| Mutation ID |
7 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000422285 |
| Start |
19354565:19354565(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.585C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
8 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000422285 |
| Start |
19353111:19353111(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.448G>T |
| AA Mutation |
p.Gly150Ter(p.G150*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PDHA1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000422285 |
| Start |
19350071:19350071(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.252G>T |
| AA Mutation |
p.Gln84His(p.Q84H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000422285 |
| Start |
19355438:19355438(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs138237215
|
| CDS Mutation |
c.693G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|