Variant #0000163721 (NC_000012.11:g.32884296C>T, NM_001278464.1:c.1246C>T (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.32884296C>T
DNA change (hg38) g.32731362C>T
Published as -
ISCN -
DB-ID DNM1L_000009 See all 5 reported entries
Variant remarks mouse embryonic fibroblasts cDNA expression dear8LOVcloning reduces shows reduced oligomerization, mitochondrial fission activity and mitochondrial recruitment of DRP1 (to lesser extent as A395D)
Reference PubMed: Fahrner 2016, Journal: Fahrner 2016, OMIM:var0006
ClinVar ID -
dbSNP ID rs863223953
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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-03-10 12:05:42 +01:00 (CET)
Date last edited 2025-10-06 12:10:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNM1L NM_001278464.1 +/. - c.1246C>T r.(?) p.(Arg416Cys)
DNM1L NM_012062.3 +/. - c.1207C>T r.(?) p.(Arg403Cys)


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