| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000227752 |
| Start |
117993256:117993256(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs748186383
|
| CDS Mutation |
c.383G>A |
| AA Mutation |
p.Gly128Asp(p.G128D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000227752 |
| Start |
117999611:117999611(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1707C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> IL10RA
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000227752 |
| Start |
117998863:117998863(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.959G>A |
| AA Mutation |
p.Gly320Asp(p.G320D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000227752 |
| Start |
117988486:117988486(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.172G>T |
| AA Mutation |
p.Glu58Ter(p.E58*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|