"Ambry Genetics"[submitter] AND "LRRC59"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2210815	NM_018509.4(LRRC59):c.910G>A (p.Asp304Asn)	LRRC59 (D304N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376091	NM_018509.4(LRRC59):c.860C>T (p.Ala287Val)	LRRC59 (A287V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120842	NM_018509.4(LRRC59):c.819G>C (p.Gln273His)	LRRC59 (Q273H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225004	NM_018509.4(LRRC59):c.800G>A (p.Arg267Gln)	LRRC59 (R267Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540638	NM_018509.4(LRRC59):c.779C>T (p.Ala260Val)	LRRC59 (A260V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253109	NM_018509.4(LRRC59):c.728G>A (p.Arg243His)	LRRC59 (R243H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554411	NM_018509.4(LRRC59):c.722A>G (p.His241Arg)	LRRC59 (H241R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468034	NM_018509.4(LRRC59):c.709C>T (p.Pro237Ser)	LRRC59 (P237S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492067	NM_018509.4(LRRC59):c.697C>T (p.Pro233Ser)	LRRC59 (P233S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271850	NM_018509.4(LRRC59):c.674C>T (p.Pro225Leu)	LRRC59 (P225L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324659	NM_018509.4(LRRC59):c.638A>C (p.Gln213Pro)	LRRC59 (Q213P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291709	NM_018509.4(LRRC59):c.533G>A (p.Arg178Gln)	LRRC59 (R178Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120840	NM_018509.4(LRRC59):c.514A>C (p.Lys172Gln)	LRRC59 (K172Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556247	NM_018509.4(LRRC59):c.481C>T (p.Arg161Trp)	LRRC59 (R161W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209519	NM_018509.4(LRRC59):c.469C>T (p.Arg157Trp)	LRRC59 (R157W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291708	NM_018509.4(LRRC59):c.455A>G (p.Gln152Arg)	LRRC59 (Q152R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120838	NM_018509.4(LRRC59):c.421G>A (p.Ala141Thr)	LRRC59 (A141T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378102	NM_018509.4(LRRC59):c.409T>C (p.Cys137Arg)	LRRC59 (C137R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120837	NM_018509.4(LRRC59):c.325A>T (p.Asn109Tyr)	LRRC59 (N109Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299027	NM_018509.4(LRRC59):c.287A>G (p.Lys96Arg)	LRRC59 (K96R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2495321	NM_018509.4(LRRC59):c.179G>A (p.Gly60Asp)	LRRC59 (G60D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466494	NM_018509.4(LRRC59):c.155C>T (p.Thr52Ile)	LRRC59 (T52I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465140	NM_018509.4(LRRC59):c.125C>T (p.Thr42Ile)	LRRC59 (T42I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253643	NM_018509.4(LRRC59):c.87G>C (p.Glu29Asp)	LRRC59 (E29D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537831	NM_018509.4(LRRC59):c.30C>A (p.Asn10Lys)	LRRC59 (N10K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25