| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299529 |
| Start |
78343598:78343598(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs771972939
|
| CDS Mutation |
c.349G>A |
| AA Mutation |
p.Asp117Asn(p.D117N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000299529 |
| Start |
78341113:78341113(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.141C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CRABP1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299529 |
| Start |
78341117:78341117(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.145G>A |
| AA Mutation |
p.Asp49Asn(p.D49N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000299529 |
| Start |
78347935:78347935(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201099878
|
| CDS Mutation |
c.372C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|