Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41583585T>ACA399476463KRT14c.1019A>T (p.Asn340Ile)
n.469A>T
dbSNP gnomAD v4
17g.41583585T>CCA399476465KRT14c.1019A>G (p.Asn340Ser)
n.469A>G
gnomAD v4
17g.41583585T>GCA399476468KRT14c.1019A>C (p.Asn340Thr)
n.469A>C
dbSNP
17g.41583585T=CA2260085465KRT14c.1019A= (p.Asn340=)
n.469A=
17g.41583586T>ACA399476471KRT14c.1018A>T (p.Asn340Tyr)
n.468A>T
17g.41583586T>CCA399476473KRT14c.1018A>G (p.Asn340Asp)
n.468A>G
17g.41583586T>GCA399476475KRT14c.1018A>C (p.Asn340His)
n.468A>C
17g.41583587C>ACA399476478KRT14c.1017G>T (p.Gln339His)
n.467G>T
17g.41583587C>GCA399476480KRT14c.1017G>C (p.Gln339His)
n.467G>C
17g.41583587C>TCA500205375KRT14c.1017G>A (p.Gln339=)
n.467G>A
17g.41583588T>ACA399476483KRT14c.1016A>T (p.Gln339Leu)
n.466A>T
17g.41583588T>CCA399476484KRT14c.1016A>G (p.Gln339Arg)
n.466A>G
17g.41583588T>GCA399476486KRT14c.1016A>C (p.Gln339Pro)
n.466A>C
17g.41583589G>ACA399476492KRT14c.1015C>T (p.Gln339Ter)
n.465C>T
17g.41583589G>CCA399476490KRT14c.1015C>G (p.Gln339Glu)
n.465C>G
dbSNP gnomAD v2 gnomAD v4
17g.41583589G=CA2260085466KRT14c.1015C= (p.Gln339=)
n.465C=
17g.41583589G>TCA399476489KRT14c.1015C>A (p.Gln339Lys)
n.465C>A
17g.41583590C>ACA399476496KRT14c.1014G>T (p.Met338Ile)
n.464G>T
17g.41583590C=CA2260085467KRT14c.1014G= (p.Met338=)
n.464G=
17g.41583590C>GCA399476498KRT14c.1014G>C (p.Met338Ile)
n.464G>C
gnomAD v4
17g.41583590C>TCA399476500KRT14c.1014G>A (p.Met338Ile)
n.464G>A
dbSNP gnomAD v2 gnomAD v4
17g.41583591A=CA2260085468KRT14c.1013T= (p.Met338=)
n.463T=
17g.41583591A>CCA8562536KRT14c.1013T>G (p.Met338Arg)
n.463T>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583591A>GCA8562537KRT14c.1013T>C (p.Met338Thr)
n.463T>C
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583591A>TCA399476507KRT14c.1013T>A (p.Met338Lys)
n.463T>A
17g.41583592T>ACA399476511KRT14c.1012A>T (p.Met338Leu)
n.462A>T
17g.41583592T>CCA399476513KRT14c.1012A>G (p.Met338Val)
n.462A>G
dbSNP
17g.41583592T>GCA399476515KRT14c.1012A>C (p.Met338Leu)
n.462A>C
17g.41583592_41583600delinsTGGTGCGCCCA2260085469KRT14c.1004_1012delinsGGCGCACCA (p.Arg335=)
n.454_462delinsGGCGCACCA
17g.41583593G>ACA500205377KRT14c.1011C>T (p.Thr337=)
n.461C>T
dbSNP gnomAD v3 gnomAD v4
17g.41583593G>CCA8562538KRT14c.1011C>G (p.Thr337=)
n.461C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583593G=CA2260085471KRT14c.1011C= (p.Thr337=)
n.461C=
17g.41583593G>TCA500205376KRT14c.1011C>A (p.Thr337=)
n.461C>A
17g.41583595_41583602delCA2260085470KRT14c.1004_1011del (p.Arg335HisfsTer7)
n.454_461del
dbSNP
17g.41583594G>ACA399476520KRT14c.1010C>T (p.Thr337Ile)
n.460C>T
COSMIC
17g.41583594G>CCA399476523KRT14c.1010C>G (p.Thr337Ser)
n.460C>G
17g.41583594G>TCA399476526KRT14c.1010C>A (p.Thr337Asn)
n.460C>A
17g.41583595T>ACA399476533KRT14c.1009A>T (p.Thr337Ser)
n.459A>T
COSMIC
17g.41583595T>CCA399476529KRT14c.1009A>G (p.Thr337Ala)
n.459A>G
dbSNP gnomAD v4
17g.41583595T>GCA399476531KRT14c.1009A>C (p.Thr337Pro)
n.459A>C
dbSNP gnomAD v2 gnomAD v4
17g.41583595T=CA2260085472KRT14c.1009A= (p.Thr337=)
n.459A=
17g.41583596G>ACA500205378KRT14c.1008C>T (p.Arg336=)
n.458C>T
dbSNP gnomAD v3 gnomAD v4
17g.41583596G>CCA500205379KRT14c.1008C>G (p.Arg336=)
n.458C>G
17g.41583596G=CA2260085473KRT14c.1008C= (p.Arg336=)
n.458C=
17g.41583596G>TCA500205380KRT14c.1008C>A (p.Arg336=)
n.458C>A
17g.41583597C>ACA399476534KRT14c.1007G>T (p.Arg336Leu)
n.457G>T
17g.41583597C=CA2260085474KRT14c.1007G= (p.Arg336=)
n.457G=
17g.41583597C>GCA399476536KRT14c.1007G>C (p.Arg336Pro)
n.457G>C
dbSNP
17g.41583597C>TCA8562539KRT14c.1007G>A (p.Arg336His)
n.457G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.41583598G>ACA8562540KRT14c.1006C>T (p.Arg336Cys)
n.456C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched