
n.7756T>C
c.7660T>C (p.Trp2554Arg)
 ClinVar gnomAD v4
13g.32357880T>GCA387745791BRCA2c.7756T>G (p.Trp2586Gly)
c.7387T>G (p.Trp2463Gly)
c.223T>G (p.Trp75Gly)
c.321T>G
n.7756T>G
c.7660T>G (p.Trp2554Gly)
13g.32357881G>ACA025259BRCA2c.7757G>A (p.Trp2586Ter)
c.7388G>A (p.Trp2463Ter)
c.224G>A (p.Trp75Ter)
c.322G>A
n.7757G>A
c.7661G>A (p.Trp2554Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32357881G>CCA387745809BRCA2c.7757G>C (p.Trp2586Ser)
c.7388G>C (p.Trp2463Ser)
c.224G>C (p.Trp75Ser)
c.322G>C
n.7757G>C
c.7661G>C (p.Trp2554Ser)
 ClinVar
13g.32357881G=CA2082818735BRCA2c.7757G= (p.Trp2586=)
c.7388G= (p.Trp2463=)
c.224G= (p.Trp75=)
c.322G=
n.7757G=
c.7661G= (p.Trp2554=)
13g.32357881G>TCA387745814BRCA2c.7757G>T (p.Trp2586Leu)
c.7388G>T (p.Trp2463Leu)
c.224G>T (p.Trp75Leu)
c.322G>T
n.7757G>T
c.7661G>T (p.Trp2554Leu)
 dbSNP
13g.32357882G>ACA025260BRCA2c.7758G>A (p.Trp2586Ter)
c.7389G>A (p.Trp2463Ter)
c.225G>A (p.Trp75Ter)
c.323G>A
n.7758G>A
c.7662G>A (p.Trp2554Ter)
 ClinVar dbSNP COSMIC COSMIC
13g.32357882G>CCA247471160BRCA2c.7758G>C (p.Trp2586Cys)
c.7389G>C (p.Trp2463Cys)
c.225G>C (p.Trp75Cys)
c.323G>C
n.7758G>C
c.7662G>C (p.Trp2554Cys)
 dbSNP gnomAD v4
13g.32357882G=CA2082818751BRCA2c.7758G= (p.Trp2586=)
c.7389G= (p.Trp2463=)
c.225G= (p.Trp75=)
c.323G=
n.7758G=
c.7662G= (p.Trp2554=)
13g.32357882G>TCA387745820BRCA2c.7758G>T (p.Trp2586Cys)
c.7389G>T (p.Trp2463Cys)
c.225G>T (p.Trp75Cys)
c.323G>T
n.7758G>T
c.7662G>T (p.Trp2554Cys)
 ClinVar dbSNP
13g.32357882_32357883dupCA16619769BRCA2c.7758_7759dup (p.Leu2587ArgfsTer?)
c.7389_7390dup (p.Leu2464ArgfsTer?)
c.225_226dup (p.Leu76ArgfsTer?)
c.7758_7759dup (p.Leu2587ArgfsTer23)
c.323_324dup
n.7758_7759dup
c.7662_7663dup (p.Leu2555ArgfsTer?)
 ClinVar dbSNP
13g.32357882_32357885delCA2695217925BRCA2c.7758_7761del (p.Trp2586Ter)
c.7389_7392del (p.Trp2463Ter)
c.225_228del (p.Trp75Ter)
c.323_326del
n.7758_7761del
c.7662_7665del (p.Trp2554Ter)
13g.32357883C>ACA387745838BRCA2c.7759C>A (p.Leu2587Ile)
c.7390C>A (p.Leu2464Ile)
c.226C>A (p.Leu76Ile)
c.324C>A
n.7759C>A
c.7663C>A (p.Leu2555Ile)
 dbSNP
13g.32357883C=CA2082818761BRCA2c.7759C= (p.Leu2587=)
c.7390C= (p.Leu2464=)
c.226C= (p.Leu76=)
c.324C=
n.7759C=
c.7663C= (p.Leu2555=)
13g.32357883C>GCA387745841BRCA2c.7759C>G (p.Leu2587Val)
c.7390C>G (p.Leu2464Val)
c.226C>G (p.Leu76Val)
c.324C>G
n.7759C>G
c.7663C>G (p.Leu2555Val)
 dbSNP gnomAD v4
13g.32357883C>TCA025261BRCA2c.7759C>T (p.Leu2587Phe)
c.7390C>T (p.Leu2464Phe)
c.226C>T (p.Leu76Phe)
c.324C>T
n.7759C>T
c.7663C>T (p.Leu2555Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32357884T>ACA387745851BRCA2c.7760T>A (p.Leu2587His)
c.7391T>A (p.Leu2464His)
c.227T>A (p.Leu76His)
c.325T>A
n.7760T>A
c.7664T>A (p.Leu2555His)
 ClinVar dbSNP
13g.32357884T>CCA387745849BRCA2c.7760T>C (p.Leu2587Pro)
c.7391T>C (p.Leu2464Pro)
c.227T>C (p.Leu76Pro)
c.325T>C
n.7760T>C
c.7664T>C (p.Leu2555Pro)
 dbSNP
13g.32357884T>GCA387745848BRCA2c.7760T>G (p.Leu2587Arg)
c.7391T>G (p.Leu2464Arg)
c.227T>G (p.Leu76Arg)
c.325T>G
n.7760T>G
c.7664T>G (p.Leu2555Arg)
13g.32357884T=CA2082818769BRCA2c.7760T= (p.Leu2587=)
c.7391T= (p.Leu2464=)
c.227T= (p.Leu76=)
c.325T=
n.7760T=
c.7664T= (p.Leu2555=)
13g.32357884_32357885delinsTCCA2082818768BRCA2c.7760_7761delinsTC (p.Leu2587=)
c.7391_7392delinsTC (p.Leu2464=)
c.227_228delinsTC (p.Leu76=)
c.325_326delinsTC
n.7760_7761delinsTC
c.7664_7665delinsTC (p.Leu2555=)
13g.32357885delCA025264BRCA2c.7761del (p.Ile2588TyrfsTer?)
c.7392del (p.Ile2465TyrfsTer?)
c.228del (p.Ile77TyrfsTer?)
c.7761del (p.Ile2588TyrfsTer21)
c.326del
n.7761del
c.7665del (p.Ile2556TyrfsTer?)
 ClinVar dbSNP
13g.32357885C>ACA483439255BRCA2c.7761C>A (p.Leu2587=)
c.7392C>A (p.Leu2464=)
c.228C>A (p.Leu76=)
c.326C>A
n.7761C>A
c.7665C>A (p.Leu2555=)
 ClinVar dbSNP
13g.32357885C=CA2082818793BRCA2c.7761C= (p.Leu2587=)
c.7392C= (p.Leu2464=)
c.228C= (p.Leu76=)
c.326C=
n.7761C=
c.7665C= (p.Leu2555=)
13g.32357885C>GCA483439256BRCA2c.7761C>G (p.Leu2587=)
c.7392C>G (p.Leu2464=)
c.228C>G (p.Leu76=)
c.326C>G
n.7761C>G
c.7665C>G (p.Leu2555=)
 ClinVar dbSNP
13g.32357885C>TCA483439257BRCA2c.7761C>T (p.Leu2587=)
c.7392C>T (p.Leu2464=)
c.228C>T (p.Leu76=)
c.326C>T
n.7761C>T
c.7665C>T (p.Leu2555=)
 ClinVar dbSNP COSMIC COSMIC
13g.32357885_32357886delinsCACA2082818795BRCA2c.7761_7762delinsCA (p.Leu2587=)
c.7392_7393delinsCA (p.Leu2464=)
c.228_229delinsCA (p.Leu76=)
c.326_327delinsCA
n.7761_7762delinsCA
c.7665_7666delinsCA (p.Leu2555=)
13g.32357885_32357888delinsCATACA2082818783BRCA2c.7761_7764delinsCATA (p.Leu2587=)
c.7392_7395delinsCATA (p.Leu2464=)
c.228_231delinsCATA (p.Leu76=)
c.326_329delinsCATA
n.7761_7764delinsCATA
c.7665_7668delinsCATA (p.Leu2555=)
13g.32357886_32357890dupCA10589449BRCA2c.7762_7766dup (p.Ser2590TyrfsTer?)
c.7393_7397dup (p.Ser2467TyrfsTer?)
c.229_233dup (p.Ser79TyrfsTer?)
c.7762_7766dup (p.Ser2590TyrfsTer21)
c.327_331dup
n.7762_7766dup
c.7666_7670dup (p.Ser2558TyrfsTer?)
 ClinVar dbSNP
13g.32357886delCA025265BRCA2c.7762del (p.Ile2588TyrfsTer?)
c.7393del (p.Ile2465TyrfsTer?)
c.229del (p.Ile77TyrfsTer?)
c.7762del (p.Ile2588TyrfsTer21)
c.327del
n.7762del
c.7666del (p.Ile2556TyrfsTer?)
 ClinVar dbSNP gnomAD v4
13g.32357886A>CCA387745858BRCA2c.7762A>C (p.Ile2588Leu)
c.7393A>C (p.Ile2465Leu)
c.229A>C (p.Ile77Leu)
c.327A>C
n.7762A>C
c.7666A>C (p.Ile2556Leu)
 ClinVar
13g.32357886A>GCA387745862BRCA2c.7762A>G (p.Ile2588Val)
c.7393A>G (p.Ile2465Val)
c.229A>G (p.Ile77Val)
c.327A>G
n.7762A>G
c.7666A>G (p.Ile2556Val)
 ClinVar dbSNP gnomAD v4
13g.32357886A>TCA387745864BRCA2c.7762A>T (p.Ile2588Leu)
c.7393A>T (p.Ile2465Leu)
c.229A>T (p.Ile77Leu)
c.327A>T
n.7762A>T
c.7666A>T (p.Ile2556Leu)
13g.32357886delinsTTCA2695217926BRCA2c.7762delinsTT (p.Ile2588PhefsTer5)
c.7393delinsTT (p.Ile2465PhefsTer5)
c.229delinsTT (p.Ile77PhefsTer5)
c.327delinsTT
n.7762delinsTT
c.7666delinsTT (p.Ile2556PhefsTer5)
13g.32357886_32357888delinsCCCA2580087360BRCA2c.7762_7764delinsCC (p.Ile2588ProfsTer?)
c.7393_7395delinsCC (p.Ile2465ProfsTer?)
c.229_231delinsCC (p.Ile77ProfsTer?)
c.7762_7764delinsCC (p.Ile2588ProfsTer21)
c.327_329delinsCC
n.7762_7764delinsCC
c.7666_7668delinsCC (p.Ile2556ProfsTer?)
 ClinVar
13g.32357886_32357888delinsTTCA090898BRCA2c.7762_7764delinsTT (p.Ile2588PhefsTer?)
c.7393_7395delinsTT (p.Ile2465PhefsTer?)
c.229_231delinsTT (p.Ile77PhefsTer?)
c.7762_7764delinsTT (p.Ile2588PhefsTer21)
c.327_329delinsTT
n.7762_7764delinsTT
c.7666_7668delinsTT (p.Ile2556PhefsTer?)
 ClinVar dbSNP
13g.32357887T>ACA387745870BRCA2c.7763T>A (p.Ile2588Lys)
c.7394T>A (p.Ile2465Lys)
c.230T>A (p.Ile77Lys)
c.328T>A
n.7763T>A
c.7667T>A (p.Ile2556Lys)
 dbSNP
13g.32357887T>CCA387745871BRCA2c.7763T>C (p.Ile2588Thr)
c.7394T>C (p.Ile2465Thr)
c.230T>C (p.Ile77Thr)
c.328T>C
n.7763T>C
c.7667T>C (p.Ile2556Thr)
 dbSNP
13g.32357887T>GCA387745873BRCA2c.7763T>G (p.Ile2588Arg)
c.7394T>G (p.Ile2465Arg)
c.230T>G (p.Ile77Arg)
c.328T>G
n.7763T>G
c.7667T>G (p.Ile2556Arg)
13g.32357887T=CA2082818821BRCA2c.7763T= (p.Ile2588=)
c.7394T= (p.Ile2465=)
c.230T= (p.Ile77=)
c.328T=
n.7763T=
c.7667T= (p.Ile2556=)
13g.32357888delCA2695217929BRCA2c.7764del (p.Ser2590ProfsTer?)
c.7395del (p.Ser2467ProfsTer?)
c.231del (p.Ser79ProfsTer?)
c.7764del (p.Ser2590ProfsTer19)
c.329del
n.7764del
c.7668del (p.Ser2558ProfsTer?)
13g.32357888A=CA2082818835BRCA2c.7764A= (p.Ile2588=)
c.7395A= (p.Ile2465=)
c.231A= (p.Ile77=)
c.329A=
n.7764A=
c.7668A= (p.Ile2556=)
13g.32357888A>CCA483439260BRCA2c.7764A>C (p.Ile2588=)
c.7395A>C (p.Ile2465=)
c.231A>C (p.Ile77=)
c.329A>C
n.7764A>C
c.7668A>C (p.Ile2556=)
13g.32357888A>GCA387745876BRCA2c.7764A>G (p.Ile2588Met)
c.7395A>G (p.Ile2465Met)
c.231A>G (p.Ile77Met)
c.329A>G
n.7764A>G
c.7668A>G (p.Ile2556Met)
13g.32357888A>TCA025266BRCA2c.7764A>T (p.Ile2588=)
c.7395A>T (p.Ile2465=)
c.231A>T (p.Ile77=)
c.329A>T
n.7764A>T
c.7668A>T (p.Ile2556=)
 ClinVar dbSNP gnomAD v4
13g.32357889C>ACA6941137BRCA2c.7765C>A (p.Pro2589Thr)
c.7396C>A (p.Pro2466Thr)
c.232C>A (p.Pro78Thr)
c.330C>A
n.7765C>A
c.7669C>A (p.Pro2557Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357889C=CA2082818848BRCA2c.7765C= (p.Pro2589=)
c.7396C= (p.Pro2466=)
c.232C= (p.Pro78=)
c.330C=
n.7765C=
c.7669C= (p.Pro2557=)
13g.32357889C>GCA387745884BRCA2c.7765C>G (p.Pro2589Ala)
c.7396C>G (p.Pro2466Ala)
c.232C>G (p.Pro78Ala)
c.330C>G
n.7765C>G
c.7669C>G (p.Pro2557Ala)
 dbSNP
13g.32357889C>TCA387745881BRCA2c.7765C>T (p.Pro2589Ser)
c.7396C>T (p.Pro2466Ser)
c.232C>T (p.Pro78Ser)
c.330C>T
n.7765C>T
c.7669C>T (p.Pro2557Ser)
 ClinVar dbSNP
13g.32357891delCA2499222306BRCA2c.7767del (p.Ser2590ProfsTer?)
c.7398del (p.Ser2467ProfsTer?)
c.234del (p.Ser79ProfsTer?)
c.7767del (p.Ser2590ProfsTer19)
c.332del
n.7767del
c.7671del (p.Ser2558ProfsTer?)
 ClinVar dbSNP
13g.32357890C>ACA025267BRCA2c.7766C>A (p.Pro2589His)
c.7397C>A (p.Pro2466His)
c.233C>A (p.Pro78His)
c.331C>A
n.7766C>A
c.7670C>A (p.Pro2557His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357890C=CA2082818874BRCA2c.7766C= (p.Pro2589=)
c.7397C= (p.Pro2466=)
c.233C= (p.Pro78=)
c.331C=
n.7766C=
c.7670C= (p.Pro2557=)
13g.32357890C>GCA387745888BRCA2c.7766C>G (p.Pro2589Arg)
c.7397C>G (p.Pro2466Arg)
c.233C>G (p.Pro78Arg)
c.331C>G
n.7766C>G
c.7670C>G (p.Pro2557Arg)
 dbSNP
13g.32357890C>TCA10579752BRCA2c.7766C>T (p.Pro2589Leu)
c.7397C>T (p.Pro2466Leu)
c.233C>T (p.Pro78Leu)
c.331C>T
n.7766C>T
c.7670C>T (p.Pro2557Leu)
 ClinVar dbSNP
13g.32357891C>ACA483439266BRCA2c.7767C>A (p.Pro2589=)
c.7398C>A (p.Pro2466=)
c.234C>A (p.Pro78=)
c.332C>A
n.7767C>A
c.7671C>A (p.Pro2557=)
 dbSNP
13g.32357891C=CA2082818885BRCA2c.7767C= (p.Pro2589=)
c.7398C= (p.Pro2466=)
c.234C= (p.Pro78=)
c.332C=
n.7767C=
c.7671C= (p.Pro2557=)
13g.32357891C>GCA483439267BRCA2c.7767C>G (p.Pro2589=)
c.7398C>G (p.Pro2466=)
c.234C>G (p.Pro78=)
c.332C>G
n.7767C>G
c.7671C>G (p.Pro2557=)
 ClinVar dbSNP gnomAD v4
13g.32357891C>TCA483439268BRCA2c.7767C>T (p.Pro2589=)
c.7398C>T (p.Pro2466=)
c.234C>T (p.Pro78=)
c.332C>T
n.7767C>T
c.7671C>T (p.Pro2557=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357892_32357893dupCA2499222307BRCA2c.7768_7769dup (p.Asn2591ProfsTer?)
c.7399_7400dup (p.Asn2468ProfsTer?)
c.235_236dup (p.Asn80ProfsTer?)
c.7768_7769dup (p.Asn2591ProfsTer19)
c.333_334dup
n.7768_7769dup
c.7672_7673dup (p.Asn2559ProfsTer?)
 ClinVar dbSNP
13g.32357892T>ACA025268BRCA2c.7768T>A (p.Ser2590Thr)
c.7399T>A (p.Ser2467Thr)
c.235T>A (p.Ser79Thr)
c.333T>A
n.7768T>A
c.7672T>A (p.Ser2558Thr)
 ClinVar dbSNP
13g.32357892T>CCA10579753BRCA2c.7768T>C (p.Ser2590Pro)
c.7399T>C (p.Ser2467Pro)
c.235T>C (p.Ser79Pro)
c.333T>C
n.7768T>C
c.7672T>C (p.Ser2558Pro)
 ClinVar dbSNP gnomAD v4
13g.32357892T>GCA387745893BRCA2c.7768T>G (p.Ser2590Ala)
c.7399T>G (p.Ser2467Ala)
c.235T>G (p.Ser79Ala)
c.333T>G
n.7768T>G
c.7672T>G (p.Ser2558Ala)
13g.32357892T=CA2082818892BRCA2c.7768T= (p.Ser2590=)
c.7399T= (p.Ser2467=)
c.235T= (p.Ser79=)
c.333T=
n.7768T=
c.7672T= (p.Ser2558=)
13g.32357893C>ACA387745895BRCA2c.7769C>A (p.Ser2590Tyr)
c.7400C>A (p.Ser2467Tyr)
c.236C>A (p.Ser79Tyr)
c.334C>A
n.7769C>A
c.7673C>A (p.Ser2558Tyr)
13g.32357893C=CA2082818900BRCA2c.7769C= (p.Ser2590=)
c.7400C= (p.Ser2467=)
c.236C= (p.Ser79=)
c.334C=
n.7769C=
c.7673C= (p.Ser2558=)
13g.32357893C>GCA025269BRCA2c.7769C>G (p.Ser2590Cys)
c.7400C>G (p.Ser2467Cys)
c.236C>G (p.Ser79Cys)
c.334C>G
n.7769C>G
c.7673C>G (p.Ser2558Cys)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357893C>TCA387745900BRCA2c.7769C>T (p.Ser2590Phe)
c.7400C>T (p.Ser2467Phe)
c.236C>T (p.Ser79Phe)
c.334C>T
n.7769C>T
c.7673C>T (p.Ser2558Phe)
 ClinVar
13g.32357894C>ACA483439272BRCA2c.7770C>A (p.Ser2590=)
c.7401C>A (p.Ser2467=)
c.237C>A (p.Ser79=)
c.335C>A
n.7770C>A
c.7674C>A (p.Ser2558=)
 dbSNP
13g.32357894C>GCA483439274BRCA2c.7770C>G (p.Ser2590=)
c.7401C>G (p.Ser2467=)
c.237C>G (p.Ser79=)
c.335C>G
n.7770C>G
c.7674C>G (p.Ser2558=)
 dbSNP
13g.32357894C>TCA483439275BRCA2c.7770C>T (p.Ser2590=)
c.7401C>T (p.Ser2467=)
c.237C>T (p.Ser79=)
c.335C>T
n.7770C>T
c.7674C>T (p.Ser2558=)
 dbSNP
13g.32357895A=CA2082818905BRCA2c.7771A= (p.Asn2591=)
c.7402A= (p.Asn2468=)
c.238A= (p.Asn80=)
c.336A=
n.7771A=
c.7675A= (p.Asn2559=)
13g.32357895A>CCA6941138BRCA2c.7771A>C (p.Asn2591His)
c.7402A>C (p.Asn2468His)
c.238A>C (p.Asn80His)
c.336A>C
n.7771A>C
c.7675A>C (p.Asn2559His)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357895A>GCA16619770BRCA2c.7771A>G (p.Asn2591Asp)
c.7402A>G (p.Asn2468Asp)
c.238A>G (p.Asn80Asp)
c.336A>G
n.7771A>G
c.7675A>G (p.Asn2559Asp)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357895A>TCA387745907BRCA2c.7771A>T (p.Asn2591Tyr)
c.7402A>T (p.Asn2468Tyr)
c.238A>T (p.Asn80Tyr)
c.336A>T
n.7771A>T
c.7675A>T (p.Asn2559Tyr)
13g.32357896A=CA2082818912BRCA2c.7772A= (p.Asn2591=)
c.7403A= (p.Asn2468=)
c.239A= (p.Asn80=)
c.337A=
n.7772A=
c.7676A= (p.Asn2559=)
13g.32357896A>CCA387745922BRCA2c.7772A>C (p.Asn2591Thr)
c.7403A>C (p.Asn2468Thr)
c.239A>C (p.Asn80Thr)
c.337A>C
n.7772A>C
c.7676A>C (p.Asn2559Thr)
13g.32357896A>GCA025270BRCA2c.7772A>G (p.Asn2591Ser)
c.7403A>G (p.Asn2468Ser)
c.239A>G (p.Asn80Ser)
c.337A>G
n.7772A>G
c.7676A>G (p.Asn2559Ser)
 ClinVar dbSNP gnomAD v4
13g.32357896A>TCA387745916BRCA2c.7772A>T (p.Asn2591Ile)
c.7403A>T (p.Asn2468Ile)
c.239A>T (p.Asn80Ile)
c.337A>T
n.7772A>T
c.7676A>T (p.Asn2559Ile)
 dbSNP
13g.32357897T>ACA387745927BRCA2c.7773T>A (p.Asn2591Lys)
c.7404T>A (p.Asn2468Lys)
c.240T>A (p.Asn80Lys)
c.338T>A
n.7773T>A
c.7677T>A (p.Asn2559Lys)
 dbSNP
13g.32357897T>CCA483439276BRCA2c.7773T>C (p.Asn2591=)
c.7404T>C (p.Asn2468=)
c.240T>C (p.Asn80=)
c.338T>C
n.7773T>C
c.7677T>C (p.Asn2559=)
 ClinVar dbSNP gnomAD v4
13g.32357897T>GCA387745930BRCA2c.7773T>G (p.Asn2591Lys)
c.7404T>G (p.Asn2468Lys)
c.240T>G (p.Asn80Lys)
c.338T>G
n.7773T>G
c.7677T>G (p.Asn2559Lys)
13g.32357897T=CA2082818921BRCA2c.7773T= (p.Asn2591=)
c.7404T= (p.Asn2468=)
c.240T= (p.Asn80=)
c.338T=
n.7773T=
c.7677T= (p.Asn2559=)
13g.32357898G>ACA387745936BRCA2c.7774G>A (p.Asp2592Asn)
c.7405G>A (p.Asp2469Asn)
c.241G>A (p.Asp81Asn)
c.339G>A
n.7774G>A
c.7678G>A (p.Asp2560Asn)
 ClinVar dbSNP
13g.32357898G>CCA387745939BRCA2c.7774G>C (p.Asp2592His)
c.7405G>C (p.Asp2469His)
c.241G>C (p.Asp81His)
c.339G>C
n.7774G>C
c.7678G>C (p.Asp2560His)
 dbSNP
13g.32357898G>TCA387745942BRCA2c.7774G>T (p.Asp2592Tyr)
c.7405G>T (p.Asp2469Tyr)
c.241G>T (p.Asp81Tyr)
c.339G>T
n.7774G>T
c.7678G>T (p.Asp2560Tyr)
 dbSNP
13g.32357899A=CA2082818931BRCA2c.7775A= (p.Asp2592=)
c.7406A= (p.Asp2469=)
c.242A= (p.Asp81=)
c.340A=
n.7775A=
c.7679A= (p.Asp2560=)
13g.32357899A>CCA387745944BRCA2c.7775A>C (p.Asp2592Ala)
c.7406A>C (p.Asp2469Ala)
c.242A>C (p.Asp81Ala)
c.340A>C
n.7775A>C
c.7679A>C (p.Asp2560Ala)
13g.32357899A>GCA387745947BRCA2c.7775A>G (p.Asp2592Gly)
c.7406A>G (p.Asp2469Gly)
c.242A>G (p.Asp81Gly)
c.340A>G
n.7775A>G
c.7679A>G (p.Asp2560Gly)
 ClinVar dbSNP gnomAD v4
13g.32357899A>TCA387745950BRCA2c.7775A>T (p.Asp2592Val)
c.7406A>T (p.Asp2469Val)
c.242A>T (p.Asp81Val)
c.340A>T
n.7775A>T
c.7679A>T (p.Asp2560Val)
13g.32357900T>ACA387745954BRCA2c.7776T>A (p.Asp2592Glu)
c.7407T>A (p.Asp2469Glu)
c.243T>A (p.Asp81Glu)
c.341T>A
n.7776T>A
c.7680T>A (p.Asp2560Glu)
 dbSNP
13g.32357900T>CCA483439282BRCA2c.7776T>C (p.Asp2592=)
c.7407T>C (p.Asp2469=)
c.243T>C (p.Asp81=)
c.341T>C
n.7776T>C
c.7680T>C (p.Asp2560=)
 ClinVar dbSNP
13g.32357900T>GCA387745958BRCA2c.7776T>G (p.Asp2592Glu)
c.7407T>G (p.Asp2469Glu)
c.243T>G (p.Asp81Glu)
c.341T>G
n.7776T>G
c.7680T>G (p.Asp2560Glu)
13g.32357901G>ACA387745960BRCA2c.7777G>A (p.Gly2593Arg)
c.7408G>A (p.Gly2470Arg)
c.244G>A (p.Gly82Arg)
c.342G>A
n.7777G>A
c.7681G>A (p.Gly2561Arg)
 ClinVar gnomAD v4
13g.32357901G>CCA387745961BRCA2c.7777G>C (p.Gly2593Arg)
c.7408G>C (p.Gly2470Arg)
c.244G>C (p.Gly82Arg)
c.342G>C
n.7777G>C
c.7681G>C (p.Gly2561Arg)
13g.32357901G=CA2082818940BRCA2c.7777G= (p.Gly2593=)
c.7408G= (p.Gly2470=)
c.244G= (p.Gly82=)
c.342G=
n.7777G=
c.7681G= (p.Gly2561=)
13g.32357901G>TCA025271BRCA2c.7777G>T (p.Gly2593Ter)
c.7408G>T (p.Gly2470Ter)
c.244G>T (p.Gly82Ter)
c.342G>T
n.7777G>T
c.7681G>T (p.Gly2561Ter)
 ClinVar dbSNP COSMIC COSMIC
13g.32357902G>ACA387745964BRCA2c.7778G>A (p.Gly2593Glu)
c.7409G>A (p.Gly2470Glu)
c.245G>A (p.Gly82Glu)
c.343G>A
n.7778G>A
c.7682G>A (p.Gly2561Glu)
 ClinVar dbSNP
13g.32357902G>CCA387745966BRCA2c.7778G>C (p.Gly2593Ala)
c.7409G>C (p.Gly2470Ala)
c.245G>C (p.Gly82Ala)
c.343G>C
n.7778G>C
c.7682G>C (p.Gly2561Ala)
 dbSNP
13g.32357902G=CA2082818945BRCA2c.7778G= (p.Gly2593=)
c.7409G= (p.Gly2470=)
c.245G= (p.Gly82=)
c.343G=
n.7778G=
c.7682G= (p.Gly2561=)
13g.32357902G>TCA387745963BRCA2c.7778G>T (p.Gly2593Val)
c.7409G>T (p.Gly2470Val)
c.245G>T (p.Gly82Val)
c.343G>T
n.7778G>T
c.7682G>T (p.Gly2561Val)
13g.32357903A=CA2082818953BRCA2c.7779A= (p.Gly2593=)
c.7410A= (p.Gly2470=)
c.246A= (p.Gly82=)
c.344A=
n.7779A=
c.7683A= (p.Gly2561=)
13g.32357903A>CCA483439283BRCA2c.7779A>C (p.Gly2593=)
c.7410A>C (p.Gly2470=)
c.246A>C (p.Gly82=)
c.344A>C
n.7779A>C
c.7683A>C (p.Gly2561=)
13g.32357903A>GCA483439284BRCA2c.7779A>G (p.Gly2593=)
c.7410A>G (p.Gly2470=)
c.246A>G (p.Gly82=)
c.344A>G
n.7779A>G
c.7683A>G (p.Gly2561=)
 dbSNP
13g.32357903A>TCA483439285BRCA2c.7779A>T (p.Gly2593=)
c.7410A>T (p.Gly2470=)
c.246A>T (p.Gly82=)
c.344A>T
n.7779A>T
c.7683A>T (p.Gly2561=)
 ClinVar dbSNP
13g.32357905dupCA10589450BRCA2c.7781dup (p.Ala2595GlyfsTer8)
c.7412dup (p.Ala2472GlyfsTer8)
c.248dup (p.Ala84GlyfsTer8)
c.346dup
n.7781dup
c.7685dup (p.Ala2563GlyfsTer8)
 ClinVar dbSNP
13g.32357905delCA2573149412BRCA2c.7781del (p.Lys2594ArgfsTer?)
c.7412del (p.Lys2471ArgfsTer?)
c.248del (p.Lys83ArgfsTer?)
c.7781del (p.Lys2594ArgfsTer15)
c.346del
n.7781del
c.7685del (p.Lys2562ArgfsTer?)
 ClinVar dbSNP
13g.32357904A>CCA387745970BRCA2c.7780A>C (p.Lys2594Gln)
c.7411A>C (p.Lys2471Gln)
c.247A>C (p.Lys83Gln)
c.345A>C
n.7780A>C
c.7684A>C (p.Lys2562Gln)
13g.32357904A>GCA387745967BRCA2c.7780A>G (p.Lys2594Glu)
c.7411A>G (p.Lys2471Glu)
c.247A>G (p.Lys83Glu)
c.345A>G
n.7780A>G
c.7684A>G (p.Lys2562Glu)
13g.32357904A>TCA387745972BRCA2c.7780A>T (p.Lys2594Ter)
c.7411A>T (p.Lys2471Ter)
c.247A>T (p.Lys83Ter)
c.345A>T
n.7780A>T
c.7684A>T (p.Lys2562Ter)
 dbSNP
13g.32357905A=CA2082818957BRCA2c.7781A= (p.Lys2594=)
c.7412A= (p.Lys2471=)
c.248A= (p.Lys83=)
c.346A=
n.7781A=
c.7685A= (p.Lys2562=)
13g.32357905A>CCA387745974BRCA2c.7781A>C (p.Lys2594Thr)
c.7412A>C (p.Lys2471Thr)
c.248A>C (p.Lys83Thr)
c.346A>C
n.7781A>C
c.7685A>C (p.Lys2562Thr)
13g.32357905A>GCA10579754BRCA2c.7781A>G (p.Lys2594Arg)
c.7412A>G (p.Lys2471Arg)
c.248A>G (p.Lys83Arg)
c.346A>G
n.7781A>G
c.7685A>G (p.Lys2562Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32357905A>TCA387745975BRCA2c.7781A>T (p.Lys2594Met)
c.7412A>T (p.Lys2471Met)
c.248A>T (p.Lys83Met)
c.346A>T
n.7781A>T
c.7685A>T (p.Lys2562Met)
13g.32357906G>ACA483439288BRCA2c.7782G>A (p.Lys2594=)
c.7413G>A (p.Lys2471=)
c.249G>A (p.Lys83=)
c.347G>A
n.7782G>A
c.7686G>A (p.Lys2562=)
 dbSNP
13g.32357906G>CCA387745983BRCA2c.7782G>C (p.Lys2594Asn)
c.7413G>C (p.Lys2471Asn)
c.249G>C (p.Lys83Asn)
c.347G>C
n.7782G>C
c.7686G>C (p.Lys2562Asn)
 dbSNP
13g.32357906G>TCA387745986BRCA2c.7782G>T (p.Lys2594Asn)
c.7413G>T (p.Lys2471Asn)
c.249G>T (p.Lys83Asn)
c.347G>T
n.7782G>T
c.7686G>T (p.Lys2562Asn)
 gnomAD v4
13g.32357907delCA2695202250BRCA2c.7783del (p.Ala2595LeufsTer?)
c.7414del (p.Ala2472LeufsTer?)
c.250del (p.Ala84LeufsTer?)
c.7783del (p.Ala2595LeufsTer14)
c.348del
n.7783del
c.7687del (p.Ala2563LeufsTer?)
13g.32357907G>ACA10579755BRCA2c.7783G>A (p.Ala2595Thr)
c.7414G>A (p.Ala2472Thr)
c.250G>A (p.Ala84Thr)
c.348G>A
n.7783G>A
c.7687G>A (p.Ala2563Thr)
 ClinVar dbSNP
13g.32357907G>CCA387745989BRCA2c.7783G>C (p.Ala2595Pro)
c.7414G>C (p.Ala2472Pro)
c.250G>C (p.Ala84Pro)
c.348G>C
n.7783G>C
c.7687G>C (p.Ala2563Pro)
 gnomAD v4
13g.32357907G=CA2082818971BRCA2c.7783G= (p.Ala2595=)
c.7414G= (p.Ala2472=)
c.250G= (p.Ala84=)
c.348G=
n.7783G=
c.7687G= (p.Ala2563=)
13g.32357907G>TCA025273BRCA2c.7783G>T (p.Ala2595Ser)
c.7414G>T (p.Ala2472Ser)
c.250G>T (p.Ala84Ser)
c.348G>T
n.7783G>T
c.7687G>T (p.Ala2563Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357908C>ACA387745994BRCA2c.7784C>A (p.Ala2595Asp)
c.7415C>A (p.Ala2472Asp)
c.251C>A (p.Ala84Asp)
c.349C>A
n.7784C>A
c.7688C>A (p.Ala2563Asp)
 dbSNP
13g.32357908C=CA2082818984BRCA2c.7784C= (p.Ala2595=)
c.7415C= (p.Ala2472=)
c.251C= (p.Ala84=)
c.349C=
n.7784C=
c.7688C= (p.Ala2563=)
13g.32357908C>GCA387745996BRCA2c.7784C>G (p.Ala2595Gly)
c.7415C>G (p.Ala2472Gly)
c.251C>G (p.Ala84Gly)
c.349C>G
n.7784C>G
c.7688C>G (p.Ala2563Gly)
 ClinVar dbSNP COSMIC COSMIC
13g.32357908C>TCA387745999BRCA2c.7784C>T (p.Ala2595Val)
c.7415C>T (p.Ala2472Val)
c.251C>T (p.Ala84Val)
c.349C>T
n.7784C>T
c.7688C>T (p.Ala2563Val)
 dbSNP
13g.32357909T>ACA16613938BRCA2c.7785T>A (p.Ala2595=)
c.7416T>A (p.Ala2472=)
c.252T>A (p.Ala84=)
c.350T>A
n.7785T>A
c.7689T>A (p.Ala2563=)
 ClinVar dbSNP
13g.32357909T>CCA483439294BRCA2c.7785T>C (p.Ala2595=)
c.7416T>C (p.Ala2472=)
c.252T>C (p.Ala84=)
c.350T>C
n.7785T>C
c.7689T>C (p.Ala2563=)
 ClinVar dbSNP
13g.32357909T>GCA483439293BRCA2c.7785T>G (p.Ala2595=)
c.7416T>G (p.Ala2472=)
c.252T>G (p.Ala84=)
c.350T>G
n.7785T>G
c.7689T>G (p.Ala2563=)
13g.32357909T=CA2082818993BRCA2c.7785T= (p.Ala2595=)
c.7416T= (p.Ala2472=)
c.252T= (p.Ala84=)
c.350T=
n.7785T=
c.7689T= (p.Ala2563=)
13g.32357910G>ACA025274BRCA2c.7786G>A (p.Gly2596Arg)
c.7417G>A (p.Gly2473Arg)
c.253G>A (p.Gly85Arg)
c.351G>A
n.7786G>A
c.7690G>A (p.Gly2564Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357910G>CCA387746004BRCA2c.7786G>C (p.Gly2596Arg)
c.7417G>C (p.Gly2473Arg)
c.253G>C (p.Gly85Arg)
c.351G>C
n.7786G>C
c.7690G>C (p.Gly2564Arg)
 ClinVar dbSNP
13g.32357910G=CA2082819003BRCA2c.7786G= (p.Gly2596=)
c.7417G= (p.Gly2473=)
c.253G= (p.Gly85=)
c.351G=
n.7786G=
c.7690G= (p.Gly2564=)
13g.32357910G>TCA387746007BRCA2c.7786G>T (p.Gly2596Ter)
c.7417G>T (p.Gly2473Ter)
c.253G>T (p.Gly85Ter)
c.351G>T
n.7786G>T
c.7690G>T (p.Gly2564Ter)
13g.32357911_32357912insGGGCA2622572192BRCA2c.7787_7788insGGG (p.Gly2596_Lys2597insGly)
c.7418_7419insGGG (p.Gly2473_Lys2474insGly)
c.254_255insGGG (p.Gly85_Lys86insGly)
c.352_353insGGG
n.7787_7788insGGG
c.7691_7692insGGG (p.Gly2564_Lys2565insGly)
 gnomAD v4
13g.32357911G>ACA16619771BRCA2c.7787G>A (p.Gly2596Glu)
c.7418G>A (p.Gly2473Glu)
c.254G>A (p.Gly85Glu)
c.352G>A
n.7787G>A
c.7691G>A (p.Gly2564Glu)
 ClinVar dbSNP
13g.32357911G>CCA387746017BRCA2c.7787G>C (p.Gly2596Ala)
c.7418G>C (p.Gly2473Ala)
c.254G>C (p.Gly85Ala)
c.352G>C
n.7787G>C
c.7691G>C (p.Gly2564Ala)
 ClinVar dbSNP
13g.32357911G=CA2082819012BRCA2c.7787G= (p.Gly2596=)
c.7418G= (p.Gly2473=)
c.254G= (p.Gly85=)
c.352G=
n.7787G=
c.7691G= (p.Gly2564=)
13g.32357911G>TCA387746014BRCA2c.7787G>T (p.Gly2596Val)
c.7418G>T (p.Gly2473Val)
c.254G>T (p.Gly85Val)
c.352G>T
n.7787G>T
c.7691G>T (p.Gly2564Val)
 ClinVar dbSNP
13g.32357911_32357912delinsGACA2082819014BRCA2c.7787_7788delinsGA (p.Gly2596=)
c.7418_7419delinsGA (p.Gly2473=)
c.254_255delinsGA (p.Gly85=)
c.352_353delinsGA
n.7787_7788delinsGA
c.7691_7692delinsGA (p.Gly2564=)
13g.32357912A=CA2082819037BRCA2c.7788A= (p.Gly2596=)
c.7419A= (p.Gly2473=)
c.255A= (p.Gly85=)
c.353A=
n.7788A=
c.7692A= (p.Gly2564=)
13g.32357912A>CCA483439300BRCA2c.7788A>C (p.Gly2596=)
c.7419A>C (p.Gly2473=)
c.255A>C (p.Gly85=)
c.353A>C
n.7788A>C
c.7692A>C (p.Gly2564=)
13g.32357912A>GCA483439301BRCA2c.7788A>G (p.Gly2596=)
c.7419A>G (p.Gly2473=)
c.255A>G (p.Gly85=)
c.353A>G
n.7788A>G
c.7692A>G (p.Gly2564=)
13g.32357912A>TCA483439303BRCA2c.7788A>T (p.Gly2596=)
c.7419A>T (p.Gly2473=)
c.255A>T (p.Gly85=)
c.353A>T
n.7788A>T
c.7692A>T (p.Gly2564=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32357912delinsGGGTCA913188540BRCA2c.7788delinsGGGT (p.Gly2596_Lys2597insGly)
c.7419delinsGGGT (p.Gly2473_Lys2474insGly)
c.255delinsGGGT (p.Gly85_Lys86insGly)
c.353delinsGGGT
n.7788delinsGGGT
c.7692delinsGGGT (p.Gly2564_Lys2565insGly)
 ClinVar dbSNP
13g.32357915dupCA025276BRCA2c.7791dup (p.Glu2598ArgfsTer5)
c.7422dup (p.Glu2475ArgfsTer5)
c.258dup (p.Glu87ArgfsTer5)
c.356dup
n.7791dup
c.7695dup (p.Glu2566ArgfsTer5)
 ClinVar dbSNP
13g.32357915delCA658823756BRCA2c.7791del (p.Glu2598LysfsTer?)
c.7422del (p.Glu2475LysfsTer?)
c.258del (p.Glu87LysfsTer?)
c.7791del (p.Glu2598LysfsTer11)
c.356del
n.7791del
c.7695del (p.Glu2566LysfsTer?)
 ClinVar dbSNP
13g.32357913A>CCA387746018BRCA2c.7789A>C (p.Lys2597Gln)
c.7420A>C (p.Lys2474Gln)
c.256A>C (p.Lys86Gln)
c.354A>C
n.7789A>C
c.7693A>C (p.Lys2565Gln)
13g.32357913A>GCA387746019BRCA2c.7789A>G (p.Lys2597Glu)
c.7420A>G (p.Lys2474Glu)
c.256A>G (p.Lys86Glu)
c.354A>G
n.7789A>G
c.7693A>G (p.Lys2565Glu)
 dbSNP
13g.32357913A>TCA387746020BRCA2c.7789A>T (p.Lys2597Ter)
c.7420A>T (p.Lys2474Ter)
c.256A>T (p.Lys86Ter)
c.354A>T
n.7789A>T
c.7693A>T (p.Lys2565Ter)
 dbSNP
13g.32357913_32357916delinsAAAGCA2082819048BRCA2c.7789_7792delinsAAAG (p.Lys2597=)
c.7420_7423delinsAAAG (p.Lys2474=)
c.256_259delinsAAAG (p.Lys86=)
c.354_357delinsAAAG
n.7789_7792delinsAAAG
c.7693_7696delinsAAAG (p.Lys2565=)
13g.32357914A>CCA387746023BRCA2c.7790A>C (p.Lys2597Thr)
c.7421A>C (p.Lys2474Thr)
c.257A>C (p.Lys86Thr)
c.355A>C
n.7790A>C
c.7694A>C (p.Lys2565Thr)
13g.32357914A>GCA387746025BRCA2c.7790A>G (p.Lys2597Arg)
c.7421A>G (p.Lys2474Arg)
c.257A>G (p.Lys86Arg)
c.355A>G
n.7790A>G
c.7694A>G (p.Lys2565Arg)
 dbSNP
13g.32357914A>TCA387746026BRCA2c.7790A>T (p.Lys2597Ile)
c.7421A>T (p.Lys2474Ile)
c.257A>T (p.Lys86Ile)
c.355A>T
n.7790A>T
c.7694A>T (p.Lys2565Ile)
13g.32357919_32357921delCA025277BRCA2c.7795_7797del (p.Glu2599del)
c.7426_7428del (p.Glu2476del)
c.262_264del (p.Glu88del)
c.360_362del
n.7795_7797del
c.7699_7701del (p.Glu2567del)
 ClinVar dbSNP gnomAD v4
13g.32357915A=CA2082819059BRCA2c.7791A= (p.Lys2597=)
c.7422A= (p.Lys2474=)
c.258A= (p.Lys86=)
c.356A=
n.7791A=
c.7695A= (p.Lys2565=)
13g.32357915A>CCA387746031BRCA2c.7791A>C (p.Lys2597Asn)
c.7422A>C (p.Lys2474Asn)
c.258A>C (p.Lys86Asn)
c.356A>C
n.7791A>C
c.7695A>C (p.Lys2565Asn)
 ClinVar dbSNP
13g.32357915A>GCA483439307BRCA2c.7791A>G (p.Lys2597=)
c.7422A>G (p.Lys2474=)
c.258A>G (p.Lys86=)
c.356A>G
n.7791A>G
c.7695A>G (p.Lys2565=)
 dbSNP
13g.32357915A>TCA387746033BRCA2c.7791A>T (p.Lys2597Asn)
c.7422A>T (p.Lys2474Asn)
c.258A>T (p.Lys86Asn)
c.356A>T
n.7791A>T
c.7695A>T (p.Lys2565Asn)
13g.32357916G>ACA387746035BRCA2c.7792G>A (p.Glu2598Lys)
c.7423G>A (p.Glu2475Lys)
c.259G>A (p.Glu87Lys)
c.357G>A
n.7792G>A
c.7696G>A (p.Glu2566Lys)
 dbSNP
13g.32357916G>CCA387746037BRCA2c.7792G>C (p.Glu2598Gln)
c.7423G>C (p.Glu2475Gln)
c.259G>C (p.Glu87Gln)
c.357G>C
n.7792G>C
c.7696G>C (p.Glu2566Gln)
 dbSNP
13g.32357916G=CA2082819070BRCA2c.7792G= (p.Glu2598=)
c.7423G= (p.Glu2475=)
c.259G= (p.Glu87=)
c.357G=
n.7792G=
c.7696G= (p.Glu2566=)
13g.32357916G>TCA387746039BRCA2c.7792G>T (p.Glu2598Ter)
c.7423G>T (p.Glu2475Ter)
c.259G>T (p.Glu87Ter)
c.357G>T
n.7792G>T
c.7696G>T (p.Glu2566Ter)
 ClinVar dbSNP
13g.32357917A=CA2082819083BRCA2c.7793A= (p.Glu2598=)
c.7424A= (p.Glu2475=)
c.260A= (p.Glu87=)
c.358A=
n.7793A=
c.7697A= (p.Glu2566=)
13g.32357917A>CCA387746056BRCA2c.7793A>C (p.Glu2598Ala)
c.7424A>C (p.Glu2475Ala)
c.260A>C (p.Glu87Ala)
c.358A>C
n.7793A>C
c.7697A>C (p.Glu2566Ala)
13g.32357917A>GCA387746059BRCA2c.7793A>G (p.Glu2598Gly)
c.7424A>G (p.Glu2475Gly)
c.260A>G (p.Glu87Gly)
c.358A>G
n.7793A>G
c.7697A>G (p.Glu2566Gly)
13g.32357917A>TCA387746043BRCA2c.7793A>T (p.Glu2598Val)
c.7424A>T (p.Glu2475Val)
c.260A>T (p.Glu87Val)
c.358A>T
n.7793A>T
c.7697A>T (p.Glu2566Val)
 dbSNP
13g.32357917_32357918insCTCTGCATTTTTGCTGTTCA2082819092BRCA2c.7793_7794insCTCTGCATTTTTGCTGTT (p.Glu2598delinsAspSerAlaPheLeuLeuLeu)
c.7424_7425insCTCTGCATTTTTGCTGTT (p.Glu2475delinsAspSerAlaPheLeuLeuLeu)
c.260_261insCTCTGCATTTTTGCTGTT (p.Glu87delinsAspSerAlaPheLeuLeuLeu)
c.358_359insCTCTGCATTTTTGCTGTT
n.7793_7794insCTCTGCATTTTTGCTGTT
c.7697_7698insCTCTGCATTTTTGCTGTT (p.Glu2566delinsAspSerAlaPheLeuLeuLeu)
 dbSNP
13g.32357918A=CA2082819088BRCA2c.7794A= (p.Glu2598=)
c.7425A= (p.Glu2475=)
c.261A= (p.Glu87=)
c.359A=
n.7794A=
c.7698A= (p.Glu2566=)
13g.32357918A>CCA387746062BRCA2c.7794A>C (p.Glu2598Asp)
c.7425A>C (p.Glu2475Asp)
c.261A>C (p.Glu87Asp)
c.359A>C
n.7794A>C
c.7698A>C (p.Glu2566Asp)
13g.32357918A>GCA483439309BRCA2c.7794A>G (p.Glu2598=)
c.7425A>G (p.Glu2475=)
c.261A>G (p.Glu87=)
c.359A>G
n.7794A>G
c.7698A>G (p.Glu2566=)
13g.32357918A>TCA387746066BRCA2c.7794A>T (p.Glu2598Asp)
c.7425A>T (p.Glu2475Asp)
c.261A>T (p.Glu87Asp)
c.359A>T
n.7794A>T
c.7698A>T (p.Glu2566Asp)
13g.32357919_32357920delCA1139770845BRCA2c.7795_7796del (p.Glu2599IlefsTer3)
c.7426_7427del (p.Glu2476IlefsTer3)
c.262_263del (p.Glu88IlefsTer3)
c.360_361del
n.7795_7796del
c.7699_7700del (p.Glu2567IlefsTer3)
13g.32357919G>ACA10579756BRCA2c.7795G>A (p.Glu2599Lys)
c.7426G>A (p.Glu2476Lys)
c.262G>A (p.Glu88Lys)
c.360G>A
n.7795G>A
c.7699G>A (p.Glu2567Lys)
 ClinVar dbSNP
13g.32357919G>CCA387746073BRCA2c.7795G>C (p.Glu2599Gln)
c.7426G>C (p.Glu2476Gln)
c.262G>C (p.Glu88Gln)
c.360G>C
n.7795G>C
c.7699G>C (p.Glu2567Gln)
 dbSNP
13g.32357919G=CA2082819102BRCA2c.7795G= (p.Glu2599=)
c.7426G= (p.Glu2476=)
c.262G= (p.Glu88=)
c.360G=
n.7795G=
c.7699G= (p.Glu2567=)
13g.32357919G>TCA10589451BRCA2c.7795G>T (p.Glu2599Ter)
c.7426G>T (p.Glu2476Ter)
c.262G>T (p.Glu88Ter)
c.360G>T
n.7795G>T
c.7699G>T (p.Glu2567Ter)
 ClinVar dbSNP COSMIC COSMIC
13g.32357919dupCA247471267BRCA2c.7795dup (p.Glu2599GlyfsTer4)
c.7426dup (p.Glu2476GlyfsTer4)
c.262dup (p.Glu88GlyfsTer4)
c.360dup
n.7795dup
c.7699dup (p.Glu2567GlyfsTer4)
 dbSNP
13g.32357919_32357920insTCA247471293BRCA2c.7795_7796insT (p.Glu2599ValfsTer4)
c.7426_7427insT (p.Glu2476ValfsTer4)
c.262_263insT (p.Glu88ValfsTer4)
c.360_361insT
n.7795_7796insT
c.7699_7700insT (p.Glu2567ValfsTer4)
 dbSNP
13g.32357920A=CA2082819114BRCA2c.7796A= (p.Glu2599=)
c.7427A= (p.Glu2476=)
c.263A= (p.Glu88=)
c.361A=
n.7796A=
c.7700A= (p.Glu2567=)
13g.32357920A>CCA6941139BRCA2c.7796A>C (p.Glu2599Ala)
c.7427A>C (p.Glu2476Ala)
c.263A>C (p.Glu88Ala)
c.361A>C
n.7796A>C
c.7700A>C (p.Glu2567Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357920A>GCA387746086BRCA2c.7796A>G (p.Glu2599Gly)
c.7427A>G (p.Glu2476Gly)
c.263A>G (p.Glu88Gly)
c.361A>G
n.7796A>G
c.7700A>G (p.Glu2567Gly)
 ClinVar dbSNP
13g.32357920A>TCA387746106BRCA2c.7796A>T (p.Glu2599Val)
c.7427A>T (p.Glu2476Val)
c.263A>T (p.Glu88Val)
c.361A>T
n.7796A>T
c.7700A>T (p.Glu2567Val)
 ClinVar dbSNP
13g.32357921A=CA2082819122BRCA2c.7797A= (p.Glu2599=)
c.7428A= (p.Glu2476=)
c.264A= (p.Glu88=)
c.362A=
n.7797A=
c.7701A= (p.Glu2567=)
13g.32357921A>CCA387746113BRCA2c.7797A>C (p.Glu2599Asp)
c.7428A>C (p.Glu2476Asp)
c.264A>C (p.Glu88Asp)
c.362A>C
n.7797A>C
c.7701A>C (p.Glu2567Asp)
 ClinVar dbSNP
13g.32357921A>GCA483439314BRCA2c.7797A>G (p.Glu2599=)
c.7428A>G (p.Glu2476=)
c.264A>G (p.Glu88=)
c.362A>G
n.7797A>G
c.7701A>G (p.Glu2567=)
13g.32357921A>TCA387746114BRCA2c.7797A>T (p.Glu2599Asp)
c.7428A>T (p.Glu2476Asp)
c.264A>T (p.Glu88Asp)
c.362A>T
n.7797A>T
c.7701A>T (p.Glu2567Asp)
13g.32357922T>ACA387746120BRCA2c.7798T>A (p.Phe2600Ile)
c.7429T>A (p.Phe2477Ile)
c.265T>A (p.Phe89Ile)
c.363T>A
n.7798T>A
c.7702T>A (p.Phe2568Ile)
 dbSNP
13g.32357922T>CCA387746117BRCA2c.7798T>C (p.Phe2600Leu)
c.7429T>C (p.Phe2477Leu)
c.265T>C (p.Phe89Leu)
c.363T>C
n.7798T>C
c.7702T>C (p.Phe2568Leu)
 dbSNP
13g.32357922T>GCA387746119BRCA2c.7798T>G (p.Phe2600Val)
c.7429T>G (p.Phe2477Val)
c.265T>G (p.Phe89Val)
c.363T>G
n.7798T>G
c.7702T>G (p.Phe2568Val)
13g.32357925delCA2727914535BRCA2c.7801del (p.Tyr2601IlefsTer?)
c.7432del (p.Tyr2478IlefsTer?)
c.268del (p.Tyr90IlefsTer?)
c.7801del (p.Tyr2601IlefsTer8)
c.366del
n.7801del
c.7705del (p.Tyr2569IlefsTer?)
 dbSNP
13g.32357923T>ACA387746124BRCA2c.7799T>A (p.Phe2600Tyr)
c.7430T>A (p.Phe2477Tyr)
c.266T>A (p.Phe89Tyr)
c.364T>A
n.7799T>A
c.7703T>A (p.Phe2568Tyr)
13g.32357923T>CCA387746126BRCA2c.7799T>C (p.Phe2600Ser)
c.7430T>C (p.Phe2477Ser)
c.266T>C (p.Phe89Ser)
c.364T>C
n.7799T>C
c.7703T>C (p.Phe2568Ser)
13g.32357923T>GCA387746128BRCA2c.7799T>G (p.Phe2600Cys)
c.7430T>G (p.Phe2477Cys)
c.266T>G (p.Phe89Cys)
c.364T>G
n.7799T>G
c.7703T>G (p.Phe2568Cys)
 ClinVar dbSNP
13g.32357923T=CA2082819129BRCA2c.7799T= (p.Phe2600=)
c.7430T= (p.Phe2477=)
c.266T= (p.Phe89=)
c.364T=
n.7799T=
c.7703T= (p.Phe2568=)
13g.32357924T>ACA387746132BRCA2c.7800T>A (p.Phe2600Leu)
c.7431T>A (p.Phe2477Leu)
c.267T>A (p.Phe89Leu)
c.365T>A
n.7800T>A
c.7704T>A (p.Phe2568Leu)
13g.32357924T>CCA483439318BRCA2c.7800T>C (p.Phe2600=)
c.7431T>C (p.Phe2477=)
c.267T>C (p.Phe89=)
c.365T>C
n.7800T>C
c.7704T>C (p.Phe2568=)
13g.32357924T>GCA16614214BRCA2c.7800T>G (p.Phe2600Leu)
c.7431T>G (p.Phe2477Leu)
c.267T>G (p.Phe89Leu)
c.365T>G
n.7800T>G
c.7704T>G (p.Phe2568Leu)
 ClinVar dbSNP
13g.32357924T=CA2082819138BRCA2c.7800T= (p.Phe2600=)
c.7431T= (p.Phe2477=)
c.267T= (p.Phe89=)
c.365T=
n.7800T=
c.7704T= (p.Phe2568=)
13g.32357924_32357925insAAAGTAAACATGCA609453902BRCA2c.7800_7801insAAAGTAAACATG (p.Phe2600_Tyr2601insLysValAsnMet)
c.7431_7432insAAAGTAAACATG (p.Phe2477_Tyr2478insLysValAsnMet)
c.267_268insAAAGTAAACATG (p.Phe89_Tyr90insLysValAsnMet)
c.365_366insAAAGTAAACATG
n.7800_7801insAAAGTAAACATG
c.7704_7705insAAAGTAAACATG (p.Phe2568_Tyr2569insLysValAsnMet)
 dbSNP gnomAD v2
13g.32357925T>ACA387746137BRCA2c.7801T>A (p.Tyr2601Asn)
c.7432T>A (p.Tyr2478Asn)
c.268T>A (p.Tyr90Asn)
c.366T>A
n.7801T>A
c.7705T>A (p.Tyr2569Asn)
13g.32357925T>CCA387746146BRCA2c.7801T>C (p.Tyr2601His)
c.7432T>C (p.Tyr2478His)
c.268T>C (p.Tyr90His)
c.366T>C
n.7801T>C
c.7705T>C (p.Tyr2569His)
13g.32357925T>GCA387746148BRCA2c.7801T>G (p.Tyr2601Asp)
c.7432T>G (p.Tyr2478Asp)
c.268T>G (p.Tyr90Asp)
c.366T>G
n.7801T>G
c.7705T>G (p.Tyr2569Asp)
13g.32357928_32357938delCA2580087366BRCA2c.7804_7805+9del
c.7435_7436+9del
c.271_272+9del
c.369_370+9del
n.7804_7805+9del
c.7708_7709+9del
 ClinVar
13g.32357926A=CA2082819146BRCA2c.7802A= (p.Tyr2601=)
c.7433A= (p.Tyr2478=)
c.269A= (p.Tyr90=)
c.367A=
n.7802A=
c.7706A= (p.Tyr2569=)
13g.32357926A>CCA387746150BRCA2c.7802A>C (p.Tyr2601Ser)
c.7433A>C (p.Tyr2478Ser)
c.269A>C (p.Tyr90Ser)
c.367A>C
n.7802A>C
c.7706A>C (p.Tyr2569Ser)
 dbSNP
13g.32357926A>GCA025278BRCA2c.7802A>G (p.Tyr2601Cys)
c.7433A>G (p.Tyr2478Cys)
c.269A>G (p.Tyr90Cys)
c.367A>G
n.7802A>G
c.7706A>G (p.Tyr2569Cys)
 ClinVar dbSNP
13g.32357926A>TCA387746155BRCA2c.7802A>T (p.Tyr2601Phe)
c.7433A>T (p.Tyr2478Phe)
c.269A>T (p.Tyr90Phe)
c.367A>T
n.7802A>T
c.7706A>T (p.Tyr2569Phe)
 dbSNP
13g.32357927delCA2582341811BRCA2c.7803del (p.Tyr2601Ter)
c.7434del (p.Tyr2478Ter)
c.270del (p.Tyr90Ter)
c.368del
n.7803del
c.7707del (p.Tyr2569Ter)
 ClinVar
13g.32357927T>ACA387746158BRCA2c.7803T>A (p.Tyr2601Ter)
c.7434T>A (p.Tyr2478Ter)
c.270T>A (p.Tyr90Ter)
c.368T>A
n.7803T>A
c.7707T>A (p.Tyr2569Ter)
 dbSNP
13g.32357927T>CCA483439324BRCA2c.7803T>C (p.Tyr2601=)
c.7434T>C (p.Tyr2478=)
c.270T>C (p.Tyr90=)
c.368T>C
n.7803T>C
c.7707T>C (p.Tyr2569=)
 ClinVar dbSNP
13g.32357927T>GCA387746160BRCA2c.7803T>G (p.Tyr2601Ter)
c.7434T>G (p.Tyr2478Ter)
c.270T>G (p.Tyr90Ter)
c.368T>G
n.7803T>G
c.7707T>G (p.Tyr2569Ter)
13g.32357927T=CA2082819161BRCA2c.7803T= (p.Tyr2601=)
c.7434T= (p.Tyr2478=)
c.270T= (p.Tyr90=)
c.368T=
n.7803T=
c.7707T= (p.Tyr2569=)
13g.32357928A=CA2082819165BRCA2c.7804A= (p.Arg2602=)
c.7435A= (p.Arg2479=)
c.271A= (p.Arg91=)
c.7804A= (p.Ser2602=)
c.369A=
n.7804A=
c.7708A= (p.Arg2570=)
13g.32357928A>CCA483439325BRCA2c.7804A>C (p.Arg2602=)
c.7435A>C (p.Arg2479=)
c.271A>C (p.Arg91=)
c.7804A>C (p.Ser2602Arg)
c.369A>C
n.7804A>C
c.7708A>C (p.Arg2570=)
13g.32357928A>GCA387746163BRCA2c.7804A>G (p.Arg2602Gly)
c.7435A>G (p.Arg2479Gly)
c.271A>G (p.Arg91Gly)
c.7804A>G (p.Ser2602Gly)
c.369A>G
n.7804A>G
c.7708A>G (p.Arg2570Gly)
 dbSNP gnomAD v4
13g.32357928A>TCA387746166BRCA2c.7804A>T (p.Arg2602Trp)
c.7435A>T (p.Arg2479Trp)
c.271A>T (p.Arg91Trp)
c.7804A>T (p.Ser2602Cys)
c.369A>T
n.7804A>T
c.7708A>T (p.Arg2570Trp)
 dbSNP
13g.32357928_32357929insTTGTTCAGCA919242800BRCA2c.7804_7805insTTGTTCAG (p.Arg2602IlefsTer?)
c.7435_7436insTTGTTCAG (p.Arg2479IlefsTer?)
c.271_272insTTGTTCAG (p.Arg91IlefsTer?)
c.7804_7805insTTGTTCAG (p.Ser2602IlefsTer10)
c.369_370insTTGTTCAG
n.7804_7805insTTGTTCAG
c.7708_7709insTTGTTCAG (p.Arg2570IlefsTer?)
 dbSNP
13g.32357929G>ACA387746169BRCA2c.7805G>A (p.Arg2602Lys)
c.7436G>A (p.Arg2479Lys)
c.272G>A (p.Arg91Lys)
c.7805G>A (p.Ser2602Asn)
c.370G>A
n.7805G>A
c.7709G>A (p.Arg2570Lys)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357929G>CCA025285BRCA2c.7805G>C (p.Arg2602Thr)
c.7436G>C (p.Arg2479Thr)
c.272G>C (p.Arg91Thr)
c.7805G>C (p.Ser2602Thr)
c.370G>C
n.7805G>C
c.7709G>C (p.Arg2570Thr)
 ClinVar dbSNP
13g.32357929G=CA2082819172BRCA2c.7805G= (p.Arg2602=)
c.7436G= (p.Arg2479=)
c.272G= (p.Arg91=)
c.7805G= (p.Ser2602=)
c.370G=
n.7805G=
c.7709G= (p.Arg2570=)
13g.32357929G>TCA387746172BRCA2c.7805G>T (p.Arg2602Met)
c.7436G>T (p.Arg2479Met)
c.272G>T (p.Arg91Met)
c.7805G>T (p.Ser2602Ile)
c.370G>T
n.7805G>T
c.7709G>T (p.Arg2570Met)
 dbSNP
13g.32357930G>ACA025280BRCA2c.7805+1G>A (n.7805+1G>A)
c.7436+1G>A (n.7436+1G>A)
c.272+1G>A (n.272+1G>A)
c.370+1G>A
n.7805+1G>A
c.7709+1G>A (n.7709+1G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
13g.32357930G>CCA387746183BRCA2c.7805+1G>C (n.7805+1G>C)
c.7436+1G>C (n.7436+1G>C)
c.272+1G>C (n.272+1G>C)
c.370+1G>C
n.7805+1G>C
c.7709+1G>C (n.7709+1G>C)
 dbSNP
13g.32357930G=CA2082819185BRCA2c.7805+1G= (n.7805+1G=)
c.7436+1G= (n.7436+1G=)
c.272+1G= (n.272+1G=)
c.370+1G=
n.7805+1G=
c.7709+1G= (n.7709+1G=)
13g.32357930G>TCA387746185BRCA2c.7805+1G>T (n.7805+1G>T)
c.7436+1G>T (n.7436+1G>T)
c.272+1G>T (n.272+1G>T)
c.370+1G>T
n.7805+1G>T
c.7709+1G>T (n.7709+1G>T)
 dbSNP
13g.32357930_32357932delinsGTACA2082819188BRCA2c.7805+1_7805+3delinsGTA (n.7805+1_7805+3delinsGTA)
c.7436+1_7436+3delinsGTA (n.7436+1_7436+3delinsGTA)
c.272+1_272+3delinsGTA (n.272+1_272+3delinsGTA)
c.370+1_370+3delinsGTA
n.7805+1_7805+3delinsGTA
c.7709+1_7709+3delinsGTA (n.7709+1_7709+3delinsGTA)
13g.32357931T>ACA387746187BRCA2c.7805+2T>A (n.7805+2T>A)
c.7436+2T>A (n.7436+2T>A)
c.272+2T>A (n.272+2T>A)
c.370+2T>A
n.7805+2T>A
c.7709+2T>A (n.7709+2T>A)
 ClinVar dbSNP
13g.32357931T>CCA387746189BRCA2c.7805+2T>C (n.7805+2T>C)
c.7436+2T>C (n.7436+2T>C)
c.272+2T>C (n.272+2T>C)
c.370+2T>C
n.7805+2T>C
c.7709+2T>C (n.7709+2T>C)
 ClinVar dbSNP
13g.32357931T>GCA10602541BRCA2c.7805+2T>G (n.7805+2T>G)
c.7436+2T>G (n.7436+2T>G)
c.272+2T>G (n.272+2T>G)
c.370+2T>G
n.7805+2T>G
c.7709+2T>G (n.7709+2T>G)
 ClinVar dbSNP
13g.32357931T=CA2082819202BRCA2c.7805+2T= (n.7805+2T=)
c.7436+2T= (n.7436+2T=)
c.272+2T= (n.272+2T=)
c.370+2T=
n.7805+2T=
c.7709+2T= (n.7709+2T=)
13g.32357931_32357932delCA1139663207BRCA2c.7805+2_7805+3del (n.7805+2_7805+3del)
c.7436+2_7436+3del (n.7436+2_7436+3del)
c.272+2_272+3del (n.272+2_272+3del)
c.370+2_370+3del
n.7805+2_7805+3del
c.7709+2_7709+3del (n.7709+2_7709+3del)
 ClinVar dbSNP
13g.32357932A=CA2082819207BRCA2c.7805+3A= (n.7805+3A=)
c.7436+3A= (n.7436+3A=)
c.272+3A= (n.272+3A=)
c.370+3A=
n.7805+3A=
c.7709+3A= (n.7709+3A=)
13g.32357932A>CCA025281BRCA2c.7805+3A>C (n.7805+3A>C)
c.7436+3A>C (n.7436+3A>C)
c.272+3A>C (n.272+3A>C)
c.370+3A>C
n.7805+3A>C
c.7709+3A>C (n.7709+3A>C)
 ClinVar dbSNP gnomAD v4
13g.32357932A>GCA2727833969BRCA2c.7805+3A>G (n.7805+3A>G)
c.7436+3A>G (n.7436+3A>G)
c.272+3A>G (n.272+3A>G)
c.370+3A>G
n.7805+3A>G
c.7709+3A>G (n.7709+3A>G)
 dbSNP
13g.32357932A>TCA2727833968BRCA2c.7805+3A>T (n.7805+3A>T)
c.7436+3A>T (n.7436+3A>T)
c.272+3A>T (n.272+3A>T)
c.370+3A>T
n.7805+3A>T
c.7709+3A>T (n.7709+3A>T)
 dbSNP
13g.32357933C>ACA915946878BRCA2c.7805+4C>A (n.7805+4C>A)
c.7436+4C>A (n.7436+4C>A)
c.272+4C>A (n.272+4C>A)
c.370+4C>A
n.7805+4C>A
c.7709+4C>A (n.7709+4C>A)
 ClinVar dbSNP
13g.32357933C=CA2082819216BRCA2c.7805+4C= (n.7805+4C=)
c.7436+4C= (n.7436+4C=)
c.272+4C= (n.272+4C=)
c.370+4C=
n.7805+4C=
c.7709+4C= (n.7709+4C=)
13g.32357933C>GCA2727840307BRCA2c.7805+4C>G (n.7805+4C>G)
c.7436+4C>G (n.7436+4C>G)
c.272+4C>G (n.272+4C>G)
c.370+4C>G
n.7805+4C>G
c.7709+4C>G (n.7709+4C>G)
 dbSNP
13g.32357933C>TCA6941140BRCA2c.7805+4C>T (n.7805+4C>T)
c.7436+4C>T (n.7436+4C>T)
c.272+4C>T (n.272+4C>T)
c.370+4C>T
n.7805+4C>T
c.7709+4C>T (n.7709+4C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357934T>ACA2727914551BRCA2c.7805+5T>A (n.7805+5T>A)
c.7436+5T>A (n.7436+5T>A)
c.272+5T>A (n.272+5T>A)
c.370+5T>A
n.7805+5T>A
c.7709+5T>A (n.7709+5T>A)
 dbSNP
13g.32357934T>GCA2580087369BRCA2c.7805+5T>G (n.7805+5T>G)
c.7436+5T>G (n.7436+5T>G)
c.272+5T>G (n.272+5T>G)
c.370+5T>G
n.7805+5T>G
c.7709+5T>G (n.7709+5T>G)
 ClinVar
13g.32357935C>ACA2727833970BRCA2c.7805+6C>A (n.7805+6C>A)
c.7436+6C>A (n.7436+6C>A)
c.272+6C>A (n.272+6C>A)
c.370+6C>A
n.7805+6C>A
c.7709+6C>A (n.7709+6C>A)
 dbSNP
13g.32357935C=CA2082819227BRCA2c.7805+6C= (n.7805+6C=)
c.7436+6C= (n.7436+6C=)
c.272+6C= (n.272+6C=)
c.370+6C=
n.7805+6C=
c.7709+6C= (n.7709+6C=)
13g.32357935C>GCA025282BRCA2c.7805+6C>G (n.7805+6C>G)
c.7436+6C>G (n.7436+6C>G)
c.272+6C>G (n.272+6C>G)
c.370+6C>G
n.7805+6C>G
c.7709+6C>G (n.7709+6C>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32357935C>TCA913188544BRCA2c.7805+6C>T (n.7805+6C>T)
c.7436+6C>T (n.7436+6C>T)
c.272+6C>T (n.272+6C>T)
c.370+6C>T
n.7805+6C>T
c.7709+6C>T (n.7709+6C>T)
 ClinVar dbSNP
13g.32357935_32357937delinsCTACA2082819233BRCA2c.7805+6_7805+8delinsCTA (n.7805+6_7805+8delinsCTA)
c.7436+6_7436+8delinsCTA (n.7436+6_7436+8delinsCTA)
c.272+6_272+8delinsCTA (n.272+6_272+8delinsCTA)
c.370+6_370+8delinsCTA
n.7805+6_7805+8delinsCTA
c.7709+6_7709+8delinsCTA (n.7709+6_7709+8delinsCTA)
13g.32357936T>ACA025283BRCA2c.7805+7T>A (n.7805+7T>A)
c.7436+7T>A (n.7436+7T>A)
c.272+7T>A (n.272+7T>A)
c.370+7T>A
n.7805+7T>A
c.7709+7T>A (n.7709+7T>A)
 ClinVar dbSNP
13g.32357936T=CA2082819241BRCA2c.7805+7T= (n.7805+7T=)
c.7436+7T= (n.7436+7T=)
c.272+7T= (n.272+7T=)
c.370+7T=
n.7805+7T=
c.7709+7T= (n.7709+7T=)
13g.32357937_32357938delCA954697467BRCA2c.7805+8_7805+9del (n.7805+8_7805+9del)
c.7436+8_7436+9del (n.7436+8_7436+9del)
c.272+8_272+9del (n.272+8_272+9del)
c.370+8_370+9del
n.7805+8_7805+9del
c.7709+8_7709+9del (n.7709+8_7709+9del)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357937A=CA2082819290BRCA2c.7805+8A= (n.7805+8A=)
c.7436+8A= (n.7436+8A=)
c.272+8A= (n.272+8A=)
c.370+8A=
n.7805+8A=
c.7709+8A= (n.7709+8A=)
13g.32357937A>CCA913188545BRCA2c.7805+8A>C (n.7805+8A>C)
c.7436+8A>C (n.7436+8A>C)
c.272+8A>C (n.272+8A>C)
c.370+8A>C
n.7805+8A>C
c.7709+8A>C (n.7709+8A>C)
 ClinVar dbSNP
13g.32357937A>GCA025284BRCA2c.7805+8A>G (n.7805+8A>G)
c.7436+8A>G (n.7436+8A>G)
c.272+8A>G (n.272+8A>G)
c.370+8A>G
n.7805+8A>G
c.7709+8A>G (n.7709+8A>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32357938T>ACA350397BRCA2c.7805+9T>A (n.7805+9T>A)
c.7436+9T>A (n.7436+9T>A)
c.272+9T>A (n.272+9T>A)
c.370+9T>A
n.7805+9T>A
c.7709+9T>A (n.7709+9T>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32357938T>CCA2499222308BRCA2c.7805+9T>C (n.7805+9T>C)
c.7436+9T>C (n.7436+9T>C)
c.272+9T>C (n.272+9T>C)
c.370+9T>C
n.7805+9T>C
c.7709+9T>C (n.7709+9T>C)
 ClinVar dbSNP
13g.32357938T=CA2082819304BRCA2c.7805+9T= (n.7805+9T=)
c.7436+9T= (n.7436+9T=)
c.272+9T= (n.272+9T=)
c.370+9T=
n.7805+9T=
c.7709+9T= (n.7709+9T=)
13g.32357939G>ACA658798124BRCA2c.7805+10G>A (n.7805+10G>A)
c.7436+10G>A (n.7436+10G>A)
c.272+10G>A (n.272+10G>A)
c.370+10G>A
n.7805+10G>A
c.7709+10G>A (n.7709+10G>A)
 ClinVar dbSNP gnomAD v4
13g.32357939G>CCA2727853380BRCA2c.7805+10G>C (n.7805+10G>C)
c.7436+10G>C (n.7436+10G>C)
c.272+10G>C (n.272+10G>C)
c.370+10G>C
n.7805+10G>C
c.7709+10G>C (n.7709+10G>C)
 dbSNP
13g.32357939G=CA2082819313BRCA2c.7805+10G= (n.7805+10G=)
c.7436+10G= (n.7436+10G=)
c.272+10G= (n.272+10G=)
c.370+10G=
n.7805+10G=
c.7709+10G= (n.7709+10G=)
13g.32357939G>TCA16606817BRCA2c.7805+10G>T (n.7805+10G>T)
c.7436+10G>T (n.7436+10G>T)
c.272+10G>T (n.272+10G>T)
c.370+10G>T
n.7805+10G>T
c.7709+10G>T (n.7709+10G>T)
 ClinVar dbSNP gnomAD v4
13g.32357940C>ACA16614357BRCA2c.7805+11C>A (n.7805+11C>A)
c.7436+11C>A (n.7436+11C>A)
c.272+11C>A (n.272+11C>A)
c.370+11C>A
n.7805+11C>A
c.7709+11C>A (n.7709+11C>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32357940C=CA2082819327BRCA2c.7805+11C= (n.7805+11C=)
c.7436+11C= (n.7436+11C=)
c.272+11C= (n.272+11C=)
c.370+11C=
n.7805+11C=
c.7709+11C= (n.7709+11C=)
13g.32357942A=CA2082819330BRCA2c.7805+13A= (n.7805+13A=)
c.7436+13A= (n.7436+13A=)
c.272+13A= (n.272+13A=)
c.370+13A=
n.7805+13A=
c.7709+13A= (n.7709+13A=)
13g.32357942A>GCA025279BRCA2c.7805+13A>G (n.7805+13A>G)
c.7436+13A>G (n.7436+13A>G)
c.272+13A>G (n.272+13A>G)
c.370+13A>G
n.7805+13A>G
c.7709+13A>G (n.7709+13A>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32357943A>GCA2499222309BRCA2c.7805+14A>G (n.7805+14A>G)
c.7436+14A>G (n.7436+14A>G)
c.272+14A>G (n.272+14A>G)
c.370+14A>G
n.7805+14A>G
c.7709+14A>G (n.7709+14A>G)
 ClinVar dbSNP
13g.32357943A>TCA2727914555BRCA2c.7805+14A>T (n.7805+14A>T)
c.7436+14A>T (n.7436+14A>T)
c.272+14A>T (n.272+14A>T)
c.370+14A>T
n.7805+14A>T
c.7709+14A>T (n.7709+14A>T)
 dbSNP
13g.32357944A>GCA2727914556BRCA2c.7805+15A>G (n.7805+15A>G)
c.7436+15A>G (n.7436+15A>G)
c.272+15A>G (n.272+15A>G)
c.370+15A>G
n.7805+15A>G
c.7709+15A>G (n.7709+15A>G)
 dbSNP
13g.32357946G>ACA337126BRCA2c.7805+17G>A (n.7805+17G>A)
c.7436+17G>A (n.7436+17G>A)
c.272+17G>A (n.272+17G>A)
c.370+17G>A
n.7805+17G>A
c.7709+17G>A (n.7709+17G>A)
 ClinVar dbSNP gnomAD v4
13g.32357946G>CCA2727836150BRCA2c.7805+17G>C (n.7805+17G>C)
c.7436+17G>C (n.7436+17G>C)
c.272+17G>C (n.272+17G>C)
c.370+17G>C
n.7805+17G>C
c.7709+17G>C (n.7709+17G>C)
 dbSNP
13g.32357946G=CA2082819342BRCA2c.7805+17G= (n.7805+17G=)
c.7436+17G= (n.7436+17G=)
c.272+17G= (n.272+17G=)
c.370+17G=
n.7805+17G=
c.7709+17G= (n.7709+17G=)
13g.32357946G>TCA697352007BRCA2c.7805+17G>T (n.7805+17G>T)
c.7436+17G>T (n.7436+17G>T)
c.272+17G>T (n.272+17G>T)
c.370+17G>T
n.7805+17G>T
c.7709+17G>T (n.7709+17G>T)
 dbSNP
13g.32357947A>GCA2697551789BRCA2c.7805+18A>G (n.7805+18A>G)
c.7436+18A>G (n.7436+18A>G)
c.272+18A>G (n.272+18A>G)
c.370+18A>G
n.7805+18A>G
c.7709+18A>G (n.7709+18A>G)
 ClinVar
13g.32357947A>TCA2727914558BRCA2c.7805+18A>T (n.7805+18A>T)
c.7436+18A>T (n.7436+18A>T)
c.272+18A>T (n.272+18A>T)
c.370+18A>T
n.7805+18A>T
c.7709+18A>T (n.7709+18A>T)
 dbSNP
13g.32357948T>ACA2727912939BRCA2c.7805+19T>A (n.7805+19T>A)
c.7436+19T>A (n.7436+19T>A)
c.272+19T>A (n.272+19T>A)
c.370+19T>A
n.7805+19T>A
c.7709+19T>A (n.7709+19T>A)
 dbSNP
13g.32357948T>GCA2082819363BRCA2c.7805+19T>G (n.7805+19T>G)
c.7436+19T>G (n.7436+19T>G)
c.272+19T>G (n.272+19T>G)
c.370+19T>G
n.7805+19T>G
c.7709+19T>G (n.7709+19T>G)
 ClinVar dbSNP
13g.32357948T=CA2082819346BRCA2c.7805+19T= (n.7805+19T=)
c.7436+19T= (n.7436+19T=)
c.272+19T= (n.272+19T=)
c.370+19T=
n.7805+19T=
c.7709+19T= (n.7709+19T=)
13g.32357949T>ACA6941141BRCA2c.7805+20T>A (n.7805+20T>A)
c.7436+20T>A (n.7436+20T>A)
c.272+20T>A (n.272+20T>A)
c.370+20T>A
n.7805+20T>A
c.7709+20T>A (n.7709+20T>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357949T>GCA2573149413BRCA2c.7805+20T>G (n.7805+20T>G)
c.7436+20T>G (n.7436+20T>G)
c.272+20T>G (n.272+20T>G)
c.370+20T>G
n.7805+20T>G
c.7709+20T>G (n.7709+20T>G)
 ClinVar dbSNP
13g.32357949T=CA2082819365BRCA2c.7805+20T= (n.7805+20T=)
c.7436+20T= (n.7436+20T=)
c.272+20T= (n.272+20T=)
c.370+20T=
n.7805+20T=
c.7709+20T= (n.7709+20T=)
13g.32357950G>CCA2727914559BRCA2c.7805+21G>C (n.7805+21G>C)
c.7436+21G>C (n.7436+21G>C)
c.272+21G>C (n.272+21G>C)
c.370+21G>C
n.7805+21G>C
c.7709+21G>C (n.7709+21G>C)
 dbSNP
13g.32357951T>ACA2727914561BRCA2c.7805+22T>A (n.7805+22T>A)
c.7436+22T>A (n.7436+22T>A)
c.272+22T>A (n.272+22T>A)
c.370+22T>A
n.7805+22T>A
c.7709+22T>A (n.7709+22T>A)
 dbSNP
13g.32357951T>CCA2622572256BRCA2c.7805+22T>C (n.7805+22T>C)
c.7436+22T>C (n.7436+22T>C)
c.272+22T>C (n.272+22T>C)
c.370+22T>C
n.7805+22T>C
c.7709+22T>C (n.7709+22T>C)
 gnomAD v4
13g.32357951T>GCA2727914563BRCA2c.7805+22T>G (n.7805+22T>G)
c.7436+22T>G (n.7436+22T>G)
c.272+22T>G (n.272+22T>G)
c.370+22T>G
n.7805+22T>G
c.7709+22T>G (n.7709+22T>G)
 dbSNP
13g.32357952G>ACA6941142BRCA2c.7805+23G>A (n.7805+23G>A)
c.7436+23G>A (n.7436+23G>A)
c.272+23G>A (n.272+23G>A)
c.370+23G>A
n.7805+23G>A
c.7709+23G>A (n.7709+23G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32357952G>CCA2727833971BRCA2c.7805+23G>C (n.7805+23G>C)
c.7436+23G>C (n.7436+23G>C)
c.272+23G>C (n.272+23G>C)
c.370+23G>C
n.7805+23G>C
c.7709+23G>C (n.7709+23G>C)
 dbSNP
13g.32357952G=CA2082819370BRCA2c.7805+23G= (n.7805+23G=)
c.7436+23G= (n.7436+23G=)
c.272+23G= (n.272+23G=)
c.370+23G=
n.7805+23G=
c.7709+23G= (n.7709+23G=)
13g.32357954G>ACA2622572264BRCA2c.7805+25G>A (n.7805+25G>A)
c.7436+25G>A (n.7436+25G>A)
c.272+25G>A (n.272+25G>A)
c.370+25G>A
n.7805+25G>A
c.7709+25G>A (n.7709+25G>A)
 dbSNP gnomAD v4
13g.32357954G>CCA2727841189BRCA2c.7805+25G>C (n.7805+25G>C)
c.7436+25G>C (n.7436+25G>C)
c.272+25G>C (n.272+25G>C)
c.370+25G>C
n.7805+25G>C
c.7709+25G>C (n.7709+25G>C)
 dbSNP
13g.32357954G=CA2082819376BRCA2c.7805+25G= (n.7805+25G=)
c.7436+25G= (n.7436+25G=)
c.272+25G= (n.272+25G=)
c.370+25G=
n.7805+25G=
c.7709+25G= (n.7709+25G=)
13g.32357954G>TCA6941143BRCA2c.7805+25G>T (n.7805+25G>T)
c.7436+25G>T (n.7436+25G>T)
c.272+25G>T (n.272+25G>T)
c.370+25G>T
n.7805+25G>T
c.7709+25G>T (n.7709+25G>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32357955T>ACA2727914565BRCA2c.7805+26T>A (n.7805+26T>A)
c.7436+26T>A (n.7436+26T>A)
c.272+26T>A (n.272+26T>A)
c.370+26T>A
n.7805+26T>A
c.7709+26T>A (n.7709+26T>A)
 dbSNP
13g.32357955T>CCA2622572273BRCA2c.7805+26T>C (n.7805+26T>C)
c.7436+26T>C (n.7436+26T>C)
c.272+26T>C (n.272+26T>C)
c.370+26T>C
n.7805+26T>C
c.7709+26T>C (n.7709+26T>C)
 gnomAD v4
13g.32357956T>ACA2727914567BRCA2c.7805+27T>A (n.7805+27T>A)
c.7436+27T>A (n.7436+27T>A)
c.272+27T>A (n.272+27T>A)
c.370+27T>A
n.7805+27T>A
c.7709+27T>A (n.7709+27T>A)
 dbSNP
13g.32357956T>CCA2622572277BRCA2c.7805+27T>C (n.7805+27T>C)
c.7436+27T>C (n.7436+27T>C)
c.272+27T>C (n.272+27T>C)
c.370+27T>C
n.7805+27T>C
c.7709+27T>C (n.7709+27T>C)
 gnomAD v4
13g.32357958A=CA2082819380BRCA2c.7805+29A= (n.7805+29A=)
c.7436+29A= (n.7436+29A=)
c.272+29A= (n.272+29A=)
c.370+29A=
n.7805+29A=
c.7709+29A= (n.7709+29A=)
13g.32357958A>CCA954697490BRCA2c.7805+29A>C (n.7805+29A>C)
c.7436+29A>C (n.7436+29A>C)
c.272+29A>C (n.272+29A>C)
c.370+29A>C
n.7805+29A>C
c.7709+29A>C (n.7709+29A>C)
 dbSNP gnomAD v3 gnomAD v4
13g.32357958A>TCA2727912941BRCA2c.7805+29A>T (n.7805+29A>T)
c.7436+29A>T (n.7436+29A>T)
c.272+29A>T (n.272+29A>T)
c.370+29A>T
n.7805+29A>T
c.7709+29A>T (n.7709+29A>T)
 dbSNP
13g.32357959C=CA2082819386BRCA2c.7805+30C= (n.7805+30C=)
c.7436+30C= (n.7436+30C=)
c.272+30C= (n.272+30C=)
c.370+30C=
n.7805+30C=
c.7709+30C= (n.7709+30C=)
13g.32357959C>TCA2082819392BRCA2c.7805+30C>T (n.7805+30C>T)
c.7436+30C>T (n.7436+30C>T)
c.272+30C>T (n.272+30C>T)
c.370+30C>T
n.7805+30C>T
c.7709+30C>T (n.7709+30C>T)
 dbSNP
13g.32357960_32357963delCA2622572278BRCA2c.7805+31_7805+34del (n.7805+31_7805+34del)
c.7436+31_7436+34del (n.7436+31_7436+34del)
c.272+31_272+34del (n.272+31_272+34del)
c.370+31_370+34del
n.7805+31_7805+34del
c.7709+31_7709+34del (n.7709+31_7709+34del)
 gnomAD v4
13g.32357961T>ACA2082819398BRCA2c.7805+32T>A (n.7805+32T>A)
c.7436+32T>A (n.7436+32T>A)
c.272+32T>A (n.272+32T>A)
c.370+32T>A
n.7805+32T>A
c.7709+32T>A (n.7709+32T>A)
 dbSNP
13g.32357961T>GCA2082819399BRCA2c.7805+32T>G (n.7805+32T>G)
c.7436+32T>G (n.7436+32T>G)
c.272+32T>G (n.272+32T>G)
c.370+32T>G
n.7805+32T>G
c.7709+32T>G (n.7709+32T>G)
 dbSNP
13g.32357961T=CA2082819397BRCA2c.7805+32T= (n.7805+32T=)
c.7436+32T= (n.7436+32T=)
c.272+32T= (n.272+32T=)
c.370+32T=
n.7805+32T=
c.7709+32T= (n.7709+32T=)
13g.32357962T>CCA6941144BRCA2c.7805+33T>C (n.7805+33T>C)
c.7436+33T>C (n.7436+33T>C)
c.272+33T>C (n.272+33T>C)
c.370+33T>C
n.7805+33T>C
c.7709+33T>C (n.7709+33T>C)
 dbSNP ExAC gnomAD v2
13g.32357962T=CA2082819401BRCA2c.7805+33T= (n.7805+33T=)
c.7436+33T= (n.7436+33T=)
c.272+33T= (n.272+33T=)
c.370+33T=
n.7805+33T=
c.7709+33T= (n.7709+33T=)
13g.32357963T>GCA6941145BRCA2c.7805+34T>G (n.7805+34T>G)
c.7436+34T>G (n.7436+34T>G)
c.272+34T>G (n.272+34T>G)
c.370+34T>G
n.7805+34T>G
c.7709+34T>G (n.7709+34T>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32357963T=CA2082819404BRCA2c.7805+34T= (n.7805+34T=)
c.7436+34T= (n.7436+34T=)
c.272+34T= (n.272+34T=)
c.370+34T=
n.7805+34T=
c.7709+34T= (n.7709+34T=)
13g.32357964A=CA2082819410BRCA2c.7805+35A= (n.7805+35A=)
c.7436+35A= (n.7436+35A=)
c.272+35A= (n.272+35A=)
c.370+35A=
n.7805+35A=
c.7709+35A= (n.7709+35A=)
13g.32357964A>GCA2622572280BRCA2c.7805+35A>G (n.7805+35A>G)
c.7436+35A>G (n.7436+35A>G)
c.272+35A>G (n.272+35A>G)
c.370+35A>G
n.7805+35A>G
c.7709+35A>G (n.7709+35A>G)
 gnomAD v4
13g.32357964A>TCA2082819412BRCA2c.7805+35A>T (n.7805+35A>T)
c.7436+35A>T (n.7436+35A>T)
c.272+35A>T (n.272+35A>T)
c.370+35A>T
n.7805+35A>T
c.7709+35A>T (n.7709+35A>T)
 dbSNP
13g.32357965T>GCA2575388219BRCA2c.7805+36T>G (n.7805+36T>G)
c.7436+36T>G (n.7436+36T>G)
c.272+36T>G (n.272+36T>G)
c.370+36T>G
n.7805+36T>G
c.7709+36T>G (n.7709+36T>G)
13g.32357966G>ACA483260664BRCA2c.7805+37G>A (n.7805+37G>A)
c.7436+37G>A (n.7436+37G>A)
c.272+37G>A (n.272+37G>A)
c.370+37G>A
n.7805+37G>A
c.7709+37G>A (n.7709+37G>A)
 gnomAD v4
13g.32357966G>CCA2727914570BRCA2c.7805+37G>C (n.7805+37G>C)
c.7436+37G>C (n.7436+37G>C)
c.272+37G>C (n.272+37G>C)
c.370+37G>C
n.7805+37G>C
c.7709+37G>C (n.7709+37G>C)
 dbSNP
13g.32357966G>TCA2622572283BRCA2c.7805+37G>T (n.7805+37G>T)
c.7436+37G>T (n.7436+37G>T)
c.272+37G>T (n.272+37G>T)
c.370+37G>T
n.7805+37G>T
c.7709+37G>T (n.7709+37G>T)
 gnomAD v4

Number of alleles fetched