rs149051148

Description

This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). Publications were found based on this search. However, the evidence from the literature, in combination with allele frequency data from public databases where available, was not sufficient to rule this variant in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.

The MKKS p.Arg518His variant was identified in 1 of 163 pedigrees with Bardet-Biedl syndrome (Beales_2001_PMID:11179009). The variant was also identified in dbSNP (ID: rs149051148), ClinVar (classified as likely benign by Invitae) and LOVD 3.0 (classified as likely benign and benign). The variant was identified in control databases in 82 of 282826 chromosomes at a frequency of 0.00029 (Genome Aggregation Database Feb 27, 2017). The variant was observed in the following populations: East Asian in 14 of 19954 chromosomes (freq: 0.000702), European (non-Finnish) in 54 of 129138 chromosomes (freq: 0.000418), South Asian in 10 of 30616 chromosomes (freq: 0.000327) and Latino in 4 of 35430 chromosomes (freq: 0.000113), while the variant was not observed in the African, Ashkenazi Jewish, European (Finnish), and Other populations. Functional studies of the R518H variant show no effect on the protein compared to wildtype (Hirayama_2008_PMID:18094050; Zaghloul_2010_PMID:20498079). The p.Arg518 residue is not conserved in mammals and computational analyses (PolyPhen-2, SIFT, AlignGVGD, BLOSUM, MutationTaster) do not suggest a high likelihood of impact to the protein; however, this information is not predictive enough to rule out pathogenicity. The variant occurs outside of the splicing consensus sequence and in silico or computational prediction software programs (SpliceSiteFinder, MaxEntScan, NNSPLICE, and GeneSplicer) do not predict a difference in splicing. In summary, based on the above information the clinical significance of this variant cannot be determined with certainty at this time although we would lean towards a more benign role for this variant. This variant is classified as likely benign.

This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). Publications were found based on this search. However, the evidence from the literature, in combination with allele frequency data from public databases where available, was not sufficient to rule this variant in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.