Colon Cancer: Gene >> ALDOC
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226253 |
| Start |
28575435:28575435(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs775893117
|
| CDS Mutation |
c.98C>T |
| AA Mutation |
p.Ala33Val(p.A33V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226253 |
| Start |
28574719:28574719(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs747367976
|
| CDS Mutation |
c.517C>T |
| AA Mutation |
p.Arg173Cys(p.R173C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> ALDOC
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226253 |
| Start |
28574093:28574093(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs145665688
|
| CDS Mutation |
c.773G>A |
| AA Mutation |
p.Arg258His(p.R258H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226253 |
| Start |
28574090:28574090(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs765845189
|
| CDS Mutation |
c.776G>A |
| AA Mutation |
p.Arg259His(p.R259H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|