Tnfrsf12a Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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13 records found for search term Tnfrsf12a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156188655	CV2346856	single nucleotide variant	NM_016639.3(TNFRSF12A):c.8G>A (p.Arg3Gln)	not specified [RCV004199853]	uncertain significance	16	3020405	3020405	Human		name
156086726	CV2289987	single nucleotide variant	NM_016639.3(TNFRSF12A):c.22C>G (p.Arg8Gly)	not specified [RCV004150632]	uncertain significance	16	3020419	3020419	Human		name
156040825	CV2387654	single nucleotide variant	NM_016639.3(TNFRSF12A):c.58G>A (p.Ala20Thr)	not specified [RCV004234201]	uncertain significance	16	3020455	3020455	Human		name
15181178	CV714865	single nucleotide variant	NM_016639.3(TNFRSF12A):c.384C>A (p.Ile128=)	not provided [RCV000974329]	benign	16	3021820	3021820	Human		name
156197218	CV2293543	single nucleotide variant	NM_016639.3(TNFRSF12A):c.149T>C (p.Met50Thr)	not specified [RCV004153072]	uncertain significance	16	3021269	3021269	Human		name
156257138	CV2322043	single nucleotide variant	NM_016639.3(TNFRSF12A):c.211C>T (p.Pro71Ser)	not specified [RCV004173793]	uncertain significance	16	3021566	3021566	Human		name
156143197	CV2358555	single nucleotide variant	NM_016639.3(TNFRSF12A):c.278G>C (p.Gly93Ala)	not specified [RCV004207437]	uncertain significance	16	3021633	3021633	Human		name
401774219	CV2691559	single nucleotide variant	NM_016639.3(TNFRSF12A):c.197G>C (p.Gly66Ala)	not specified [RCV004305391]	uncertain significance	16	3021317	3021317	Human		name
405787438	CV3339901	single nucleotide variant	NM_016639.3(TNFRSF12A):c.272T>C (p.Val91Ala)	not specified [RCV004473137]	uncertain significance	16	3021627	3021627	Human		name
597673786	CV3620752	single nucleotide variant	NM_016639.3(TNFRSF12A):c.157G>A (p.Ala53Thr)	not specified [RCV004882795]	uncertain significance	16	3021277	3021277	Human		name
598229346	CV3935129	single nucleotide variant	NM_016639.3(TNFRSF12A):c.144G>C (p.Lys48Asn)	not specified [RCV005294871]	uncertain significance	16	3021264	3021264	Human		name
598253226	CV3935130	single nucleotide variant	NM_016639.3(TNFRSF12A):c.208G>A (p.Ala70Thr)	not specified [RCV005278213]	uncertain significance	16	3021563	3021563	Human		name
405787443	CV3339902	single nucleotide variant	NM_016639.3(TNFRSF12A):c.298G>A (p.Val100Ile)	not specified [RCV004473138]	uncertain significance	16	3021653	3021653	Human		name