Colon Cancer: Gene >> CDC42
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000344548 |
| Start |
22091452:22091452(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.511G>A |
| AA Mutation |
p.Glu171Lys(p.E171K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000344548 |
| Start |
22091439:22091439(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.498G>T |
| AA Mutation |
p.Lys166Asn(p.K166N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CDC42
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000344548 |
| Start |
22081786:22081786(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.170A>G |
| AA Mutation |
p.Asp57Gly(p.D57G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000344548 |
| Start |
22091498:22091498(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs756680625
|
| CDS Mutation |
c.557G>A |
| AA Mutation |
p.Arg186His(p.R186H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000344548 |
| Start |
22078558:22078558(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.80A>C |
| AA Mutation |
p.Lys27Thr(p.K27T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|