ClinVar Genomic variation as it relates to human health
NM_022765.4(MICAL1):c.326G>A (p.Arg109Gln)
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 | |||
MICAL1 | - | - |
GRCh38 GRCh37 |
1004 | 1057 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Oct 28, 2023 | RCV003063091.2 | |
Uncertain significance (1) |
|
Sep 20, 2023 | RCV004070349.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024