| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263598 |
| Start |
135524893:135524893(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.467G>A |
| AA Mutation |
p.Gly156Glu(p.G156E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263598 |
| Start |
135523914:135523914(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs373587388
|
| CDS Mutation |
c.327G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> LCN1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263598 |
| Start |
135524845:135524845(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.419A>C |
| AA Mutation |
p.Asn140Thr(p.N140T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|