ClinVar Genomic variation as it relates to human health
NM_001369598.1(ST7):c.1395G>A (p.Thr465=)
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 | |||
ST7 | - | - |
GRCh38 GRCh37 |
10 | 59 | |
ST7-OT3 | - | - | - |
GRCh38 GRCh37 |
- | 34 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
ST7-related disorder
|
Likely benign (1) |
|
Oct 1, 2019 | RCV003931812.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 13, 2024