| Mutation ID |
6 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000320334 |
| Start |
113980997:113980997(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs376475211
|
| CDS Mutation |
c.449G>A |
| AA Mutation |
p.Arg150Gln(p.R150Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
7 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000320334 |
| Start |
113981337:113981337(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
rs761283199
|
| CDS Mutation |
c.795delC |
| AA Mutation |
p.Tyr266ThrfsTer3(p.Y266Tfs*3) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> OLFML3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000320334 |
| Start |
113980483:113980483(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs775272671
|
| CDS Mutation |
c.266G>A |
| AA Mutation |
p.Arg89His(p.R89H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000320334 |
| Start |
113980579:113980579(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.362G>A |
| AA Mutation |
p.Gly121Asp(p.G121D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000320334 |
| Start |
113981256:113981256(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs57320081
|
| CDS Mutation |
c.708G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|