Colon Cancer: Gene >> TMEM11
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317635 |
| Start |
21198341:21198341(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs775552645
|
| CDS Mutation |
c.562G>A |
| AA Mutation |
p.Glu188Lys(p.E188K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000317635 |
| Start |
21198420:21198420(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.483G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TMEM11
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317635 |
| Start |
21198341:21198341(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs775552645
|
| CDS Mutation |
c.562G>A |
| AA Mutation |
p.Glu188Lys(p.E188K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317635 |
| Start |
21198470:21198470(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.433C>T |
| AA Mutation |
p.Arg145Cys(p.R145C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000317635 |
| Start |
21198384:21198384(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs765996667
|
| CDS Mutation |
c.519G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|