Colon Cancer: Gene >> STH
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000537309 |
| Start |
45999296:45999296(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.17G>A |
| AA Mutation |
p.Gly6Asp(p.G6D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000537309 |
| Start |
45999360:45999360(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763740965
|
| CDS Mutation |
c.81C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> STH
| Mutation ID |
1 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000537309 |
| Start |
45999298:45999298(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.19C>T |
| AA Mutation |
p.Gln7Ter(p.Q7*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|