Gene >> NLK
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000407008 |
| Start |
28168578:28168578(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.968A>G |
| AA Mutation |
p.Asp323Gly(p.D323G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000407008 |
| Start |
28168616:28168616(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1006G>A |
| AA Mutation |
p.Gly336Arg(p.G336R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |