Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.186285723C>TCA16040948F11c.1390C>T (p.Gln464Ter)
c.86C>T
c.1228C>T (p.Gln410Ter)
c.1393C>T (p.Gln465Ter)
c.1123C>T (p.Gln375Ter)
c.1345C>T (p.Gln449Ter)
n.1798C>T
n.1864C>T
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
4g.186285723C=CA1519938520F11c.1390C= (p.Gln464=)
c.86C=
c.1228C= (p.Gln410=)
c.1393C= (p.Gln465=)
c.1123C= (p.Gln375=)
c.1345C= (p.Gln449=)
n.1798C=
n.1864C=
dbSNP

Number of alleles fetched