Variant #0001078718 (NC_000010.10:g.71038467G>C, NM_001358263.1:c.-270G>C (HK1))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.71038467G>C
DNA change (hg38) g.69278711G>C
Published as -
ISCN -
DB-ID HK1_000021 See all 35 reported entries
Variant remarks in vitro expression analysis suggests inability to bind to VDAC, inducing a sustained release of mitochondrial calcium in the cytoplasm, leaving mSC prone to demyelination, which may explain the demyelinating peripheral neuropathy affects CMT4G patients
Reference PubMed: Ceprian 2024
ClinVar ID -
dbSNP ID -
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 2026-06-27 13:58:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HK1 NM_000188.2 +?/. - c.-40237G>C r.(?) p.(=)
HK1 NM_001358263.1 +?/. - c.-270G>C r.(?) p.(?)


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