ClinVar Genomic variation as it relates to human health
GRCh37/hg19 4q35.1-35.2(chr4:185211271-190957473)x1
Germline
Classification
(1)
Pathogenic
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 | |||
ACSL1 | - | - |
GRCh38 GRCh37 |
35 | 147 | |
ANKRD37 | - | - |
GRCh38 GRCh37 |
- | 142 | |
CASP3 | - | - |
GRCh38 GRCh37 |
13 | 125 | |
CCDC110 | - | - |
GRCh38 GRCh37 |
39 | 180 | |
CENPU | - | - |
GRCh38 GRCh37 |
30 | 149 | |
CFAP96 | - | - | - |
GRCh38 GRCh37 |
5 | 161 |
CFAP97 | - | - |
GRCh38 GRCh37 |
44 | 174 | |
CYP4V2 | - | - |
GRCh38 GRCh37 |
446 | 700 | |
F11 | - | - |
GRCh38 GRCh37 |
490 | 805 | |
FAM149A | - | - | - |
GRCh38 GRCh37 |
54 | 191 |
There are 18 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Pathogenic (1) |
|
- | RCV002292211.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023