Colon Cancer: Gene >> NCR1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000291890 |
| Start |
54906305:54906305(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769495093
|
| CDS Mutation |
c.41G>A |
| AA Mutation |
p.Cys14Tyr(p.C14Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000291890 |
| Start |
54910058:54910058(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.675C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> NCR1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000291890 |
| Start |
54912728:54912728(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs766273248
|
| CDS Mutation |
c.772C>T |
| AA Mutation |
p.Arg258Trp(p.R258W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000291890 |
| Start |
54912174:54912175(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.691dupT |
| AA Mutation |
p.Trp231LeufsTer45(p.W231Lfs*45) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
|