| Mutation ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000267938 |
| Start |
75869007:75869007(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.444T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
inframe_insertion |
| Transcription ID |
ENST00000267938 |
| Start |
75868976:75868977(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.420_422dupAGA |
| AA Mutation |
p.Glu146dup(p.E146dup) |
| Mutation Classification |
In_Frame_Ins |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> UBE2Q2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000267938 |
| Start |
75854437:75854437(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.232A>C |
| AA Mutation |
p.Asn78His(p.N78H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|