| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.35851260A>G | CA16041983 | NPHS1 | c.397+2T>C (n.397+2T>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.35851260A>T | CA405410442 | NPHS1 | c.397+2T>A (n.397+2T>A) | ClinVar dbSNP |
| 19 | g.35851260A= | CA2333851744 | NPHS1 | c.397+2T= (n.397+2T=) | dbSNP |