ClinVar Genomic variation as it relates to human health
GRCh37/hg19 5p15.33(chr5:26141-2537457)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 | |||
TERT | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
2971 | 3413 | |
SLC6A18 | Dosage sensitivity unlikely | No evidence available |
GRCh38 GRCh37 |
86 | 243 | |
AHRR | - | - |
GRCh38 GRCh37 |
1 | 241 | |
BRD9 | - | - |
GRCh38 GRCh37 |
38 | 196 | |
CCDC127 | - | - | - |
GRCh38 GRCh37 |
27 | 178 |
CEP72 | - | - |
GRCh38 GRCh38 GRCh37 |
58 | 241 | |
CLPTM1L | - | - |
GRCh38 GRCh38 GRCh37 |
60 | 207 | |
EXOC3 | - | - |
GRCh38 GRCh37 |
58 | 210 | |
EXOC3-AS1 | - | - | - |
GRCh38 GRCh37 |
- | 150 |
IRX4 | - | - |
GRCh38 GRCh37 |
68 | 205 |
There are 16 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) |
|
Jun 19, 2022 | RCV002284255.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 13, 2023