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

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3290204	NM_178834.5(LAYN):c.17C>T (p.Ala6Val)	LAYN (A6V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2285947	NM_178834.5(LAYN):c.35T>G (p.Leu12Arg)	LAYN (L12R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3117977	NM_178834.5(LAYN):c.59G>A (p.Arg20Gln)	LAYN (R20Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3290203	NM_178834.5(LAYN):c.74G>T (p.Arg25Leu)	LAYN (R25L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3290198	NM_178834.5(LAYN):c.116G>A (p.Arg39Lys)	LAYN (R39K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543926	NM_178834.5(LAYN):c.130G>A (p.Val44Ile)	LAYN (V44I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2231693	NM_178834.5(LAYN):c.167T>G (p.Phe56Cys)	LAYN (F64C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3290201	NM_178834.5(LAYN):c.223T>G (p.Ser75Ala)	LAYN (S75A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117974	NM_178834.5(LAYN):c.307C>T (p.Arg103Cys)	LAYN (R111C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2367908	NM_178834.5(LAYN):c.308G>A (p.Arg103His)	LAYN (R103H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3290200	NM_178834.5(LAYN):c.359C>G (p.Thr120Ser)	LAYN (L28V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558608	NM_178834.5(LAYN):c.433A>T (p.Met145Leu)	LAYN (M153L +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3117975	NM_178834.5(LAYN):c.463A>G (p.Ile155Val)	LAYN (I11V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509720	NM_178834.5(LAYN):c.473C>T (p.Pro158Leu)	LAYN (P14L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466993	NM_178834.5(LAYN):c.500G>A (p.Arg167Gln)	LAYN (R175Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542360	NM_178834.5(LAYN):c.593C>A (p.Thr198Lys)	LAYN, LOC126861337 (T53K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221576	NM_178834.5(LAYN):c.631G>A (p.Ala211Thr)	LAYN, LOC126861337 (A66T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290199	NM_178834.5(LAYN):c.653G>A (p.Ser218Asn)	LAYN, LOC126861337 (S218N +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2368276	NM_178834.5(LAYN):c.721G>A (p.Val241Ile)	LAYN (V249I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208576	NM_178834.5(LAYN):c.766C>T (p.Arg256Trp)	LAYN (R256W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361355	NM_178834.5(LAYN):c.781C>T (p.Pro261Ser)	LAYN (P269S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265543	NM_178834.5(LAYN):c.803C>G (p.Thr268Ser)	LAYN (T268S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117978	NM_178834.5(LAYN):c.805A>G (p.Ile269Val)	LAYN (I125V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262478	NM_178834.5(LAYN):c.856G>A (p.Val286Ile)	LAYN (V286I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618271	NM_178834.5(LAYN):c.893C>T (p.Thr298Ile)	LAYN (T154I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600462	NM_178834.5(LAYN):c.895C>T (p.Arg299Trp)	LAYN (R307W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492882	NM_178834.5(LAYN):c.998G>A (p.Ser333Asn)	LAYN (S188N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396533	NM_178834.5(LAYN):c.1021G>A (p.Val341Met)	LAYN (V196M +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3117973	NM_178834.5(LAYN):c.1085A>G (p.Lys362Arg)	LAYN (K218R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 29