Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Neuberg Centre For Genomic Medicine, |
RCV005055521 | SCV005690639 | pathogenic | Microphthalmia, syndromic 1 | criteria provided, single submitter | clinical testing | The missense c.109T>C (p.Ser37Pro) variant in NAA10 gene has been reported in multiple individuals from two families affected with NAA10-related Ogden syndrome (Rope et al., 2011). It has also been observed to segregate with disease in related individuals (Rope et al., 2011). Experimental studies showed that this variant impairs both NatA complex formation and NatA catalytic activity (Myklebust et al., 2015). This variant is absent in the gnomAD Exomes. This variant has been submitted to the ClinVar database as Pathogenic. Multiple lines of computational evidence (Polyphen - Probably Damaging, SIFT - Damaging and MutationTaster - Disease causing) predict a damaging effect on protein structure and function for this variant. The reference amino acid at this position in NAA10 is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. The amino acid Ser at position 37 is changed to a Pro changing protein sequence and it might alter its composition and physico-chemical properties. For these reasons, this variant has been classified as Pathogenic. | |
OMIM | RCV000022818 | SCV000044107 | pathogenic | Ogden syndrome | 2011-07-15 | no assertion criteria provided | literature only |