Gene >> CCR1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296140 |
| Start |
46203967:46203967(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.347G>T |
| AA Mutation |
p.Gly116Val(p.G116V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296140 |
| Start |
46203472:46203472(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.842T>A |
| AA Mutation |
p.Leu281Gln(p.L281Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |