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

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1981142	NM_002579.3(PALM):c.14C>T (p.Ala5Val)	PALM (A5V)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2296474	NM_002579.3(PALM):c.70C>T (p.Arg24Trp)	PALM (R24W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 431724	NM_002579.3(PALM):c.71G>A (p.Arg24Gln)	PALM (R24Q)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 2488747	NM_002579.3(PALM):c.77C>T (p.Ala26Val)	PALM (A26V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3208136	NM_002579.3(PALM):c.97C>T (p.Arg33Trp)	PALM (R33W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2177072	NM_002579.3(PALM):c.176C>T (p.Thr59Met)	PALM (T59M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2978203	NM_002579.3(PALM):c.245G>A (p.Arg82Gln)	PALM (R82Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2174519	NM_002579.3(PALM):c.256G>T (p.Asp86Tyr)	PALM (D86Y)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1392510	NM_002579.3(PALM):c.310G>A (p.Ala104Thr)	PALM (A104T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2301416	NM_002579.3(PALM):c.359C>A (p.Ala120Asp)	PALM (A120D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1447925	NM_002579.3(PALM):c.422C>T (p.Thr141Met)	PALM (T141M)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2311153	NM_002579.3(PALM):c.430G>A (p.Gly144Ser)	PALM (G144S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1504927	NM_002579.3(PALM):c.434C>T (p.Thr145Met)	PALM (T145M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2208844	NM_002579.3(PALM):c.446A>T (p.Lys149Met)	PALM (K149M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2520071	NM_002579.3(PALM):c.574A>T (p.Thr192Ser)	PALM (T192S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2326471	NM_002579.3(PALM):c.619G>A (p.Glu207Lys)	PALM (E207K)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2312082	NM_002579.3(PALM):c.635T>G (p.Val212Gly)	PALM (V212G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529878	NM_002579.3(PALM):c.667G>A (p.Gly223Arg)	PALM (G223R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3208134	NM_002579.3(PALM):c.670A>C (p.Ile224Leu)	PALM (I180L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218990	NM_002579.3(PALM):c.695T>G (p.Val232Gly)	PALM (V188G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403340	NM_002579.3(PALM):c.706A>G (p.Ile236Val)	PALM (I192V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595043	NM_002579.3(PALM):c.721G>A (p.Glu241Lys)	PALM (E197K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559596	NM_002579.3(PALM):c.739G>A (p.Ala247Thr)	PALM (A203T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536432	NM_002579.3(PALM):c.752C>T (p.Ala251Val)	PALM (A251V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304127	NM_002579.3(PALM):c.758C>T (p.Ala253Val)	PALM (A209V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490703	NM_002579.3(PALM):c.772G>C (p.Gly258Arg)	PALM (G214R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207327	NM_002579.3(PALM):c.791C>T (p.Ala264Val)	PALM (A220V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2189989	NM_002579.3(PALM):c.809G>A (p.Arg270Gln)	PALM (R226Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1516521	NM_002579.3(PALM):c.851C>T (p.Thr284Met)	PALM (T240M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2357914	NM_002579.3(PALM):c.874C>T (p.Pro292Ser)	PALM (P248S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330548	NM_002579.3(PALM):c.881A>C (p.Gln294Pro)	PALM (Q250P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313768	NM_002579.3(PALM):c.937G>A (p.Glu313Lys)	PALM (E269K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607948	NM_002579.3(PALM):c.996A>C (p.Glu332Asp)	PALM (E332D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1897394	NM_002579.3(PALM):c.1042G>T (p.Ala348Ser)	PALM (A304S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3208133	NM_002579.3(PALM):c.1093G>A (p.Glu365Lys)	PALM (E365K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1519758	NM_002579.3(PALM):c.1095G>T (p.Glu365Asp)	PALM (E321D +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance

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Items: 36