ClinVar Genomic variation as it relates to human health
GRCh37/hg19 14q32.31-32.33(chr14:102615953-107285437)x1
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 | |||
CDC42BPB | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
192 | 259 | |
AKT1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
764 | 833 | |
ADSS1 | - | - |
GRCh38 GRCh37 |
392 | 472 | |
AHNAK2 | - | - |
GRCh38 GRCh37 |
1061 | 1129 | |
AMN | - | - |
GRCh38 GRCh37 |
453 | 628 | |
ANKRD9 | - | - |
GRCh38 GRCh37 |
31 | 86 | |
ASPG | - | - |
GRCh38 GRCh37 |
38 | 98 | |
ATP5MJ | - | - |
GRCh38 GRCh37 |
1 | 59 | |
BAG5 | - | - |
GRCh38 GRCh37 |
32 | 93 | |
BRF1 | - | - |
GRCh38 GRCh37 |
145 | 328 |
There are 54 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 |
---|---|---|---|---|
Pathogenic (1) |
|
Jul 27, 2019 | RCV001259801.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022