Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.106036488C>G | CA413876303 | SERPINA7 | c.571G>C (p.Asp191His) | dbSNP gnomAD v2 gnomAD v4 |
X | g.106036488C>T | CA120665 | SERPINA7 | c.571G>A (p.Asp191Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
X | g.106036488C= | CA2449829297 | SERPINA7 | c.571G= (p.Asp191=) | dbSNP |