ClinVar Genomic variation as it relates to human health
NM_152259.4(TICRR):c.5342A>G (p.Glu1781Gly)
Germline
Classification
(2)
Uncertain significance
criteria provided, multiple submitters, no conflicts
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 | |||
KIF7 | - | - |
GRCh38 GRCh37 |
1273 | 1542 | |
TICRR | - | - |
GRCh38 GRCh37 |
73 | 206 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Sep 17, 2021 | RCV004082735.1 | |
Uncertain significance (1) |
|
- | RCV004695355.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 17, 2024