| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367990 |
| Start |
161222501:161222501(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.207G>T |
| AA Mutation |
p.Lys69Asn(p.K69N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000367990 |
| Start |
161223390:161223390(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs761252493
|
| CDS Mutation |
c.12C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> APOA2
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000367990 |
| Start |
161222438:161222438(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs752976925
|
| CDS Mutation |
c.270C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|