Colon Cancer: Gene >> CXCL11
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306621 |
| Start |
76035966:76035966(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.22A>G |
| AA Mutation |
p.Ile8Val(p.I8V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306621 |
| Start |
76034802:76034802(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.276G>T |
| AA Mutation |
p.Lys92Asn(p.K92N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CXCL11
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306621 |
| Start |
76035237:76035237(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.167A>G |
| AA Mutation |
p.Asn56Ser(p.N56S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306621 |
| Start |
76035072:76035072(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs372692015
|
| CDS Mutation |
c.236C>T |
| AA Mutation |
p.Ser79Leu(p.S79L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|