Sfrp2 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

24 records found for search term Sfrp2

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15196706	CV777311	single nucleotide variant	NM_003013.3(SFRP2):c.584-4A>T	not provided [RCV000956262]	benign	4	153781759	153781759	Human		name
407489881	CV3484014	single nucleotide variant	NM_003013.3(SFRP2):c.11G>A (p.Gly4Asp)	not specified [RCV004666179]	uncertain significance	4	153788825	153788825	Human		name
15196710	CV698398	single nucleotide variant	NM_003013.3(SFRP2):c.246G>A (p.Leu82=)	not provided [RCV000956263]	benign	4	153788590	153788590	Human		name
156074172	CV2247769	single nucleotide variant	NM_003013.3(SFRP2):c.79C>G (p.Leu27Val)	not specified [RCV004121239]	uncertain significance	4	153788757	153788757	Human		name
329361748	CV2468271	single nucleotide variant	NM_003013.3(SFRP2):c.47A>G (p.His16Arg)	not specified [RCV004275833]	uncertain significance	4	153788789	153788789	Human		name
405763891	CV3321498	single nucleotide variant	NM_003013.3(SFRP2):c.91C>G (p.Pro31Ala)	not specified [RCV004455790]	uncertain significance	4	153788745	153788745	Human		name
407489894	CV3484017	single nucleotide variant	NM_003013.3(SFRP2):c.51C>G (p.Cys17Trp)	not specified [RCV004666181]	uncertain significance	4	153788785	153788785	Human		name
15185898	CV764359	single nucleotide variant	NM_003013.3(SFRP2):c.675C>T (p.Asn225=)	not provided [RCV000931192]	likely benign	4	153781664	153781664	Human		name
155926525	CV2230636	single nucleotide variant	NM_003013.3(SFRP2):c.205A>G (p.Met69Val)	not specified [RCV004097590]	uncertain significance	4	153788631	153788631	Human		name
407492617	CV3484015	single nucleotide variant	NM_003013.3(SFRP2):c.194G>T (p.Gly65Val)	not specified [RCV004667204]	uncertain significance	4	153788642	153788642	Human		name
407489887	CV3484016	single nucleotide variant	NM_003013.3(SFRP2):c.220G>C (p.Glu74Gln)	not specified [RCV004666180]	uncertain significance	4	153788616	153788616	Human		name
11040236	CV223618	single nucleotide variant	NM_003013.3(SFRP2):c.626A>G (p.Asp209Gly)	Anophthalmia-microphthalmia syndrome [RCV000207374]\|not specified [RCV005278538]	pathogenic\|likely benign\|uncertain significance	4	153781713	153781713	Human	1	name
156267940	CV2275585	single nucleotide variant	NM_003013.3(SFRP2):c.607A>T (p.Ile203Leu)	not specified [RCV004137221]	uncertain significance	4	153781732	153781732	Human		name
156338445	CV2370647	single nucleotide variant	NM_003013.3(SFRP2):c.544G>T (p.Asp182Tyr)	not specified [RCV004215968]	uncertain significance	4	153785903	153785903	Human		name
401745319	CV2698513	single nucleotide variant	NM_003013.3(SFRP2):c.539A>G (p.Asp180Gly)	not specified [RCV004299011]	uncertain significance	4	153785908	153785908	Human		name
401719121	CV2731189	single nucleotide variant	NM_003013.3(SFRP2):c.772C>G (p.Leu258Val)	not specified [RCV004332672]	uncertain significance	4	153781567	153781567	Human		name
405763872	CV3321495	single nucleotide variant	NM_003013.3(SFRP2):c.331A>C (p.Ile111Leu)	not specified [RCV004455787]	uncertain significance	4	153788505	153788505	Human		name
405763879	CV3321496	single nucleotide variant	NM_003013.3(SFRP2):c.799G>A (p.Glu267Lys)	not specified [RCV004455788]	uncertain significance	4	153781540	153781540	Human		name
405763885	CV3321497	single nucleotide variant	NM_003013.3(SFRP2):c.872G>A (p.Arg291His)	not specified [RCV004455789]	uncertain significance	4	153781467	153781467	Human		name
407489899	CV3484018	single nucleotide variant	NM_003013.3(SFRP2):c.754G>A (p.Asp252Asn)	not specified [RCV004666182]	uncertain significance	4	153781585	153781585	Human		name
407489905	CV3484019	single nucleotide variant	NM_003013.3(SFRP2):c.578A>G (p.Asp193Gly)	not specified [RCV004666183]	uncertain significance	4	153785869	153785869	Human		name
598198523	CV3921135	single nucleotide variant	NM_003013.3(SFRP2):c.550G>A (p.Asp184Asn)	not specified [RCV005268260]	uncertain significance	4	153785897	153785897	Human		name
598166364	CV3921136	single nucleotide variant	NM_003013.3(SFRP2):c.376G>T (p.Ala126Ser)	not specified [RCV005283657]	uncertain significance	4	153788460	153788460	Human		name
598166371	CV3921137	single nucleotide variant	NM_003013.3(SFRP2):c.419T>C (p.Leu140Pro)	not specified [RCV005283658]	uncertain significance	4	153788417	153788417	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