Colon Cancer: Gene >> CCL22
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000219235 |
| Start |
57358869:57358869(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs146388634
|
| CDS Mutation |
c.53C>T |
| AA Mutation |
p.Ala18Val(p.A18V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000219235 |
| Start |
57360482:57360482(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.119A>G |
| AA Mutation |
p.Tyr40Cys(p.Y40C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CCL22
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000219235 |
| Start |
57363564:57363564(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.258G>T |
| AA Mutation |
p.Met86Ile(p.M86I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|