ClinVar Genomic variation as it relates to human health
GRCh38/hg38 5q23.3-33.2(chr5:129847794-153353546)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 | |||
CTNNA1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
2866 | 2925 | |
POU4F3 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1 | 195 | |
PURA | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
468 | 526 | |
SPINK1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
202 | 223 | |
TCOF1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
808 | 846 | |
CAMK2A | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
118 | 130 | |
PCDHGA8 | Dosage sensitivity unlikely | No evidence available |
GRCh38 GRCh37 |
- | 639 | |
TIGD6 | - | Dosage sensitivity unlikely | No evidence available |
GRCh38 GRCh37 |
45 | 59 |
ABLIM3 | - | - |
GRCh38 GRCh37 |
59 | 74 | |
ACSL6 | - | - |
GRCh38 GRCh37 |
33 | 52 |
There are 1149 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) |
|
Sep 21, 2012 | RCV000138808.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024