Colon Cancer: Gene >> TRH
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000302649 |
| Start |
129976027:129976027(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.211G>A |
| AA Mutation |
p.Ala71Thr(p.A71T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302649 |
| Start |
129975956:129975956(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.140G>A |
| AA Mutation |
p.Arg47His(p.R47H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TRH
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302649 |
| Start |
129976848:129976848(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.361G>T |
| AA Mutation |
p.Asp121Tyr(p.D121Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|