Gene >> CCR8
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000326306 |
| Start |
39332912:39332912(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.581G>T |
| AA Mutation |
p.Trp194Leu(p.W194L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000326306 |
| Start |
39332856:39332856(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.525C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |