ClinVar Genomic variation as it relates to human health
NM_032353.4(VPS25):c.514G>A (p.Gly172Ser)
Germline
Classification
(1)
Likely pathogenic
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 | |||
VPS25 | - | - |
GRCh38 GRCh37 |
10 | 17 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
VPS25-related neurodevelopmental delay
|
Likely pathogenic (1) |
|
- | RCV004577399.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 04, 2024