Gene >> C1R
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000542285 |
| Start |
7080681:7080681(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764633353
|
| CDS Mutation |
c.1969G>A |
| AA Mutation |
p.Val657Ile(p.V657I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000542285 |
| Start |
7088879:7088879(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs570489350
|
| CDS Mutation |
c.876G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |