ClinVar Genomic variation as it relates to human health
GRCh38/hg38 5p15.31-15.2(chr5:8824306-14246099)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 | |||
TRIO | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1259 | 1442 | |
CTNND2 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
279 | 391 | |
ANKRD33B | - | - | - |
GRCh38 GRCh37 |
50 | 156 |
ATPSCKMT | - | - |
GRCh38 GRCh37 |
19 | 121 | |
CCT5 | - | - |
GRCh38 GRCh37 |
314 | 417 | |
CMBL | - | - |
GRCh38 GRCh37 |
26 | 127 | |
CTD-2154B17.1 | - | - | - | GRCh38 | - | 42 |
DAP | - | - |
GRCh38 GRCh37 |
8 | 114 | |
DAP-DT | - | - | - | GRCh38 | - | 42 |
DNAH5 | - | - |
GRCh38 GRCh37 |
5624 | 5870 |
There are 105 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
|
Pathogenic (1) |
|
Dec 22, 2010 | RCV000137141.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024