ClinVar Genomic variation as it relates to human health
GRCh37/hg19 5p15.33(chr5:676464-972978)x3
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 | |||
BRD9 | - | - |
GRCh38 GRCh37 |
29 | 187 | |
TPPP | - | - |
GRCh38 GRCh37 |
7 | 189 | |
TRIP13 | - | - |
GRCh38 GRCh37 |
113 | 270 | |
ZDHHC11 | - | - | - |
GRCh38 GRCh37 |
63 | 227 |
ZDHHC11B | - | - | - |
GRCh38 GRCh37 |
2 | 167 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jul 27, 2022 | RCV003484600.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024