Colon Cancer: Gene >> AMN
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299155 |
| Start |
102923965:102923965(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.193G>A |
| AA Mutation |
p.Ala65Thr(p.A65T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> AMN
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299155 |
| Start |
102923753:102923753(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.86A>G |
| AA Mutation |
p.Asp29Gly(p.D29G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299155 |
| Start |
102923723:102923723(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.56C>T |
| AA Mutation |
p.Ala19Val(p.A19V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|