ClinVar for Gene (Select 57647) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3365499	NM_032656.4(DHX37):c.2212G>T (p.Glu738Ter)	DHX37 (E738*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 3363220	NM_032656.4(DHX37):c.2570T>C (p.Val857Ala)	DHX37 (V857A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361438	NM_032656.4(DHX37):c.2330_2331inv (p.Thr777Met)	DHX37 (T777M)	Inversion (missense variant)	not provided	GUncertain significance
Select item 3360752	NM_032656.4(DHX37):c.1739A>G (p.Glu580Gly)	DHX37 (E580G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3355395	NM_032656.4(DHX37):c.3050C>T (p.Pro1017Leu)	DHX37 (P1017L)	Single nucleotide variant (missense variant)	DHX37-related disorder	GUncertain significance
Select item 3271907	NM_032656.4(DHX37):c.2543C>T (p.Ala848Val)	DHX37 (A848V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3271905	NM_032656.4(DHX37):c.460C>T (p.Arg154Cys)	DHX37 (R154C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3271904	NM_032656.4(DHX37):c.503A>G (p.Glu168Gly)	DHX37 (E168G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3244437	NC_000012.11:g.(?_125263013)_(125473568_?)dup	DHX37, SCARB1 +1 more	Duplication	not provided	GUncertain significance
Select item 3082276	NM_032656.4(DHX37):c.952G>A (p.Val318Met)	DHX37 (V318M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3082275	NM_032656.4(DHX37):c.920G>A (p.Arg307His)	DHX37 (R307H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3082274	NM_032656.4(DHX37):c.683G>C (p.Arg228Thr)	DHX37 (R228T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3082273	NM_032656.4(DHX37):c.3127G>A (p.Val1043Met)	DHX37 (V1043M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3082272	NM_032656.4(DHX37):c.2929C>T (p.Pro977Ser)	DHX37 (P977S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3082271	NM_032656.4(DHX37):c.2884G>A (p.Asp962Asn)	DHX37 (D962N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3082270	NM_032656.4(DHX37):c.2747C>T (p.Pro916Leu)	DHX37 (P916L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3082269	NM_032656.4(DHX37):c.2653A>G (p.Met885Val)	DHX37 (M885V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3082267	NM_032656.4(DHX37):c.2166C>A (p.Asn722Lys)	DHX37 (N722K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3082266	NM_032656.4(DHX37):c.1731T>G (p.Asp577Glu)	DHX37 (D577E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3082264	NM_032656.4(DHX37):c.143C>T (p.Ala48Val)	DHX37 (A48V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3067862	NM_032656.4(DHX37):c.1829C>T (p.Pro610Leu)	DHX37 (P610L)	Single nucleotide variant (missense variant)	46,XY sex reversal 11	GUncertain significance
Select item 3067308	NM_032656.4(DHX37):c.399C>G (p.Asp133Glu)	DHX37 (D133E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3051964	NM_032656.4(DHX37):c.2559C>T (p.Gly853=)	DHX37	Single nucleotide variant (synonymous variant)	DHX37-related disorder	GLikely benign
Select item 3025788	NM_032656.4(DHX37):c.3301C>T (p.Arg1101Cys)	DHX37 (R1101C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3013240	NM_032656.4(DHX37):c.392A>T (p.Lys131Met)	DHX37 (K131M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3007241	NM_032656.4(DHX37):c.2703C>T (p.Ala901=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2977694	NM_032656.4(DHX37):c.2142G>A (p.Ala714=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2974076	NM_032656.4(DHX37):c.699C>G (p.Pro233=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2956451	NM_032656.4(DHX37):c.3327G>C (p.Leu1109=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2914752	NM_032656.4(DHX37):c.3061C>A (p.Pro1021Thr)	DHX37 (P1021T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2912153	NM_032656.4(DHX37):c.2470G>A (p.Glu824Lys)	DHX37 (E824K)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2903469	NM_032656.4(DHX37):c.127G>A (p.Val43Ile)	DHX37 (V43I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2903286	NM_032656.4(DHX37):c.3427A>G (p.Met1143Val)	DHX37 (M1143V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2902827	NM_032656.4(DHX37):c.1581G>A (p.Ala527=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2901694	NM_032656.4(DHX37):c.2795G>C (p.Gly932Ala)	DHX37 (G932A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2901005	NM_032656.4(DHX37):c.2265-8A>G	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2899543	NM_032656.4(DHX37):c.377A>G (p.Tyr126Cys)	DHX37 (Y126C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2892828	NM_032656.4(DHX37):c.586G>A (p.Val196Met)	DHX37 (V196M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2892078	NM_032656.4(DHX37):c.955G>A (p.Ala319Thr)	DHX37 (A319T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2891660	NM_032656.4(DHX37):c.837C>T (p.Ser279=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2889057	NM_032656.4(DHX37):c.311A>G (p.Gln104Arg)	DHX37 (Q104R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2888618	NM_032656.4(DHX37):c.2032G>A (p.Gly678Ser)	DHX37 (G678S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2888010	NM_032656.4(DHX37):c.488A>G (p.Glu163Gly)	DHX37 (E163G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2880842	NM_032656.4(DHX37):c.318C>T (p.Ser106=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2880788	NM_032656.4(DHX37):c.2148C>A (p.Asn716Lys)	DHX37 (N716K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2878407	NM_032656.4(DHX37):c.2695+20C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2878031	NM_032656.4(DHX37):c.1094G>A (p.Arg365Gln)	DHX37 (R365Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2876920	NM_032656.4(DHX37):c.276+15G>A	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2875638	NM_032656.4(DHX37):c.3217-18C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2875292	NM_032656.4(DHX37):c.214C>T (p.Leu72=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2874562	NM_032656.4(DHX37):c.1504+17G>A	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2872793	NM_032656.4(DHX37):c.1409-17G>A	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2870934	NM_032656.4(DHX37):c.1908G>A (p.Val636=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2870721	NM_032656.4(DHX37):c.1590+12G>A	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869754	NM_032656.4(DHX37):c.2784C>T (p.Ile928=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2869188	NM_032656.4(DHX37):c.3216+15G>A	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869067	NM_032656.4(DHX37):c.650C>G (p.Pro217Arg)	DHX37 (P217R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2868418	NM_032656.4(DHX37):c.1191+17G>A	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2868400	NM_032656.4(DHX37):c.2983+14C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2868308	NM_032656.4(DHX37):c.1504+12G>A	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2868198	NM_032656.4(DHX37):c.3290+12G>A	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867865	NM_032656.4(DHX37):c.277-14G>C	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867433	NM_032656.4(DHX37):c.3121+13A>G	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867427	NM_032656.4(DHX37):c.1736-17_1736-15dup	DHX37	Duplication (intron variant)	not provided	GLikely benign
Select item 2867321	NM_032656.4(DHX37):c.3150C>T (p.Ile1050=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2867159	NM_032656.4(DHX37):c.2265-18C>A	DHX37	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2861000	NM_032656.4(DHX37):c.750G>A (p.Leu250=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2857096	NM_032656.4(DHX37):c.2453+20G>C	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2854461	NM_032656.4(DHX37):c.14G>T (p.Arg5Leu)	DHX37, LOC130009166 (R5L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2854412	NM_032656.4(DHX37):c.3290+8C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2845655	NM_032656.4(DHX37):c.2590G>T (p.Ala864Ser)	DHX37 (A864S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2832210	NM_032656.4(DHX37):c.278G>T (p.Arg93Leu)	DHX37 (R93L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2831965	NM_032656.4(DHX37):c.2498_2499delinsTC (p.Arg833Leu)	DHX37 (R833L)	Indel (missense variant)	not provided	GUncertain significance
Select item 2821956	NM_032656.4(DHX37):c.888-35_888-19del	DHX37	Deletion (intron variant)	not provided	GLikely benign
Select item 2814798	NM_032656.4(DHX37):c.1293+10G>A	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2809296	NM_032656.4(DHX37):c.2454-6_2454-5del	DHX37	Deletion (intron variant)	not provided	GUncertain significance
Select item 2805945	NM_032656.4(DHX37):c.1987G>A (p.Ala663Thr)	DHX37 (A663T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2800163	NM_032656.4(DHX37):c.627C>T (p.Pro209=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2791740	NM_032656.4(DHX37):c.1192-9C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2785600	NM_032656.4(DHX37):c.968A>G (p.Asn323Ser)	DHX37 (N323S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2783318	NM_032656.4(DHX37):c.3197G>A (p.Arg1066Gln)	DHX37 (R1066Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2782238	NM_032656.4(DHX37):c.2382C>T (p.His794=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2780642	NM_032656.4(DHX37):c.2459C>T (p.Ala820Val)	DHX37 (A820V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2779405	NM_032656.4(DHX37):c.3283T>C (p.Trp1095Arg)	DHX37 (W1095R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2775722	NM_032656.4(DHX37):c.2442G>A (p.Glu814=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2775658	NM_032656.4(DHX37):c.2830G>A (p.Glu944Lys)	DHX37 (E944K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2773192	NM_032656.4(DHX37):c.1197C>T (p.Asn399=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2755225	NM_032656.4(DHX37):c.2335C>T (p.Pro779Ser)	DHX37 (P779S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2753950	NM_032656.4(DHX37):c.1513G>A (p.Asp505Asn)	DHX37 (D505N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2750133	NM_032656.4(DHX37):c.1920G>C (p.Lys640Asn)	DHX37 (K640N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2728144	NM_032656.4(DHX37):c.3442G>A (p.Glu1148Lys)	DHX37 (E1148K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2726543	NM_032656.4(DHX37):c.2674C>T (p.Arg892Trp)	DHX37 (R892W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2722322	NM_032656.4(DHX37):c.1047G>A (p.Thr349=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2720575	NM_032656.4(DHX37):c.1149C>T (p.Ile383=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2720438	NM_032656.4(DHX37):c.2931C>T (p.Pro977=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2717408	NM_032656.4(DHX37):c.640A>G (p.Met214Val)	DHX37 (M214V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2713741	NM_032656.4(DHX37):c.2190C>T (p.Ser730=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2712684	NM_032656.4(DHX37):c.2985C>T (p.Gly995=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2709672	NM_032656.4(DHX37):c.3224G>A (p.Arg1075His)	DHX37 (R1075H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2690986	NM_032656.4(DHX37):c.2698A>G (p.Asn900Asp)	DHX37 (N900D)	Single nucleotide variant (missense variant)	Male infertility with azoospermia or oligozoospermia due to single gene mutation	GLikely pathogenic

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