Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107690200G>ACA261401SLC26A4c.1226G>A (p.Arg409His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107690200G>CCA261402SLC26A4c.1226G>C (p.Arg409Pro)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.107690200G>TCA368839267SLC26A4c.1226G>T (p.Arg409Leu)
ClinVar dbSNP gnomAD v4
7g.107690200G=CA1732748383SLC26A4c.1226G= (p.Arg409=)
dbSNP

Number of alleles fetched