Gene >> CHAF1B
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000314103 |
| Start |
36413111:36413111(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1289C>A |
| AA Mutation |
p.Pro430His(p.P430H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000314103 |
| Start |
36413121:36413121(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1299T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |