Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.166228971A>T | CA118143 | SCN1A-AS1,SCN9A | c.3926T>A (p.Val1309Asp) c.3770T>A (p.Val1257Asp) c.3893T>A (p.Val1298Asp) n.612-19224A>T c.3539T>A (p.Val1180Asp) c.3182T>A (p.Val1061Asp) | ClinVar dbSNP |
2 | g.166228971A= | CA1304943724 | SCN1A-AS1,SCN9A | c.3926T= (p.Val1309=) c.3770T= (p.Val1257=) c.3893T= (p.Val1298=) n.612-19224A= c.3539T= (p.Val1180=) c.3182T= (p.Val1061=) | dbSNP |