| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.139561749G>A | CA414445661 | F9 | c.1064G>A (p.Gly355Asp) n.1723+8G>A c.950G>A (p.Gly317Asp) c.935G>A (p.Gly312Asp) | dbSNP |
| X | g.139561749G>T | CA255386 | F9 | c.1064G>T (p.Gly355Val) n.1723+8G>T c.950G>T (p.Gly317Val) c.935G>T (p.Gly312Val) | ClinVar dbSNP |