Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.29226961G>ACA346467602ALKc.3028C>T (p.His1010Tyr)
c.194C>T
c.1897C>T (p.His633Tyr)
c.181C>T (p.His61Tyr)
n.3884C>T
 dbSNP
2g.29226961G>CCA346467603ALKc.3028C>G (p.His1010Asp)
c.194C>G
c.1897C>G (p.His633Asp)
c.181C>G (p.His61Asp)
n.3884C>G
 dbSNP
2g.29226961G>TCA346467604ALKc.3028C>A (p.His1010Asn)
c.194C>A
c.1897C>A (p.His633Asn)
c.181C>A (p.His61Asn)
n.3884C>A
 dbSNP
2g.29226962G>ACA425435938ALKc.3027C>T (p.Asp1009=)
c.193C>T
c.1896C>T (p.Asp632=)
c.180C>T (p.Asp60=)
n.3883C>T
 ClinVar
2g.29226962G>CCA346467605ALKc.3027C>G (p.Asp1009Glu)
c.193C>G
c.1896C>G (p.Asp632Glu)
c.180C>G (p.Asp60Glu)
n.3883C>G
 dbSNP
2g.29226962G>TCA346467606ALKc.3027C>A (p.Asp1009Glu)
c.193C>A
c.1896C>A (p.Asp632Glu)
c.180C>A (p.Asp60Glu)
n.3883C>A
 ClinVar dbSNP
2g.29226963T>ACA346467607ALKc.3026A>T (p.Asp1009Val)
c.192A>T
c.1895A>T (p.Asp632Val)
c.179A>T (p.Asp60Val)
n.3882A>T
2g.29226963T>CCA346467608ALKc.3026A>G (p.Asp1009Gly)
c.192A>G
c.1895A>G (p.Asp632Gly)
c.179A>G (p.Asp60Gly)
n.3882A>G
 dbSNP
2g.29226963T>GCA346467609ALKc.3026A>C (p.Asp1009Ala)
c.192A>C
c.1895A>C (p.Asp632Ala)
c.179A>C (p.Asp60Ala)
n.3882A>C
2g.29226964C>ACA346467611ALKc.3025G>T (p.Asp1009Tyr)
c.191G>T
c.1894G>T (p.Asp632Tyr)
c.178G>T (p.Asp60Tyr)
n.3881G>T
 dbSNP
2g.29226964C=CA1241092849ALKc.3025G= (p.Asp1009=)
c.191G=
c.1894G= (p.Asp632=)
c.178G= (p.Asp60=)
n.3881G=
2g.29226964C>GCA1594112ALKc.3025G>C (p.Asp1009His)
c.191G>C
c.1894G>C (p.Asp632His)
c.178G>C (p.Asp60His)
n.3881G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.29226964C>TCA346467610ALKc.3025G>A (p.Asp1009Asn)
c.191G>A
c.1894G>A (p.Asp632Asn)
c.178G>A (p.Asp60Asn)
n.3881G>A
 dbSNP COSMIC
2g.29226965A>CCA346467612ALKc.3024T>G (p.Cys1008Trp)
c.190T>G
c.1893T>G (p.Cys631Trp)
c.177T>G (p.Cys59Trp)
n.3880T>G
 dbSNP
2g.29226965A>GCA425435942ALKc.3024T>C (p.Cys1008=)
c.190T>C
c.1893T>C (p.Cys631=)
c.177T>C (p.Cys59=)
n.3880T>C
 gnomAD v4
2g.29226965A>TCA346467613ALKc.3024T>A (p.Cys1008Ter)
c.190T>A
c.1893T>A (p.Cys631Ter)
c.177T>A (p.Cys59Ter)
n.3880T>A
 dbSNP
2g.29226966C>ACA346467614ALKc.3023G>T (p.Cys1008Phe)
c.189G>T
c.1892G>T (p.Cys631Phe)
c.176G>T (p.Cys59Phe)
n.3879G>T
2g.29226966C>GCA346467615ALKc.3023G>C (p.Cys1008Ser)
c.189G>C
c.1892G>C (p.Cys631Ser)
c.176G>C (p.Cys59Ser)
n.3879G>C
 dbSNP
2g.29226966C>TCA346467616ALKc.3023G>A (p.Cys1008Tyr)
c.189G>A
c.1892G>A (p.Cys631Tyr)
c.176G>A (p.Cys59Tyr)
n.3879G>A
 dbSNP
2g.29226967A>CCA346467619ALKc.3022T>G (p.Cys1008Gly)
c.188T>G
c.1891T>G (p.Cys631Gly)
c.175T>G (p.Cys59Gly)
n.3878T>G
2g.29226967A>GCA346467617ALKc.3022T>C (p.Cys1008Arg)
c.188T>C
c.1891T>C (p.Cys631Arg)
c.175T>C (p.Cys59Arg)
n.3878T>C
 dbSNP
2g.29226967A>TCA346467618ALKc.3022T>A (p.Cys1008Ser)
c.188T>A
c.1891T>A (p.Cys631Ser)
c.175T>A (p.Cys59Ser)
n.3878T>A
2g.29226968G>ACA425435946ALKc.3021C>T (p.Phe1007=)
c.187C>T
c.1890C>T (p.Phe630=)
c.174C>T (p.Phe58=)
n.3877C>T
 dbSNP
2g.29226968G>CCA346467620ALKc.3021C>G (p.Phe1007Leu)
c.187C>G
c.1890C>G (p.Phe630Leu)
c.174C>G (p.Phe58Leu)
n.3877C>G
 dbSNP
2g.29226968G>TCA346467621ALKc.3021C>A (p.Phe1007Leu)
c.187C>A
c.1890C>A (p.Phe630Leu)
c.174C>A (p.Phe58Leu)
n.3877C>A
2g.29226969A=CA1241092850ALKc.3020T= (p.Phe1007=)
c.186T=
c.1889T= (p.Phe630=)
c.173T= (p.Phe58=)
n.3876T=
2g.29226969A>CCA346467622ALKc.3020T>G (p.Phe1007Cys)
c.186T>G
c.1889T>G (p.Phe630Cys)
c.173T>G (p.Phe58Cys)
n.3876T>G
2g.29226969A>GCA346467623ALKc.3020T>C (p.Phe1007Ser)
c.186T>C
c.1889T>C (p.Phe630Ser)
c.173T>C (p.Phe58Ser)
n.3876T>C
 ClinVar dbSNP
2g.29226969A>TCA346467624ALKc.3020T>A (p.Phe1007Tyr)
c.186T>A
c.1889T>A (p.Phe630Tyr)
c.173T>A (p.Phe58Tyr)
n.3876T>A
 dbSNP
2g.29226970A=CA1241092851ALKc.3019T= (p.Phe1007=)
c.185T=
c.1888T= (p.Phe630=)
c.172T= (p.Phe58=)
n.3875T=
2g.29226970A>CCA346467627ALKc.3019T>G (p.Phe1007Val)
c.185T>G
c.1888T>G (p.Phe630Val)
c.172T>G (p.Phe58Val)
n.3875T>G
 ClinVar dbSNP gnomAD v4
2g.29226970A>GCA346467626ALKc.3019T>C (p.Phe1007Leu)
c.185T>C
c.1888T>C (p.Phe630Leu)
c.172T>C (p.Phe58Leu)
n.3875T>C
2g.29226970A>TCA346467625ALKc.3019T>A (p.Phe1007Ile)
c.185T>A
c.1888T>A (p.Phe630Ile)
c.172T>A (p.Phe58Ile)
n.3875T>A
2g.29226971G>ACA425435949ALKc.3018C>T (p.Cys1006=)
c.184C>T
c.1887C>T (p.Cys629=)
c.171C>T (p.Cys57=)
n.3874C>T
 ClinVar dbSNP
2g.29226971G>CCA346467628ALKc.3018C>G (p.Cys1006Trp)
c.184C>G
c.1887C>G (p.Cys629Trp)
c.171C>G (p.Cys57Trp)
n.3874C>G
 dbSNP
2g.29226971G=CA1241092852ALKc.3018C= (p.Cys1006=)
c.184C=
c.1887C= (p.Cys629=)
c.171C= (p.Cys57=)
n.3874C=
2g.29226971G>TCA346467629ALKc.3018C>A (p.Cys1006Ter)
c.184C>A
c.1887C>A (p.Cys629Ter)
c.171C>A (p.Cys57Ter)
n.3874C>A
 dbSNP
2g.29226972C>ACA346467630ALKc.3017G>T (p.Cys1006Phe)
c.183G>T
c.1886G>T (p.Cys629Phe)
c.170G>T (p.Cys57Phe)
n.3873G>T
 ClinVar dbSNP gnomAD v4
2g.29226972C=CA1241092853ALKc.3017G= (p.Cys1006=)
c.183G=
c.1886G= (p.Cys629=)
c.170G= (p.Cys57=)
n.3873G=
2g.29226972C>GCA346467631ALKc.3017G>C (p.Cys1006Ser)
c.183G>C
c.1886G>C (p.Cys629Ser)
c.170G>C (p.Cys57Ser)
n.3873G>C
 dbSNP
2g.29226972C>TCA346467632ALKc.3017G>A (p.Cys1006Tyr)
c.183G>A
c.1886G>A (p.Cys629Tyr)
c.170G>A (p.Cys57Tyr)
n.3873G>A
 dbSNP COSMIC
2g.29226973A>CCA346467633ALKc.3016T>G (p.Cys1006Gly)
c.182T>G
c.1885T>G (p.Cys629Gly)
c.169T>G (p.Cys57Gly)
n.3872T>G
2g.29226973A>GCA346467634ALKc.3016T>C (p.Cys1006Arg)
c.182T>C
c.1885T>C (p.Cys629Arg)
c.169T>C (p.Cys57Arg)
n.3872T>C
 gnomAD v4
2g.29226973A>TCA346467635ALKc.3016T>A (p.Cys1006Ser)
c.182T>A
c.1885T>A (p.Cys629Ser)
c.169T>A (p.Cys57Ser)
n.3872T>A
2g.29226974G>ACA425435954ALKc.3015C>T (p.Ile1005=)
c.181C>T
c.1884C>T (p.Ile628=)
c.168C>T (p.Ile56=)
n.3871C>T
 dbSNP
2g.29226974G>CCA346467636ALKc.3015C>G (p.Ile1005Met)
c.181C>G
c.1884C>G (p.Ile628Met)
c.168C>G (p.Ile56Met)
n.3871C>G
 dbSNP
2g.29226974G>TCA425435953ALKc.3015C>A (p.Ile1005=)
c.181C>A
c.1884C>A (p.Ile628=)
c.168C>A (p.Ile56=)
n.3871C>A
2g.29226975A=CA1241092854ALKc.3014T= (p.Ile1005=)
c.180T=
c.1883T= (p.Ile628=)
c.167T= (p.Ile56=)
n.3870T=
2g.29226975A>CCA346467637ALKc.3014T>G (p.Ile1005Ser)
c.180T>G
c.1883T>G (p.Ile628Ser)
c.167T>G (p.Ile56Ser)
n.3870T>G
 dbSNP
2g.29226975A>GCA346467638ALKc.3014T>C (p.Ile1005Thr)
c.180T>C
c.1883T>C (p.Ile628Thr)
c.167T>C (p.Ile56Thr)
n.3870T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched