Variant #0000163722 (NC_000012.11:g.32884052C>A, DNM1L(NM_001278464.1):c.1223C>A)
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 |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |

Variant on transcripts
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