Related gene-specific medical variations for Gene (Select 56647) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3082192	NM_018180.3(DHX32):c.2083C>G (p.Gln695Glu)	BCCIP, DHX32 (Q695E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3082190	NM_018180.3(DHX32):c.1928A>G (p.His643Arg)	BCCIP, DHX32 (H643R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3082188	NM_018180.3(DHX32):c.1537G>T (p.Val513Leu)	BCCIP, DHX32 (V513L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3022967	NM_018180.3(DHX32):c.2157T>C (p.Pro719=)	DHX32, BCCIP	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3020197	NM_018180.3(DHX32):c.1910A>G (p.Asn637Ser)	BCCIP, DHX32 (N637S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3001282	NM_018180.3(DHX32):c.1696T>C (p.Cys566Arg)	BCCIP, DHX32 (C566R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2999643	NM_018180.3(DHX32):c.2063+12G>A	BCCIP, DHX32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2986277	NM_018180.3(DHX32):c.1645A>G (p.Ser549Gly)	BCCIP, DHX32 (S549G)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2975386	NM_018180.3(DHX32):c.1755T>C (p.Asp585=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2975247	NM_018180.3(DHX32):c.1425T>C (p.Ser475=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2971488	NM_018180.3(DHX32):c.1192+5T>C	BCCIP, DHX32	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2965224	NM_018180.3(DHX32):c.1487C>T (p.Ala496Val)	BCCIP, DHX32 (A496V)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2960232	NM_018180.3(DHX32):c.1490_1494del (p.Ala496_Ser497insTer)	BCCIP, DHX32	Deletion (nonsense +2 more)	not provided	GUncertain significance
Select item 2956658	NM_018180.3(DHX32):c.1693+16G>A	BCCIP, DHX32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2906041	NM_018180.3(DHX32):c.1119C>T (p.Asn373=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2904121	NM_018180.3(DHX32):c.1420C>A (p.Leu474Ile)	BCCIP, DHX32 (L474I)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2867371	NM_018180.3(DHX32):c.2133G>C (p.Gln711His)	BCCIP, DHX32 (Q711H)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2843889	NM_018180.3(DHX32):c.1694-18del	BCCIP, DHX32	Deletion (intron variant)	not provided	GLikely benign
Select item 2837463	NM_018180.3(DHX32):c.1093-11T>C	BCCIP, DHX32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2820389	NM_018180.3(DHX32):c.1805A>G (p.Tyr602Cys)	BCCIP, DHX32 (Y602C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2818929	NM_018180.3(DHX32):c.2218T>A (p.Cys740Ser)	BCCIP, DHX32 (C740S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2817409	NM_018180.3(DHX32):c.1890G>C (p.Arg630=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2812856	NM_018180.3(DHX32):c.2193G>T (p.Glu731Asp)	BCCIP, DHX32 (E731D)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2811168	NM_018180.3(DHX32):c.1370A>C (p.Gln457Pro)	BCCIP, DHX32 (Q457P)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2797478	NM_018180.3(DHX32):c.2141T>C (p.Val714Ala)	BCCIP, DHX32 (V714A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2792458	NM_018180.3(DHX32):c.1313T>C (p.Ile438Thr)	BCCIP, DHX32 (I438T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2782827	NM_018180.3(DHX32):c.2109T>C (p.Pro703=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2754904	NM_018180.3(DHX32):c.1249A>C (p.Lys417Gln)	BCCIP, DHX32 (K417Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2745454	NM_018180.3(DHX32):c.1379A>G (p.Glu460Gly)	BCCIP, DHX32 (E460G)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2743141	NM_018180.3(DHX32):c.1142G>A (p.Ser381Asn)	BCCIP, DHX32 (S381N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2737584	NM_018180.3(DHX32):c.2093del (p.Phe698fs)	BCCIP, DHX32 (F698fs)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2735884	NM_018180.3(DHX32):c.1693+6T>C	BCCIP, DHX32	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2712114	NM_018180.3(DHX32):c.1344C>G (p.Asn448Lys)	BCCIP, DHX32 (N448K)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2710471	NM_018180.3(DHX32):c.1670C>T (p.Thr557Ile)	BCCIP, DHX32 (T557I)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2704361	NM_018180.3(DHX32):c.1290G>A (p.Val430=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 2702315	NM_018180.3(DHX32):c.2085A>G (p.Gln695=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2604606	NM_018180.3(DHX32):c.2090A>G (p.Tyr697Cys)	BCCIP, DHX32 (Y697C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541755	NM_018180.3(DHX32):c.1102C>T (p.Pro368Ser)	BCCIP, DHX32 (P368S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528045	NM_018180.3(DHX32):c.2172T>A (p.Asn724Lys)	BCCIP, DHX32 (N724K)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2492295	NM_018180.3(DHX32):c.1985C>T (p.Pro662Leu)	BCCIP, DHX32 (P662L)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2477968	NM_018180.3(DHX32):c.1939G>A (p.Ala647Thr)	BCCIP, DHX32 (A647T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2428344	NM_018180.3(DHX32):c.1121C>T (p.Ser374Leu)	BCCIP, DHX32 (S374L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2428342	NM_018180.3(DHX32):c.1773C>G (p.Leu591=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2421540	NM_018180.3(DHX32):c.1585G>T (p.Ala529Ser)	BCCIP, DHX32 (A529S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2419043	NM_018180.3(DHX32):c.1171A>T (p.Ile391Phe)	BCCIP, DHX32 (I391F)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2418403	NM_018180.3(DHX32):c.1103C>T (p.Pro368Leu)	BCCIP, DHX32 (P368L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2274686	NM_018180.3(DHX32):c.1160T>C (p.Ile387Thr)	BCCIP, DHX32 (I387T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2274685	NM_018180.3(DHX32):c.1158G>T (p.Glu386Asp)	BCCIP, DHX32 (E386D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269898	NM_018180.3(DHX32):c.1802C>T (p.Pro601Leu)	BCCIP, DHX32 (P601L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226022	NM_018180.3(DHX32):c.1417A>C (p.Asn473His)	BCCIP, DHX32 (N473H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2209815	NM_018180.3(DHX32):c.1855G>A (p.Ala619Thr)	BCCIP, DHX32 (A619T)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2200766	NM_018180.3(DHX32):c.1987G>C (p.Glu663Gln)	BCCIP, DHX32 (E663Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2195659	NM_018180.3(DHX32):c.1380A>G (p.Glu460=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2192944	NM_018180.3(DHX32):c.2217A>G (p.Arg739=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2191141	NM_018180.3(DHX32):c.2064-8A>G	BCCIP, DHX32	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2189059	NM_018180.3(DHX32):c.1954_1955del (p.Leu652fs)	BCCIP, DHX32 (L652fs)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2188619	NM_018180.3(DHX32):c.1093-7T>C	BCCIP, DHX32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2181272	NM_018180.3(DHX32):c.1790G>A (p.Arg597Gln)	BCCIP, DHX32 (R597Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2178505	NM_018180.3(DHX32):c.2064-7_2064-4del	BCCIP, DHX32	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2172036	NM_018180.3(DHX32):c.1927C>T (p.His643Tyr)	BCCIP, DHX32 (H643Y)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2155331	NM_018180.3(DHX32):c.2196G>A (p.Thr732=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2144795	NM_018180.3(DHX32):c.1794C>T (p.Ile598=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2139673	NM_018180.3(DHX32):c.1754A>C (p.Asp585Ala)	BCCIP, DHX32 (D585A)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2136941	NM_018180.3(DHX32):c.2176del (p.Glu726fs)	BCCIP, DHX32 (E726fs)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2131268	NM_018180.3(DHX32):c.1703A>C (p.Glu568Ala)	BCCIP, DHX32 (E568A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2126752	NM_018180.3(DHX32):c.1351+18T>C	BCCIP, DHX32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2125104	NM_018180.3(DHX32):c.1534dup (p.Met512fs)	BCCIP, DHX32 (M512fs)	Duplication (frameshift variant +2 more)	not provided	GUncertain significance
Select item 2117554	NM_018180.3(DHX32):c.1125C>T (p.Leu375=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2113854	NM_018180.3(DHX32):c.1121C>G (p.Ser374Trp)	BCCIP, DHX32 (S374W)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2110820	NM_018180.3(DHX32):c.1352-24ATT[2]	DHX32, BCCIP	Microsatellite (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2110025	NM_018180.3(DHX32):c.1774T>C (p.Leu592=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2103893	NM_018180.3(DHX32):c.1833A>G (p.Glu611=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2103168	NM_018180.3(DHX32):c.2063+17A>G	BCCIP, DHX32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2099686	NM_018180.3(DHX32):c.1882-20T>C	BCCIP, DHX32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2097161	NM_018180.3(DHX32):c.1334A>T (p.Asp445Val)	BCCIP, DHX32 (D445V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2090290	NM_018180.3(DHX32):c.1570C>T (p.His524Tyr)	BCCIP, DHX32 (H524Y)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2085859	NM_018180.3(DHX32):c.1693+7G>A	BCCIP, DHX32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2084966	NM_018180.3(DHX32):c.1599T>C (p.Cys533=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2076754	NM_018180.3(DHX32):c.1228T>A (p.Ser410Thr)	BCCIP, DHX32 (S410T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2074288	NM_018180.3(DHX32):c.2191G>C (p.Glu731Gln)	BCCIP, DHX32 (E731Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2074058	NM_018180.3(DHX32):c.1692_1693+2del	BCCIP, DHX32	Deletion (intron variant +1 more)	not provided	GUncertain significance
Select item 2073978	NM_018180.3(DHX32):c.1653C>T (p.Tyr551=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2073977	NM_018180.3(DHX32):c.2018C>T (p.Ser673Phe)	BCCIP, DHX32 (S673F)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2072647	NM_018180.3(DHX32):c.1437CAT[1] (p.Ile480del)	BCCIP, DHX32 (I480del)	Microsatellite (inframe_deletion +2 more)	not provided	GUncertain significance
Select item 2069752	NM_018180.3(DHX32):c.1875T>C (p.Phe625=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2069617	NM_018180.3(DHX32):c.1882-7C>T	BCCIP, DHX32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2061965	NM_018180.3(DHX32):c.1857T>C (p.Ala619=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2050910	NM_018180.3(DHX32):c.1752A>C (p.Ala584=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2045616	NM_018180.3(DHX32):c.1671A>C (p.Thr557=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2042157	NM_018180.3(DHX32):c.2160_2161del (p.Ser721fs)	BCCIP, DHX32 (S721fs)	Microsatellite (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2035064	NM_018180.3(DHX32):c.1312A>G (p.Ile438Val)	BCCIP, DHX32 (I438V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2034614	NM_018180.3(DHX32):c.1979del (p.Lys660fs)	BCCIP, DHX32 (K660fs)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2032285	NM_018180.3(DHX32):c.1272C>T (p.Ala424=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2026885	NM_018180.3(DHX32):c.2110A>G (p.Ser704Gly)	BCCIP, DHX32 (S704G)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2021216	NM_018180.3(DHX32):c.1646G>A (p.Ser549Asn)	DHX32, BCCIP (S549N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2016564	NM_018180.3(DHX32):c.1172T>C (p.Ile391Thr)	BCCIP, DHX32 (I391T)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2016226	NM_018180.3(DHX32):c.2037G>A (p.Arg679=)	BCCIP, DHX32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2004773	NM_018180.3(DHX32):c.2192A>T (p.Glu731Val)	BCCIP, DHX32 (E731V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2001780	NM_018180.3(DHX32):c.1882-9G>A	BCCIP, DHX32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1998890	NM_018180.3(DHX32):c.1143C>G (p.Ser381Arg)	BCCIP, DHX32 (S381R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

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