Gene >> C9
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263408 |
| Start |
39341226:39341226(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.396T>G |
| AA Mutation |
p.Asp132Glu(p.D132E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263408 |
| Start |
39331763:39331763(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.528C>G |
| AA Mutation |
p.Phe176Leu(p.F176L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |