ClinVar Genomic variation as it relates to human health
GRCh38/hg38 5q23.3-33.2(chr5:130860928-155321811)x3
Germline
Classification
(1)
Pathogenic
criteria provided, single submitter
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 |
2755 | 2809 | |
PURA | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
459 | 518 | |
SPINK1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
186 | 208 | |
TCOF1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
769 | 810 | |
CAMK2A | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
107 | 122 | |
PCDHGA8 | Dosage sensitivity unlikely | No evidence available |
GRCh38 GRCh37 |
- | 433 | |
TIGD6 | - | Dosage sensitivity unlikely | No evidence available |
GRCh38 GRCh37 |
29 | 46 |
ABLIM3 | - | - |
GRCh38 GRCh37 |
44 | 62 | |
ACSL6 | - | - |
GRCh38 GRCh37 |
20 | 41 | |
ACSL6-AS1 | - | - | - | GRCh38 | - | 7 |
There are 1210 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 |
---|---|---|---|---|
Pathogenic (1) |
|
Aug 12, 2011 | RCV000051193.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023