Related gene-specific medical variations for Gene (Select 80196) - ClinVar

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Links from Gene

Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3314902	NM_025126.4(RNF34):c.613A>G (p.Arg205Gly)	KDM2B, RNF34 (R13G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3314901	NM_025126.4(RNF34):c.103G>A (p.Ala35Thr)	KDM2B, RNF34 (A35T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3314900	NM_025126.4(RNF34):c.752T>A (p.Val251Glu)	KDM2B, RNF34 (V251E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314899	NM_025126.4(RNF34):c.301A>G (p.Thr101Ala)	KDM2B, RNF34 (T101A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3314898	NM_025126.4(RNF34):c.1001A>G (p.Asp334Gly)	KDM2B, RNF34 (D335G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314896	NM_025126.4(RNF34):c.262G>A (p.Val88Ile)	KDM2B, RNF34 (V89I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3155414	NM_025126.4(RNF34):c.934G>A (p.Glu312Lys)	KDM2B, RNF34 (E312K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3155413	NM_025126.4(RNF34):c.829G>T (p.Ala277Ser)	KDM2B, RNF34 (A277S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3155412	NM_025126.4(RNF34):c.687T>G (p.Asp229Glu)	KDM2B, RNF34 (D230E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3155411	NM_025126.4(RNF34):c.533C>T (p.Ser178Leu)	KDM2B, RNF34 (S178L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3155409	NM_025126.4(RNF34):c.22A>G (p.Met8Val)	KDM2B, RNF34 (M9V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3155408	NM_025126.4(RNF34):c.160G>A (p.Ala54Thr)	KDM2B, RNF34 (A54T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2610423	NM_025126.4(RNF34):c.429G>T (p.Leu143Phe)	KDM2B, RNF34 (L143F +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2595100	NM_025126.4(RNF34):c.833G>A (p.Arg278Gln)	KDM2B, RNF34 (R279Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2515801	NM_025126.4(RNF34):c.184T>G (p.Cys62Gly)	KDM2B, RNF34 (C62G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2476983	NM_025126.4(RNF34):c.893G>A (p.Arg298Gln)	KDM2B, RNF34 (R298Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2387622	NM_025126.4(RNF34):c.412C>T (p.Arg138Cys)	KDM2B, RNF34 (R138C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2377433	NM_025126.4(RNF34):c.705A>T (p.Glu235Asp)	KDM2B, RNF34 (E236D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2310229	NM_025126.4(RNF34):c.289C>T (p.Arg97Cys)	KDM2B, RNF34 (R98C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2267604	NM_025126.4(RNF34):c.446G>A (p.Cys149Tyr)	KDM2B, RNF34 (C149Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2264515	NM_025126.4(RNF34):c.693T>G (p.Asp231Glu)	KDM2B, RNF34 (D231E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2209947	NM_025126.4(RNF34):c.616T>C (p.Ser206Pro)	KDM2B, RNF34 (S14P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 778448	NM_025126.4(RNF34):c.530G>A (p.Arg177His)	KDM2B, RNF34 (R178H +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign

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Links from Gene

Items: 23