Colon Cancer: Gene >> IL18BP
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260049 |
| Start |
72001843:72001843(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.567T>A |
| AA Mutation |
p.Ser189Arg(p.S189R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000260049 |
| Start |
72000442:72000442(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.120C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> IL18BP
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260049 |
| Start |
72001535:72001535(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs768554589
|
| CDS Mutation |
c.490G>A |
| AA Mutation |
p.Val164Ile(p.V164I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260049 |
| Start |
72001240:72001240(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.275T>C |
| AA Mutation |
p.Phe92Ser(p.F92S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260049 |
| Start |
72001252:72001252(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.287G>T |
| AA Mutation |
p.Ser96Ile(p.S96I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|