ClinVar Genomic variation as it relates to human health
NM_031372.4(HNRNPDL):c.31C>A (p.Pro11Thr)
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 | |||
HNRNPDL | - | - |
GRCh38 GRCh37 |
388 | 430 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jan 29, 2023 | RCV003846806.1 | |
HNRNPDL-related disorder
|
Uncertain significance (1) |
|
Feb 26, 2024 | RCV003939235.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 12, 2024