Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129529049G>TCA256669RHOc.316G>T (p.Gly106Trp)
ClinVar dbSNP
3g.129529049G>CCA354496864RHOc.316G>C (p.Gly106Arg)
ClinVar dbSNP
3g.129529049G>ACA256683RHOc.316G>A (p.Gly106Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129529049G=CA1401206060RHOc.316G= (p.Gly106=)
dbSNP

Number of alleles fetched