ClinVar Genomic variation as it relates to human health
NM_001080414.4(CCDC88C):c.6075C>T (p.Tyr2025=)
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 | |||
CCDC88C | - | - |
GRCh38 GRCh37 |
1497 | 1544 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Nov 29, 2023 | RCV003873827.2 | |
Likely benign (1) |
|
May 24, 2024 | RCV004690493.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 30, 2024