ClinVar Genomic variation as it relates to human health
NM_178040.4(ERC1):c.1026C>T (p.His342=)
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 | |||
ERC1 | - | - |
GRCh38 GRCh38 GRCh37 |
80 | 170 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
ERC1-related disorder
|
Likely benign (1) |
|
Feb 25, 2019 | RCV003947239.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 13, 2024