Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154947846G>C | CA255133 | F8 | c.1965C>G (p.Tyr655Ter) c.*1779+6046C>G (n.*1779+6046C>G) c.1860C>G (p.Tyr620Ter) | ClinVar dbSNP |
X | g.154947846G= | CA2466842566 | F8 | c.1965C= (p.Tyr655=) c.*1779+6046C= (n.*1779+6046C=) c.1860C= (p.Tyr620=) | dbSNP |