ClinVar Genomic variation as it relates to human health
NM_003632.3(CNTNAP1):c.716-31_716-9dup
Germline
Classification
(1)
Likely benign
no assertion criteria provided
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 | |||
CNTNAP1 | - | - |
GRCh38 GRCh37 |
455 | 505 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
CNTNAP1-related disorder
|
Likely benign (1) |
|
Mar 22, 2019 | RCV004543971.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Nov 25, 2024