Colon Cancer: Gene >> NCR3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340027 |
| Start |
31590091:31590091(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.79A>T |
| AA Mutation |
p.Ile27Phe(p.I27F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000340027 |
| Start |
31590095:31590096(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.74dupC |
| AA Mutation |
p.Glu26Ter(p.E26*) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> NCR3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340027 |
| Start |
31589883:31589883(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs143363686
|
| CDS Mutation |
c.287G>A |
| AA Mutation |
p.Arg96Gln(p.R96Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|