Thap3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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23 records found for search term Thap3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156131310	CV2206334	single nucleotide variant	NM_001195753.2(THAP3):c.22C>T (p.Arg8Trp)	not specified [RCV004078671]	uncertain significance	1	6625240	6625240	Human		name
156330701	CV2210682	single nucleotide variant	NM_001195753.2(THAP3):c.16G>A (p.Ala6Thr)	not specified [RCV004083823]	uncertain significance	1	6625234	6625234	Human		name
156325636	CV2195442	single nucleotide variant	NM_001195753.2(THAP3):c.40T>C (p.Tyr14His)	not specified [RCV004080347]	uncertain significance	1	6625258	6625258	Human		name
407497772	CV3478829	single nucleotide variant	NM_001195753.2(THAP3):c.50G>T (p.Arg17Leu)	not specified [RCV004668490]	uncertain significance	1	6625268	6625268	Human		name
407497776	CV3478830	single nucleotide variant	NM_001195753.2(THAP3):c.59A>G (p.Gln20Arg)	not specified [RCV004668491]	uncertain significance	1	6625277	6625277	Human		name
407497786	CV3478832	single nucleotide variant	NM_001195753.2(THAP3):c.80C>T (p.Pro27Leu)	not specified [RCV004668493]	uncertain significance	1	6628504	6628504	Human		name
156247689	CV2263902	single nucleotide variant	NM_001195753.2(THAP3):c.208C>T (p.Arg70Cys)	not specified [RCV004137950]	uncertain significance	1	6628632	6628632	Human		name
155968496	CV2337849	single nucleotide variant	NM_001195753.2(THAP3):c.256G>A (p.Asp86Asn)	not specified [RCV004183859]	uncertain significance	1	6628680	6628680	Human		name
597752435	CV3616342	single nucleotide variant	NM_001195753.2(THAP3):c.140A>C (p.Lys47Thr)	not specified [RCV004867151]	uncertain significance	1	6628564	6628564	Human		name
597752439	CV3616343	single nucleotide variant	NM_001195753.2(THAP3):c.138C>G (p.Phe46Leu)	not specified [RCV004867152]	uncertain significance	1	6628562	6628562	Human		name
156344766	CV2346208	single nucleotide variant	NM_001195753.2(THAP3):c.661C>T (p.Arg221Cys)	not specified [RCV004201661]	uncertain significance	1	6633018	6633018	Human		name
329361685	CV2468204	single nucleotide variant	NM_001195753.2(THAP3):c.448C>T (p.Arg150Trp)	not specified [RCV004275785]	likely benign	1	6632805	6632805	Human		name
401896402	CV2781265	single nucleotide variant	NM_001195753.2(THAP3):c.590A>G (p.Lys197Arg)	not specified [RCV004352297]	uncertain significance	1	6632947	6632947	Human		name
405792969	CV3339140	single nucleotide variant	NM_001195753.2(THAP3):c.455C>T (p.Pro152Leu)	not specified [RCV004474742]	uncertain significance	1	6632812	6632812	Human		name
405792972	CV3339141	single nucleotide variant	NM_001195753.2(THAP3):c.494C>A (p.Ala165Glu)	not specified [RCV004474743]	uncertain significance	1	6632851	6632851	Human		name
405792975	CV3339142	single nucleotide variant	NM_001195753.2(THAP3):c.613C>T (p.Arg205Cys)	not specified [RCV004474744]	uncertain significance	1	6632970	6632970	Human		name
405792978	CV3339143	single nucleotide variant	NM_001195753.2(THAP3):c.653G>T (p.Ser218Ile)	not specified [RCV004474745]	uncertain significance	1	6633010	6633010	Human		name
407497781	CV3478831	single nucleotide variant	NM_001195753.2(THAP3):c.584C>T (p.Thr195Ile)	not specified [RCV004668492]	uncertain significance	1	6632941	6632941	Human		name
597752450	CV3616345	single nucleotide variant	NM_001195753.2(THAP3):c.662G>A (p.Arg221His)	not specified [RCV004867154]	uncertain significance	1	6633019	6633019	Human		name
597752455	CV3616346	single nucleotide variant	NM_001195753.2(THAP3):c.347C>T (p.Ala116Val)	not specified [RCV004867155]	likely benign	1	6632404	6632404	Human		name
598184589	CV3913461	single nucleotide variant	NM_001195753.2(THAP3):c.331A>G (p.Lys111Glu)	not specified [RCV005287299]	uncertain significance	1	6630351	6630351	Human		name
598184596	CV3913462	single nucleotide variant	NM_001195753.2(THAP3):c.337C>T (p.Leu113Phe)	not specified [RCV005287300]	uncertain significance	1	6632394	6632394	Human		name
598184604	CV3913463	single nucleotide variant	NM_001195753.2(THAP3):c.583A>G (p.Thr195Ala)	not specified [RCV005287301]	uncertain significance	1	6632940	6632940	Human		name

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