Colon Cancer: Gene >> IL9
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000274520 |
| Start |
135895558:135895558(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.147T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> IL9
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274520 |
| Start |
135892474:135892474(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.352G>A |
| AA Mutation |
p.Ala118Thr(p.A118T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274520 |
| Start |
135894035:135894035(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.300G>T |
| AA Mutation |
p.Lys100Asn(p.K100N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|