Colon Cancer: Gene >> GPR55
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000392039 |
| Start |
230910652:230910652(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.311G>A |
| AA Mutation |
p.Ser104Asn(p.S104N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> GPR55
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000392039 |
| Start |
230910401:230910401(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.562T>A |
| AA Mutation |
p.Phe188Ile(p.F188I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000392039 |
| Start |
230910505:230910505(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs541186477
|
| CDS Mutation |
c.458G>A |
| AA Mutation |
p.Ser153Asn(p.S153N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000392039 |
| Start |
230910690:230910690(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370767476
|
| CDS Mutation |
c.273G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|