Colon Cancer: Gene >> RGN
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336169 |
| Start |
47081194:47081194(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.50G>A |
| AA Mutation |
p.Gly17Asp(p.G17D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336169 |
| Start |
47089936:47089936(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.507C>A |
| AA Mutation |
p.Asp169Glu(p.D169E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> RGN
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336169 |
| Start |
47091792:47091792(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.677G>A |
| AA Mutation |
p.Arg226His(p.R226H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|