ClinVar Genomic variation as it relates to human health
NM_033550.4(TP53RK):c.36C>T (p.Gly12=)
Germline
Classification
(1)
Likely benign
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 | |||
LOC130065998 | - | - | - | GRCh38 | - | 19 |
TP53RK | - | - |
GRCh38 GRCh37 |
55 | 82 | |
TP53RK-DT | - | - | - | GRCh38 | - | 19 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Nov 1, 2022 | RCV002580704.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 29, 2024