| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.41348306C>T | CA308515302 | TGFB1 | c.505G>A (p.Glu169Lys) n.36G>A | dbSNP |
| 19 | g.41348306C>G | CA9460083 | TGFB1 | c.505G>C (p.Glu169Gln) n.36G>C | ClinVar dbSNP ExAC gnomAD v4 |
| 19 | g.41348306C= | CA2336423944 | TGFB1 | c.505G= (p.Glu169=) n.36G= | dbSNP |