Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.36219873del | CA16041309 | CLTA,GNE | c.1874del (p.Met625ArgfsTer?) c.1604del (p.Met535ArgfsTer?) c.1781del (p.Met594ArgfsTer?) c.1559del (p.Met520ArgfsTer?) c.485+15694del (n.485+15694del) c.1451del (p.Met484ArgfsTer?) c.1766del (p.Met589ArgfsTer?) c.1721del (p.Met574ArgfsTer?) c.1628del (p.Met543ArgfsTer?) | ClinVar dbSNP |
9 | g.36219873A= | CA1846328501 | CLTA,GNE | c.1874T= (p.Met625=) c.1604T= (p.Met535=) c.1781T= (p.Met594=) c.1559T= (p.Met520=) c.485+15694A= (n.485+15694A=) c.1451T= (p.Met484=) c.1766T= (p.Met589=) c.1721T= (p.Met574=) c.1628T= (p.Met543=) | dbSNP dbSNP |