Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.81752250C>TCA257399HGFc.495G>A (p.Ser165=)
c.483-3G>A (n.483-3G>A)
n.511-3G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
7g.81752250C>ACA456129497HGFc.495G>T (p.Ser165=)
c.483-3G>T (n.483-3G>T)
n.511-3G>T
dbSNP
7g.81752250C>GCA456129498HGFc.495G>C (p.Ser165=)
c.483-3G>C (n.483-3G>C)
n.511-3G>C
dbSNP

Number of alleles fetched