ClinVar Genomic variation as it relates to human health
NM_000996.4(RPL35A):c.204A>G (p.Arg68=)
Germline
Classification
(2)
Likely 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 | |||
IQCG | - | - |
GRCh38 GRCh37 |
29 | 208 | |
RPL35A | - | - |
GRCh38 GRCh37 |
- | 172 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
May 8, 2023 | RCV003516257.1 | |
RPL35A-related disorder
|
Likely benign (1) |
|
Apr 30, 2019 | RCV003980998.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 01, 2024