| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.108580543G>A | CA258325 | COL4A5 | c.791G>A (p.Gly264Asp) c.467G>A (p.Gly156Asp) c.806G>A (p.Gly269Asp) | dbSNP |
| X | g.108580543G= | CA2450683019 | COL4A5 | c.791G= (p.Gly264=) c.467G= (p.Gly156=) c.806G= (p.Gly269=) | dbSNP |
| X | g.108580543G>T | CA413925603 | COL4A5 | c.791G>T (p.Gly264Val) c.467G>T (p.Gly156Val) c.806G>T (p.Gly269Val) | dbSNP COSMIC COSMIC |