"Ambry Genetics"[submitter] AND "SNX4"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2557978	NM_003794.4(SNX4):c.1344C>G (p.Ser448Arg)	SNX4 (S448R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596681	NM_003794.4(SNX4):c.1247G>A (p.Arg416Gln)	SNX4 (R416Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167315	NM_003794.4(SNX4):c.1213G>A (p.Ala405Thr)	SNX4 (A405T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167314	NM_003794.4(SNX4):c.1208C>T (p.Ala403Val)	SNX4 (A403V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204131	NM_003794.4(SNX4):c.1100C>T (p.Thr367Ile)	SNX4 (T367I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377308	NM_003794.4(SNX4):c.935A>G (p.Glu312Gly)	SNX4 (E312G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2412246	NM_003794.4(SNX4):c.878T>G (p.Ile293Ser)	SNX4 (I293S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208727	NM_003794.4(SNX4):c.848T>C (p.Met283Thr)	SNX4 (M283T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3321332	NM_003794.4(SNX4):c.823G>A (p.Gly275Arg)	SNX4 (G275R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3321333	NM_003794.4(SNX4):c.740G>A (p.Arg247Gln)	SNX4 (R247Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408709	NM_003794.4(SNX4):c.673C>T (p.His225Tyr)	SNX4 (H225Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167320	NM_003794.4(SNX4):c.665A>G (p.Asp222Gly)	SNX4 (D222G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167319	NM_003794.4(SNX4):c.649G>T (p.Asp217Tyr)	SNX4 (D217Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167318	NM_003794.4(SNX4):c.519A>C (p.Arg173Ser)	SNX4 (R173S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167317	NM_003794.4(SNX4):c.340A>G (p.Arg114Gly)	SNX4 (R114G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477728	NM_003794.4(SNX4):c.310T>G (p.Trp104Gly)	SNX4 (W104G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512492	NM_003794.4(SNX4):c.209G>A (p.Gly70Glu)	SNX4 (G70E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3321331	NM_003794.4(SNX4):c.140C>G (p.Thr47Arg)	SNX4 (T47R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2387983	NM_003794.4(SNX4):c.133G>A (p.Val45Ile)	SNX4 (V45I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331679	NM_003794.4(SNX4):c.112G>A (p.Ala38Thr)	SNX4 (A38T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167321	NM_003794.4(SNX4):c.68C>G (p.Pro23Arg)	LOC129937448, SNX4 (P23R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2589826	NM_003794.4(SNX4):c.65C>T (p.Ser22Phe)	LOC129937448, SNX4 (S22F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590530	NM_003794.4(SNX4):c.56C>G (p.Pro19Arg)	LOC129937448, SNX4 (P19R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2240733	NM_003794.4(SNX4):c.38A>G (p.Gln13Arg)	LOC129937448, SNX4 (Q13R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405566	NM_003794.4(SNX4):c.34C>T (p.Leu12Phe)	LOC129937448, SNX4 (L12F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2240732	NM_003794.4(SNX4):c.19G>T (p.Asp7Tyr)	LOC129937448, SNX4 (D7Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 26