Variant #0000983675 (NC_000019.9:g.5893196_5893197del, NM_175614.4:c.*1559_*1560del (NDUFA11))
Chromosome |
19 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5893196_5893197del |
DNA change (hg38) |
- |
Published as |
NDUFA11(NM_001193375.3):c.421_422del (p.(Val141Thrfs*286)) |
ISCN |
- |
DB-ID |
NDUFA11_000019 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2024-04-19 20:27:30 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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