Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.119509176A>GCA3382214HSD17B4c.1369A>G (p.Asn457Asp)
c.1444A>G (p.Asn482Asp)
c.1315A>G (p.Asn439Asp)
c.1297A>G (p.Asn433Asp)
c.949A>G (p.Asn317Asp)
c.583A>G (p.Asn195Asp)
c.958A>G (p.Asn320Asp)
n.3122A>G
n.503A>G
n.152A>G
n.36A>G
ClinVar dbSNP ExAC gnomAD
5g.119509176A>TCA118961HSD17B4c.1369A>T (p.Asn457Tyr)
c.1444A>T (p.Asn482Tyr)
c.1315A>T (p.Asn439Tyr)
c.1297A>T (p.Asn433Tyr)
c.949A>T (p.Asn317Tyr)
c.583A>T (p.Asn195Tyr)
c.958A>T (p.Asn320Tyr)
n.3122A>T
n.503A>T
n.152A>T
n.36A>T
ClinVar dbSNP ExAC gnomAD

Number of alleles fetched