ClinVar Genomic variation as it relates to human health
NM_001144967.3(NEDD4L):c.980G>T (p.Ser327Ile)
Germline
Classification
(2)
Uncertain significance
criteria provided, multiple submitters, no conflicts
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 | |||
NEDD4L | - | - |
GRCh38 GRCh37 |
898 | 1030 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Apr 9, 2022 | RCV002594637.2 | |
Uncertain significance (1) |
|
Jun 26, 2023 | RCV003340520.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 01, 2024