| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000295822 |
| Start |
170893414:170893414(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.408T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000295822 |
| Start |
170894330:170894330(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.364G>T |
| AA Mutation |
p.Glu122Ter(p.E122*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> EIF5A2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295822 |
| Start |
170907002:170907002(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.257G>T |
| AA Mutation |
p.Arg86Ile(p.R86I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295822 |
| Start |
170907797:170907797(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs747942434
|
| CDS Mutation |
c.10G>A |
| AA Mutation |
p.Glu4Lys(p.E4K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|