Related gene-specific medical variations for Gene (Select 8744) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3180345	NM_003811.4(TNFSF9):c.692G>A (p.Gly231Asp)	LOC130063305, TNFSF9 (G231D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180344	NM_003811.4(TNFSF9):c.625G>A (p.Gly209Ser)	LOC130063305, TNFSF9 (G209S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180343	NM_003811.4(TNFSF9):c.604C>G (p.Arg202Gly)	LOC130063305, TNFSF9 (R202G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180342	NM_003811.4(TNFSF9):c.194C>G (p.Ala65Gly)	LOC130063303, TNFSF9 (A65G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180341	NM_003811.4(TNFSF9):c.10G>A (p.Ala4Thr)	LOC130063302, TNFSF9 (A4T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514778	NM_003811.4(TNFSF9):c.673G>A (p.Ala225Thr)	LOC130063305, TNFSF9 (A225T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380113	NM_003811.4(TNFSF9):c.16G>A (p.Asp6Asn)	LOC130063302, TNFSF9 (D6N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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