Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107663427C>TCA4432413SLC26A4c.296C>T (p.Thr99Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
7g.107663427C>ACA164209206SLC26A4c.296C>A (p.Thr99Lys)
 dbSNP gnomAD v2 gnomAD v4
7g.107663427C>GCA16616708SLC26A4c.296C>G (p.Thr99Arg)
 ClinVar dbSNP

Number of alleles fetched