ClinVar Genomic variation as it relates to human health
NM_001190274.2(FBXO11):c.77_118del (p.Gln26_Gln39del)
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 | |||
FBXO11 | - | - |
GRCh38 GRCh37 |
664 | 1000 | |
LOC100506235 | - | - | - | GRCh38 | - | 159 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Nov 8, 2022 | RCV002871873.10 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 07, 2024