Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154906468C>G | CA255160 | F8 | c.5325G>C (p.Leu1775Phe) c.5220G>C (p.Leu1740Phe) | ClinVar dbSNP |
X | g.154906468C>T | CA519357998 | F8 | c.5325G>A (p.Leu1775=) c.5220G>A (p.Leu1740=) | dbSNP gnomAD v4 |
X | g.154906468C= | CA2466828925 | F8 | c.5325G= (p.Leu1775=) c.5220G= (p.Leu1740=) | dbSNP |