Colon Cancer: Gene >> CXCL10
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306602 |
| Start |
76022395:76022395(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.249G>T |
| AA Mutation |
p.Lys83Asn(p.K83N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306602 |
| Start |
76022408:76022408(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs755610178
|
| CDS Mutation |
c.236C>T |
| AA Mutation |
p.Ser79Leu(p.S79L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CXCL10
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306602 |
| Start |
76022369:76022369(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.275A>T |
| AA Mutation |
p.Glu92Val(p.E92V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306602 |
| Start |
76022739:76022739(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.140A>C |
| AA Mutation |
p.Lys47Thr(p.K47T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|