"PreventionGenetics, part of Exact Sciences"[submitter] AND "DHX34"[ge - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3056984	NM_014681.6(DHX34):c.49C>T (p.Arg17Trp)	DHX34 (R17W)	Single nucleotide variant (missense variant)	DHX34-related disorder	GBenign
Select item 721876	NM_014681.6(DHX34):c.249T>C (p.Pro83=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder +1 more	GBenign/Likely benign
Select item 712250	NM_014681.6(DHX34):c.256C>T (p.Pro86Ser)	DHX34 (P86S)	Single nucleotide variant (missense variant)	DHX34-related disorder +1 more	GBenign
Select item 789121	NM_014681.6(DHX34):c.350G>A (p.Gly117Asp)	DHX34 (G117D)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 775417	NM_014681.6(DHX34):c.508C>T (p.Arg170Cys)	DHX34 (R170C)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3059175	NM_014681.6(DHX34):c.834G>A (p.Val278=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder	GBenign
Select item 3050604	NM_014681.6(DHX34):c.864C>T (p.Asn288=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder	GBenign
Select item 3056792	NM_014681.6(DHX34):c.899C>G (p.Pro300Arg)	DHX34 (P300R)	Single nucleotide variant (missense variant)	DHX34-related disorder	GBenign
Select item 3038863	NM_014681.6(DHX34):c.927C>T (p.Leu309=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder	GLikely benign
Select item 3039476	NM_014681.6(DHX34):c.1122G>A (p.Pro374=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder	GBenign
Select item 712251	NM_014681.6(DHX34):c.1491C>T (p.Pro497=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder +1 more	GBenign
Select item 3059415	NM_014681.6(DHX34):c.1554A>G (p.Pro518=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder	GBenign
Select item 786355	NM_014681.6(DHX34):c.1582T>C (p.Leu528=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder +1 more	GBenign/Likely benign
Select item 3039035	NM_014681.6(DHX34):c.1590G>A (p.Leu530=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder	GBenign
Select item 3060131	NM_014681.6(DHX34):c.1593+9T>C	DHX34	Single nucleotide variant (intron variant)	DHX34-related disorder	GBenign
Select item 718689	NM_014681.6(DHX34):c.1839C>T (p.Ser613=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder +1 more	GLikely benign
Select item 791481	NM_014681.6(DHX34):c.1863C>T (p.Ser621=)	DHX34	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 781510	NM_014681.6(DHX34):c.2184C>T (p.His728=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder +1 more	GBenign
Select item 3055698	NM_014681.6(DHX34):c.2200C>T (p.Arg734Cys)	DHX34 (R734C)	Single nucleotide variant (missense variant)	DHX34-related disorder	GBenign
Select item 770294	NM_014681.6(DHX34):c.2219G>A (p.Arg740Gln)	DHX34 (R740Q)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2330276	NM_014681.6(DHX34):c.2278C>T (p.Pro760Ser)	DHX34 (P760S)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3059865	NM_014681.6(DHX34):c.2406G>A (p.Leu802=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder	GBenign
Select item 3044313	NM_014681.6(DHX34):c.2419G>A (p.Gly807Ser)	DHX34 (G807S)	Single nucleotide variant (missense variant)	DHX34-related disorder	GBenign
Select item 786356	NM_014681.6(DHX34):c.2449G>A (p.Ala817Thr)	DHX34 (A817T)	Single nucleotide variant (missense variant)	DHX34-related disorder +1 more	GBenign
Select item 3050758	NM_014681.6(DHX34):c.2482-5C>T	DHX34	Single nucleotide variant (intron variant)	DHX34-related disorder	GBenign
Select item 3045088	NM_014681.6(DHX34):c.2568G>A (p.Glu856=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder	GBenign
Select item 3060534	NM_014681.6(DHX34):c.2707-10T>C	DHX34	Single nucleotide variant (intron variant)	DHX34-related disorder	GBenign
Select item 3057123	NM_014681.6(DHX34):c.2826T>G (p.Ala942=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder	GBenign
Select item 3037806	NM_014681.6(DHX34):c.2836C>T (p.Leu946Phe)	DHX34 (L946F)	Single nucleotide variant (missense variant)	DHX34-related disorder	GBenign
Select item 717090	NM_014681.6(DHX34):c.2898GGA[7] (p.Glu971dup)	DHX34	Microsatellite (inframe_insertion)	DHX34-related disorder +1 more	GBenign
Select item 778602	NM_014681.6(DHX34):c.2898GGA[4] (p.Glu970_Glu971del)	DHX34	Microsatellite (inframe_deletion)	DHX34-related disorder +1 more	GBenign
Select item 3038245	NM_014681.6(DHX34):c.2999G>A (p.Arg1000Gln)	DHX34 (R1000Q)	Single nucleotide variant (missense variant)	DHX34-related disorder	GLikely benign
Select item 789669	NM_014681.6(DHX34):c.3180C>T (p.Ser1060=)	DHX34	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 769460	NM_014681.6(DHX34):c.3299-3T>C	DHX34	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 3034375	NM_014681.6(DHX34):c.3402G>A (p.Glu1134=)	DHX34	Single nucleotide variant (synonymous variant)	DHX34-related disorder	GLikely benign

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Items: 35