"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "IFT70B"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2651567	NM_152517.3(IFT70B):c.1613A>G (p.Lys538Arg)	IFT70B (K538R)	Single nucleotide variant (missense variant)	IFT70B-related condition +1 more	GLikely benign
Select item 2651568	NM_152517.3(IFT70B):c.777T>C (p.Ala259=)	IFT70B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign