Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.92476153T>G | CA341147856 | GFI1 | c.1145A>C (p.Asn382Thr) c.193A>C (p.Thr65Pro) | dbSNP |
1 | g.92476153T>C | CA119872 | GFI1 | c.1145A>G (p.Asn382Ser) c.193A>G (p.Thr65Ala) | ClinVar dbSNP |
1 | g.92476153T= | CA1140495682 | GFI1 | c.1145A= (p.Asn382=) c.193A= (p.Thr65=) | dbSNP |