Related gene-specific medical variations for Gene (Select 57447) - ClinVar

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Links from Gene

Items: 49

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3314640	NM_138331.2(RNASE8):c.44T>G (p.Leu15Arg)	NDRG2, RNASE8 (L15R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314639	NM_032572.4(RNASE7):c.201C>G (p.Asp67Glu)	NDRG2, RNASE7 (D67E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314634	NM_001012264.4(RNASE13):c.359C>G (p.Pro120Arg)	NDRG2, RNASE13 +1 more (P120R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314633	NM_001012264.4(RNASE13):c.145C>T (p.Arg49Trp)	NDRG2, RNASE13 +1 more (R49W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3298984	NM_001320329.2(NDRG2):c.635A>G (p.Glu212Gly)	LOC126861884, NDRG2 (E152G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186273	NM_001320329.2(NDRG2):c.655A>C (p.Asn219His)	LOC126861884, NDRG2 (N219H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186269	NM_001320329.2(NDRG2):c.641T>C (p.Ile214Thr)	LOC126861884, NDRG2 (I210T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181579	NM_173846.5(TPPP2):c.406G>C (p.Glu136Gln)	NDRG2, TPPP2 (E136Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181578	NM_173846.5(TPPP2):c.32G>A (p.Arg11Gln)	NDRG2, TPPP2 (R11Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181577	NM_173846.5(TPPP2):c.306C>G (p.Asp102Glu)	NDRG2, TPPP2 (D102E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181576	NM_173846.5(TPPP2):c.305A>G (p.Asp102Gly)	NDRG2, TPPP2 (D102G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181575	NM_173846.5(TPPP2):c.227A>T (p.Glu76Val)	NDRG2, TPPP2 (E76V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181574	NM_173846.5(TPPP2):c.197C>T (p.Thr66Met)	NDRG2, TPPP2 (T66M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154857	NM_138331.2(RNASE8):c.370C>A (p.His124Asn)	NDRG2, RNASE8 (H124N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154856	NM_032572.4(RNASE7):c.280G>A (p.Asp94Asn)	NDRG2, RNASE7 (D94N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154844	NM_001012264.4(RNASE13):c.301A>G (p.Thr101Ala)	NDRG2, RNASE13 +1 more (T101A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154842	NM_001012264.4(RNASE13):c.20G>A (p.Arg7Gln)	NDRG2, RNASE13 +1 more (R7Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2605760	NM_001012264.4(RNASE13):c.317C>G (p.Ser106Cys)	NDRG2, RNASE13 +1 more (S106C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592754	NM_032572.4(RNASE7):c.265G>T (p.Ala89Ser)	NDRG2, RNASE7 (A89S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2551071	NM_001320329.2(NDRG2):c.551A>G (p.His184Arg)	LOC126861884, NDRG2 (H184R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547811	NM_173846.5(TPPP2):c.188G>A (p.Arg63Gln)	NDRG2, TPPP2 (R63Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513152	NM_001012264.4(RNASE13):c.83G>A (p.Gly28Asp)	NDRG2, RNASE13 +1 more (G28D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493976	NM_173846.5(TPPP2):c.184G>A (p.Ala62Thr)	NDRG2, TPPP2 (A62T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476808	NM_173846.5(TPPP2):c.395A>C (p.Glu132Ala)	NDRG2, TPPP2 (E132A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456275	NM_173846.5(TPPP2):c.157G>A (p.Val53Met)	NDRG2, TPPP2 (V53M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456133	NM_173846.5(TPPP2):c.437G>A (p.Arg146Gln)	NDRG2, TPPP2 (R146Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2409012	NM_032572.4(RNASE7):c.190C>T (p.Arg64Trp)	NDRG2, RNASE7 (R64W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395903	NM_001012264.4(RNASE13):c.371A>G (p.Tyr124Cys)	NDRG2, RNASE13 +1 more (Y124C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393910	NM_138331.2(RNASE8):c.161T>C (p.Met54Thr)	NDRG2, RNASE8 (M54T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393747	NM_032572.4(RNASE7):c.460A>G (p.Arg154Gly)	NDRG2, RNASE7 (R154G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392596	NM_138331.2(RNASE8):c.220C>T (p.Pro74Ser)	NDRG2, RNASE8 (P74S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2391006	NM_032572.4(RNASE7):c.429G>C (p.Gln143His)	NDRG2, RNASE7 (Q143H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383153	NM_001012264.4(RNASE13):c.400C>T (p.Leu134Phe)	NDRG2, RNASE13 +1 more (L134F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361741	NM_173846.5(TPPP2):c.436C>T (p.Arg146Trp)	NDRG2, TPPP2 (R146W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359244	NM_001012264.4(RNASE13):c.75G>A (p.Met25Ile)	NDRG2, RNASE13 +1 more (M25I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2356849	NM_001012264.4(RNASE13):c.461C>T (p.Ser154Leu)	NDRG2, RNASE13 +1 more (S154L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342231	NM_138331.2(RNASE8):c.115A>C (p.Lys39Gln)	NDRG2, RNASE8 (K39Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340895	NM_173846.5(TPPP2):c.148G>A (p.Val50Met)	NDRG2, TPPP2 (V50M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322801	NM_001320329.2(NDRG2):c.668A>G (p.His223Arg)	LOC126861884, NDRG2 (H223R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317285	NM_032572.4(RNASE7):c.467T>C (p.Leu156Pro)	NDRG2, RNASE7 (L156P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299067	NM_032572.4(RNASE7):c.76G>C (p.Val26Leu)	NDRG2, RNASE7 (V26L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294045	NM_032572.4(RNASE7):c.265G>A (p.Ala89Thr)	NDRG2, RNASE7 (A89T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2276525	NM_001012264.4(RNASE13):c.228T>A (p.His76Gln)	NDRG2, RNASE13 +1 more (H76Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250476	NM_001012264.4(RNASE13):c.7C>T (p.Pro3Ser)	NDRG2, RNASE13 +1 more (P3S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244797	NM_173846.5(TPPP2):c.218C>T (p.Ala73Val)	NDRG2, TPPP2 (A73V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2233943	NM_032572.4(RNASE7):c.191G>A (p.Arg64Gln)	NDRG2, RNASE7 (R64Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2217061	NM_173846.5(TPPP2):c.251G>A (p.Gly84Glu)	NDRG2, TPPP2 (G84E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206778	NM_173846.5(TPPP2):c.476A>G (p.Tyr159Cys)	NDRG2, TPPP2 (Y159C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 776817	NM_173846.5(TPPP2):c.495C>G (p.Tyr165Ter)	NDRG2, TPPP2 (Y165*)	Single nucleotide variant (nonsense +1 more)	not provided	GBenign

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Links from Gene

Items: 49