Gene >> C3
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000245907 |
| Start |
6697552:6697552(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2588G>C |
| AA Mutation |
p.Arg863Thr(p.R863T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000245907 |
| Start |
6678249:6678249(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4753A>G |
| AA Mutation |
p.Ile1585Val(p.I1585V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |