| Mutation ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000241651 |
| Start |
203085871:203085871(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs768292063
|
| CDS Mutation |
c.91G>A |
| AA Mutation |
p.Glu31Lys(p.E31K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000241651 |
| Start |
203085507:203085507(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.455delG |
| AA Mutation |
p.Gly152AlafsTer101(p.G152Afs*101) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> MYOG
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000241651 |
| Start |
203085871:203085871(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs768292063
|
| CDS Mutation |
c.91G>A |
| AA Mutation |
p.Glu31Lys(p.E31K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|