ClinVar Genomic variation as it relates to human health
NM_002495.4(NDUFS4):c.60G>C (p.Val20=)
Germline
Classification
(1)
Likely benign
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
LOC129993885 | - | - | - | GRCh38 | - | 52 |
NDUFS4 | - | - |
GRCh38 GRCh37 |
167 | 227 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
NDUFS4-related disorder
|
Likely benign (1) |
|
May 2, 2019 | RCV003919716.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 12, 2024