Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.43100480C>GCA376770079RETc.95C>G (p.Ser32Trp)
c.74-10727C>G (n.74-10727C>G)
c.74-11619C>G (n.74-11619C>G)
ClinVar dbSNP
10g.43100480C>ACA376770078RETc.95C>A (p.Ser32Ter)
c.74-10727C>A (n.74-10727C>A)
c.74-11619C>A (n.74-11619C>A)
dbSNP
10g.43100480C>TCA009398RETc.95C>T (p.Ser32Leu)
c.74-10727C>T (n.74-10727C>T)
c.74-11619C>T (n.74-11619C>T)
ClinVar dbSNP gnomAD v4
10g.43100480C=CA1905836755RETc.95C= (p.Ser32=)
c.74-10727C= (n.74-10727C=)
c.74-11619C= (n.74-11619C=)
dbSNP

Number of alleles fetched