Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Neuberg Centre For Genomic Medicine, |
RCV003340840 | SCV004047608 | uncertain significance | Mucopolysaccharidosis, MPS-IV-A | criteria provided, single submitter | clinical testing | The missense variant c.779A>T (p.Glu260Val) in GALNS gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The p.Glu260Val variant is novel (not in any individuals) in gnomAD Exomes and 1000 Genomes. This variant has not been reported to the ClinVar database. The amino acid Glu at position 260 is changed to a Val changing protein sequence and it might alter its composition and physico-chemical properties. The amino acid change p.Glu260Val in GALNS is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. For these reasons, this variant has been classified as Uncertain Significance (VUS). |