ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7q34-35(chr7:140061285-144622893)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 | |||
BRAF | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1254 | 1368 | |
PRSS1 | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh37 |
2 | 826 | |
ADCK2 | - | - | - |
GRCh38 GRCh37 |
47 | 91 |
AGK | - | - |
GRCh38 GRCh38 GRCh37 |
349 | 398 | |
AGK-DT | - | - | - | GRCh38 | - | 23 |
ARHGEF35 | - | - | - |
GRCh38 GRCh38 GRCh37 |
40 | 98 |
ARHGEF35-AS1 | - | - | - |
GRCh38 GRCh38 |
- | 55 |
ARHGEF5 | - | - |
GRCh38 GRCh38 GRCh37 |
52 | 108 | |
CASP2 | - | - |
GRCh38 GRCh37 |
35 | 86 | |
CLCN1 | - | - |
GRCh38 GRCh37 |
1397 | 1549 |
There are 222 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
May 18, 2015 | RCV000143724.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024