Colon Cancer: Gene >> RNASE2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000304625 |
| Start |
20956083:20956083(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.312G>T |
| AA Mutation |
p.Gln104His(p.Q104H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> RNASE2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000304625 |
| Start |
20955808:20955808(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.37C>T |
| AA Mutation |
p.Leu13Phe(p.L13F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000304625 |
| Start |
20955939:20955939(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200694912
|
| CDS Mutation |
c.168C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000304625 |
| Start |
20956204:20956204(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.433C>T |
| AA Mutation |
p.Arg145Ter(p.R145*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|