Tnfsf13b Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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14 records found for search term Tnfsf13b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150514685	CV1212097	single nucleotide variant	NM_006573.5(TNFSF13B):c.482-137C>G	not provided [RCV001599166]	benign	13	108303116	108303116	Human		name
150505913	CV1226215	single nucleotide variant	NM_006573.5(TNFSF13B):c.745+217T>A	not provided [RCV001635583]	benign	13	108303821	108303821	Human		name
597674421	CV3620829	single nucleotide variant	NM_006573.5(TNFSF13B):c.98G>A (p.Arg33Gln)	not specified [RCV004882866]	likely benign	13	108269993	108269993	Human		name
15135268	CV713819	single nucleotide variant	NM_006573.5(TNFSF13B):c.726T>C (p.Asn242=)	not provided [RCV000965260]	benign	13	108303585	108303585	Human		name
15116258	CV753690	single nucleotide variant	NM_006573.5(TNFSF13B):c.495T>C (p.Phe165=)	not provided [RCV000917595]	likely benign	13	108303266	108303266	Human		name
156276079	CV2255747	single nucleotide variant	NM_006573.5(TNFSF13B):c.143T>A (p.Leu48Gln)	not specified [RCV004120133]	uncertain significance	13	108270038	108270038	Human		name
155954420	CV2274321	single nucleotide variant	NM_006573.5(TNFSF13B):c.205G>A (p.Val69Met)	not specified [RCV004136712]	uncertain significance	13	108270100	108270100	Human		name
329375737	CV2468790	single nucleotide variant	NM_006573.5(TNFSF13B):c.152C>G (p.Thr51Ser)	not specified [RCV004280106]	uncertain significance	13	108270047	108270047	Human		name
407459054	CV3479243	single nucleotide variant	NM_006573.5(TNFSF13B):c.184A>G (p.Thr62Ala)	not specified [RCV004687012]	uncertain significance	13	108270079	108270079	Human		name
597674411	CV3620828	single nucleotide variant	NM_006573.5(TNFSF13B):c.283G>A (p.Ala95Thr)	not specified [RCV004882865]	uncertain significance	13	108270178	108270178	Human		name
598229569	CV3935192	single nucleotide variant	NM_006573.5(TNFSF13B):c.233G>T (p.Ser78Ile)	not specified [RCV005294911]	uncertain significance	13	108270128	108270128	Human		name
156356237	CV2320749	single nucleotide variant	NM_006573.5(TNFSF13B):c.472A>G (p.Ile158Val)	not specified [RCV004172591]	uncertain significance	13	108286850	108286850	Human		name
598229563	CV3935191	single nucleotide variant	NM_006573.5(TNFSF13B):c.340A>T (p.Ile114Phe)	not specified [RCV005294910]	uncertain significance	13	108270340	108270340	Human		name
15181152	CV713818	single nucleotide variant	NM_006573.5(TNFSF13B):c.313G>A (p.Ala105Thr)	not provided [RCV000974323]	benign	13	108270208	108270208	Human		name