Related gene-specific medical variations for Gene (Select 8764) - ClinVar

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Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3257857	NM_003820.4(TNFRSF14):c.36G>A (p.Trp12Ter)	TNFRSF14, TNFRSF14-AS1 (W12*)	Single nucleotide variant (nonsense)	Neoplasm	OLikely oncogenic
Select item 3180245	NM_003820.4(TNFRSF14):c.37A>G (p.Arg13Gly)	TNFRSF14, TNFRSF14-AS1 (R13G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180244	NM_003820.4(TNFRSF14):c.31C>T (p.Pro11Ser)	TNFRSF14, TNFRSF14-AS1 (P11S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 787525	NM_003820.4(TNFRSF14):c.9T>C (p.Pro3=)	TNFRSF14, TNFRSF14-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 135357	NM_003820.4(TNFRSF14):c.797C>T (p.Thr266Met)	TNFRSF14 (T266M)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	Gnot provided
Select item 135356	NM_003820.4(TNFRSF14):c.785C>T (p.Pro262Leu)	TNFRSF14 (P262L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	Gnot provided
Select item 135355	NM_003820.4(TNFRSF14):c.721G>A (p.Val241Ile)	TNFRSF14 (V241I)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	Gnot provided
Select item 135354	NM_003820.4(TNFRSF14):c.521G>A (p.Gly174Glu)	TNFRSF14 (G174E)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135353	NM_003820.4(TNFRSF14):c.349G>A (p.Ala117Thr)	TNFRSF14 (A117T)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 135352	NM_003820.4(TNFRSF14):c.408C>T (p.Ala136=)	TNFRSF14	Single nucleotide variant (synonymous variant)	not specified	Gnot provided
Select item 135351	NM_003820.4(TNFRSF14):c.405C>T (p.Cys135=)	TNFRSF14	Single nucleotide variant (synonymous variant)	not specified	Gnot provided
Select item 135350	NM_003820.4(TNFRSF14):c.348C>T (p.Asn116=)	TNFRSF14	Single nucleotide variant (synonymous variant)	not specified	Gnot provided
Select item 135349	NM_003820.4(TNFRSF14):c.50A>G (p.Lys17Arg)	TNFRSF14, TNFRSF14-AS1 (K17R)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 133417	NM_003820.4(TNFRSF14):c.552-140C>T	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133416	NM_003820.4(TNFRSF14):c.552-165del	TNFRSF14	Deletion (intron variant)	not specified	Gnot provided
Select item 133415	NM_003820.4(TNFRSF14):c.305-59_305-57delinsACT	TNFRSF14	Indel (intron variant)	not specified	Gnot provided
Select item 133414	NM_003820.4(TNFRSF14):c.305-57C>T	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133413	NM_003820.4(TNFRSF14):c.305-98G>A	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133412	NM_003820.4(TNFRSF14):c.305-171G>A	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133411	NM_003820.4(TNFRSF14):c.305-191C>T	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133410	NM_003820.4(TNFRSF14):c.305-191C>G	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133409	NM_003820.4(TNFRSF14):c.305-201G>A	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133408	NM_003820.4(TNFRSF14):c.305-249C>T	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133407	NM_003820.4(TNFRSF14):c.305-308C>T	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133406	NM_003820.4(TNFRSF14):c.305-320C>A	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133405	NM_003820.4(TNFRSF14):c.305-328C>A	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133404	NM_003820.4(TNFRSF14):c.305-364C>A	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133403	NM_003820.4(TNFRSF14):c.305-397T>A	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133402	NM_003820.4(TNFRSF14):c.305-401G>T	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133401	NM_003820.4(TNFRSF14):c.305-462G>T	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133400	NM_003820.4(TNFRSF14):c.305-476C>T	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133399	NM_003820.4(TNFRSF14):c.305-653T>C	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133398	NM_003820.4(TNFRSF14):c.305-654A>G	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133397	NM_003820.4(TNFRSF14):c.304+642C>T	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133396	NM_003820.4(TNFRSF14):c.304+624C>T	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133395	NM_003820.4(TNFRSF14):c.304+606C>G	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 133394	NM_003820.4(TNFRSF14):c.304+545C>T	TNFRSF14	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 91954	NM_003820.4(TNFRSF14):c.558C>G (p.Ser186Arg)	TNFRSF14 (S186R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

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Links from Gene

Items: 38