Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.20425445del | CA170612 | SCARF2 | c.2531del (p.Gln844ArgfsTer?) c.2543del (p.Gln848ArgfsTer?) c.2546del (p.Gln849ArgfsTer?) | ClinVar dbSNP |
22 | g.20425445T= | CA3244240238 | SCARF2 | c.2531A= (p.Gln844=) c.2543A= (p.Gln848=) c.2546A= (p.Gln849=) | dbSNP |