"Ambry Genetics"[submitter] AND "DISP1"[gene] - ClinVar

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Items: 70

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2300159	NM_001377229.1(DISP1):c.7A>G (p.Met3Val)	DISP1 (M3V)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 3082584	NM_001377229.1(DISP1):c.182C>T (p.Thr61Met)	DISP1 (T61M)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2538101	NM_001377229.1(DISP1):c.213C>A (p.Asn71Lys)	DISP1 (N71K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2049879	NM_001377229.1(DISP1):c.281A>G (p.His94Arg)	DISP1 (H94R)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 1499747	NM_001377229.1(DISP1):c.341C>T (p.Ser114Leu)	DISP1 (S114L)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 2228096	NM_001377229.1(DISP1):c.349A>G (p.Met117Val)	DISP1 (M117V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2381716	NM_001377229.1(DISP1):c.413C>A (p.Thr138Lys)	DISP1 (T138K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2239723	NM_001377229.1(DISP1):c.597C>G (p.Phe199Leu)	DISP1 (F199L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2231199	NM_001377229.1(DISP1):c.718A>G (p.Met240Val)	DISP1 (M240V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2559655	NM_001377229.1(DISP1):c.721G>A (p.Val241Met)	DISP1 (V241M)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2263793	NM_001377229.1(DISP1):c.805A>G (p.Arg269Gly)	DISP1 (R26G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082595	NM_001377229.1(DISP1):c.830G>A (p.Arg277Lys)	DISP1 (R277K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554829	NM_001377229.1(DISP1):c.860A>T (p.His287Leu)	DISP1 (H287L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534893	NM_001377229.1(DISP1):c.1022A>G (p.Gln341Arg)	DISP1 (Q98R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508775	NM_001377229.1(DISP1):c.1094C>G (p.Ser365Trp)	DISP1 (S365W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272164	NM_001377229.1(DISP1):c.1118G>A (p.Arg373Gln)	DISP1 (R130Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272163	NM_001377229.1(DISP1):c.1147C>T (p.Arg383Trp)	DISP1 (R140W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543084	NM_001377229.1(DISP1):c.1238A>G (p.Asn413Ser)	DISP1 (N170S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252628	NM_001377229.1(DISP1):c.1240G>A (p.Val414Met)	DISP1 (V414M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082580	NM_001377229.1(DISP1):c.1250A>G (p.Lys417Arg)	DISP1 (K417R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1450864	NM_001377229.1(DISP1):c.1337C>T (p.Thr446Met)	DISP1 (T446M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2596690	NM_001377229.1(DISP1):c.1432T>C (p.Ser478Pro)	DISP1 (S478P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358362	NM_001377229.1(DISP1):c.1441G>A (p.Val481Met)	DISP1 (V238M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253797	NM_001377229.1(DISP1):c.1630T>C (p.Phe544Leu)	DISP1 (F544L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401253	NM_001377229.1(DISP1):c.1678C>T (p.Leu560Phe)	DISP1 (L560F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082582	NM_001377229.1(DISP1):c.1694T>C (p.Ile565Thr)	DISP1 (I322T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2040586	NM_001377229.1(DISP1):c.1781C>T (p.Ser594Leu)	DISP1 (S351L +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1174810	NM_001377229.1(DISP1):c.1804C>A (p.Gln602Lys)	DISP1 (Q359K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082583	NM_001377229.1(DISP1):c.1822A>G (p.Met608Val)	DISP1 (M608V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082585	NM_001377229.1(DISP1):c.1910C>T (p.Ala637Val)	DISP1 (A394V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082586	NM_001377229.1(DISP1):c.1982G>C (p.Arg661Pro)	DISP1 (R418P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515892	NM_001377229.1(DISP1):c.2032T>G (p.Tyr678Asp)	DISP1 (Y435D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082587	NM_001377229.1(DISP1):c.2050T>C (p.Trp684Arg)	DISP1 (W441R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558594	NM_001377229.1(DISP1):c.2108G>A (p.Arg703Gln)	DISP1 (R703Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2041501	NM_001377229.1(DISP1):c.2119G>A (p.Glu707Lys)	DISP1 (E464K +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2516005	NM_001377229.1(DISP1):c.2153G>A (p.Arg718His)	DISP1 (R475H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2367704	NM_001377229.1(DISP1):c.2266C>T (p.Arg756Trp)	DISP1 (R513W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082588	NM_001377229.1(DISP1):c.2270C>T (p.Ser757Leu)	DISP1 (S757L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220063	NM_001377229.1(DISP1):c.2319G>A (p.Met773Ile)	DISP1 (M530I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2711675	NM_001377229.1(DISP1):c.2377G>A (p.Val793Met)	DISP1 (V550M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2471586	NM_001377229.1(DISP1):c.2518T>C (p.Phe840Leu)	DISP1 (F840L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272161	NM_001377229.1(DISP1):c.2569A>C (p.Lys857Gln)	DISP1 (K614Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272160	NM_001377229.1(DISP1):c.2663T>G (p.Leu888Arg)	DISP1 (L645R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264175	NM_001377229.1(DISP1):c.2705G>A (p.Gly902Glu)	DISP1 (G902E +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2255013	NM_001377229.1(DISP1):c.2756C>G (p.Thr919Ser)	DISP1 (T676S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1991107	NM_001377229.1(DISP1):c.2902G>T (p.Val968Phe)	DISP1 (V968F +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2516463	NM_001377229.1(DISP1):c.2921A>G (p.Tyr974Cys)	DISP1 (Y731C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278971	NM_001377229.1(DISP1):c.2953C>G (p.Leu985Val)	DISP1 (L742V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353968	NM_001377229.1(DISP1):c.3016A>G (p.Ile1006Val)	DISP1 (I1006V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2492358	NM_001377229.1(DISP1):c.3128C>T (p.Ser1043Leu)	DISP1 (S1043L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468928	NM_001377229.1(DISP1):c.3232C>T (p.Arg1078Cys)	DISP1 (R835C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343231	NM_001377229.1(DISP1):c.3274G>A (p.Val1092Met)	DISP1 (V1092M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304859	NM_001377229.1(DISP1):c.3275T>G (p.Val1092Gly)	DISP1 (V1092G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318901	NM_001377229.1(DISP1):c.3384G>C (p.Gln1128His)	DISP1 (Q1128H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242246	NM_001377229.1(DISP1):c.3531T>G (p.His1177Gln)	DISP1 (H934Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353969	NM_001377229.1(DISP1):c.3610G>A (p.Ala1204Thr)	DISP1 (A1204T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2414910	NM_001377229.1(DISP1):c.3688C>T (p.Pro1230Ser)	DISP1 (P1230S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3272159	NM_001377229.1(DISP1):c.3934G>A (p.Val1312Met)	DISP1 (V1069M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2062939	NM_001377229.1(DISP1):c.3967G>A (p.Glu1323Lys)	DISP1 (E1080K +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2220909	NM_001377229.1(DISP1):c.3985A>G (p.Ile1329Val)	DISP1 (I1329V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1702962	NM_001377229.1(DISP1):c.4054C>T (p.Pro1352Ser)	DISP1 (P1109S +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2378610	NM_001377229.1(DISP1):c.4189A>G (p.Arg1397Gly)	DISP1 (R1154G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082589	NM_001377229.1(DISP1):c.4214C>T (p.Thr1405Met)	DISP1 (T1162M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272162	NM_001377229.1(DISP1):c.4283G>A (p.Ser1428Asn)	DISP1 (S1185N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356639	NM_001377229.1(DISP1):c.4321C>G (p.Leu1441Val)	DISP1 (L1198V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545447	NM_001377229.1(DISP1):c.4347T>G (p.Ser1449Arg)	DISP1 (S1449R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082590	NM_001377229.1(DISP1):c.4352A>C (p.Asn1451Thr)	DISP1 (N1208T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355951	NM_001377229.1(DISP1):c.4396C>A (p.His1466Asn)	DISP1 (H1466N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082591	NM_001377229.1(DISP1):c.4432A>G (p.Asn1478Asp)	DISP1 (N1235D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082592	NM_001377229.1(DISP1):c.4550A>C (p.Glu1517Ala)	DISP1 (E1274A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 70