ClinVar Genomic variation as it relates to human health
GRCh37/hg19 14q24.3(chr14:74883763-77219310)x1
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 | |||
ACYP1 | - | - |
GRCh38 GRCh37 |
1 | 20 | |
AREL1 | - | - |
GRCh38 GRCh37 |
54 | 71 | |
BATF | - | - |
GRCh38 GRCh37 |
2 | 21 | |
DLST | - | - |
GRCh38 GRCh37 |
62 | 80 | |
EIF2B2 | - | - |
GRCh38 GRCh37 |
276 | 300 | |
ERG28 | - | - |
GRCh38 GRCh37 |
1 | 22 | |
ESRRB | - | - |
GRCh38 GRCh37 |
250 | 273 | |
FCF1 | - | - | - |
GRCh38 GRCh37 |
11 | 26 |
FLVCR2 | - | - |
GRCh38 GRCh37 |
141 | 212 | |
FOS | - | - |
GRCh38 GRCh37 |
25 | 41 |
There are 17 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jul 8, 2022 | RCV003483211.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024