ClinVar Genomic variation as it relates to human health
NC_000005.9:g.(?_136957787)_(140078137_?)dup
Germline
Classification
(1)
Uncertain significance
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 |
2824 | 2880 | |
PURA | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
464 | 521 | |
ANKHD1 | - | - |
GRCh38 GRCh37 |
- | 29 | |
ANKHD1-EIF4EBP3 | - | - | - |
GRCh38 GRCh37 |
5 | 45 |
APBB3 | - | - |
GRCh38 GRCh37 |
36 | 54 | |
BRD8 | - | - |
GRCh38 GRCh37 |
43 | 63 | |
CD14 | - | - |
GRCh38 GRCh37 |
- | 41 | |
CDC23 | - | - |
GRCh38 GRCh37 |
14 | 34 | |
CDC25C | - | - |
GRCh38 GRCh37 |
30 | 49 | |
CXXC5 | - | - |
GRCh38 GRCh37 |
21 | 40 |
There are 45 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Sep 5, 2021 | RCV003116437.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jan 26, 2024