Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.17821329T>A | CA404761565 | INSL3 | c.178A>T (p.Thr60Ser) c.177A>T | dbSNP gnomAD v4 |
19 | g.17821329T>C | CA9301295 | INSL3 | c.178A>G (p.Thr60Ala) c.177A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.17821329T>G | CA404761567 | INSL3 | c.178A>C (p.Thr60Pro) c.177A>C | dbSNP gnomAD v4 |