Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.36234106G>ACA340501CLTA,GNEc.889C>T (p.Arg297Trp)
c.619C>T (p.Arg207Trp)
c.796C>T (p.Arg266Trp)
c.486-29092G>A (n.486-29092G>A)
c.466C>T (p.Arg156Trp)
c.781C>T (p.Arg261Trp)
c.736C>T (p.Arg246Trp)
c.643C>T (p.Arg215Trp)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC
9g.36234106G=CA1846355728CLTA,GNEc.889C= (p.Arg297=)
c.619C= (p.Arg207=)
c.796C= (p.Arg266=)
c.486-29092G= (n.486-29092G=)
c.466C= (p.Arg156=)
c.781C= (p.Arg261=)
c.736C= (p.Arg246=)
c.643C= (p.Arg215=)
dbSNP

Number of alleles fetched