Variant #0000163722 (NC_000012.11:g.32884052C>A, NM_001278464.1:c.1223C>A (DNM1L))
| Chromosome |
12 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32884052C>A |
| DNA change (hg38) |
g.32731118C>A |
| Published as |
A395D |
| ISCN |
- |
| DB-ID |
DNM1L_000006 See all 4 reported entries |
| Variant remarks |
mouse embryonic fibroblasts cDNA expression cloning reduces shows reduced oligomerization, mitochondrial fission activity and mitochondrial recruitment of DRP1 (stronger effect compared to R403C) |
| Reference |
PubMed: Fahrner 2016, Journal: Fahrner 2016 |
| ClinVar ID |
- |
| dbSNP ID |
rs121908531 |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2017-03-10 12:09:29 +01:00 (CET) |
| Date last edited |
2025-10-06 12:10:18 +02:00 (CEST) |

Variant on transcripts
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