Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.122506796G>A | CA342726 | HTRA1 | c.883G>A (p.Gly295Arg) c.565G>A (p.Gly189Arg) c.106G>A (p.Gly36Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
10 | g.122506796G>C | CA5725960 | HTRA1 | c.883G>C (p.Gly295Arg) c.565G>C (p.Gly189Arg) c.106G>C (p.Gly36Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |