Colon Cancer: Gene >> TIMP1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000218388 |
| Start |
47585281:47585281(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.278G>A |
| AA Mutation |
p.Cys93Tyr(p.C93Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> TIMP1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000218388 |
| Start |
47585308:47585308(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs140600134
|
| CDS Mutation |
c.305G>A |
| AA Mutation |
p.Arg102His(p.R102H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000218388 |
| Start |
47584944:47584944(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.130G>A |
| AA Mutation |
p.Ala44Thr(p.A44T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000218388 |
| Start |
47584952:47584952(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.138C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|