ClinVar Genomic variation as it relates to human health
NM_018719.5(CDCA7L):c.*1333_*1334del
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 | |||
CDCA7L | - | - |
GRCh38 GRCh37 |
30 | 206 | |
DNAH11 | - | - |
GRCh38 GRCh37 |
5377 | 5757 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Apr 20, 2023 | RCV003818395.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jul 15, 2024