Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.35849310G>A | CA250273 | NPHS1 | c.766C>T (p.Arg256Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35849310G>C | CA9390664 | NPHS1 | c.766C>G (p.Arg256Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35849310G= | CA2333850839 | NPHS1 | c.766C= (p.Arg256=) | dbSNP |