Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.149487072A>T | CA348624 | IDS | c.1033T>A (p.Trp345Arg) c.400T>A (p.Trp134Arg) n.140T>A c.763T>A (p.Trp255Arg) | ClinVar dbSNP |
X | g.149487072A= | CA2465005594 | IDS | c.1033T= (p.Trp345=) c.400T= (p.Trp134=) n.140T= c.763T= (p.Trp255=) | dbSNP |