ClinVar Genomic variation as it relates to human health
GRCh38/hg38 14q11.2(chr14:22130104-22343431)x3
Germline
Classification
(1)
Benign
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 | |||
TRA | - | - | - |
GRCh38 GRCh37 |
2 | 102 |
TRAV26-2 | - | - | - | GRCh38 | - | 25 |
TRAV27 | - | - | - | GRCh38 | - | 26 |
TRAV29DV5 | - | - | - | GRCh38 | - | 26 |
TRAV30 | - | - | - | GRCh38 | - | 26 |
TRAV34 | - | - | - | GRCh38 | - | 25 |
TRAV35 | - | - | - | GRCh38 | - | 25 |
TRAV36DV7 | - | - | - | GRCh38 | - | 25 |
TRAV38-1 | - | - | - | GRCh38 | - | 26 |
TRAV38-2DV8 | - | - | - | GRCh38 | - | 26 |
There are 4 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Sep 21, 2012 | RCV000138458.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024