ClinVar Genomic variation as it relates to human health
NM_001350814.2(GRB10):c.1485C>T (p.His495=)
Germline
Classification
(2)
Benign
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 | |||
GRB10 | No evidence available | No evidence available |
GRCh38 GRCh37 |
49 | 62 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Aug 1, 2023 | RCV003433831.5 | |
Benign (1) |
|
Mar 1, 2019 | RCV003966427.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 12, 2024