ClinVar Genomic variation as it relates to human health
NM_002863.5(PYGL):c.1964_1969inv (p.Glu655_Val657delinsAlaPhePhe)
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
PYGL | - | - |
GRCh38 GRCh37 |
345 | 364 |
Conditions - Germline
There are no conditions for this variant because no interpretation for the single variant has been submitted to ClinVar yet.
Citations for germline classification of this variant
HelpConditions - Somatic
There are no conditions for this variant because no interpretation for the single variant has been submitted to ClinVar yet.
Citations for somatic classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 25, 2024