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 International |
| Created by |
Johan den Dunnen |
| Date created |
2026-06-27 13:58:49 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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