Ugt2a1 Variant Search Result - Rat Genome Database

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32 records found for search term Ugt2a1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405805064	CV3338087	single nucleotide variant	NM_001252275.3(UGT2A1):c.997-1026C>T	not specified [RCV004479544]	uncertain significance	4	69596275	69596275	Human		name
329379959	CV2466340	single nucleotide variant	NM_001252275.3(UGT2A1):c.68T>C (p.Val23Ala)	not specified [RCV004280256]	uncertain significance	4	69647577	69647577	Human		name
401779388	CV2718528	single nucleotide variant	NM_001252275.3(UGT2A1):c.82A>G (p.Met28Val)	not specified [RCV004318333]	uncertain significance	4	69647563	69647563	Human		name
598190515	CV3929259	single nucleotide variant	NM_001252275.3(UGT2A1):c.84G>C (p.Met28Ile)	not specified [RCV005288221]	uncertain significance	4	69647561	69647561	Human		name
15101206	CV749043	single nucleotide variant	NM_001252275.3(UGT2A1):c.930T>G (p.Arg310=)	not provided [RCV000914739]	likely benign	4	69599312	69599312	Human		name
156248650	CV2264000	single nucleotide variant	NM_001252275.3(UGT2A1):c.241G>A (p.Glu81Lys)	not specified [RCV004138023]	uncertain significance	4	69647404	69647404	Human		name
155956095	CV2303987	single nucleotide variant	NM_001252275.3(UGT2A1):c.200C>A (p.Pro67Gln)	not specified [RCV004170042]	uncertain significance	4	69647445	69647445	Human		name
156046847	CV2340277	single nucleotide variant	NM_001252275.3(UGT2A1):c.167C>T (p.Ser56Phe)	not specified [RCV004194547]	uncertain significance	4	69647478	69647478	Human		name
329373887	CV2434648	single nucleotide variant	NM_001252275.3(UGT2A1):c.254G>A (p.Gly85Glu)	not provided [RCV004696331]\|not specified [RCV004248369]	uncertain significance	4	69647391	69647391	Human		name
405805051	CV3338081	single nucleotide variant	NM_001252275.3(UGT2A1):c.122A>G (p.Asp41Gly)	not specified [RCV004479538]	uncertain significance	4	69647523	69647523	Human		name
405805053	CV3338082	single nucleotide variant	NM_001252275.3(UGT2A1):c.143A>G (p.His48Arg)	not specified [RCV004479539]	uncertain significance	4	69647502	69647502	Human		name
407523480	CV3491322	single nucleotide variant	NM_001252275.3(UGT2A1):c.128T>C (p.Leu43Pro)	not specified [RCV004678025]	uncertain significance	4	69647517	69647517	Human		name
598266187	CV3929260	single nucleotide variant	NM_001252275.3(UGT2A1):c.296C>A (p.Pro99Gln)	not specified [RCV005301885]	uncertain significance	4	69647349	69647349	Human		name
598190524	CV3929261	single nucleotide variant	NM_001252275.3(UGT2A1):c.118A>G (p.Ile40Val)	not specified [RCV005288222]	uncertain significance	4	69647527	69647527	Human		name
15185026	CV698609	single nucleotide variant	NM_001252275.3(UGT2A1):c.164C>T (p.Ala55Val)	not provided [RCV000952859]	benign	4	69647481	69647481	Human		name
15166852	CV709431	single nucleotide variant	NM_001252275.3(UGT2A1):c.1170A>T (p.Gly390=)	not provided [RCV000971274]	benign	4	69594611	69594611	Human		name
15101202	CV749042	single nucleotide variant	NM_001252275.3(UGT2A1):c.1041C>T (p.Asn347=)	not provided [RCV000914738]	likely benign	4	69595205	69595205	Human		name
156399184	CV2204964	single nucleotide variant	NM_001252275.3(UGT2A1):c.575A>G (p.Tyr192Cys)	not specified [RCV004077586]	uncertain significance	4	69647070	69647070	Human		name
156180503	CV2225945	single nucleotide variant	NM_001252275.3(UGT2A1):c.426C>A (p.Ser142Arg)	not specified [RCV004105115]	uncertain significance	4	69647219	69647219	Human		name
155917569	CV2274926	single nucleotide variant	NM_001252275.3(UGT2A1):c.644C>T (p.Ser215Phe)	not specified [RCV004134986]	uncertain significance	4	69647001	69647001	Human		name
156396789	CV2330272	single nucleotide variant	NM_001252275.3(UGT2A1):c.476T>G (p.Val159Gly)	not specified [RCV004187721]	uncertain significance	4	69647169	69647169	Human		name
401768304	CV2720048	single nucleotide variant	NM_001252275.3(UGT2A1):c.686C>T (p.Ser229Leu)	not specified [RCV004323622]	uncertain significance	4	69646959	69646959	Human		name
405805055	CV3338083	single nucleotide variant	NM_001252275.3(UGT2A1):c.349G>A (p.Asp117Asn)	not specified [RCV004479540]	likely benign	4	69647296	69647296	Human		name
405805057	CV3338084	single nucleotide variant	NM_001252275.3(UGT2A1):c.467G>A (p.Gly156Asp)	not specified [RCV004479541]	uncertain significance	4	69647178	69647178	Human		name
405805059	CV3338085	single nucleotide variant	NM_001252275.3(UGT2A1):c.504G>A (p.Met168Ile)	not specified [RCV004479542]	likely benign	4	69647141	69647141	Human		name
407462423	CV3491323	single nucleotide variant	NM_001252275.3(UGT2A1):c.556G>A (p.Val186Ile)	not specified [RCV004687957]	uncertain significance	4	69647089	69647089	Human		name
12896339	CV389665	single nucleotide variant	NM_001252275.3(UGT2A1):c.576T>A (p.Tyr192Ter)	not provided [RCV004711109]\|not specified [RCV000455213]	likely benign	4	69647069	69647069	Human		name
155930951	CV2362399	single nucleotide variant	NM_001252275.3(UGT2A1):c.1463C>A (p.Ser488Tyr)	not specified [RCV004213025]	uncertain significance	4	69589493	69589493	Human		name
15171620	CV709429	single nucleotide variant	NM_001252275.3(UGT2A1):c.1369C>T (p.Arg457Ter)	not provided [RCV000972235]	likely benign	4	69589587	69589587	Human		name
15113662	CV709430	single nucleotide variant	NM_001252275.3(UGT2A1):c.1179G>A (p.Met393Ile)	not provided [RCV000961532]	benign	4	69594602	69594602	Human		name
15199787	CV721052	single nucleotide variant	NM_001252275.3(UGT2A1):c.1020G>T (p.Lys340Asn)	not provided [RCV000890729]	likely benign	4	69595226	69595226	Human		name
598128661	CV3887866	insertion	NM_001252275.3(UGT2A1):c.716-7_716-6insTTTTTTTTTTTTTTTTTTTTTTT	not provided [RCV005244040]	likely benign	4	69635828	69635829	Human		name

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