| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000272274 |
| Start |
27254242:27254242(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs371046119
|
| CDS Mutation |
c.90T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000272274 |
| Start |
27256217:27256217(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.276T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> RPL21
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000272274 |
| Start |
27254247:27254247(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs587777527
|
| CDS Mutation |
c.95G>A |
| AA Mutation |
p.Arg32Gln(p.R32Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000272274 |
| Start |
27254259:27254259(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.107A>C |
| AA Mutation |
p.Lys36Thr(p.K36T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|