Colon Cancer: Gene >> PRSS50
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000315170 |
| Start |
46717761:46717761(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763693848
|
| CDS Mutation |
c.64G>A |
| AA Mutation |
p.Ala22Thr(p.A22T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> PRSS50
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000315170 |
| Start |
46717439:46717439(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.305G>A |
| AA Mutation |
p.Arg102His(p.R102H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000315170 |
| Start |
46712913:46712913(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.909G>C |
| AA Mutation |
p.Glu303Asp(p.E303D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000315170 |
| Start |
46712270:46712270(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1134C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|