Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.151289853C>T | CA1088645 | ZNF687 | c.2810C>T (p.Pro937Leu) c.1618C>T c.*112C>T (n.*112C>T) c.2837C>T (p.Pro946Leu) c.2633C>T (p.Pro878Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.151289853C>G | CA072935 | ZNF687 | c.2810C>G (p.Pro937Arg) c.1618C>G c.*112C>G (n.*112C>G) c.2837C>G (p.Pro946Arg) c.2633C>G (p.Pro878Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.151289853C>A | CA1088644 | ZNF687 | c.2810C>A (p.Pro937His) c.1618C>A c.*112C>A (n.*112C>A) c.2837C>A (p.Pro946His) c.2633C>A (p.Pro878His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |