"Ambry Genetics"[submitter] AND "STK35"[gene] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2291209	NM_080836.4(STK35):c.61A>T (p.Arg21Trp)	STK35 (R21W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351149	NM_080836.4(STK35):c.101G>A (p.Ser34Asn)	STK35 (S34N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323323	NM_080836.4(STK35):c.173C>A (p.Ala58Asp)	LOC130065299, STK35 (A58D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243626	NM_080836.4(STK35):c.176G>A (p.Arg59Gln)	LOC130065299, STK35 (R59Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390671	NM_080836.4(STK35):c.187T>G (p.Ser63Ala)	LOC130065299, STK35 (S63A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323322	NM_080836.4(STK35):c.199C>G (p.Arg67Gly)	LOC130065299, STK35 (R67G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291836	NM_080836.4(STK35):c.229G>C (p.Asp77His)	LOC130065299, STK35 (D77H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525619	NM_080836.4(STK35):c.235C>A (p.Pro79Thr)	LOC130065299, STK35 (P79T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323325	NM_080836.4(STK35):c.248C>T (p.Ala83Val)	LOC130065299, STK35 (A83V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323324	NM_080836.4(STK35):c.250C>G (p.Pro84Ala)	LOC130065299, STK35 (P84A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171386	NM_080836.4(STK35):c.310C>T (p.Pro104Ser)	STK35 (P104S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171387	NM_080836.4(STK35):c.355G>A (p.Gly119Arg)	STK35 (G119R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310243	NM_080836.4(STK35):c.356G>C (p.Gly119Ala)	STK35 (G119A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285969	NM_080836.4(STK35):c.359C>T (p.Ala120Val)	STK35 (A120V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311000	NM_080836.4(STK35):c.362G>C (p.Arg121Pro)	STK35 (R121P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569552	NM_080836.4(STK35):c.392C>T (p.Pro131Leu)	STK35 (P131L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548216	NM_080836.4(STK35):c.409G>A (p.Gly137Arg)	STK35 (G137R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461741	NM_080836.4(STK35):c.434C>A (p.Thr145Lys)	STK35 (T145K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256302	NM_080836.4(STK35):c.442C>T (p.Pro148Ser)	STK35 (P148S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534646	NM_080836.4(STK35):c.479C>T (p.Pro160Leu)	STK35 (P160L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534647	NM_080836.4(STK35):c.484A>G (p.Thr162Ala)	STK35 (T162A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171388	NM_080836.4(STK35):c.497C>T (p.Pro166Leu)	STK35 (P166L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534648	NM_080836.4(STK35):c.512G>A (p.Arg171Gln)	STK35 (R171Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2534650	NM_080836.4(STK35):c.533C>T (p.Ala178Val)	STK35 (A178V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534651	NM_080836.4(STK35):c.554T>A (p.Phe185Tyr)	STK35 (F185Y)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3323326	NM_080836.4(STK35):c.562C>G (p.Arg188Gly)	STK35 (R188G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171389	NM_080836.4(STK35):c.664G>A (p.Gly222Arg)	STK35 (G222R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171390	NM_080836.4(STK35):c.667C>G (p.Arg223Gly)	STK35 (R223G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204325	NM_080836.4(STK35):c.898A>G (p.Arg300Gly)	STK35 (R300G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603996	NM_080836.4(STK35):c.1204A>C (p.Asn402His)	STK35 (N402H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323327	NM_080836.4(STK35):c.1249G>A (p.Gly417Ser)	STK35 (G417S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 31