"PreventionGenetics, part of Exact Sciences"[submitter] AND "IFT57"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 774602	NM_018010.4(IFT57):c.1232A>G (p.Asn411Ser)	IFT57 (N411S)	Single nucleotide variant (missense variant)	IFT57-related disorder +1 more	GBenign
Select item 1652906	NM_018010.4(IFT57):c.1197C>T (p.His399=)	IFT57	Single nucleotide variant (synonymous variant)	IFT57-related disorder +1 more	GLikely benign
Select item 1672902	NM_018010.4(IFT57):c.1044+7A>G	IFT57	Single nucleotide variant (intron variant)	IFT57-related disorder +1 more	GBenign/Likely benign
Select item 2060868	NM_018010.4(IFT57):c.96G>C (p.Arg32=)	IFT57	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1094046	NM_018010.4(IFT57):c.35G>C (p.Gly12Ala)	IFT57 (G12A)	Single nucleotide variant (missense variant)	IFT57-related disorder +1 more	GLikely benign
Select item 1550808	NM_018010.4(IFT57):c.7G>A (p.Ala3Thr)	IFT57 (A3T)	Single nucleotide variant (missense variant)	IFT57-related disorder +1 more	GBenign

ClinVar