ClinVar Genomic variation as it relates to human health
NM_178828.5(SPATA31E1):c.4028A>G (p.Asn1343Ser)
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 | |||
LOC497256 | - | - | - | GRCh38 | - | 167 |
SPATA31E1 | - | - | - |
GRCh38 GRCh37 |
1 | 178 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Apr 26, 2024 | RCV004672883.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 11, 2024