| Mutation ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000359864 |
| Start |
2994836:2994836(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs527238579
|
| CDS Mutation |
c.70G>A |
| AA Mutation |
p.Ala24Thr(p.A24T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000359864 |
| Start |
3018576:3018576(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.515G>A |
| AA Mutation |
p.Gly172Glu(p.G172E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TEAD4
| Mutation ID |
1 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000359864 |
| Start |
3038067:3038067(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.997A>T |
| AA Mutation |
p.Lys333Ter(p.K333*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|