| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361523 |
| Start |
42813989:42813989(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1000G>A |
| AA Mutation |
p.Gly334Arg(p.G334R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361523 |
| Start |
42818573:42818573(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs111283520
|
| CDS Mutation |
c.459C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> BECN1
| Mutation ID |
1 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000361523 |
| Start |
42816044:42816044(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.694G>T |
| AA Mutation |
p.Glu232Ter(p.E232*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000361523 |
| Start |
42819553:42819554(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.254dupC |
| AA Mutation |
p.Ala86SerfsTer20(p.A86Sfs*20) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
|