Ctsg Variant Search Result - Rat Genome Database

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26 records found for search term Ctsg

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156226199	CV2215902	single nucleotide variant	NM_001911.3(CTSG):c.58G>A (p.Glu20Lys)	not specified [RCV004096986]	uncertain significance	14	24575410	24575410	Human		name
156097609	CV2310279	single nucleotide variant	NM_001911.3(CTSG):c.91T>G (p.Ser31Ala)	not specified [RCV004157025]	uncertain significance	14	24575377	24575377	Human		name
15200006	CV702847	single nucleotide variant	NM_001911.3(CTSG):c.44G>C (p.Gly15Ala)	not provided [RCV000957206]	benign	14	24576180	24576180	Human		name
15135297	CV714096	single nucleotide variant	NM_001911.3(CTSG):c.528C>T (p.Phe176=)	not provided [RCV000965265]	benign	14	24574311	24574311	Human		name
401861725	CV2756453	single nucleotide variant	NM_001911.3(CTSG):c.171C>G (p.Asp57Glu)	not specified [RCV004342987]	uncertain significance	14	24575297	24575297	Human		name
401863955	CV2770944	single nucleotide variant	NM_001911.3(CTSG):c.251A>C (p.Asn84Thr)	not specified [RCV004343610]	uncertain significance	14	24574763	24574763	Human		name
405700003	CV3246326	single nucleotide variant	NM_001911.3(CTSG):c.193T>G (p.Cys65Gly)	not specified [RCV004375062]	uncertain significance	14	24575275	24575275	Human		name
405700008	CV3246327	single nucleotide variant	NM_001911.3(CTSG):c.224G>A (p.Gly75Asp)	not specified [RCV004375063]	uncertain significance	14	24574790	24574790	Human		name
597653078	CV3661402	single nucleotide variant	NM_001911.3(CTSG):c.124A>G (p.Ser42Gly)	not specified [RCV004910764]	uncertain significance	14	24575344	24575344	Human		name
597653094	CV3661404	single nucleotide variant	NM_001911.3(CTSG):c.286C>T (p.Arg96Cys)	not specified [RCV004910766]	uncertain significance	14	24574728	24574728	Human		name
598221666	CV3955903	single nucleotide variant	NM_001911.3(CTSG):c.195C>G (p.Cys65Trp)	not specified [RCV005317739]	uncertain significance	14	24575273	24575273	Human		name
15200004	CV702846	single nucleotide variant	NM_001911.3(CTSG):c.269C>T (p.Thr90Ile)	not provided [RCV000957205]	benign	14	24574745	24574745	Human		name
155961396	CV2200631	single nucleotide variant	NM_001911.3(CTSG):c.336G>T (p.Leu112Phe)	not specified [RCV004079317]	uncertain significance	14	24574678	24574678	Human		name
156303626	CV2308416	single nucleotide variant	NM_001911.3(CTSG):c.626A>G (p.Asn209Ser)	not specified [RCV004166716]	uncertain significance	14	24573779	24573779	Human		name
156129986	CV2364810	single nucleotide variant	NM_001911.3(CTSG):c.751A>G (p.Met251Val)	not specified [RCV004219676]	uncertain significance	14	24573654	24573654	Human		name
156208946	CV2370051	single nucleotide variant	NM_001911.3(CTSG):c.758C>G (p.Thr253Ser)	not specified [RCV004210947]	uncertain significance	14	24573647	24573647	Human		name
329399836	CV2467646	single nucleotide variant	NM_001911.3(CTSG):c.463G>C (p.Gly155Arg)	not specified [RCV004287496]	likely benign	14	24574376	24574376	Human		name
401761225	CV2706262	single nucleotide variant	NM_001911.3(CTSG):c.461G>A (p.Arg154Lys)	not specified [RCV004314927]	uncertain significance	14	24574378	24574378	Human		name
405700014	CV3246328	single nucleotide variant	NM_001911.3(CTSG):c.369C>A (p.Asn123Lys)	not specified [RCV004375064]	uncertain significance	14	24574470	24574470	Human		name
405700020	CV3246329	single nucleotide variant	NM_001911.3(CTSG):c.428C>G (p.Thr143Ser)	not specified [RCV004375065]	uncertain significance	14	24574411	24574411	Human		name
407472713	CV3426398	single nucleotide variant	NM_001911.3(CTSG):c.346A>G (p.Arg116Gly)	not specified [RCV004616006]	uncertain significance	14	24574493	24574493	Human		name
597653086	CV3661403	single nucleotide variant	NM_001911.3(CTSG):c.463G>A (p.Gly155Arg)	not specified [RCV004910765]	likely benign	14	24574376	24574376	Human		name
12896883	CV390189	single nucleotide variant	NM_001911.3(CTSG):c.374A>G (p.Asn125Ser)	not provided [RCV004716470]\|not specified [RCV000455949]	benign	14	24574465	24574465	Human		name
598221649	CV3955901	single nucleotide variant	NM_001911.3(CTSG):c.647C>T (p.Ser216Phe)	not specified [RCV005317737]	uncertain significance	14	24573758	24573758	Human		name
598221658	CV3955902	single nucleotide variant	NM_001911.3(CTSG):c.691G>A (p.Val231Ile)	not specified [RCV005317738]	likely benign	14	24573714	24573714	Human		name
8635200	CV90422	single nucleotide variant	NM_001911.2(CTSG):c.668T>C (p.Val223Ala)	Malignant melanoma [RCV000070520]	not provided	14	24573737	24573737	Human		name

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