Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.108208948A>G | CA16609403 | LIG4 | c.2120T>C (p.Leu707Pro) c.2321T>C (p.Leu774Pro) c.2357T>C (p.Leu786Pro) c.2333T>C (p.Leu778Pro) | ClinVar dbSNP gnomAD v4 |
13 | g.108208948A= | CA2117793985 | LIG4 | c.2120T= (p.Leu707=) c.2321T= (p.Leu774=) c.2357T= (p.Leu786=) c.2333T= (p.Leu778=) | dbSNP |