ClinVar Genomic variation as it relates to human health
NM_001004051.4(GPRASP2):c.2363G>T (p.Ser788Ile)
Germline
Classification
(1)
Likely pathogenic
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 | |||
ARMCX5-GPRASP2 | - | - | - |
GRCh38 GRCh37 |
- | 359 |
GPRASP2 | - | - |
GRCh38 GRCh37 |
- | 221 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely pathogenic (1) |
|
Jan 12, 2022 | RCV002474263.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 01, 2024