ClinVar Genomic variation as it relates to human health
NM_014049.5(ACAD9):c.843T>C (p.Pro281=)
Germline
Classification
(2)
Likely benign
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 | |||
ACAD9 | - | - |
GRCh38 GRCh37 |
771 | 1039 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Feb 21, 2023 | RCV003725118.1 | |
ACAD9-related disorder
|
Likely benign (1) |
|
Jul 12, 2019 | RCV003956510.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 19, 2024