| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.142541008C>A | CA345955 | ATR | c.3477G>T (p.Met1159Ile) c.*2251G>T (n.*2251G>T) n.3506G>T n.736G>T c.2267G>T c.3285G>T (p.Met1095Ile) n.3566G>T | ClinVar dbSNP gnomAD v4 |
| 3 | g.142541008C= | CA1407019850 | ATR | c.3477G= (p.Met1159=) c.*2251G= (n.*2251G=) n.3506G= n.736G= c.2267G= c.3285G= (p.Met1095=) n.3566G= | dbSNP |