ClinVar Genomic variation as it relates to human health
NM_017757.3(ZNF407):c.2761G>T (p.Val921Phe)
Germline
Classification
(3)
Uncertain significance
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 | |||
ZNF407 | No evidence available | No evidence available |
GRCh38 GRCh37 |
281 | 496 | |
LOC126862798 | - | - | - | GRCh38 | - | 113 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jun 16, 2022 | RCV002469892.1 | |
Uncertain significance (1) |
|
Feb 13, 2024 | RCV003933796.1 | |
Uncertain significance (1) |
|
May 31, 2022 | RCV004067582.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 19, 2024