Colon Cancer: Gene >> RIT1
No Mutation Annotation! |
Rectum Cancer: Gene >> RIT1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368323 |
| Start |
155904789:155904789(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.179T>G |
| AA Mutation |
p.Ile60Ser(p.I60S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368323 |
| Start |
155900402:155900402(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.646G>T |
| AA Mutation |
p.Asp216Tyr(p.D216Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368323 |
| Start |
155904788:155904788(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.180C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000368323 |
| Start |
155900585:155900585(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.463G>T |
| AA Mutation |
p.Glu155Ter(p.E155*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000368323 |
| Start |
155900564:155900565(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.483dupT |
| AA Mutation |
p.Glu162Ter(p.E162*) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
|