ClinVar Genomic variation as it relates to human health
GRCh38/hg38 16q24.3(chr16:89665706-90081985)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 | |||
TUBB3 | No evidence available | No evidence available |
GRCh38 GRCh37 |
288 | 354 | |
CDK10 | - | - |
GRCh38 GRCh37 |
83 | 159 | |
CENPBD1 | - | - | - |
GRCh38 GRCh37 |
14 | 67 |
DBNDD1 | - | - |
GRCh38 GRCh37 |
16 | 69 | |
DEF8 | - | - | - |
GRCh38 GRCh37 |
40 | 94 |
FANCA | - | - |
GRCh38 GRCh37 |
4078 | 5203 | |
GAS8 | - | - |
GRCh38 GRCh37 |
358 | 425 | |
GAS8-AS1 | - | - |
GRCh38 GRCh37 |
- | 64 | |
LINC02166 | - | - | - | GRCh38 | - | 33 |
LOC112486223 | - | - | - | GRCh38 | - | 177 |
There are 60 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Aug 12, 2011 | RCV000053937.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024