ClinVar Genomic variation as it relates to human health
GRCh38/hg38 4q35.1-35.2(chr4:184406972-188915538)x3
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 |
- | 141 | |
CASP3 | - | - |
GRCh38 GRCh37 |
13 | 125 | |
CCDC110 | - | - |
GRCh38 GRCh37 |
39 | 178 | |
CENPU | - | - |
GRCh38 GRCh37 |
30 | 149 | |
CFAP96 | - | - | - |
GRCh38 GRCh37 |
5 | 160 |
CFAP97 | - | - |
GRCh38 GRCh37 |
44 | 173 | |
CYP4V2 | - | - |
GRCh38 GRCh37 |
445 | 698 | |
F11 | - | - |
GRCh38 GRCh37 |
485 | 799 | |
F11-AS1 | - | - | - | GRCh38 | - | 232 |
There are 154 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Aug 19, 2010 | RCV000134158.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024