St6gal2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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50 records found for search term St6gal2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8648969	CV110597	single nucleotide variant	NM_032528.2(ST6GAL2):c.944-4002C>G	Lung cancer [RCV000091120]	uncertain significance	2	106838148	106838148	Human		name
8648970	CV110598	single nucleotide variant	NM_032528.2(ST6GAL2):c.-58+20776T>G	Lung cancer [RCV000091121]	uncertain significance	2	106866200	106866200	Human		name
405867094	CV2842611	single nucleotide variant	NM_001142351.2(ST6GAL2):c.1319-6204A>G	EBV-positive nodal T- and NK-cell lymphoma [RCV004557968]	likely benign	2	106813153	106813153	Human		name
8629781	CV84928	single nucleotide variant	NM_032528.2(ST6GAL2):c.141G>A (p.Glu47=)	Malignant melanoma [RCV000065010]	not provided	2	106843837	106843837	Human		name
8625094	CV80213	single nucleotide variant	NM_032528.2(ST6GAL2):c.439A>G (p.Thr147Ala)	Malignant melanoma [RCV000060289]	not provided	2	106843539	106843539	Human		name
156169081	CV2247291	single nucleotide variant	NM_001142351.2(ST6GAL2):c.36G>T (p.Met12Ile)	not specified [RCV004115065]	uncertain significance	2	106843942	106843942	Human		name
156370185	CV2263494	single nucleotide variant	NM_001142351.2(ST6GAL2):c.83T>C (p.Ile28Thr)	not specified [RCV004133730]	uncertain significance	2	106843895	106843895	Human		name
405867090	CV2842610	single nucleotide variant	NM_001142351.2(ST6GAL2):c.873C>T (p.Arg291=)	EBV-positive nodal T- and NK-cell lymphoma [RCV004557967]	likely benign	2	106843105	106843105	Human		name
597745989	CV3608612	single nucleotide variant	NM_001142351.2(ST6GAL2):c.51C>G (p.Phe17Leu)	not specified [RCV004865774]	uncertain significance	2	106843927	106843927	Human		name
8629779	CV84926	single nucleotide variant	NM_032528.2(ST6GAL2):c.1048A>G (p.Thr350Ala)	Malignant melanoma [RCV000065008]	not provided	2	106832660	106832660	Human		name
8629780	CV84927	single nucleotide variant	NM_032528.2(ST6GAL2):c.1000G>A (p.Asp334Asn)	Malignant melanoma [RCV000065009]	not provided	2	106834090	106834090	Human		name
156057331	CV2239077	single nucleotide variant	NM_001142351.2(ST6GAL2):c.127C>T (p.Leu43Phe)	not specified [RCV004112082]	likely benign	2	106843851	106843851	Human		name
156285746	CV2289097	single nucleotide variant	NM_001142351.2(ST6GAL2):c.283G>T (p.Asp95Tyr)	not specified [RCV004150036]	uncertain significance	2	106843695	106843695	Human		name
156175354	CV2346008	single nucleotide variant	NM_001142351.2(ST6GAL2):c.297G>C (p.Trp99Cys)	not specified [RCV004199040]	uncertain significance	2	106843681	106843681	Human		name
401733518	CV2713118	single nucleotide variant	NM_001142351.2(ST6GAL2):c.130T>A (p.Ser44Thr)	not specified [RCV004316669]	uncertain significance	2	106843848	106843848	Human		name
401748632	CV2713119	single nucleotide variant	NM_001142351.2(ST6GAL2):c.131C>G (p.Ser44Cys)	not specified [RCV004316670]	uncertain significance	2	106843847	106843847	Human		name
401859354	CV2771545	single nucleotide variant	NM_001142351.2(ST6GAL2):c.281G>C (p.Gly94Ala)	not specified [RCV004348572]	uncertain significance	2	106843697	106843697	Human		name
597745979	CV3608608	single nucleotide variant	NM_001142351.2(ST6GAL2):c.274G>C (p.Gly92Arg)	not specified [RCV004865772]	uncertain significance	2	106843704	106843704	Human		name
598249110	CV3923095	single nucleotide variant	NM_001142351.2(ST6GAL2):c.223G>T (p.Asp75Tyr)	not specified [RCV005277536]	uncertain significance	2	106843755	106843755	Human		name
598249118	CV3923096	single nucleotide variant	NM_001142351.2(ST6GAL2):c.209C>T (p.Pro70Leu)	not specified [RCV005277537]	likely benign	2	106843769	106843769	Human		name
156278529	CV2227555	single nucleotide variant	NM_001142351.2(ST6GAL2):c.536G>A (p.Arg179Lys)	not specified [RCV004092200]	uncertain significance	2	106843442	106843442	Human		name
155919081	CV2279352	single nucleotide variant	NM_001142351.2(ST6GAL2):c.729G>T (p.Glu243Asp)	not specified [RCV004139866]	uncertain significance	2	106843249	106843249	Human		name
155904889	CV2285730	single nucleotide variant	NM_001142351.2(ST6GAL2):c.314G>A (p.Gly105Glu)	not specified [RCV004141877]	uncertain significance	2	106843664	106843664	Human		name
156241119	CV2286097	single nucleotide variant	NM_001142351.2(ST6GAL2):c.682T>A (p.Tyr228Asn)	not specified [RCV004143985]	uncertain significance	2	106843296	106843296	Human		name
156249922	CV2311176	single nucleotide variant	NM_001142351.2(ST6GAL2):c.733G>A (p.Gly245Arg)	not specified [RCV004166274]	likely benign	2	106843245	106843245	Human		name
156287650	CV2327338	single nucleotide variant	NM_001142351.2(ST6GAL2):c.508A>G (p.Arg170Gly)	not specified [RCV004174775]	uncertain significance	2	106843470	106843470	Human		name
156051239	CV2386300	single nucleotide variant	NM_001142351.2(ST6GAL2):c.395T>C (p.Phe132Ser)	not specified [RCV004228644]	uncertain significance	2	106843583	106843583	Human		name
401855811	CV2757482	single nucleotide variant	NM_001142351.2(ST6GAL2):c.484G>C (p.Ala162Pro)	not specified [RCV004340869]	uncertain significance	2	106843494	106843494	Human		name
401859949	CV2765217	single nucleotide variant	NM_001142351.2(ST6GAL2):c.754C>G (p.Leu252Val)	not specified [RCV004339744]	uncertain significance	2	106843224	106843224	Human		name
405720488	CV3323462	single nucleotide variant	NM_001142351.2(ST6GAL2):c.578A>G (p.Asp193Gly)	not specified [RCV004463063]	uncertain significance	2	106843400	106843400	Human		name
405720494	CV3323463	single nucleotide variant	NM_001142351.2(ST6GAL2):c.771C>G (p.Ser257Arg)	not specified [RCV004463064]	likely benign	2	106843207	106843207	Human		name
407517243	CV3475079	single nucleotide variant	NM_001142351.2(ST6GAL2):c.689C>T (p.Thr230Ile)	not specified [RCV004675577]	uncertain significance	2	106843289	106843289	Human		name
407517246	CV3475080	single nucleotide variant	NM_001142351.2(ST6GAL2):c.860A>G (p.Gln287Arg)	not specified [RCV004675578]	uncertain significance	2	106843118	106843118	Human		name
597745968	CV3608605	single nucleotide variant	NM_001142351.2(ST6GAL2):c.458C>G (p.Pro153Arg)	not specified [RCV004865770]	uncertain significance	2	106843520	106843520	Human		name
597681850	CV3608609	single nucleotide variant	NM_001142351.2(ST6GAL2):c.952G>A (p.Asp318Asn)	not specified [RCV004857608]	uncertain significance	2	106834138	106834138	Human		name
597745984	CV3608610	single nucleotide variant	NM_001142351.2(ST6GAL2):c.451C>T (p.Pro151Ser)	not specified [RCV004865773]	uncertain significance	2	106843527	106843527	Human		name
597681860	CV3608611	single nucleotide variant	NM_001142351.2(ST6GAL2):c.644A>G (p.Lys215Arg)	not specified [RCV004857609]	uncertain significance	2	106843334	106843334	Human		name
597745997	CV3608615	single nucleotide variant	NM_001142351.2(ST6GAL2):c.728A>T (p.Glu243Val)	not specified [RCV004865776]	uncertain significance	2	106843250	106843250	Human		name
598213982	CV3923093	single nucleotide variant	NM_001142351.2(ST6GAL2):c.956C>T (p.Ala319Val)	not specified [RCV005271070]	uncertain significance	2	106834134	106834134	Human		name
156149975	CV2197625	single nucleotide variant	NM_001142351.2(ST6GAL2):c.1009A>C (p.Asn337His)	not specified [RCV004074841]	uncertain significance	2	106834081	106834081	Human		name
156200900	CV2350943	single nucleotide variant	NM_001142351.2(ST6GAL2):c.1423G>A (p.Ala475Thr)	not specified [RCV004211774]	uncertain significance	2	106806845	106806845	Human		name
329351578	CV2462125	single nucleotide variant	NM_001142351.2(ST6GAL2):c.1127C>T (p.Ser376Phe)	not specified [RCV004266150]	uncertain significance	2	106832581	106832581	Human		name
405720464	CV3323459	single nucleotide variant	NM_001142351.2(ST6GAL2):c.1059C>G (p.Ser353Arg)	not specified [RCV004463060]	uncertain significance	2	106832649	106832649	Human		name
405720471	CV3323460	single nucleotide variant	NM_001142351.2(ST6GAL2):c.1255G>T (p.Asp419Tyr)	not specified [RCV004463061]	uncertain significance	2	106830129	106830129	Human		name
405720480	CV3323461	single nucleotide variant	NM_001142351.2(ST6GAL2):c.1459T>C (p.Tyr487His)	not specified [RCV004463062]	uncertain significance	2	106806809	106806809	Human		name
597681840	CV3608604	single nucleotide variant	NM_001142351.2(ST6GAL2):c.1093G>A (p.Val365Ile)	not specified [RCV004857607]	uncertain significance	2	106832615	106832615	Human		name
597745973	CV3608607	single nucleotide variant	NM_001142351.2(ST6GAL2):c.1065C>G (p.His355Gln)	not specified [RCV004865771]	uncertain significance	2	106832643	106832643	Human		name
597745994	CV3608613	single nucleotide variant	NM_001142351.2(ST6GAL2):c.1077T>A (p.Ser359Arg)	not specified [RCV004865775]	uncertain significance	2	106832631	106832631	Human		name
597681869	CV3608614	single nucleotide variant	NM_001142351.2(ST6GAL2):c.1193G>A (p.Arg398His)	not specified [RCV004857610]	uncertain significance	2	106830191	106830191	Human		name
598175601	CV3923094	single nucleotide variant	NM_001142351.2(ST6GAL2):c.1535C>T (p.Pro512Leu)	not specified [RCV005285513]	uncertain significance	2	106806733	106806733	Human		name

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