Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.106036712A>T | CA120670 | SERPINA7 | c.347T>A (p.Ile116Asn) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
X | g.106036712A= | CA2449829381 | SERPINA7 | c.347T= (p.Ile116=) | dbSNP |
X | g.106036712A>G | CA413876797 | SERPINA7 | c.347T>C (p.Ile116Thr) | dbSNP gnomAD v4 |