Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32328077_32337667delCA2580087045BRCA2c.632-1366_3312del
c.263-1366_2943del
n.632-1366_3312del
ClinVar
13g.32330917_32331031delCA2499222059BRCA2c.682-2_793+1del
c.313-2_424+1del
c.*461-2_*572+1del
n.880-2_991+1del
n.682-2_793+1del
ClinVar dbSNP
13g.32331010_32331017delinsAAAGAGAACA2082759680BRCA2c.773_780delinsAAAGAGAA (p.Gln258=)
c.404_411delinsAAAGAGAA (p.Gln135=)
c.*552_*559delinsAAAGAGAA (n.*552_*559delinsAAAGAGAA)
n.971_978delinsAAAGAGAA
n.773_780delinsAAAGAGAA
13g.32331012_32331017delCA2573149308BRCA2c.775_780del (p.Arg259_Glu260del)
c.406_411del (p.Arg136_Glu137del)
c.*554_*559del (n.*554_*559del)
n.973_978del
n.775_780del
dbSNP
13g.32331011_32331017delinsTCA025253BRCA2c.774_780delinsT (p.Gln258_Glu260delinsHis)
c.405_411delinsT (p.Gln135_Glu137delinsHis)
c.*553_*559delinsT (n.*553_*559delinsT)
n.972_978delinsT
n.774_780delinsT
ClinVar dbSNP
13g.32331015_32331016delCA025258BRCA2c.778_779del (p.Glu260SerfsTer15)
c.409_410del (p.Glu137SerfsTer15)
c.*557_*558del (n.*557_*558del)
n.976_977del
n.778_779del
dbSNP
13g.32331013_32331016delCA2622599904BRCA2c.776_779del (p.Arg259LysfsTer17)
c.407_410del (p.Arg136LysfsTer17)
c.*555_*558del (n.*555_*558del)
n.974_977del
n.776_779del
gnomAD v4
13g.32331015_32331016delinsTCCA2580087095BRCA2c.778_779delinsTC (p.Glu260Ser)
c.409_410delinsTC (p.Glu137Ser)
c.*557_*558delinsTC (n.*557_*558delinsTC)
n.976_977delinsTC
n.778_779delinsTC
ClinVar
13g.32331016A=CA2082759737BRCA2c.779A= (p.Glu260=)
c.410A= (p.Glu137=)
c.*558A= (n.*558A=)
n.977A=
n.779A=
13g.32331016A>CCA387760207BRCA2c.779A>C (p.Glu260Ala)
c.410A>C (p.Glu137Ala)
c.*558A>C (n.*558A>C)
n.977A>C
n.779A>C
13g.32331016A>GCA387760209BRCA2c.779A>G (p.Glu260Gly)
c.410A>G (p.Glu137Gly)
c.*558A>G (n.*558A>G)
n.977A>G
n.779A>G
ClinVar dbSNP gnomAD v4
13g.32331016A>TCA387760206BRCA2c.779A>T (p.Glu260Val)
c.410A>T (p.Glu137Val)
c.*558A>T (n.*558A>T)
n.977A>T
n.779A>T
13g.32331017A>CCA387760213BRCA2c.780A>C (p.Glu260Asp)
c.411A>C (p.Glu137Asp)
c.*559A>C (n.*559A>C)
n.978A>C
n.780A>C
ClinVar
13g.32331017A>GCA483274537BRCA2c.780A>G (p.Glu260=)
c.411A>G (p.Glu137=)
c.*559A>G (n.*559A>G)
n.978A>G
n.780A>G
dbSNP
13g.32331017A>TCA387760211BRCA2c.780A>T (p.Glu260Asp)
c.411A>T (p.Glu137Asp)
c.*559A>T (n.*559A>T)
n.978A>T
n.780A>T
dbSNP
13g.32331018G>ACA387760214BRCA2c.781G>A (p.Ala261Thr)
c.412G>A (p.Ala138Thr)
c.*560G>A (n.*560G>A)
n.979G>A
n.781G>A
ClinVar dbSNP gnomAD v4
13g.32331018G>CCA387760216BRCA2c.781G>C (p.Ala261Pro)
c.412G>C (p.Ala138Pro)
c.*560G>C (n.*560G>C)
n.979G>C
n.781G>C
ClinVar dbSNP
13g.32331018G=CA2082759746BRCA2c.781G= (p.Ala261=)
c.412G= (p.Ala138=)
c.*560G= (n.*560G=)
n.979G=
n.781G=
13g.32331018G>TCA387760219BRCA2c.781G>T (p.Ala261Ser)
c.412G>T (p.Ala138Ser)
c.*560G>T (n.*560G>T)
n.979G>T
n.781G>T
13g.32331019delCA2695199245BRCA2c.782del (p.Ala261ValfsTer16)
c.413del (p.Ala138ValfsTer16)
c.*561del (n.*561del)
n.980del
n.782del
13g.32331019C>ACA387760220BRCA2c.782C>A (p.Ala261Asp)
c.413C>A (p.Ala138Asp)
c.*561C>A (n.*561C>A)
n.980C>A
n.782C>A
dbSNP gnomAD v4
13g.32331019C>GCA387760222BRCA2c.782C>G (p.Ala261Gly)
c.413C>G (p.Ala138Gly)
c.*561C>G (n.*561C>G)
n.980C>G
n.782C>G
dbSNP
13g.32331019C>TCA387760224BRCA2c.782C>T (p.Ala261Val)
c.413C>T (p.Ala138Val)
c.*561C>T (n.*561C>T)
n.980C>T
n.782C>T
ClinVar dbSNP gnomAD v4
13g.32331020T>ACA483274544BRCA2c.783T>A (p.Ala261=)
c.414T>A (p.Ala138=)
c.*562T>A (n.*562T>A)
n.981T>A
n.783T>A
dbSNP
13g.32331020T>CCA483274542BRCA2c.783T>C (p.Ala261=)
c.414T>C (p.Ala138=)
c.*562T>C (n.*562T>C)
n.981T>C
n.783T>C
dbSNP
13g.32331020T>GCA483274539BRCA2c.783T>G (p.Ala261=)
c.414T>G (p.Ala138=)
c.*562T>G (n.*562T>G)
n.981T>G
n.783T>G
gnomAD v4
13g.32331021delCA2499222061BRCA2c.784del (p.Ala262GlnfsTer15)
c.415del (p.Ala139GlnfsTer15)
c.*563del (n.*563del)
n.982del
n.784del
13g.32331021G>ACA025308BRCA2c.784G>A (p.Ala262Thr)
c.415G>A (p.Ala139Thr)
c.*563G>A (n.*563G>A)
n.982G>A
n.784G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32331021G>CCA387760226BRCA2c.784G>C (p.Ala262Pro)
c.415G>C (p.Ala139Pro)
c.*563G>C (n.*563G>C)
n.982G>C
n.784G>C
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32331021G=CA2082759760BRCA2c.784G= (p.Ala262=)
c.415G= (p.Ala139=)
c.*563G= (n.*563G=)
n.982G=
n.784G=
13g.32331021G>TCA387760228BRCA2c.784G>T (p.Ala262Ser)
c.415G>T (p.Ala139Ser)
c.*563G>T (n.*563G>T)
n.982G>T
n.784G>T
13g.32331022C>ACA387760230BRCA2c.785C>A (p.Ala262Glu)
c.416C>A (p.Ala139Glu)
c.*564C>A (n.*564C>A)
n.983C>A
n.785C>A
dbSNP gnomAD v4
13g.32331022C=CA2082759765BRCA2c.785C= (p.Ala262=)
c.416C= (p.Ala139=)
c.*564C= (n.*564C=)
n.983C=
n.785C=
13g.32331022C>GCA387760232BRCA2c.785C>G (p.Ala262Gly)
c.416C>G (p.Ala139Gly)
c.*564C>G (n.*564C>G)
n.983C>G
n.785C>G
dbSNP
13g.32331022C>TCA10579472BRCA2c.785C>T (p.Ala262Val)
c.416C>T (p.Ala139Val)
c.*564C>T (n.*564C>T)
n.983C>T
n.785C>T
ClinVar dbSNP COSMIC
13g.32331023A>CCA483274554BRCA2c.786A>C (p.Ala262=)
c.417A>C (p.Ala139=)
c.*565A>C (n.*565A>C)
n.984A>C
n.786A>C
13g.32331023A>GCA483274553BRCA2c.786A>G (p.Ala262=)
c.417A>G (p.Ala139=)
c.*565A>G (n.*565A>G)
n.984A>G
n.786A>G
dbSNP
13g.32331023A>TCA483274551BRCA2c.786A>T (p.Ala262=)
c.417A>T (p.Ala139=)
c.*565A>T (n.*565A>T)
n.984A>T
n.786A>T
dbSNP
13g.32331024dupCA273049BRCA2c.787dup (p.Ser263LysfsTer13)
c.418dup (p.Ser140LysfsTer13)
c.*566dup (n.*566dup)
n.985dup
n.787dup
ClinVar dbSNP
13g.32331024A>CCA387760242BRCA2c.787A>C (p.Ser263Arg)
c.418A>C (p.Ser140Arg)
c.*566A>C (n.*566A>C)
n.985A>C
n.787A>C
ClinVar
13g.32331024A>GCA387760234BRCA2c.787A>G (p.Ser263Gly)
c.418A>G (p.Ser140Gly)
c.*566A>G (n.*566A>G)
n.985A>G
n.787A>G
ClinVar dbSNP
13g.32331024A>TCA387760240BRCA2c.787A>T (p.Ser263Cys)
c.418A>T (p.Ser140Cys)
c.*566A>T (n.*566A>T)
n.985A>T
n.787A>T
dbSNP
13g.32331025G>ACA387760244BRCA2c.788G>A (p.Ser263Asn)
c.419G>A (p.Ser140Asn)
c.*567G>A (n.*567G>A)
n.986G>A
n.788G>A
ClinVar dbSNP
13g.32331025G>CCA387760245BRCA2c.788G>C (p.Ser263Thr)
c.419G>C (p.Ser140Thr)
c.*567G>C (n.*567G>C)
n.986G>C
n.788G>C
ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32331025G=CA2082759782BRCA2c.788G= (p.Ser263=)
c.419G= (p.Ser140=)
c.*567G= (n.*567G=)
n.986G=
n.788G=
13g.32331025G>TCA387760247BRCA2c.788G>T (p.Ser263Ile)
c.419G>T (p.Ser140Ile)
c.*567G>T (n.*567G>T)
n.986G>T
n.788G>T
13g.32331026T>ACA387760249BRCA2c.789T>A (p.Ser263Arg)
c.420T>A (p.Ser140Arg)
c.*568T>A (n.*568T>A)
n.987T>A
n.789T>A
13g.32331026T>CCA483274561BRCA2c.789T>C (p.Ser263=)
c.420T>C (p.Ser140=)
c.*568T>C (n.*568T>C)
n.987T>C
n.789T>C
13g.32331026T>GCA387760253BRCA2c.789T>G (p.Ser263Arg)
c.420T>G (p.Ser140Arg)
c.*568T>G (n.*568T>G)
n.987T>G
n.789T>G
dbSNP gnomAD v4
13g.32331027C>ACA387760255BRCA2c.790C>A (p.His264Asn)
c.421C>A (p.His141Asn)
c.*569C>A (n.*569C>A)
n.988C>A
n.790C>A
ClinVar dbSNP

Number of alleles fetched