Related gene-specific medical variations for Gene (Select 122664) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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)	RNASE13, TPPP2 +1 more (R49W)	Single nucleotide variant (missense variant +1 more)	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)	TPPP2, NDRG2 (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 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 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 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 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 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 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 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

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Links from Gene

Items: 29