Gene >> TTK
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369798 |
| Start |
80013358:80013358(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.976A>C |
| AA Mutation |
p.Asn326His(p.N326H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369798 |
| Start |
80010900:80010900(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.556A>T |
| AA Mutation |
p.Asn186Tyr(p.N186Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |