Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.77453359C>T | CA235912 | VIPAS39 | c.136G>A (p.Val46Met) n.26G>A c.214G>A (p.Val72Met) c.136G>A n.258G>A n.243G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.77453359C>A | CA390699658 | VIPAS39 | c.136G>T (p.Val46Leu) n.26G>T c.214G>T (p.Val72Leu) c.136G>T n.258G>T n.243G>T | dbSNP gnomAD v4 |
14 | g.77453359C= | CA2148401099 | VIPAS39 | c.136G= (p.Val46=) n.26G= c.214G= (p.Val72=) c.136G= n.258G= n.243G= | dbSNP |