| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.116277089C>A | CA16606071 | MED13L | c.43G>T (p.Glu15Ter) | ClinVar dbSNP gnomAD v4 |
| 12 | g.116277089C= | CA2065529013 | MED13L | c.43G= (p.Glu15=) | dbSNP |
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.116277089C>A | CA16606071 | MED13L | c.43G>T (p.Glu15Ter) | ClinVar dbSNP gnomAD v4 |
| 12 | g.116277089C= | CA2065529013 | MED13L | c.43G= (p.Glu15=) | dbSNP |