ClinVar Genomic variation as it relates to human health
NM_130468.4(CHST14):c.403C>G (p.Arg135Gly)
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
CHST14 | - | - |
GRCh38 GRCh37 |
206 | 283 |
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 rs267606727 ...
HelpRecord last updated Jan 26, 2024