DHX37[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1931135	NM_032656.4(DHX37):c.3459C>G (p.Pro1153=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 735695	NM_032656.4(DHX37):c.3440T>C (p.Ile1147Thr)	DHX37 (I1147T)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2177300	NM_032656.4(DHX37):c.3436G>A (p.Asp1146Asn)	DHX37 (D1146N)	Single nucleotide variant (missense variant)	not provided	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 1678357	NM_032656.4(DHX37):c.3425C>G (p.Ala1142Gly)	DHX37 (A1142G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2204950	NM_032656.4(DHX37):c.3407G>A (p.Cys1136Tyr)	DHX37 (C1136Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2582138	NM_032656.4(DHX37):c.3390C>A (p.Tyr1130Ter)	DHX37 (Y1130*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1971107	NM_032656.4(DHX37):c.3389-11C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1921907	NM_032656.4(DHX37):c.3388+12C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2956451	NM_032656.4(DHX37):c.3327G>C (p.Leu1109=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2063687	NM_032656.4(DHX37):c.3322G>T (p.Ala1108Ser)	DHX37 (A1108S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1978724	NM_032656.4(DHX37):c.3313C>T (p.Leu1105Phe)	DHX37 (L1105F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2086178	NM_032656.4(DHX37):c.3306G>A (p.Thr1102=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2031398	NM_032656.4(DHX37):c.3302G>T (p.Arg1101Leu)	DHX37 (R1101L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1030048	NM_032656.4(DHX37):c.3302G>A (p.Arg1101His)	DHX37 (R1101H)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
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 2018185	NM_032656.4(DHX37):c.3291-20C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1972010	NM_032656.4(DHX37):c.3290+15G>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 2116489	NM_032656.4(DHX37):c.3290+12G>T	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1974690	NM_032656.4(DHX37):c.3290+11C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2854412	NM_032656.4(DHX37):c.3290+8C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
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 691930	NM_032656.4(DHX37):c.3281C>T (p.Thr1094Met)	DHX37 (T1094M)	Single nucleotide variant (missense variant)	Neurodevelopmental delay +2 more	GLikely pathogenic
Select item 1910687	NM_032656.4(DHX37):c.3268A>G (p.Thr1090Ala)	DHX37 (T1090A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2326239	NM_032656.4(DHX37):c.3265G>A (p.Gly1089Ser)	DHX37 (G1089S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 1255483	NM_032656.4(DHX37):c.3242G>A (p.Arg1081Gln)	DHX37 (R1081Q)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 2358901	NM_032656.4(DHX37):c.3227A>C (p.Lys1076Thr)	DHX37 (K1076T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
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 2110383	NM_032656.4(DHX37):c.3223C>T (p.Arg1075Cys)	DHX37 (R1075C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1342471	NM_032656.4(DHX37):c.3217-1G>T	DHX37	Single nucleotide variant (splice acceptor variant)	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies	GLikely pathogenic
Select item 2875638	NM_032656.4(DHX37):c.3217-18C>T	DHX37	Single nucleotide variant (intron 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 1978641	NM_032656.4(DHX37):c.3216+14C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1971458	NM_032656.4(DHX37):c.3216+11C>G	DHX37	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2182100	NM_032656.4(DHX37):c.3216+3A>G	DHX37	Single nucleotide variant (intron variant)	not provided	GConflicting classifications of pathogenicity
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 1973552	NM_032656.4(DHX37):c.3196C>T (p.Arg1066Trp)	DHX37 (R1066W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1255484	NM_032656.4(DHX37):c.3195C>T (p.Ala1065=)	DHX37	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 2045021	NM_032656.4(DHX37):c.3186G>A (p.Lys1062=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1696961	NM_032656.4(DHX37):c.3185A>C (p.Lys1062Thr)	DHX37 (K1062T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2043946	NM_032656.4(DHX37):c.3179G>A (p.Arg1060His)	DHX37 (R1060H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2255128	NM_032656.4(DHX37):c.3178C>T (p.Arg1060Cys)	DHX37 (R1060C)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 1975266	NM_032656.4(DHX37):c.3178C>G (p.Arg1060Gly)	DHX37 (R1060G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2512386	NM_032656.4(DHX37):c.3151G>A (p.Glu1051Lys)	DHX37 (E1051K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2867321	NM_032656.4(DHX37):c.3150C>T (p.Ile1050=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1976864	NM_032656.4(DHX37):c.3143C>G (p.Pro1048Arg)	DHX37 (P1048R)	Single nucleotide variant (missense variant)	not provided	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 2540958	NM_032656.4(DHX37):c.3127G>C (p.Val1043Leu)	DHX37 (V1043L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2200681	NM_032656.4(DHX37):c.3125G>A (p.Arg1042His)	DHX37 (R1042H)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2066455	NM_032656.4(DHX37):c.3122-11C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2061088	NM_032656.4(DHX37):c.3121+15T>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 1675520	NM_032656.4(DHX37):c.3092G>A (p.Arg1031Gln)	DHX37 (R1031Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1917940	NM_032656.4(DHX37):c.3089G>A (p.Gly1030Glu)	DHX37 (G1030E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2599923	NM_032656.4(DHX37):c.3086G>C (p.Arg1029Pro)	DHX37 (R1029P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2098048	NM_032656.4(DHX37):c.3084G>A (p.Glu1028=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2161758	NM_032656.4(DHX37):c.3082G>A (p.Glu1028Lys)	DHX37 (E1028K)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2067915	NM_032656.4(DHX37):c.3081C>T (p.Pro1027=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2168184	NM_032656.4(DHX37):c.3078C>T (p.Cys1026=)	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 3355395	NM_032656.4(DHX37):c.3050C>T (p.Pro1017Leu)	DHX37 (P1017L)	Single nucleotide variant (missense variant)	DHX37-related disorder	GUncertain significance
Select item 2090317	NM_032656.4(DHX37):c.3046A>G (p.Lys1016Glu)	DHX37 (K1016E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1684970	NM_032656.4(DHX37):c.3045C>G (p.Asp1015Glu)	DHX37 (D1015E)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 724504	NM_032656.4(DHX37):c.3019C>G (p.Leu1007Val)	DHX37 (L1007V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2049434	NM_032656.4(DHX37):c.2995G>A (p.Val999Met)	DHX37 (V999M)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2044172	NM_032656.4(DHX37):c.2994C>T (p.Ser998=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2712684	NM_032656.4(DHX37):c.2985C>T (p.Gly995=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1318584	NM_032656.4(DHX37):c.2984G>C (p.Gly995Ala)	DHX37 (G995A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2131633	NM_032656.4(DHX37):c.2984-3del	DHX37	Deletion (intron variant)	not provided	GBenign
Select item 2051231	NM_032656.4(DHX37):c.2984-10C>T	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 1978911	NM_032656.4(DHX37):c.2983+5C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1030047	NM_032656.4(DHX37):c.2956G>A (p.Val986Met)	DHX37 (V986M)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1972311	NM_032656.4(DHX37):c.2955C>G (p.Ile985Met)	DHX37 (I985M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2720438	NM_032656.4(DHX37):c.2931C>T (p.Pro977=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 2189033	NM_032656.4(DHX37):c.2911G>A (p.Val971Ile)	DHX37 (V971I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1710815	NM_032656.4(DHX37):c.2905A>G (p.Ser969Gly)	DHX37 (S969G)	Single nucleotide variant (missense variant)	not provided	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 2074191	NM_032656.4(DHX37):c.2883C>T (p.Asp961=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1973847	NM_032656.4(DHX37):c.2880C>T (p.Leu960=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1972154	NM_032656.4(DHX37):c.2869-13C>T	DHX37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1255485	NM_032656.4(DHX37):c.2869-38G>A	DHX37	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1315790	NM_032656.4(DHX37):c.2849del (p.Lys950fs)	DHX37 (K950fs)	Deletion (frameshift variant)	not provided	GUncertain significance
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 2217582	NM_032656.4(DHX37):c.2816G>A (p.Arg939His)	DHX37 (R939H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2325372	NM_032656.4(DHX37):c.2815C>T (p.Arg939Cys)	DHX37 (R939C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2082298	NM_032656.4(DHX37):c.2799G>C (p.Leu933=)	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 1251560	NM_032656.4(DHX37):c.2793A>G (p.Ala931=)	DHX37	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 2869754	NM_032656.4(DHX37):c.2784C>T (p.Ile928=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2010140	NM_032656.4(DHX37):c.2781G>C (p.Gln927His)	DHX37 (Q927H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2690942	NM_032656.4(DHX37):c.2762A>G (p.Gln921Arg)	DHX37 (Q921R)	Single nucleotide variant (missense variant)	Male infertility with azoospermia or oligozoospermia due to single gene mutation	GLikely pathogenic
Select item 2124386	NM_032656.4(DHX37):c.2757G>C (p.Glu919Asp)	DHX37 (E919D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 775323	NM_032656.4(DHX37):c.2748G>T (p.Pro916=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GBenign
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 2145601	NM_032656.4(DHX37):c.2713G>A (p.Glu905Lys)	DHX37 (E905K)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies +2 more	GConflicting classifications of pathogenicity
Select item 3007241	NM_032656.4(DHX37):c.2703C>T (p.Ala901=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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