Submissions for variant NM_015662.3(IFT172):c.2308A>C (p.Ile770Leu)

Total submissions: 2

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	RCV002471925	SCV002767570	uncertain significance	Short-rib thoracic dysplasia 10 with or without polydactyly	2019-08-28	criteria provided, single submitter	clinical testing	A heterozygous missense variant was identified, NM_015662.2(IFT172):c.2308A>C in exon 22 of 48 of the IFT172 gene. This substitution is predicted to create a minor amino acid change from isoleucine to leucine at position 770 of the protein, NP_056477.1(IFT172):p.(Ile770Leu). The isoleucine at this position has moderate conservation (100 vertebrates, UCSC), but is not situated in a known functional domain. In silico software predictions of the pathogenicity of this variant are conflicting (Polyphen, SIFT, CADD, Mutation Taster). The variant is present in the gnomAD population database at a frequency of 0.0004% (1 heterozygotes, 0 homozygotes). The variant has not been previously reported in a clinical testing setting. Analysis of parental samples has found this variant to be paternally inherited. Based on information available at the time of curation, this variant has been classified as a VARIANT of UNCERTAIN SIGNIFICANCE (VUS).
Fulgent Genetics, Fulgent Genetics	RCV005025839	SCV005651420	uncertain significance	Short-rib thoracic dysplasia 10 with or without polydactyly; Retinitis pigmentosa 71; Bardet-Biedl syndrome 20	2024-04-24	criteria provided, single submitter	clinical testing