Colon Cancer: Gene >> MLN
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000430124 |
| Start |
33801064:33801064(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs749823669
|
| CDS Mutation |
c.100G>A |
| AA Mutation |
p.Glu34Lys(p.E34K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000430124 |
| Start |
33801053:33801053(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.111G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> MLN
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000430124 |
| Start |
33801096:33801096(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs746105078
|
| CDS Mutation |
c.68C>T |
| AA Mutation |
p.Thr23Met(p.T23M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|