ClinVar Genomic variation as it relates to human health
NM_001388465.1(TBC1D26):c.267G>A (p.Arg89=)
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 | |||
TBC1D26 | - | - | - |
GRCh38 GRCh37 |
5 | 38 |
TBC1D26-AS1 | - | - | - | GRCh38 | - | 23 |
ZNF286A-TBC1D26 | - | - | - | GRCh38 | 1 | 50 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Jun 1, 2022 | RCV003413156.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 15, 2024