Related gene-specific medical variations for Gene (Select 8797) - ClinVar - NCBI

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Links from Gene

Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3327473	NM_003844.4(TNFRSF10A):c.95C>A (p.Ala32Asp)	LOC111255645, TNFRSF10A (A32D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180212	NM_003844.4(TNFRSF10A):c.85G>A (p.Ala29Thr)	LOC111255645, TNFRSF10A (A29T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180208	NM_003844.4(TNFRSF10A):c.281T>C (p.Phe94Ser)	LOC111255645, TNFRSF10A (F94S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180207	NM_003844.4(TNFRSF10A):c.236C>T (p.Ala79Val)	LOC111255645, TNFRSF10A (A79V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180206	NM_003844.4(TNFRSF10A):c.188G>A (p.Gly63Glu)	LOC111255645, TNFRSF10A (G63E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180205	NM_003844.4(TNFRSF10A):c.142C>G (p.Arg48Gly)	LOC111255645, TNFRSF10A (R48G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517277	NM_003844.4(TNFRSF10A):c.57T>A (p.Asn19Lys)	LOC111255645, TNFRSF10A (N19K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484193	NM_003844.4(TNFRSF10A):c.92C>A (p.Ala31Glu)	LOC111255645, TNFRSF10A (A31E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362759	NM_003844.4(TNFRSF10A):c.295G>T (p.Val99Phe)	LOC111255645, TNFRSF10A (V99F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345911	NM_003844.4(TNFRSF10A):c.110T>G (p.Val37Gly)	LOC111255645, TNFRSF10A (V37G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261207	NM_003844.4(TNFRSF10A):c.21A>T (p.Arg7Ser)	LOC111255645, TNFRSF10A (R7S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249475	NM_003844.4(TNFRSF10A):c.109G>A (p.Val37Met)	LOC111255645, TNFRSF10A (V37M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237668	NM_003844.4(TNFRSF10A):c.305A>C (p.Gln102Pro)	LOC111255645, TNFRSF10A (Q102P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777635	NM_003844.4(TNFRSF10A):c.306+5G>C	LOC111255645, TNFRSF10A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 730510	NM_003844.4(TNFRSF10A):c.206G>C (p.Arg69Pro)	LOC111255645, TNFRSF10A (R69P)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 100847	NM_003844.4(TNFRSF10A):c.355G>A (p.Gly119Ser)	TNFRSF10A (G119S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance