Colon Cancer: Gene >> TOB1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268957 |
| Start |
50863225:50863225(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.793T>A |
| AA Mutation |
p.Ser265Thr(p.S265T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000268957 |
| Start |
50863197:50863198(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.820_821insACTGCATG |
| AA Mutation |
p.Phe274TyrfsTer52(p.F274Yfs*52) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TOB1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268957 |
| Start |
50863229:50863229(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.789A>C |
| AA Mutation |
p.Lys263Asn(p.K263N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000268957 |
| Start |
50863927:50863927(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.91G>T |
| AA Mutation |
p.Glu31Ter(p.E31*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|