| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.9808128G>A | CA10584394 | SBF2,SBF2-AS1 | n.799C>T c.2878C>T (p.Gln960Ter) n.851C>T c.4390C>T (p.Gln1464Ter) c.*623C>T (n.*623C>T) c.4372C>T (p.Gln1458Ter) c.3922C>T (p.Gln1308Ter) c.4411C>T (p.Gln1471Ter) c.4252C>T (p.Gln1418Ter) c.481C>T n.1486C>T c.3019C>T (p.Gln1007Ter) c.4309C>T (p.Gln1437Ter) c.522C>T n.791C>T c.4186C>T (p.Gln1396Ter) n.1234C>T c.4315C>T (p.Gln1439Ter) n.383C>T c.4174C>T (p.Gln1392Ter) n.492G>A c.4282C>T (p.Gln1428Ter) c.4297C>T (p.Gln1433Ter) c.4273C>T (p.Gln1425Ter) n.4549C>T | ClinVar dbSNP |
| 11 | g.9808128G= | CA1951779606 | SBF2,SBF2-AS1 | n.799C= c.2878C= (p.Gln960=) n.851C= c.4390C= (p.Gln1464=) c.*623C= (n.*623C=) c.4372C= (p.Gln1458=) c.3922C= (p.Gln1308=) c.4411C= (p.Gln1471=) c.4252C= (p.Gln1418=) c.481C= n.1486C= c.3019C= (p.Gln1007=) c.4309C= (p.Gln1437=) c.522C= n.791C= c.4186C= (p.Gln1396=) n.1234C= c.4315C= (p.Gln1439=) n.383C= c.4174C= (p.Gln1392=) n.492G= c.4282C= (p.Gln1428=) c.4297C= (p.Gln1433=) c.4273C= (p.Gln1425=) n.4549C= | dbSNP |