| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89268645G>A | CA204730 | ANKRD11 | c.7825C>T (p.Gln2609Ter) c.*7628C>T (n.*7628C>T) c.1099C>T (p.Gln367Ter) c.506C>T c.7723C>T (p.Gln2575Ter) c.7528C>T (p.Gln2510Ter) c.7696C>T (p.Gln2566Ter) | ClinVar dbSNP gnomAD v4 |
| 16 | g.89268645G= | CA2241594820 | ANKRD11 | c.7825C= (p.Gln2609=) c.*7628C= (n.*7628C=) c.1099C= (p.Gln367=) c.506C= c.7723C= (p.Gln2575=) c.7528C= (p.Gln2510=) c.7696C= (p.Gln2566=) | dbSNP |