Colon Cancer: Gene >> MICB
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000252229 |
| Start |
31506310:31506310(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs775923426
|
| CDS Mutation |
c.493G>A |
| AA Mutation |
p.Val165Ile(p.V165I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000252229 |
| Start |
31506302:31506302(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.485C>T |
| AA Mutation |
p.Ala162Val(p.A162V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> MICB
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000252229 |
| Start |
31505736:31505736(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs2240858
|
| CDS Mutation |
c.190C>T |
| AA Mutation |
p.Arg64Cys(p.R64C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000252229 |
| Start |
31507126:31507126(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs760425014
|
| CDS Mutation |
c.718C>T |
| AA Mutation |
p.Arg240Cys(p.R240C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000252229 |
| Start |
31506319:31506319(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.502T>A |
| AA Mutation |
p.Phe168Ile(p.F168I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|