Gene >> INCENP
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000394818 |
| Start |
62145060:62145060(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1684G>A |
| AA Mutation |
p.Asp562Asn(p.D562N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000394818 |
| Start |
62146792:62146792(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs759111475
|
| CDS Mutation |
c.2094C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |