Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154969360A>T | CA414917674 | F8 | c.980T>A (p.Leu327Gln) c.*856T>A (n.*856T>A) c.875T>A (p.Leu292Gln) | dbSNP |
X | g.154969360A>G | CA255086 | F8 | c.980T>C (p.Leu327Pro) c.*856T>C (n.*856T>C) c.875T>C (p.Leu292Pro) | ClinVar dbSNP |
X | g.154969360A= | CA2466848978 | F8 | c.980T= (p.Leu327=) c.*856T= (n.*856T=) c.875T= (p.Leu292=) | dbSNP |