| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.43109146C>A | CA007467 | RET | c.868-2061C>A (n.868-2061C>A) n.753C>A c.1179C>A (p.Phe393Leu) c.626-2061C>A (n.626-2061C>A) c.74-2061C>A (n.74-2061C>A) c.74-2953C>A (n.74-2953C>A) c.417C>A (p.Phe139Leu) | ClinVar dbSNP |
| 10 | g.43109146C= | CA1905810886 | RET | c.868-2061C= (n.868-2061C=) n.753C= c.1179C= (p.Phe393=) c.626-2061C= (n.626-2061C=) c.74-2061C= (n.74-2061C=) c.74-2953C= (n.74-2953C=) c.417C= (p.Phe139=) | dbSNP |