"Ambry Genetics"[submitter] AND "SNX25"[gene] - ClinVar

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Items: 52

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2548731	NM_001378034.2(SNX25):c.645T>A (p.Ser215Arg)	SNX25 (S215R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341275	NM_001378034.2(SNX25):c.841C>G (p.Pro281Ala)	SNX25 (P117A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351839	NM_001378034.2(SNX25):c.871C>T (p.Arg291Cys)	SNX25 (R127C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3321303	NM_001378034.2(SNX25):c.974C>T (p.Ala325Val)	SNX25 (A161V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167251	NM_001378034.2(SNX25):c.1046A>G (p.Lys349Arg)	SNX25 (K185R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359452	NM_001378034.2(SNX25):c.1048C>T (p.Leu350Phe)	SNX25 (L186F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255465	NM_001378034.2(SNX25):c.1052T>G (p.Ile351Ser)	SNX25 (I351S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258945	NM_001378034.2(SNX25):c.1093T>C (p.Tyr365His)	SNX25 (Y365H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615916	NM_001378034.2(SNX25):c.1385G>A (p.Arg462Gln)	SNX25 (R298Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374509	NM_001378034.2(SNX25):c.1417G>C (p.Asp473His)	SNX25 (D506H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3167239	NM_001378034.2(SNX25):c.1525G>A (p.Glu509Lys)	SNX25 (E345K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2365778	NM_001378034.2(SNX25):c.1538T>C (p.Ile513Thr)	SNX25 (I513T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383547	NM_001378034.2(SNX25):c.1780G>A (p.Val594Met)	SNX25 (V594M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3167240	NM_001378034.2(SNX25):c.1805A>G (p.Asn602Ser)	SNX25 (N602S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167241	NM_001378034.2(SNX25):c.1951G>A (p.Glu651Lys)	SNX25 (E487K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167242	NM_001378034.2(SNX25):c.1960C>T (p.Arg654Cys)	SNX25 (R654C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492532	NM_001378034.2(SNX25):c.2044G>A (p.Glu682Lys)	SNX25 (E715K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312123	NM_001378034.2(SNX25):c.2113G>A (p.Gly705Arg)	SNX25 (G705R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264519	NM_001378034.2(SNX25):c.2135C>G (p.Thr712Arg)	SNX25 (T548R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3167243	NM_001378034.2(SNX25):c.2224C>G (p.Leu742Val)	SNX25 (L578V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222630	NM_001378034.2(SNX25):c.2389G>A (p.Val797Met)	SNX25 (V633M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167244	NM_001378034.2(SNX25):c.2444G>A (p.Arg815His)	SNX25 (R815H +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3167245	NM_001378034.2(SNX25):c.2551A>G (p.Met851Val)	SNX25 (M687V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167246	NM_001378034.2(SNX25):c.2557A>T (p.Ile853Phe)	SNX25 (I689F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319502	NM_001378034.2(SNX25):c.2620G>C (p.Val874Leu)	SNX25 (V710L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3167247	NM_001378034.2(SNX25):c.2626G>C (p.Val876Leu)	SNX25 (V712L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167248	NM_001378034.2(SNX25):c.2737A>G (p.Asn913Asp)	SNX25 (N913D +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262081	NM_001378034.2(SNX25):c.2737A>C (p.Asn913His)	SNX25 (N858H +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3321304	NM_001378034.2(SNX25):c.2830C>T (p.Pro944Ser)	SNX25 (P977S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556111	NM_001378034.2(SNX25):c.2834A>C (p.Asp945Ala)	SNX25 (D890A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3167249	NM_001378034.2(SNX25):c.2890T>C (p.Phe964Leu)	SNX25 (F909L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252454	NM_001378034.2(SNX25):c.2897C>G (p.Ala966Gly)	SNX25 (A802G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602488	NM_001378034.2(SNX25):c.2958T>G (p.Ile986Met)	SNX25 (I1019M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2297000	NM_001377440.1(LRP2BP):c.997G>A (p.Ala333Thr)	LRP2BP, SNX25 (A235T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120273	NM_001377440.1(LRP2BP):c.979G>A (p.Ala327Thr)	LRP2BP, SNX25 (A228T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384250	NM_001377440.1(LRP2BP):c.877G>A (p.Gly293Ser)	LRP2BP, SNX25 (G292S +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2330842	NM_001377440.1(LRP2BP):c.813C>G (p.Asp271Glu)	LRP2BP, SNX25 (D172E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120272	NM_001377440.1(LRP2BP):c.800A>G (p.Lys267Arg)	LRP2BP, SNX25 (K168R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222793	NM_001377440.1(LRP2BP):c.748G>A (p.Val250Met)	LRP2BP, SNX25 (V151M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346535	NM_001377440.1(LRP2BP):c.739G>A (p.Gly247Arg)	LRP2BP, SNX25 (G246R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219699	NM_001377440.1(LRP2BP):c.718C>T (p.Arg240Cys)	LRP2BP, SNX25 (R142C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560234	NM_001377440.1(LRP2BP):c.699C>G (p.Cys233Trp)	LRP2BP, SNX25 (C135W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120270	NM_001377440.1(LRP2BP):c.680C>A (p.Thr227Lys)	LRP2BP, SNX25 (T129K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250817	NM_001377440.1(LRP2BP):c.680C>T (p.Thr227Met)	LRP2BP, SNX25 (T128M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206492	NM_001377440.1(LRP2BP):c.643C>T (p.Leu215Phe)	LRP2BP, SNX25 (L116F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120269	NM_001377440.1(LRP2BP):c.467C>G (p.Ala156Gly)	LRP2BP, SNX25 (A57G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465820	NM_001377440.1(LRP2BP):c.452G>A (p.Arg151Gln)	LRP2BP, SNX25 (R150Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530506	NM_001377440.1(LRP2BP):c.388C>A (p.His130Asn)	LRP2BP, SNX25 (H129N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274961	NM_001377440.1(LRP2BP):c.292G>T (p.Val98Leu)	LRP2BP, SNX25 (V98L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278424	NM_001377440.1(LRP2BP):c.259G>A (p.Glu87Lys)	LRP2BP, SNX25 (E87K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120268	NM_001377440.1(LRP2BP):c.164T>G (p.Leu55Arg)	LRP2BP, SNX25 (L55R)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2600450	NM_001377440.1(LRP2BP):c.13A>G (p.Ser5Gly)	LRP2BP, SNX25 (S5G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 52