Variant #0000163715 (NC_000012.11:g.32883952G>A, NM_001278464.1:c.1123G>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.32883952G>A
DNA change (hg38) g.32731018G>A
Published as -
ISCN -
DB-ID DNM1L_000007 See all 2 reported entries
Variant remarks control fibroblast cDNA overexpression cloning induced significantly altered mitochondrial morphology
Reference PubMed: Sheffer 2016, Journal: Sheffer 2016, OMIM:var0003
ClinVar ID -
dbSNP ID rs886037861
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 11:12:47 +01:00 (CET)
Date last edited 2025-10-06 12:10:15 +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.1123G>A r.(?) p.(Gly375Ser)
DNM1L NM_012062.3 +/. - c.1084G>A r.(?) p.(Gly362Ser)


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