"Ambry Genetics"[submitter] AND "LRCH3"[gene] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2520184	NM_001365715.1(LRCH3):c.67G>A (p.Gly23Ser)	LRCH3 (G23S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2210167	NM_001365715.1(LRCH3):c.86A>C (p.His29Pro)	LRCH3 (H29P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2610576	NM_001365715.1(LRCH3):c.107C>A (p.Ala36Glu)	LRCH3 (A36E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2489815	NM_001365715.1(LRCH3):c.127G>T (p.Gly43Cys)	LRCH3 (G43C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2477896	NM_001365715.1(LRCH3):c.217C>T (p.Pro73Ser)	LRCH3 (P73S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2215054	NM_001365715.1(LRCH3):c.476A>G (p.Asn159Ser)	LRCH3 (N159S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2318442	NM_001365715.1(LRCH3):c.506T>C (p.Ile169Thr)	LRCH3 (I169T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2531990	NM_001365715.1(LRCH3):c.508G>C (p.Gly170Arg)	LRCH3 (G170R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2320783	NM_001365715.1(LRCH3):c.620A>C (p.His207Pro)	LRCH3 (H207P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2454327	NM_001365715.1(LRCH3):c.662T>A (p.Ile221Lys)	LRCH3 (I221K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2303180	NM_001365715.1(LRCH3):c.827C>T (p.Ala276Val)	LRCH3 (A276V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2407398	NM_001365715.1(LRCH3):c.910C>T (p.Arg304Cys)	LRCH3 (R304C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2313806	NM_001365715.1(LRCH3):c.1012C>G (p.Arg338Gly)	LRCH3 (R338G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2495852	NM_001365715.1(LRCH3):c.1036C>G (p.Gln346Glu)	LRCH3 (Q346E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2522054	NM_001365715.1(LRCH3):c.1055G>T (p.Ser352Ile)	LRCH3 (S352I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2559423	NM_001365715.1(LRCH3):c.1073G>A (p.Arg358His)	LRCH3 (R358H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2552603	NM_001365715.1(LRCH3):c.1147G>A (p.Ala383Thr)	LRCH3 (A383T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2318918	NM_001365715.1(LRCH3):c.1152G>C (p.Glu384Asp)	LRCH3 (E384D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2487895	NM_001365715.1(LRCH3):c.1200C>A (p.Ser400Arg)	LRCH3 (S400R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2508122	NM_001365715.1(LRCH3):c.1238G>T (p.Arg413Leu)	LRCH3 (R413L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2562409	NM_001365715.1(LRCH3):c.1310G>A (p.Arg437Lys)	LRCH3 (R437K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2409298	NM_001365715.1(LRCH3):c.1546A>G (p.Ser516Gly)	LRCH3 (S516G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2232101	NM_001365715.1(LRCH3):c.1627G>T (p.Asp543Tyr)	LRCH3 (D543Y)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2622514	NM_001365715.1(LRCH3):c.1820A>T (p.Gln607Leu)	LRCH3 (Q583L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2596227	NM_001365715.1(LRCH3):c.1876C>T (p.His626Tyr)	LRCH3 (H626Y +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2558373	NM_001365715.1(LRCH3):c.1931T>G (p.Ile644Arg)	LRCH3 (I608R +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2473337	NM_001365715.1(LRCH3):c.1978G>A (p.Asp660Asn)	LRCH3 (D624N +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2370361	NM_001365715.1(LRCH3):c.1988G>A (p.Arg663His)	LRCH3 (R639H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2334137	NM_001365715.1(LRCH3):c.2075C>T (p.Ala692Val)	LRCH3 (A692V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2621301	NM_001365715.1(LRCH3):c.2104A>G (p.Ser702Gly)	LRCH3 (S666G +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 30