Variant #0001043902 (NC_000022.10:g.41940441_41940442insCGCGCACCGC, NM_001098.2:c.*15824_*15825insCGCGCACCGC (ACO2))
| Chromosome |
22 |
| 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.41940441_41940442insCGCGCACCGC |
| DNA change (hg38) |
- |
| Published as |
POLR3H(NM_001282885.2):c.-23_-22insCGGTGCGCGG |
| ISCN |
- |
| DB-ID |
ACO2_000179 |
| 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 |
2025-05-05 21:14:00 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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