Egr1 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

28 records found for search term Egr1

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
243057681	CV2404674	single nucleotide variant	NM_001964.3(EGR1):c.-205G>A	Squamous cell carcinoma [RCV003129701]	uncertain significance	5	138465557	138465557	Human	2	name
15157392	CV698801	single nucleotide variant	NM_001964.3(EGR1):c.513G>C (p.Ser171=)	not provided [RCV000946876]	benign	5	138466962	138466962	Human		name
156168972	CV2276682	single nucleotide variant	NM_001964.3(EGR1):c.149G>A (p.Gly50Asp)	not specified [RCV004146482]	uncertain significance	5	138465910	138465910	Human		name
156388651	CV2375956	single nucleotide variant	NM_001964.3(EGR1):c.142T>C (p.Phe48Leu)	not specified [RCV004218164]	uncertain significance	5	138465903	138465903	Human		name
401917861	CV2828021	single nucleotide variant	NM_001964.3(EGR1):c.1056C>T (p.Ser352=)	not provided [RCV003429779]	likely benign	5	138467505	138467505	Human		name
407498441	CV3437973	single nucleotide variant	NM_001964.3(EGR1):c.155C>T (p.Ala52Val)	not specified [RCV004622460]	uncertain significance	5	138465916	138465916	Human		name
597647435	CV3674193	single nucleotide variant	NM_001964.3(EGR1):c.271G>A (p.Asp91Asn)	not specified [RCV004910078]	uncertain significance	5	138466032	138466032	Human		name
598177846	CV3961152	single nucleotide variant	NM_001964.3(EGR1):c.117G>A (p.Met39Ile)	not specified [RCV005332254]	uncertain significance	5	138465878	138465878	Human		name
598177811	CV3965098	single nucleotide variant	NM_001964.3(EGR1):c.280G>A (p.Glu94Lys)	not specified [RCV005332249]	uncertain significance	5	138466041	138466041	Human		name
598177819	CV3965099	single nucleotide variant	NM_001964.3(EGR1):c.224G>A (p.Gly75Asp)	not specified [RCV005332250]	uncertain significance	5	138465985	138465985	Human		name
15188124	CV698802	single nucleotide variant	NM_001964.3(EGR1):c.1017T>G (p.Ala339=)	not provided [RCV000953788]	benign	5	138467466	138467466	Human		name
156183158	CV2222359	single nucleotide variant	NM_001964.3(EGR1):c.631A>C (p.Thr211Pro)	not specified [RCV004099229]	uncertain significance	5	138467080	138467080	Human		name
329373890	CV2434649	single nucleotide variant	NM_001964.3(EGR1):c.514T>G (p.Ser172Ala)	not specified [RCV004248370]	uncertain significance	5	138466963	138466963	Human		name
405716991	CV3241777	single nucleotide variant	NM_001964.3(EGR1):c.782A>G (p.Gln261Arg)	not specified [RCV004377514]	uncertain significance	5	138467231	138467231	Human		name
597647442	CV3674194	single nucleotide variant	NM_001964.3(EGR1):c.899G>T (p.Gly300Val)	not specified [RCV004910079]	uncertain significance	5	138467348	138467348	Human		name
598177833	CV3961150	single nucleotide variant	NM_001964.3(EGR1):c.301A>G (p.Thr101Ala)	not specified [RCV005332252]	uncertain significance	5	138466062	138466062	Human		name
598177855	CV3961153	single nucleotide variant	NM_001964.3(EGR1):c.313T>C (p.Phe105Leu)	not specified [RCV005332255]	uncertain significance	5	138466762	138466762	Human		name
598177861	CV3961154	single nucleotide variant	NM_001964.3(EGR1):c.577G>T (p.Ala193Ser)	not specified [RCV005332256]	uncertain significance	5	138467026	138467026	Human		name
598177867	CV3961155	single nucleotide variant	NM_001964.3(EGR1):c.322A>G (p.Ile108Val)	not specified [RCV005332257]	uncertain significance	5	138466771	138466771	Human		name
598177804	CV3965097	single nucleotide variant	NM_001964.3(EGR1):c.304G>T (p.Ala102Ser)	not specified [RCV005332248]	uncertain significance	5	138466065	138466065	Human		name
156134967	CV2284698	single nucleotide variant	NM_001964.3(EGR1):c.1072C>T (p.His358Tyr)	not specified [RCV004140850]	uncertain significance	5	138467521	138467521	Human		name
156338879	CV2351494	single nucleotide variant	NM_001964.3(EGR1):c.1570G>A (p.Ala524Thr)	not specified [RCV004193177]	uncertain significance	5	138468019	138468019	Human		name
401729589	CV2683731	single nucleotide variant	NM_001964.3(EGR1):c.1535G>T (p.Ser512Ile)	not specified [RCV004284472]	uncertain significance	5	138467984	138467984	Human		name
401731825	CV2712172	single nucleotide variant	NM_001964.3(EGR1):c.1478C>G (p.Pro493Arg)	not specified [RCV004311891]	uncertain significance	5	138467927	138467927	Human		name
405716981	CV3241776	single nucleotide variant	NM_001964.3(EGR1):c.1445A>G (p.Tyr482Cys)	not specified [RCV004377513]	uncertain significance	5	138467894	138467894	Human		name
597746373	CV3674195	single nucleotide variant	NM_001964.3(EGR1):c.1399C>A (p.Pro467Thr)	not specified [RCV004922683]	uncertain significance	5	138467848	138467848	Human		name
598177839	CV3961151	single nucleotide variant	NM_001964.3(EGR1):c.1601C>A (p.Thr534Asn)	not specified [RCV005332253]	uncertain significance	5	138468050	138468050	Human		name
15111606	CV709640	microsatellite	NM_001964.3(EGR1):c.184AGC[5] (p.Ser67del)	not provided [RCV000961140]	likely benign	5	138465944	138465946	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message