ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10q24.32(chr10:101599084-101676484)x3
Germline
Classification
(1)
Uncertain significance
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 | |||
FBXW4 | No evidence available | No evidence available |
GRCh38 GRCh37 |
70 | 148 | |
DPCD | - | - |
GRCh38 GRCh37 |
15 | 71 | |
LOC124416891 | - | - | - | GRCh38 | - | 11 |
LOC130004560 | - | - | - | GRCh38 | - | 12 |
LOC130004561 | - | - | - | GRCh38 | - | 11 |
MIR3158-1 | - | - | - | GRCh38 | - | 12 |
MIR3158-2 | - | - | - | GRCh38 | - | 12 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Dec 22, 2010 | RCV000136700.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024