Mif4gd 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 Mif4gd

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156237601	CV2224220	single nucleotide variant	NM_001370592.1(MIF4GD):c.82+717A>G	not specified [RCV004096058]	uncertain significance	17	75269397	75269397	Human		name
156264638	CV2364353	single nucleotide variant	NM_001370592.1(MIF4GD):c.82+731C>T	not specified [RCV004223571]	uncertain significance	17	75269383	75269383	Human		name
597635846	CV3560367	single nucleotide variant	NM_001370592.1(MIF4GD):c.82+689G>C	not specified [RCV004824447]	uncertain significance	17	75269425	75269425	Human		name
598254459	CV3993191	single nucleotide variant	NM_001370592.1(MIF4GD):c.82+756C>T	not specified [RCV005367204]	uncertain significance	17	75269358	75269358	Human		name
155905686	CV2393761	single nucleotide variant	NM_001370592.1(MIF4GD):c.21G>C (p.Glu7Asp)	not specified [RCV004233599]	uncertain significance	17	75270175	75270175	Human		name
401765005	CV2701698	single nucleotide variant	NM_001370592.1(MIF4GD):c.80A>T (p.Lys27Ile)	not specified [RCV004314106]	uncertain significance	17	75270116	75270116	Human		name
156281714	CV2338481	single nucleotide variant	NM_001370592.1(MIF4GD):c.255G>T (p.Gln85His)	not specified [RCV004188521]	uncertain significance	17	75267839	75267839	Human		name
401726829	CV2674562	single nucleotide variant	NM_001370592.1(MIF4GD):c.169C>T (p.Arg57Cys)	not specified [RCV004291439]	uncertain significance	17	75268106	75268106	Human		name
401865688	CV2786094	single nucleotide variant	NM_001370592.1(MIF4GD):c.105G>C (p.Glu35Asp)	not specified [RCV004359906]	uncertain significance	17	75268170	75268170	Human		name
405672619	CV3285702	single nucleotide variant	NM_001370592.1(MIF4GD):c.230G>A (p.Arg77His)	not specified [RCV004419851]	uncertain significance	17	75267864	75267864	Human		name
597646714	CV3560365	single nucleotide variant	NM_001370592.1(MIF4GD):c.245G>A (p.Arg82Gln)	not specified [RCV004833102]	uncertain significance	17	75267849	75267849	Human		name
598186441	CV3993192	single nucleotide variant	NM_001370592.1(MIF4GD):c.221T>G (p.Val74Gly)	not specified [RCV005373406]	uncertain significance	17	75267873	75267873	Human		name
156245034	CV2283397	single nucleotide variant	NM_001370592.1(MIF4GD):c.430A>G (p.Lys144Glu)	not specified [RCV004139626]	uncertain significance	17	75267549	75267549	Human		name
155905933	CV2303212	single nucleotide variant	NM_001370592.1(MIF4GD):c.658G>A (p.Val220Ile)	not specified [RCV004156971]	uncertain significance	17	75266751	75266751	Human		name
401755850	CV2675540	single nucleotide variant	NM_001370592.1(MIF4GD):c.508A>G (p.Met170Val)	not specified [RCV004295156]	uncertain significance	17	75266901	75266901	Human		name
401881644	CV2784758	single nucleotide variant	NM_001370592.1(MIF4GD):c.397C>T (p.Leu133Phe)	not specified [RCV004352554]	uncertain significance	17	75267582	75267582	Human		name
405672623	CV3285703	single nucleotide variant	NM_001370592.1(MIF4GD):c.298G>C (p.Gly100Arg)	not specified [RCV004419852]	uncertain significance	17	75267796	75267796	Human		name
407518506	CV3447016	single nucleotide variant	NM_001370592.1(MIF4GD):c.404G>A (p.Arg135Gln)	not specified [RCV004628897]	uncertain significance	17	75267575	75267575	Human		name
597646693	CV3560361	single nucleotide variant	NM_001370592.1(MIF4GD):c.596T>C (p.Ile199Thr)	not specified [RCV004833099]	uncertain significance	17	75266813	75266813	Human		name
597646699	CV3560363	single nucleotide variant	NM_001370592.1(MIF4GD):c.613G>A (p.Gly205Ser)	not specified [RCV004833100]	uncertain significance	17	75266796	75266796	Human		name
597646708	CV3560364	single nucleotide variant	NM_001370592.1(MIF4GD):c.603C>G (p.Phe201Leu)	not specified [RCV004833101]	uncertain significance	17	75266806	75266806	Human		name
597646722	CV3560366	single nucleotide variant	NM_001370592.1(MIF4GD):c.664G>A (p.Asp222Asn)	not specified [RCV004833103]	uncertain significance	17	75266745	75266745	Human		name
598186435	CV3993190	single nucleotide variant	NM_001370592.1(MIF4GD):c.472G>A (p.Val158Ile)	not specified [RCV005373405]	uncertain significance	17	75266937	75266937	Human		name
598254467	CV3993195	single nucleotide variant	NM_001370592.1(MIF4GD):c.341A>G (p.Tyr114Cys)	not specified [RCV005367205]	uncertain significance	17	75267753	75267753	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