"Ambry Genetics"[submitter] AND "IFT22"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2286288	NM_022777.4(IFT22):c.505A>G (p.Ile169Val)	IFT22 (I169V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204150	NM_022777.4(IFT22):c.473G>A (p.Arg158Gln)	IFT22 (R128Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226622	NM_022777.4(IFT22):c.392A>G (p.Lys131Arg)	IFT22 (K101R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335540	NM_022777.4(IFT22):c.329C>T (p.Pro110Leu)	IFT22 (P80L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548251	NM_022777.4(IFT22):c.287G>A (p.Arg96Gln)	IFT22 (R19Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359355	NM_022777.4(IFT22):c.286C>T (p.Arg96Trp)	IFT22 (R19W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281124	NM_022777.4(IFT22):c.283C>G (p.His95Asp)	IFT22 (H65D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281698	NM_022777.4(IFT22):c.266A>T (p.Asn89Ile)	IFT22 (N89I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108394	NM_022777.4(IFT22):c.242C>T (p.Ala81Val)	IFT22 (A81V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108393	NM_022777.4(IFT22):c.227C>T (p.Ala76Val)	IFT22 (A76V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314363	NM_022777.4(IFT22):c.218G>A (p.Cys73Tyr)	IFT22 (C73Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455240	NM_022777.4(IFT22):c.197G>C (p.Gly66Ala)	IFT22 (G66A)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2283339	NM_022777.4(IFT22):c.126A>C (p.Glu42Asp)	IFT22 (E42D)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2517890	NM_022777.4(IFT22):c.86T>C (p.Ile29Thr)	IFT22 (I29T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance