ClinVar Genomic variation as it relates to human health
NM_020778.5(ALPK3):c.904C>A (p.Leu302Met)
Germline
Classification
(3)
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 | |||
ALPK3 | - | - |
GRCh38 GRCh37 |
2292 | 2420 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Apr 25, 2022 | RCV002392199.2 | |
Uncertain significance (1) |
|
Dec 22, 2023 | RCV003095266.2 | |
Uncertain significance (1) |
|
May 7, 2021 | RCV003985028.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 01, 2024