Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.15641924T>G | CA278185 | BTD | c.266T>G (p.Val89Gly) n.1105T>G c.32T>G (p.Val11Gly) c.326T>G (p.Val109Gly) c.332T>G (p.Val111Gly) c.44T>G (p.Val15Gly) n.401T>G | dbSNP |
3 | g.15641924T= | CA1347644759 | BTD | c.266T= (p.Val89=) n.1105T= c.32T= (p.Val11=) c.326T= (p.Val109=) c.332T= (p.Val111=) c.44T= (p.Val15=) n.401T= | dbSNP |