Tnfsf10 Variant Search Result - Rat Genome Database

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26 records found for search term Tnfsf10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150511709	CV1229529	single nucleotide variant	NM_003810.4(TNFSF10):c.*207G>A	not provided [RCV001637458]	benign	3	172506285	172506285	Human		name
150331725	CV1163430	single nucleotide variant	NM_003810.4(TNFSF10):c.314-88G>A	not provided [RCV001527921]	benign	3	172509409	172509409	Human		name
150457357	CV1278614	single nucleotide variant	NM_003810.4(TNFSF10):c.132+44A>C	not provided [RCV001709229]	benign	3	172523209	172523209	Human		name
150465593	CV1277264	single nucleotide variant	NM_003810.4(TNFSF10):c.133-3652A>C	not provided [RCV001710558]	benign	3	172518650	172518650	Human		name
329400558	CV2438486	single nucleotide variant	NM_003810.4(TNFSF10):c.26G>C (p.Gly9Ala)	not specified [RCV004259634]	uncertain significance	3	172523359	172523359	Human		name
15165733	CV697933	single nucleotide variant	NM_003810.4(TNFSF10):c.105C>T (p.Tyr35=)	not provided [RCV000948663]	benign	3	172523280	172523280	Human		name
15106299	CV763732	single nucleotide variant	NM_003810.4(TNFSF10):c.261C>T (p.Leu87=)	not provided [RCV000937754]	likely benign	3	172514870	172514870	Human		name
150513832	CV1227923	single nucleotide variant	NM_003810.4(TNFSF10):c.825T>C (p.Phe275=)	not provided [RCV001638201]	benign	3	172506513	172506513	Human		name
405787864	CV3339984	single nucleotide variant	NM_003810.4(TNFSF10):c.82T>A (p.Ser28Thr)	not specified [RCV004473220]	uncertain significance	3	172523303	172523303	Human		name
15167908	CV708687	single nucleotide variant	NM_003810.4(TNFSF10):c.97G>A (p.Val33Ile)	not provided [RCV000971499]	benign	3	172523288	172523288	Human		name
405787840	CV3339979	single nucleotide variant	NM_003810.4(TNFSF10):c.149C>T (p.Ser50Phe)	not specified [RCV004473215]	uncertain significance	3	172514982	172514982	Human		name
155962527	CV2254417	single nucleotide variant	NM_003810.4(TNFSF10):c.456C>G (p.Asn152Lys)	not specified [RCV004123800]	uncertain significance	3	172506882	172506882	Human		name
156353791	CV2324144	single nucleotide variant	NM_003810.4(TNFSF10):c.434A>C (p.Lys145Thr)	not specified [RCV004176895]	uncertain significance	3	172506904	172506904	Human		name
401777986	CV2704505	single nucleotide variant	NM_003810.4(TNFSF10):c.307G>A (p.Val103Ile)	not specified [RCV004313244]	uncertain significance	3	172511623	172511623	Human		name
401777170	CV2721631	single nucleotide variant	NM_003810.4(TNFSF10):c.344G>C (p.Arg115Thr)	not specified [RCV004316130]	uncertain significance	3	172509291	172509291	Human		name
401863276	CV2779257	single nucleotide variant	NM_003810.4(TNFSF10):c.565T>G (p.Tyr189Asp)	not specified [RCV004350941]	uncertain significance	3	172506773	172506773	Human		name
405787844	CV3339980	single nucleotide variant	NM_003810.4(TNFSF10):c.533A>G (p.Glu178Gly)	not specified [RCV004473216]	uncertain significance	3	172506805	172506805	Human		name
405787848	CV3339981	single nucleotide variant	NM_003810.4(TNFSF10):c.609C>A (p.Asp203Glu)	not specified [RCV004473217]	uncertain significance	3	172506729	172506729	Human		name
405787854	CV3339982	single nucleotide variant	NM_003810.4(TNFSF10):c.726C>G (p.Ile242Met)	not specified [RCV004473218]	uncertain significance	3	172506612	172506612	Human		name
405787858	CV3339983	single nucleotide variant	NM_003810.4(TNFSF10):c.758A>G (p.Asn253Ser)	not specified [RCV004473219]	uncertain significance	3	172506580	172506580	Human		name
597674382	CV3620823	single nucleotide variant	NM_003810.4(TNFSF10):c.554A>G (p.Tyr185Cys)	not specified [RCV004882862]	uncertain significance	3	172506784	172506784	Human		name
598229528	CV3935183	single nucleotide variant	NM_003810.4(TNFSF10):c.446G>A (p.Arg149His)	not specified [RCV005294904]	uncertain significance	3	172506892	172506892	Human		name
598229532	CV3935184	single nucleotide variant	NM_003810.4(TNFSF10):c.503A>G (p.His168Arg)	not specified [RCV005294905]	uncertain significance	3	172506835	172506835	Human		name
8625567	CV80691	single nucleotide variant	NM_003810.3(TNFSF10):c.754G>A (p.Glu252Lys)	Malignant melanoma [RCV000060768]	not provided	3	172506584	172506584	Human		name
8625568	CV80692	single nucleotide variant	NM_003810.3(TNFSF10):c.592G>A (p.Glu198Lys)	Malignant melanoma [RCV000060769]	not provided	3	172506746	172506746	Human		name
8625569	CV80693	single nucleotide variant	NM_003810.3(TNFSF10):c.587T>A (p.Ile196Lys)	Malignant melanoma [RCV000060770]	not provided	3	172506751	172506751	Human		name

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