"PreventionGenetics, part of Exact Sciences"[submitter] AND "IFT81"[ge - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 731781	NM_014055.4(IFT81):c.65A>C (p.Asn22Thr)	IFT81 (N22T)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GLikely benign
Select item 734183	NM_014055.4(IFT81):c.792G>A (p.Lys264=)	IFT81	Single nucleotide variant (synonymous variant +2 more)	IFT81-related disorder +1 more	GBenign/Likely benign
Select item 1083729	NM_014055.4(IFT81):c.1731A>G (p.Gln577=)	IFT81	Single nucleotide variant (synonymous variant +1 more)	IFT81-related disorder +1 more	GLikely benign
Select item 1639822	NM_014055.4(IFT81):c.2022A>G (p.Leu674=)	IFT81	Single nucleotide variant (synonymous variant +1 more)	IFT81-related disorder +1 more	GLikely benign

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