Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.42001654A>G | CA2902149 | SLC30A9 | c.148A>G (p.Met50Val) n.273A>G n.298A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.42001654A>C | CA356745450 | SLC30A9 | c.148A>C (p.Met50Leu) n.273A>C n.298A>C | dbSNP gnomAD v4 |
4 | g.42001654A= | CA2581416045 | SLC30A9 | c.148A= (p.Met50=) n.273A= n.298A= | dbSNP |