| Mutation ID |
3 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000415083 |
| Start |
26057636:26057636(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.338delG |
| AA Mutation |
p.Gly113ValfsTer11(p.G113Vfs*11) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
inframe_insertion;splice_region_variant |
| Transcription ID |
ENST00000415083 |
| Start |
26035126:26035127(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.974_975insTGATAA |
| AA Mutation |
p.Gly325_Asn326insAspLys(p.G325_N326insDK) |
| Mutation Classification |
In_Frame_Ins |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> SS18
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000415083 |
| Start |
26035874:26035874(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs570531592
|
| CDS Mutation |
c.930C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|