| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.71401691T>C | CA279925 | TAF1 | c.3236T>C (p.Ile1079Thr) c.865T>C c.3950T>C (p.Ile1317Thr) c.544T>C c.3887T>C (p.Ile1296Thr) c.4010T>C (p.Ile1337Thr) c.3947T>C (p.Ile1316Thr) c.679T>C n.4086T>C c.4007T>C (p.Ile1336Thr) c.3629T>C (p.Ile1210Thr) n.4020T>C n.3968T>C | ClinVar dbSNP COSMIC COSMIC COSMIC |
| X | g.71401691T= | CA2436451195 | TAF1 | c.3236T= (p.Ile1079=) c.865T= c.3950T= (p.Ile1317=) c.544T= c.3887T= (p.Ile1296=) c.4010T= (p.Ile1337=) c.3947T= (p.Ile1316=) c.679T= n.4086T= c.4007T= (p.Ile1336=) c.3629T= (p.Ile1210=) n.4020T= n.3968T= | dbSNP |