Related gene-specific medical variations for Gene (Select 51330) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3180237	NM_016639.3(TNFRSF12A):c.298G>A (p.Val100Ile)	LOC126862263, TNFRSF12A (V100I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180236	NM_016639.3(TNFRSF12A):c.272T>C (p.Val91Ala)	LOC126862263, TNFRSF12A (V91A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529615	NM_016639.3(TNFRSF12A):c.197G>C (p.Gly66Ala)	LOC126862263, TNFRSF12A (G66A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401321	NM_016639.3(TNFRSF12A):c.58G>A (p.Ala20Thr)	LOC126862263, TNFRSF12A (A20T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369730	NM_016639.3(TNFRSF12A):c.278G>C (p.Gly93Ala)	LOC126862263, TNFRSF12A (G93A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364608	NM_016639.3(TNFRSF12A):c.8G>A (p.Arg3Gln)	LOC126862263, TNFRSF12A (R3Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337048	NM_016639.3(TNFRSF12A):c.211C>T (p.Pro71Ser)	LOC126862263, TNFRSF12A (P71S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305490	NM_016639.3(TNFRSF12A):c.149T>C (p.Met50Thr)	LOC126862263, TNFRSF12A (M50T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302796	NM_016639.3(TNFRSF12A):c.22C>G (p.Arg8Gly)	LOC126862263, TNFRSF12A (R8G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791372	NM_016639.3(TNFRSF12A):c.384C>A (p.Ile128=)	LOC126862263, TNFRSF12A	Single nucleotide variant (synonymous variant)	not provided	GBenign