Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.43120144T>G | CA008989 | RET | c.2275T>G (p.Ser759Ala) n.2245T>G n.2236T>G c.2671T>G (p.Ser891Ala) c.*1265T>G (n.*1265T>G) c.*20T>G (n.*20T>G) c.1909T>G (p.Ser637Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.43120144T= | CA1905819918 | RET | c.2275T= (p.Ser759=) n.2245T= n.2236T= c.2671T= (p.Ser891=) c.*1265T= (n.*1265T=) c.*20T= (n.*20T=) c.1909T= (p.Ser637=) | dbSNP |