"Ambry Genetics"[submitter] AND "IFT25"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3285427	NM_016126.4(IFT25):c.425T>C (p.Leu142Pro)	IFT25 (L76P +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2469874	NM_016126.4(IFT25):c.364G>A (p.Ala122Thr)	IFT25 (A122T +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3108397	NM_016126.4(IFT25):c.334G>A (p.Ala112Thr)	IFT25 (A89T +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3108396	NM_016126.4(IFT25):c.195A>C (p.Gln65His)	IFT25 (Q22H +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3285428	NM_016126.4(IFT25):c.167A>G (p.His56Arg)	IFT25 (H56R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469668	NM_016126.4(IFT25):c.92T>C (p.Ile31Thr)	IFT25 (I31T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3108398	NM_016126.4(IFT25):c.40G>A (p.Glu14Lys)	IFT25 (E14K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3108395	NM_016126.4(IFT25):c.11T>C (p.Ile4Thr)	IFT25 (I4T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

ClinVar