Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.94606867C>G | CA374106775 | FBP1 | c.813G>C (n.813G>C) c.653G>C (p.Arg218Thr) c.458G>C (p.Arg153Thr) c.401G>C (p.Arg134Thr) c.407G>C (p.Arg136Thr) | dbSNP |
9 | g.94606867C>A | CA374106773 | FBP1 | c.813G>T (n.813G>T) c.653G>T (p.Arg218Met) c.458G>T (p.Arg153Met) c.401G>T (p.Arg134Met) c.407G>T (p.Arg136Met) | dbSNP |
9 | g.94606867C>T | CA5136172 | FBP1 | c.813G>A (n.813G>A) c.653G>A (p.Arg218Lys) c.458G>A (p.Arg153Lys) c.401G>A (p.Arg134Lys) c.407G>A (p.Arg136Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |