Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129528783C>ACA354495380RHOc.50C>A (p.Thr17Lys)
 ClinVar dbSNP
3g.129528783C>TCA256665RHOc.50C>T (p.Thr17Met)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129528783C=CA1401205042RHOc.50C= (p.Thr17=)
 dbSNP

Number of alleles fetched