Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.40718779_40718849delCA2627842627RAD51c.436-26_480del
c.439-26_483del
c.435+9663_435+9733del (n.435+9663_435+9733del)
c.*15-26_*59del
c.226-107_226-37del (n.226-107_226-37del)
c.64-26_108del
gnomAD v4
15g.40718818G>ACA256732RAD51c.449G>A (p.Arg150Gln)
c.452G>A (p.Arg151Gln)
c.435+9702G>A (n.435+9702G>A)
c.*28G>A (n.*28G>A)
c.416G>A
c.226-68G>A (n.226-68G>A)
c.77G>A (p.Arg26Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.40718818G>CCA501077RAD51c.449G>C (p.Arg150Pro)
c.452G>C (p.Arg151Pro)
c.435+9702G>C (n.435+9702G>C)
c.*28G>C (n.*28G>C)
c.416G>C
c.226-68G>C (n.226-68G>C)
c.77G>C (p.Arg26Pro)
15g.40718818G=CA2171911651RAD51c.449G= (p.Arg150=)
c.452G= (p.Arg151=)
c.435+9702G= (n.435+9702G=)
c.*28G= (n.*28G=)
c.416G=
c.226-68G= (n.226-68G=)
c.77G= (p.Arg26=)
15g.40718818G>TCA391753276RAD51c.449G>T (p.Arg150Leu)
c.452G>T (p.Arg151Leu)
c.435+9702G>T (n.435+9702G>T)
c.*28G>T (n.*28G>T)
c.416G>T
c.226-68G>T (n.226-68G>T)
c.77G>T (p.Arg26Leu)
gnomAD v4
15g.40718819G>ACA489772874RAD51c.450G>A (p.Arg150=)
c.453G>A (p.Arg151=)
c.435+9703G>A (n.435+9703G>A)
c.*29G>A (n.*29G>A)
c.417G>A
c.226-67G>A (n.226-67G>A)
c.78G>A (p.Arg26=)
15g.40718819G>CCA268843912RAD51c.450G>C (p.Arg150=)
c.453G>C (p.Arg151=)
c.435+9703G>C (n.435+9703G>C)
c.*29G>C (n.*29G>C)
c.417G>C
c.226-67G>C (n.226-67G>C)
c.78G>C (p.Arg26=)
dbSNP gnomAD v3 gnomAD v4
15g.40718819G=CA2171911652RAD51c.450G= (p.Arg150=)
c.453G= (p.Arg151=)
c.435+9703G= (n.435+9703G=)
c.*29G= (n.*29G=)
c.417G=
c.226-67G= (n.226-67G=)
c.78G= (p.Arg26=)
15g.40718819G>TCA489772875RAD51c.450G>T (p.Arg150=)
c.453G>T (p.Arg151=)
c.435+9703G>T (n.435+9703G>T)
c.*29G>T (n.*29G>T)
c.417G>T
c.226-67G>T (n.226-67G>T)
c.78G>T (p.Arg26=)
ClinVar
15g.40718820G>ACA391753279RAD51c.451G>A (p.Gly151Ser)
c.454G>A (p.Gly152Ser)
c.435+9704G>A (n.435+9704G>A)
c.*30G>A (n.*30G>A)
c.418G>A
c.226-66G>A (n.226-66G>A)
c.79G>A (p.Gly27Ser)
ClinVar gnomAD v4
15g.40718820G>CCA391753282RAD51c.451G>C (p.Gly151Arg)
c.454G>C (p.Gly152Arg)
c.435+9704G>C (n.435+9704G>C)
c.*30G>C (n.*30G>C)
c.418G>C
c.226-66G>C (n.226-66G>C)
c.79G>C (p.Gly27Arg)
15g.40718820G=CA2171911653RAD51c.451G= (p.Gly151=)
c.454G= (p.Gly152=)
c.435+9704G= (n.435+9704G=)
c.*30G= (n.*30G=)
c.418G=
c.226-66G= (n.226-66G=)
c.79G= (p.Gly27=)
15g.40718820G>TCA391753285RAD51c.451G>T (p.Gly151Cys)
c.454G>T (p.Gly152Cys)
c.435+9704G>T (n.435+9704G>T)
c.*30G>T (n.*30G>T)
c.418G>T
c.226-66G>T (n.226-66G>T)
c.79G>T (p.Gly27Cys)
ClinVar dbSNP gnomAD v2 gnomAD v4
15g.40718821G>ACA391753287RAD51c.452G>A (p.Gly151Asp)
c.455G>A (p.Gly152Asp)
c.435+9705G>A (n.435+9705G>A)
c.*31G>A (n.*31G>A)
c.419G>A
c.226-65G>A (n.226-65G>A)
c.80G>A (p.Gly27Asp)
15g.40718821G>CCA268843915RAD51c.452G>C (p.Gly151Ala)
c.455G>C (p.Gly152Ala)
c.435+9705G>C (n.435+9705G>C)
c.*31G>C (n.*31G>C)
c.419G>C
c.226-65G>C (n.226-65G>C)
c.80G>C (p.Gly27Ala)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.40718821G=CA2171911654RAD51c.452G= (p.Gly151=)
c.455G= (p.Gly152=)
c.435+9705G= (n.435+9705G=)
c.*31G= (n.*31G=)
c.419G=
c.226-65G= (n.226-65G=)
c.80G= (p.Gly27=)
15g.40718821G>TCA391753290RAD51c.452G>T (p.Gly151Val)
c.455G>T (p.Gly152Val)
c.435+9705G>T (n.435+9705G>T)
c.*31G>T (n.*31G>T)
c.419G>T
c.226-65G>T (n.226-65G>T)
c.80G>T (p.Gly27Val)
15g.40718822T>ACA489772877RAD51c.453T>A (p.Gly151=)
c.456T>A (p.Gly152=)
c.435+9706T>A (n.435+9706T>A)
c.*32T>A (n.*32T>A)
c.420T>A
c.226-64T>A (n.226-64T>A)
c.81T>A (p.Gly27=)
15g.40718822T>CCA489772878RAD51c.453T>C (p.Gly151=)
c.456T>C (p.Gly152=)
c.435+9706T>C (n.435+9706T>C)
c.*32T>C (n.*32T>C)
c.420T>C
c.226-64T>C (n.226-64T>C)
c.81T>C (p.Gly27=)
ClinVar
15g.40718822T>GCA489772880RAD51c.453T>G (p.Gly151=)
c.456T>G (p.Gly152=)
c.435+9706T>G (n.435+9706T>G)
c.*32T>G (n.*32T>G)
c.420T>G
c.226-64T>G (n.226-64T>G)
c.81T>G (p.Gly27=)
ClinVar
15g.40718823G>ACA391753294RAD51c.454G>A (p.Gly152Arg)
c.457G>A (p.Gly153Arg)
c.435+9707G>A (n.435+9707G>A)
c.*33G>A (n.*33G>A)
c.421G>A
c.226-63G>A (n.226-63G>A)
c.82G>A (p.Gly28Arg)
15g.40718823G>CCA391753296RAD51c.454G>C (p.Gly152Arg)
c.457G>C (p.Gly153Arg)
c.435+9707G>C (n.435+9707G>C)
c.*33G>C (n.*33G>C)
c.421G>C
c.226-63G>C (n.226-63G>C)
c.82G>C (p.Gly28Arg)
15g.40718823G>TCA391753292RAD51c.454G>T (p.Gly152Ter)
c.457G>T (p.Gly153Ter)
c.435+9707G>T (n.435+9707G>T)
c.*33G>T (n.*33G>T)
c.421G>T
c.226-63G>T (n.226-63G>T)
c.82G>T (p.Gly28Ter)
15g.40718824G>ACA391753299RAD51c.455G>A (p.Gly152Glu)
c.458G>A (p.Gly153Glu)
c.435+9708G>A (n.435+9708G>A)
c.*34G>A (n.*34G>A)
c.422G>A
c.226-62G>A (n.226-62G>A)
c.83G>A (p.Gly28Glu)
15g.40718824G>CCA391753300RAD51c.455G>C (p.Gly152Ala)
c.458G>C (p.Gly153Ala)
c.435+9708G>C (n.435+9708G>C)
c.*34G>C (n.*34G>C)
c.422G>C
c.226-62G>C (n.226-62G>C)
c.83G>C (p.Gly28Ala)
15g.40718824G>TCA391753301RAD51c.455G>T (p.Gly152Val)
c.458G>T (p.Gly153Val)
c.435+9708G>T (n.435+9708G>T)
c.*34G>T (n.*34G>T)
c.422G>T
c.226-62G>T (n.226-62G>T)
c.83G>T (p.Gly28Val)
15g.40718825A=CA2171911655RAD51c.456A= (p.Gly152=)
c.459A= (p.Gly153=)
c.435+9709A= (n.435+9709A=)
c.*35A= (n.*35A=)
c.423A=
c.226-61A= (n.226-61A=)
c.84A= (p.Gly28=)
15g.40718825A>CCA489772881RAD51c.456A>C (p.Gly152=)
c.459A>C (p.Gly153=)
c.435+9709A>C (n.435+9709A>C)
c.*35A>C (n.*35A>C)
c.423A>C
c.226-61A>C (n.226-61A>C)
c.84A>C (p.Gly28=)
15g.40718825A>GCA489772882RAD51c.456A>G (p.Gly152=)
c.459A>G (p.Gly153=)
c.435+9709A>G (n.435+9709A>G)
c.*35A>G (n.*35A>G)
c.423A>G
c.226-61A>G (n.226-61A>G)
c.84A>G (p.Gly28=)
15g.40718825A>TCA268843921RAD51c.456A>T (p.Gly152=)
c.459A>T (p.Gly153=)
c.435+9709A>T (n.435+9709A>T)
c.*35A>T (n.*35A>T)
c.423A>T
c.226-61A>T (n.226-61A>T)
c.84A>T (p.Gly28=)
ClinVar dbSNP gnomAD v4
15g.40718826G>ACA391753304RAD51c.457G>A (p.Gly153Ser)
c.460G>A (p.Gly154Ser)
c.435+9710G>A (n.435+9710G>A)
c.*36G>A (n.*36G>A)
c.424G>A
c.226-60G>A (n.226-60G>A)
c.85G>A (p.Gly29Ser)
dbSNP
15g.40718826G>CCA391753306RAD51c.457G>C (p.Gly153Arg)
c.460G>C (p.Gly154Arg)
c.435+9710G>C (n.435+9710G>C)
c.*36G>C (n.*36G>C)
c.424G>C
c.226-60G>C (n.226-60G>C)
c.85G>C (p.Gly29Arg)
15g.40718826G>TCA391753308RAD51c.457G>T (p.Gly153Cys)
c.460G>T (p.Gly154Cys)
c.435+9710G>T (n.435+9710G>T)
c.*36G>T (n.*36G>T)
c.424G>T
c.226-60G>T (n.226-60G>T)
c.85G>T (p.Gly29Cys)
15g.40718827G>ACA391753310RAD51c.458G>A (p.Gly153Asp)
c.461G>A (p.Gly154Asp)
c.435+9711G>A (n.435+9711G>A)
c.*37G>A (n.*37G>A)
c.425G>A
c.226-59G>A (n.226-59G>A)
c.86G>A (p.Gly29Asp)
dbSNP gnomAD v2 gnomAD v4
15g.40718827G>CCA391753312RAD51c.458G>C (p.Gly153Ala)
c.461G>C (p.Gly154Ala)
c.435+9711G>C (n.435+9711G>C)
c.*37G>C (n.*37G>C)
c.425G>C
c.226-59G>C (n.226-59G>C)
c.86G>C (p.Gly29Ala)
15g.40718827G=CA2171911656RAD51c.458G= (p.Gly153=)
c.461G= (p.Gly154=)
c.435+9711G= (n.435+9711G=)
c.*37G= (n.*37G=)
c.425G=
c.226-59G= (n.226-59G=)
c.86G= (p.Gly29=)
15g.40718827G>TCA391753314RAD51c.458G>T (p.Gly153Val)
c.461G>T (p.Gly154Val)
c.435+9711G>T (n.435+9711G>T)
c.*37G>T (n.*37G>T)
c.425G>T
c.226-59G>T (n.226-59G>T)
c.86G>T (p.Gly29Val)
15g.40718828T>ACA489772884RAD51c.459T>A (p.Gly153=)
c.462T>A (p.Gly154=)
c.435+9712T>A (n.435+9712T>A)
c.*38T>A (n.*38T>A)
c.226-58T>A (n.226-58T>A)
c.87T>A (p.Gly29=)
15g.40718828T>CCA489772885RAD51c.459T>C (p.Gly153=)
c.462T>C (p.Gly154=)
c.435+9712T>C (n.435+9712T>C)
c.*38T>C (n.*38T>C)
c.226-58T>C (n.226-58T>C)
c.87T>C (p.Gly29=)
15g.40718828T>GCA489772886RAD51c.459T>G (p.Gly153=)
c.462T>G (p.Gly154=)
c.435+9712T>G (n.435+9712T>G)
c.*38T>G (n.*38T>G)
c.226-58T>G (n.226-58T>G)
c.87T>G (p.Gly29=)
15g.40718829G>ACA391753317RAD51c.460G>A (p.Glu154Lys)
c.463G>A (p.Glu155Lys)
c.435+9713G>A (n.435+9713G>A)
c.*39G>A (n.*39G>A)
c.226-57G>A (n.226-57G>A)
c.88G>A (p.Glu30Lys)
15g.40718829G>CCA391753320RAD51c.460G>C (p.Glu154Gln)
c.463G>C (p.Glu155Gln)
c.435+9713G>C (n.435+9713G>C)
c.*39G>C (n.*39G>C)
c.226-57G>C (n.226-57G>C)
c.88G>C (p.Glu30Gln)
15g.40718829G>TCA391753322RAD51c.460G>T (p.Glu154Ter)
c.463G>T (p.Glu155Ter)
c.435+9713G>T (n.435+9713G>T)
c.*39G>T (n.*39G>T)
c.226-57G>T (n.226-57G>T)
c.88G>T (p.Glu30Ter)
15g.40718830A>CCA391753328RAD51c.461A>C (p.Glu154Ala)
c.464A>C (p.Glu155Ala)
c.435+9714A>C (n.435+9714A>C)
c.*40A>C (n.*40A>C)
c.226-56A>C (n.226-56A>C)
c.89A>C (p.Glu30Ala)
15g.40718830A>GCA391753323RAD51c.461A>G (p.Glu154Gly)
c.464A>G (p.Glu155Gly)
c.435+9714A>G (n.435+9714A>G)
c.*40A>G (n.*40A>G)
c.226-56A>G (n.226-56A>G)
c.89A>G (p.Glu30Gly)
15g.40718830A>TCA391753326RAD51c.461A>T (p.Glu154Val)
c.464A>T (p.Glu155Val)
c.435+9714A>T (n.435+9714A>T)
c.*40A>T (n.*40A>T)
c.226-56A>T (n.226-56A>T)
c.89A>T (p.Glu30Val)
15g.40718831A>CCA391753329RAD51c.462A>C (p.Glu154Asp)
c.465A>C (p.Glu155Asp)
c.435+9715A>C (n.435+9715A>C)
c.*41A>C (n.*41A>C)
c.226-55A>C (n.226-55A>C)
c.90A>C (p.Glu30Asp)
15g.40718831A>GCA489772888RAD51c.462A>G (p.Glu154=)
c.465A>G (p.Glu155=)
c.435+9715A>G (n.435+9715A>G)
c.*41A>G (n.*41A>G)
c.226-55A>G (n.226-55A>G)
c.90A>G (p.Glu30=)
15g.40718831A>TCA391753332RAD51c.462A>T (p.Glu154Asp)
c.465A>T (p.Glu155Asp)
c.435+9715A>T (n.435+9715A>T)
c.*41A>T (n.*41A>T)
c.226-55A>T (n.226-55A>T)
c.90A>T (p.Glu30Asp)
15g.40718832G>ACA391753334RAD51c.463G>A (p.Gly155Arg)
c.466G>A (p.Gly156Arg)
c.435+9716G>A (n.435+9716G>A)
c.*42G>A (n.*42G>A)
c.226-54G>A (n.226-54G>A)
c.91G>A (p.Gly31Arg)

Number of alleles fetched