| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154997065A>T | CA255054 | F8 | c.296T>A (p.Val99Asp) c.*82T>A (n.*82T>A) c.191T>A (p.Val64Asp) c.278T>A (p.Val93Asp) | ClinVar dbSNP |
| X | g.154997065A>G | CA414920067 | F8 | c.296T>C (p.Val99Ala) c.*82T>C (n.*82T>C) c.191T>C (p.Val64Ala) c.278T>C (p.Val93Ala) | ClinVar dbSNP |
| X | g.154997065A= | CA2466857792 | F8 | c.296T= (p.Val99=) c.*82T= (n.*82T=) c.191T= (p.Val64=) c.278T= (p.Val93=) | dbSNP |