Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.36234106G>A | CA340501 | CLTA,GNE | c.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 |
9 | g.36234106G= | CA1846355728 | CLTA,GNE | c.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 |