Colon Cancer: Gene >> ISG20
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306072 |
| Start |
88655424:88655424(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.439C>T |
| AA Mutation |
p.Leu147Phe(p.L147F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306072 |
| Start |
88639548:88639548(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs371941091
|
| CDS Mutation |
c.182C>A |
| AA Mutation |
p.Pro61His(p.P61H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> ISG20
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306072 |
| Start |
88652234:88652234(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs549880749
|
| CDS Mutation |
c.353G>A |
| AA Mutation |
p.Arg118His(p.R118H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|