| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000395748 |
| Start |
74446702:74446702(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769439500
|
| CDS Mutation |
c.230C>T |
| AA Mutation |
p.Ser77Leu(p.S77L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000395748 |
| Start |
74450465:74450465(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.598G>A |
| AA Mutation |
p.Ala200Thr(p.A200T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> AREG
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000395748 |
| Start |
74452549:74452549(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.671G>T |
| AA Mutation |
p.Arg224Ile(p.R224I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|