Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.122461760G>T | CA341903 | HTRA1 | c.108G>T (p.Gly36=) c.154+3051G>T (n.154+3051G>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.122461760G>C | CA341901 | HTRA1 | c.108G>C (p.Gly36=) c.154+3051G>C (n.154+3051G>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |