Gsto1 Variant Search Result - Rat Genome Database

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19 records found for search term Gsto1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15201454	CV777865	single nucleotide variant	NM_004832.3(GSTO1):c.34+7C>A	not provided [RCV000957627]	likely benign	10	104254969	104254969	Human		name
15127609	CV779603	single nucleotide variant	NM_004832.3(GSTO1):c.34+5G>A	not provided [RCV000963935]	benign	10	104254967	104254967	Human		name
405278685	CV3220328	microsatellite	NM_004832.3(GSTO1):c.464_465+1del	GSTO1-related disorder [RCV003976559]	likely benign	10	104263072	104263074	Human		name , trait , alternate_id
15160212	CV712142	single nucleotide variant	NM_004832.3(GSTO1):c.20G>A (p.Arg7Lys)	not provided [RCV000969856]	benign	10	104254948	104254948	Human		name
407504445	CV3433492	single nucleotide variant	NM_004832.3(GSTO1):c.59C>T (p.Pro20Leu)	not specified [RCV004624076]	uncertain significance	10	104255187	104255187	Human		name
156236085	CV2245483	single nucleotide variant	NM_004832.3(GSTO1):c.269G>T (p.Cys90Phe)	not specified [RCV004109261]	uncertain significance	10	104259701	104259701	Human		name
405717303	CV3259238	single nucleotide variant	NM_004832.3(GSTO1):c.122T>C (p.Val41Ala)	not specified [RCV004388360]	uncertain significance	10	104255250	104255250	Human		name
407464245	CV3433490	single nucleotide variant	NM_004832.3(GSTO1):c.133A>G (p.Lys45Glu)	not specified [RCV004635032]	uncertain significance	10	104255261	104255261	Human		name
407464254	CV3433493	single nucleotide variant	NM_004832.3(GSTO1):c.181G>C (p.Glu61Gln)	not specified [RCV004635034]	uncertain significance	10	104259613	104259613	Human		name
156272537	CV2277533	single nucleotide variant	NM_004832.3(GSTO1):c.332C>G (p.Ala111Gly)	not specified [RCV004145222]	uncertain significance	10	104259764	104259764	Human		name
329397522	CV2463814	single nucleotide variant	NM_004832.3(GSTO1):c.442A>G (p.Lys148Glu)	not specified [RCV004279903]	uncertain significance	10	104263054	104263054	Human		name
401778618	CV2709353	single nucleotide variant	NM_004832.3(GSTO1):c.544G>A (p.Glu182Lys)	not specified [RCV004316497]	uncertain significance	10	104266162	104266162	Human		name
405276409	CV3193407	single nucleotide variant	NM_004832.3(GSTO1):c.419C>A (p.Ala140Asp)	GSTO1-related disorder [RCV003974574]	benign	10	104263031	104263031	Human		name , trait , alternate_id
405717312	CV3259239	single nucleotide variant	NM_004832.3(GSTO1):c.398G>A (p.Ser133Asn)	not specified [RCV004388361]	uncertain significance	10	104263010	104263010	Human		name
405717322	CV3259240	single nucleotide variant	NM_004832.3(GSTO1):c.458T>G (p.Leu153Arg)	not specified [RCV004388362]	uncertain significance	10	104263070	104263070	Human		name
407464241	CV3433489	single nucleotide variant	NM_004832.3(GSTO1):c.640G>A (p.Ala214Thr)	not specified [RCV004635031]	uncertain significance	10	104267319	104267319	Human		name
407464257	CV3433494	single nucleotide variant	NM_004832.3(GSTO1):c.692A>C (p.Gln231Pro)	not specified [RCV004635035]	uncertain significance	10	104267371	104267371	Human		name
598252459	CV3978505	single nucleotide variant	NM_004832.3(GSTO1):c.716A>G (p.Tyr239Cys)	not specified [RCV005346105]	uncertain significance	10	104267395	104267395	Human		name
15191316	CV723754	single nucleotide variant	NM_004832.3(GSTO1):c.488C>T (p.Thr163Ile)	not provided [RCV000888345]	likely benign	10	104266106	104266106	Human		name

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