Gene >> CXCL10
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306602 |
| Start |
76022701:76022701(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.178G>A |
| AA Mutation |
p.Val60Ile(p.V60I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000306602 |
| Start |
76023390:76023390(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.42G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |