Utp23 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 Utp23

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401780044	CV2725841	single nucleotide variant	NM_032334.3(UTP23):c.8T>A (p.Ile3Asn)	not specified [RCV004316305]	uncertain significance	8	116766611	116766611	Human		name
407529191	CV3487829	single nucleotide variant	NM_032334.3(UTP23):c.36T>G (p.His12Gln)	not specified [RCV004680775]	uncertain significance	8	116766639	116766639	Human		name
598204939	CV3933103	single nucleotide variant	NM_032334.3(UTP23):c.50G>A (p.Arg17His)	not specified [RCV005290772]	uncertain significance	8	116766653	116766653	Human		name
156292823	CV2296865	single nucleotide variant	NM_032334.3(UTP23):c.266G>A (p.Arg89Gln)	not specified [RCV004148744]	uncertain significance	8	116770269	116770269	Human		name
156070599	CV2356038	single nucleotide variant	NM_032334.3(UTP23):c.161T>G (p.Met54Arg)	not specified [RCV004201412]	uncertain significance	8	116766764	116766764	Human		name
597697451	CV3632969	single nucleotide variant	NM_032334.3(UTP23):c.280T>G (p.Phe94Val)	not specified [RCV004885268]	uncertain significance	8	116770283	116770283	Human		name
598204945	CV3933104	single nucleotide variant	NM_032334.3(UTP23):c.131A>G (p.Gln44Arg)	not specified [RCV005290773]	uncertain significance	8	116766734	116766734	Human		name
150467252	CV1277539	single nucleotide variant	NM_032334.3(UTP23):c.644C>T (p.Pro215Leu)	not provided [RCV001710834]	benign	8	116771736	116771736	Human		name
156373686	CV2201325	single nucleotide variant	NM_032334.3(UTP23):c.353T>C (p.Val118Ala)	not specified [RCV004077454]	uncertain significance	8	116770356	116770356	Human		name
155995397	CV2286524	single nucleotide variant	NM_032334.3(UTP23):c.323T>C (p.Val108Ala)	not specified [RCV004140023]	uncertain significance	8	116770326	116770326	Human		name
156010368	CV2291007	single nucleotide variant	NM_032334.3(UTP23):c.640G>T (p.Ala214Ser)	not specified [RCV004151553]	uncertain significance	8	116771732	116771732	Human		name
156208299	CV2382480	single nucleotide variant	NM_032334.3(UTP23):c.394A>C (p.Lys132Gln)	not specified [RCV004230812]	uncertain significance	8	116771486	116771486	Human		name
156257223	CV2397852	single nucleotide variant	NM_032334.3(UTP23):c.538G>C (p.Glu180Gln)	not specified [RCV004239322]	uncertain significance	8	116771630	116771630	Human		name
329376572	CV2428466	single nucleotide variant	NM_032334.3(UTP23):c.527A>G (p.Lys176Arg)	not specified [RCV004253258]	uncertain significance	8	116771619	116771619	Human		name
329380403	CV2466604	single nucleotide variant	NM_032334.3(UTP23):c.428A>T (p.Asn143Ile)	not specified [RCV004274128]	uncertain significance	8	116771520	116771520	Human		name
405801393	CV3348537	single nucleotide variant	NM_032334.3(UTP23):c.524T>C (p.Ile175Thr)	not specified [RCV004477800]	uncertain significance	8	116771616	116771616	Human		name
405801395	CV3348538	single nucleotide variant	NM_032334.3(UTP23):c.728A>G (p.Lys243Arg)	not specified [RCV004477801]	uncertain significance	8	116771820	116771820	Human		name
407529193	CV3487830	single nucleotide variant	NM_032334.3(UTP23):c.543A>T (p.Glu181Asp)	not specified [RCV004680776]	uncertain significance	8	116771635	116771635	Human		name
597803431	CV3632966	single nucleotide variant	NM_032334.3(UTP23):c.587G>A (p.Arg196His)	not specified [RCV004881732]	uncertain significance	8	116771679	116771679	Human		name
597803435	CV3632968	single nucleotide variant	NM_032334.3(UTP23):c.581A>G (p.Lys194Arg)	not specified [RCV004881734]	uncertain significance	8	116771673	116771673	Human		name
597697459	CV3632970	single nucleotide variant	NM_032334.3(UTP23):c.487T>A (p.Ser163Thr)	not specified [RCV004885269]	uncertain significance	8	116771579	116771579	Human		name
598239461	CV3933105	single nucleotide variant	NM_032334.3(UTP23):c.389A>C (p.Lys130Thr)	not specified [RCV005296594]	uncertain significance	8	116771481	116771481	Human		name
15198145	CV700357	single nucleotide variant	NM_032334.3(UTP23):c.509A>G (p.His170Arg)	not provided [RCV000956665]	benign	8	116771601	116771601	Human		name

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