ClinVar Miner

Submissions for variant NM_000180.3(GUCY2D):c.2302C>T (p.Arg768Trp) (rs61750168)

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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000084856 SCV000322380 pathogenic not provided 2016-04-04 criteria provided, single submitter clinical testing The R768W variant in the GUCY2D gene has been reported previously in the heterozygous, homozygous, and compound heterozygous state in multiple unrelated individuals with Leber congenital amaurosis, and may represent a European founder mutation (Lotery et al., 2000; Booij et al., 2005; Astuti et al., 2015; Peshenko et al., 2010; Yzer et al., 2006; Coppieters et al., 2012). Functional studies of the R768W variant in HEK293 cells resulted in a dramatic reduction in GUCY2D enzyme activation in the presence of GCAP1, diminished binding to GCAP1, and altered GCAP1 co-localization (Peshenko et al., 2010). The R768W variant was not observed with any significant frequency in approximately 6500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. The R768W variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs at a position that is conserved across species. We interpret R768W as a pathogenic variant.
Invitae RCV000543628 SCV000649515 pathogenic Cone-rod dystrophy 6; Leber congenital amaurosis 1 2018-04-16 criteria provided, single submitter clinical testing This sequence change replaces arginine with tryptophan at codon 768 of the GUCY2D protein (p.Arg768Trp). The arginine residue is highly conserved and there is a moderate physicochemical difference between arginine and tryptophan. This variant is present in population databases (rs61750168, ExAC 0.03%). This variant has been reported in the homozygous or compound heterozygous state in many individuals affected with Leber congenital amaurosis (PMID: 23035049, 17724218, 26626312, 26253563, 16505055). ClinVar contains an entry for this variant (Variation ID: 98563). Experimental studies have shown that this missense change severely impairs binding to RD3 and is enzymatically inactive, even at saturating concentrations of GCAP1 (PMID: 20050595, 25477517). For these reasons, this variant has been classified as Pathogenic.
Fulgent Genetics,Fulgent Genetics RCV000763023 SCV000893483 pathogenic Choroidal dystrophy, central areolar 1; Cone-rod dystrophy 6; Leber congenital amaurosis 1 2018-10-31 criteria provided, single submitter clinical testing
Retina International RCV000084856 SCV000116992 not provided not provided no assertion provided not provided
Medical Genetics Laboratory, Kennedy Center,Juliane Marie Center, Rigshospitalet RCV000787613 SCV000926597 likely pathogenic Leber congenital amaurosis 2018-04-01 no assertion criteria provided research
OMIM RCV000850093 SCV000992257 pathogenic Leber congenital amaurosis 1 2019-09-03 no assertion criteria provided literature only
OMIM RCV000850094 SCV000992258 pathogenic NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1I 2019-09-03 no assertion criteria provided literature only

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