| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154969518C>T | CA255072 | F8 | c.822G>A (p.Trp274Ter) c.*698G>A (n.*698G>A) c.717G>A (p.Trp239Ter) | ClinVar dbSNP |
| X | g.154969518C>A | CA337337669 | F8 | c.822G>T (p.Trp274Cys) c.*698G>T (n.*698G>T) c.717G>T (p.Trp239Cys) | dbSNP |
| X | g.154969518C= | CA2466849051 | F8 | c.822G= (p.Trp274=) c.*698G= (n.*698G=) c.717G= (p.Trp239=) | dbSNP |