Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128848680G>T | CA369202763 | FLNC | c.4700G>T (p.Arg1567Leu) | ClinVar dbSNP |
7 | g.128848680G>A | CA152865 | FLNC | c.4700G>A (p.Arg1567Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128848680G>C | CA166184144 | FLNC | c.4700G>C (p.Arg1567Pro) | dbSNP gnomAD v4 |
7 | g.128848680G= | CA1742561783 | FLNC | c.4700G= (p.Arg1567=) | dbSNP |