| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.179575761C>A | CA343553832 | NPHS2 | c.104G>T (p.Gly35Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.179575761C>T | CA10581522 | NPHS2 | c.104G>A (p.Gly35Asp) | ClinVar dbSNP gnomAD v4 |
| 1 | g.179575761C= | CA1210326721 | NPHS2 | c.104G= (p.Gly35=) | dbSNP |