Colon Cancer: Gene >> GID8
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000266069 |
| Start |
62944802:62944802(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.577G>A |
| AA Mutation |
p.Ala193Thr(p.A193T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000266069 |
| Start |
62943542:62943542(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs753601523
|
| CDS Mutation |
c.363G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> GID8
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000266069 |
| Start |
62941594:62941594(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.92G>A |
| AA Mutation |
p.Arg31His(p.R31H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000266069 |
| Start |
62941604:62941604(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.102G>T |
| AA Mutation |
p.Met34Ile(p.M34I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|