| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226730 |
| Start |
122456422:122456422(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.19C>A |
| AA Mutation |
p.Leu7Met(p.L7M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226730 |
| Start |
122456147:122456147(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.204G>T |
| AA Mutation |
p.Lys68Asn(p.K68N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> IL2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226730 |
| Start |
122453783:122453783(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.278C>T |
| AA Mutation |
p.Ala93Val(p.A93V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|