| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000285093 |
| Start |
49802810:49802810(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs151022375
|
| CDS Mutation |
c.60C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000285093 |
| Start |
49792245:49792245(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs754463910
|
| CDS Mutation |
c.660C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> ACAA2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000285093 |
| Start |
49785204:49785204(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs745865904
|
| CDS Mutation |
c.1102G>A |
| AA Mutation |
p.Glu368Lys(p.E368K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|