Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.6182121G>TCA126618F13A1c.1326C>A (p.Tyr442Ter)
c.1488C>A (p.Tyr496Ter)
ClinVar dbSNP gnomAD v4
6g.6182121G>ACA3624370F13A1c.1326C>T (p.Tyr442=)
c.1488C>T (p.Tyr496=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched