Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.153694424C>TCA10549526SLC6A8c.1473C>T (p.Cys491=)
c.402C>T (p.Cys134=)
c.1128C>T (p.Cys376=)
n.1694C>T
c.1443C>T (p.Cys481=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
Xg.153694424C>GCA256015SLC6A8c.1473C>G (p.Cys491Trp)
c.402C>G (p.Cys134Trp)
c.1128C>G (p.Cys376Trp)
n.1694C>G
c.1443C>G (p.Cys481Trp)
ClinVar dbSNP

Number of alleles fetched