Variant #0000980231 (NC_000012.11:g.32895533G>A, NM_001278464.1:c.2044G>A (DNM1L))
| Chromosome |
12 |
| 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.32895533G>A |
| DNA change (hg38) |
- |
| Published as |
DNM1L(NM_012062.5):c.2005G>A (p.(Ala669Thr)) |
| ISCN |
- |
| DB-ID |
DNM1L_000048 |
| 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 |
2025-10-06 12:06:24 +02:00 (CEST) |

Variant on transcripts
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