Gene >> CCR2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000292301 |
| Start |
46359803:46359803(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1068A>T |
| AA Mutation |
p.Lys356Asn(p.K356N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000292301 |
| Start |
46359770:46359770(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1035G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |