Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.122488926G>A | CA378579777 | HTRA1 | c.497G>A (p.Arg166His) c.179G>A (p.Arg60His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
10 | g.122488926G>T | CA350920 | HTRA1 | c.497G>T (p.Arg166Leu) c.179G>T (p.Arg60Leu) | ClinVar dbSNP |
10 | g.122488926G= | CA1941464053 | HTRA1 | c.497G= (p.Arg166=) c.179G= (p.Arg60=) | dbSNP |