ClinVar Genomic variation as it relates to human health
NM_178511.6(INAFM1):c.371C>T (p.Pro124Leu)
Germline
Classification
(1)
Likely benign
criteria provided, single submitter
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 | |||
CCDC9 | - | - | - |
GRCh38 GRCh37 |
57 | 96 |
INAFM1 | - | - | - |
GRCh38 GRCh37 |
- | 38 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Mar 2, 2023 | RCV004286874.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 27, 2024