Hmgcll1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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38 records found for search term Hmgcll1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8582004	CV116456	single nucleotide variant	NM_001042406.1(HMGCLL1):c.796-598T>A	Lung cancer [RCV000096979]	uncertain significance	6	55440157	55440157	Human		name
8626240	CV81384	single nucleotide variant	NM_001042406.1(HMGCLL1):c.720C>T (p.Ile240=)	Malignant melanoma [RCV000061462]	not provided	6	55495494	55495494	Human		name
156278561	CV2284960	single nucleotide variant	NM_001042406.2(HMGCLL1):c.265A>T (p.Thr89Ser)	not specified [RCV004143402]	uncertain significance	6	55541761	55541761	Human		name
401730889	CV2674188	single nucleotide variant	NM_001042406.2(HMGCLL1):c.284G>T (p.Arg95Ile)	not specified [RCV004289083]	uncertain significance	6	55541742	55541742	Human		name
401743065	CV2677757	single nucleotide variant	NM_001042406.2(HMGCLL1):c.259G>C (p.Glu87Gln)	not specified [RCV004291832]	uncertain significance	6	55541767	55541767	Human		name
401740077	CV2683252	single nucleotide variant	NM_001042406.2(HMGCLL1):c.166A>T (p.Arg56Trp)	not specified [RCV004288037]	uncertain significance	6	55542083	55542083	Human		name
405790884	CV3266839	single nucleotide variant	NM_001042406.2(HMGCLL1):c.163C>G (p.Pro55Ala)	not specified [RCV004399662]	uncertain significance	6	55542086	55542086	Human		name
405790887	CV3266840	single nucleotide variant	NM_001042406.2(HMGCLL1):c.278C>T (p.Ser93Phe)	not specified [RCV004399663]	uncertain significance	6	55541748	55541748	Human		name
405790890	CV3266841	single nucleotide variant	NM_001042406.2(HMGCLL1):c.284G>C (p.Arg95Thr)	not specified [RCV004399664]	uncertain significance	6	55541742	55541742	Human		name
597791283	CV3682799	single nucleotide variant	NM_001042406.2(HMGCLL1):c.256A>G (p.Ile86Val)	not specified [RCV004933455]	uncertain significance	6	55541770	55541770	Human		name
598248654	CV3975383	single nucleotide variant	NM_001042406.2(HMGCLL1):c.113C>T (p.Thr38Ile)	not specified [RCV005345474]	uncertain significance	6	55542136	55542136	Human		name
156255995	CV2219720	single nucleotide variant	NM_001042406.2(HMGCLL1):c.661A>G (p.Ile221Val)	not specified [RCV004095424]	uncertain significance	6	55495553	55495553	Human		name
156086498	CV2241242	single nucleotide variant	NM_001042406.2(HMGCLL1):c.811G>A (p.Val271Met)	not specified [RCV004102400]	uncertain significance	6	55439544	55439544	Human		name
156077384	CV2318543	single nucleotide variant	NM_001042406.2(HMGCLL1):c.883G>A (p.Asp295Asn)	not specified [RCV004173451]	uncertain significance	6	55439472	55439472	Human		name
156168884	CV2320126	single nucleotide variant	NM_001042406.2(HMGCLL1):c.722C>A (p.Pro241Gln)	not specified [RCV004167970]	uncertain significance	6	55495492	55495492	Human		name
156341561	CV2344848	single nucleotide variant	NM_001042406.2(HMGCLL1):c.880G>A (p.Glu294Lys)	not specified [RCV004190989]	uncertain significance	6	55439475	55439475	Human		name
156285495	CV2345582	single nucleotide variant	NM_001042406.2(HMGCLL1):c.400G>C (p.Ala134Pro)	not specified [RCV004205536]	uncertain significance	6	55514190	55514190	Human		name
156260028	CV2381072	single nucleotide variant	NM_001042406.2(HMGCLL1):c.853A>G (p.Lys285Glu)	not specified [RCV004225107]	uncertain significance	6	55439502	55439502	Human		name
156111135	CV2387747	single nucleotide variant	NM_001042406.2(HMGCLL1):c.618A>T (p.Arg206Ser)	not specified [RCV004234279]	uncertain significance	6	55495596	55495596	Human		name
329387675	CV2446761	single nucleotide variant	NM_001042406.2(HMGCLL1):c.349C>T (p.Arg117Cys)	not specified [RCV004257630]	uncertain significance	6	55516552	55516552	Human		name
329396233	CV2459443	single nucleotide variant	NM_001042406.2(HMGCLL1):c.518G>A (p.Arg173Lys)	not specified [RCV004275128]	uncertain significance	6	55514072	55514072	Human		name
401747926	CV2687636	single nucleotide variant	NM_001042406.2(HMGCLL1):c.440A>C (p.Glu147Ala)	not specified [RCV004300851]	uncertain significance	6	55514150	55514150	Human		name
401747384	CV2688901	single nucleotide variant	NM_001042406.2(HMGCLL1):c.514G>A (p.Ala172Thr)	not specified [RCV004303909]	uncertain significance	6	55514076	55514076	Human		name
401764511	CV2705055	single nucleotide variant	NM_001042406.2(HMGCLL1):c.784A>T (p.Thr262Ser)	not specified [RCV004309970]	uncertain significance	6	55495430	55495430	Human		name
401764524	CV2705066	single nucleotide variant	NM_001042406.2(HMGCLL1):c.785C>T (p.Thr262Met)	not specified [RCV004309980]	uncertain significance	6	55495429	55495429	Human		name
401773172	CV2716478	single nucleotide variant	NM_001042406.2(HMGCLL1):c.456G>T (p.Lys152Asn)	not specified [RCV004325783]	uncertain significance	6	55514134	55514134	Human		name
405790880	CV3266838	single nucleotide variant	NM_001042406.2(HMGCLL1):c.943A>T (p.Met315Leu)	not specified [RCV004399661]	uncertain significance	6	55435742	55435742	Human		name
405790893	CV3266842	single nucleotide variant	NM_001042406.2(HMGCLL1):c.652G>A (p.Gly218Arg)	not specified [RCV004399665]	uncertain significance	6	55495562	55495562	Human		name
405790896	CV3266843	single nucleotide variant	NM_001042406.2(HMGCLL1):c.676C>G (p.Pro226Ala)	not specified [RCV004399666]	uncertain significance	6	55495538	55495538	Human		name
597791280	CV3682798	single nucleotide variant	NM_001042406.2(HMGCLL1):c.590C>T (p.Pro197Leu)	not specified [RCV004933454]	uncertain significance	6	55499252	55499252	Human		name
597791289	CV3682801	single nucleotide variant	NM_001042406.2(HMGCLL1):c.328A>T (p.Ile110Phe)	not specified [RCV004933457]	uncertain significance	6	55516573	55516573	Human		name
597791291	CV3682802	single nucleotide variant	NM_001042406.2(HMGCLL1):c.953G>T (p.Gly318Val)	not specified [RCV004933458]	uncertain significance	6	55435732	55435732	Human		name
597791295	CV3682803	single nucleotide variant	NM_001042406.2(HMGCLL1):c.659C>T (p.Thr220Ile)	not specified [RCV004933459]	uncertain significance	6	55495555	55495555	Human		name
598190387	CV3975380	single nucleotide variant	NM_001042406.2(HMGCLL1):c.460A>G (p.Ile154Val)	not specified [RCV005354126]	uncertain significance	6	55514130	55514130	Human		name
598248646	CV3975382	single nucleotide variant	NM_001042406.2(HMGCLL1):c.623A>T (p.Tyr208Phe)	not specified [RCV005345473]	uncertain significance	6	55495591	55495591	Human		name
598190401	CV3975384	single nucleotide variant	NM_001042406.2(HMGCLL1):c.856G>T (p.Gly286Cys)	not specified [RCV005354128]	uncertain significance	6	55439499	55439499	Human		name
8626239	CV81383	single nucleotide variant	NM_001042406.1(HMGCLL1):c.778A>T (p.Ile260Phe)	Malignant melanoma [RCV000061461]	not provided	6	55495436	55495436	Human		name
156098109	CV2392758	single nucleotide variant	NM_001042406.2(HMGCLL1):c.1010C>T (p.Ser337Phe)	not specified [RCV004247126]	uncertain significance	6	55435675	55435675	Human		name

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