Gene >> NCAPG
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000251496 |
| Start |
17839757:17839757(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2548T>C |
| AA Mutation |
p.Tyr850His(p.Y850H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000251496 |
| Start |
17828345:17828345(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1721C>A |
| AA Mutation |
p.Ser574Ter(p.S574*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |