Related gene-specific medical variations for Gene (Select 27242) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3353507	NM_014452.5(TNFRSF21):c.653C>T (p.Ser218Phe)	LOC126859685, TNFRSF21 (S218F)	Single nucleotide variant (missense variant)	TNFRSF21-related condition	GUncertain significance
Select item 3327519	NM_014452.5(TNFRSF21):c.469C>T (p.Arg157Trp)	LOC126859685, TNFRSF21 (R157W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180280	NM_014452.5(TNFRSF21):c.602A>C (p.Lys201Thr)	LOC126859685, TNFRSF21 (K201T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180279	NM_014452.5(TNFRSF21):c.445G>A (p.Val149Met)	LOC126859685, TNFRSF21 (V149M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180278	NM_014452.5(TNFRSF21):c.424G>T (p.Ala142Ser)	LOC126859685, TNFRSF21 (A142S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466488	NM_014452.5(TNFRSF21):c.349A>G (p.Met117Val)	LOC126859685, TNFRSF21 (M117V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374218	NM_014452.5(TNFRSF21):c.725C>G (p.Pro242Arg)	LOC126859685, TNFRSF21 (P242R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330097	NM_014452.5(TNFRSF21):c.694C>T (p.Arg232Cys)	LOC126859685, TNFRSF21 (R232C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317418	NM_014452.5(TNFRSF21):c.517C>T (p.Arg173Trp)	LOC126859685, TNFRSF21 (R173W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314476	NM_014452.5(TNFRSF21):c.454G>T (p.Val152Leu)	LOC126859685, TNFRSF21 (V152L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280098	NM_014452.5(TNFRSF21):c.274C>A (p.Pro92Thr)	LOC126859685, TNFRSF21 (P92T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242975	NM_014452.5(TNFRSF21):c.446T>C (p.Val149Ala)	LOC126859685, TNFRSF21 (V149A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233811	NM_014452.5(TNFRSF21):c.307A>G (p.Ile103Val)	LOC126859685, TNFRSF21 (I103V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 873549	NM_014452.5(TNFRSF21):c.436C>G (p.Pro146Ala)	LOC126859685, TNFRSF21 (P146A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance