Hemgn Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

42 records found for search term Hemgn

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405802714	CV3273567	single nucleotide variant	NM_197978.3(HEMGN):c.10G>A (p.Gly4Arg)	not specified [RCV004404063]	uncertain significance	9	97938127	97938127	Human		name
407521459	CV3437043	single nucleotide variant	NM_197978.3(HEMGN):c.64G>A (p.Glu22Lys)	not specified [RCV004630371]	uncertain significance	9	97938073	97938073	Human		name
597760536	CV3689282	single nucleotide variant	NM_197978.3(HEMGN):c.91A>G (p.Thr31Ala)	not specified [RCV004925723]	uncertain significance	9	97936253	97936253	Human		name
597760541	CV3689284	single nucleotide variant	NM_197978.3(HEMGN):c.89G>A (p.Gly30Glu)	not specified [RCV004925724]	uncertain significance	9	97936255	97936255	Human		name
401758070	CV2731667	single nucleotide variant	NM_197978.3(HEMGN):c.217C>G (p.Arg73Gly)	not specified [RCV004331771]	uncertain significance	9	97931178	97931178	Human		name
405802719	CV3273570	single nucleotide variant	NM_197978.3(HEMGN):c.223G>T (p.Gly75Cys)	not specified [RCV004404066]	uncertain significance	9	97931172	97931172	Human		name
597760509	CV3689277	single nucleotide variant	NM_197978.3(HEMGN):c.263C>T (p.Pro88Leu)	not specified [RCV004925718]	uncertain significance	9	97931132	97931132	Human		name
597760525	CV3689280	single nucleotide variant	NM_197978.3(HEMGN):c.188G>A (p.Arg63His)	not specified [RCV004925721]	uncertain significance	9	97931207	97931207	Human		name
15188032	CV701103	single nucleotide variant	NM_197978.3(HEMGN):c.1347T>C (p.Tyr449=)	not provided [RCV000953762]	benign	9	97930048	97930048	Human		name
15098674	CV701104	single nucleotide variant	NM_197978.3(HEMGN):c.1029C>A (p.Ile343=)	not provided [RCV000958614]	benign	9	97930366	97930366	Human		name
156284034	CV2231116	single nucleotide variant	NM_197978.3(HEMGN):c.946C>G (p.Gln316Glu)	not specified [RCV004094332]	uncertain significance	9	97930449	97930449	Human		name
156084620	CV2244559	single nucleotide variant	NM_197978.3(HEMGN):c.559T>C (p.Ser187Pro)	not specified [RCV004102290]	likely benign	9	97930836	97930836	Human		name
156241152	CV2265686	single nucleotide variant	NM_197978.3(HEMGN):c.371C>T (p.Pro124Leu)	not specified [RCV004124407]	uncertain significance	9	97931024	97931024	Human		name
155949870	CV2267733	single nucleotide variant	NM_197978.3(HEMGN):c.855T>G (p.Asn285Lys)	not specified [RCV004134267]	uncertain significance	9	97930540	97930540	Human		name
155942806	CV2298311	single nucleotide variant	NM_197978.3(HEMGN):c.950A>C (p.Glu317Ala)	not specified [RCV004160215]	uncertain significance	9	97930445	97930445	Human		name
156299712	CV2306877	single nucleotide variant	NM_197978.3(HEMGN):c.903A>G (p.Ile301Met)	not specified [RCV004157407]	uncertain significance	9	97930492	97930492	Human		name
156306948	CV2335322	single nucleotide variant	NM_197978.3(HEMGN):c.332C>G (p.Pro111Arg)	not specified [RCV004186884]	uncertain significance	9	97931063	97931063	Human		name
156385422	CV2379630	single nucleotide variant	NM_197978.3(HEMGN):c.400T>C (p.Ser134Pro)	not specified [RCV004217327]	uncertain significance	9	97930995	97930995	Human		name
401763825	CV2700197	single nucleotide variant	NM_197978.3(HEMGN):c.304G>A (p.Ala102Thr)	not specified [RCV004309055]	uncertain significance	9	97931091	97931091	Human		name
401881757	CV2784812	single nucleotide variant	NM_197978.3(HEMGN):c.639C>G (p.Asp213Glu)	not specified [RCV004352602]	uncertain significance	9	97930756	97930756	Human		name
405802721	CV3273571	single nucleotide variant	NM_197978.3(HEMGN):c.392A>C (p.Glu131Ala)	not specified [RCV004404067]	uncertain significance	9	97931003	97931003	Human		name
405802723	CV3273572	single nucleotide variant	NM_197978.3(HEMGN):c.521C>A (p.Pro174His)	not specified [RCV004404068]	uncertain significance	9	97930874	97930874	Human		name
405802725	CV3273573	single nucleotide variant	NM_197978.3(HEMGN):c.836C>A (p.Ala279Glu)	not specified [RCV004404069]	uncertain significance	9	97930559	97930559	Human		name
597760519	CV3689279	single nucleotide variant	NM_197978.3(HEMGN):c.506C>T (p.Pro169Leu)	not specified [RCV004925720]	uncertain significance	9	97930889	97930889	Human		name
598274891	CV3968134	single nucleotide variant	NM_197978.3(HEMGN):c.638A>G (p.Asp213Gly)	not specified [RCV005351638]	uncertain significance	9	97930757	97930757	Human		name
598247505	CV3968137	single nucleotide variant	NM_197978.3(HEMGN):c.775C>A (p.Gln259Lys)	not specified [RCV005345308]	uncertain significance	9	97930620	97930620	Human		name
8633454	CV88669	single nucleotide variant	NM_018437.4(HEMGN):c.355C>T (p.Pro119Ser)	Malignant melanoma [RCV000068762]	not provided	9	97931040	97931040	Human		name
155941057	CV2294185	single nucleotide variant	NM_197978.3(HEMGN):c.1351T>C (p.Phe451Leu)	not specified [RCV004149546]	uncertain significance	9	97930044	97930044	Human		name
156164421	CV2389691	single nucleotide variant	NM_197978.3(HEMGN):c.1009G>A (p.Ala337Thr)	not specified [RCV004243742]	uncertain significance	9	97930386	97930386	Human		name
329376020	CV2431701	single nucleotide variant	NM_197978.3(HEMGN):c.1352T>C (p.Phe451Ser)	not specified [RCV004248866]	uncertain significance	9	97930043	97930043	Human		name
401744434	CV2680961	single nucleotide variant	NM_197978.3(HEMGN):c.1232A>G (p.Glu411Gly)	not specified [RCV004296032]	uncertain significance	9	97930163	97930163	Human		name
401760378	CV2695023	single nucleotide variant	NM_197978.3(HEMGN):c.1114C>A (p.Gln372Lys)	not specified [RCV004301396]	uncertain significance	9	97930281	97930281	Human		name
401771213	CV2700935	single nucleotide variant	NM_197978.3(HEMGN):c.1388C>G (p.Pro463Arg)	not specified [RCV004307197]	uncertain significance	9	97927451	97927451	Human		name
401885053	CV2786660	single nucleotide variant	NM_197978.3(HEMGN):c.1081C>A (p.Pro361Thr)	not specified [RCV004363788]	uncertain significance	9	97930314	97930314	Human		name
405802716	CV3273568	single nucleotide variant	NM_197978.3(HEMGN):c.1109C>T (p.Thr370Met)	not specified [RCV004404064]	uncertain significance	9	97930286	97930286	Human		name
405802718	CV3273569	single nucleotide variant	NM_197978.3(HEMGN):c.1154A>G (p.Tyr385Cys)	not specified [RCV004404065]	uncertain significance	9	97930241	97930241	Human		name
407521456	CV3437042	single nucleotide variant	NM_197978.3(HEMGN):c.1084G>C (p.Gly362Arg)	not specified [RCV004630370]	uncertain significance	9	97930311	97930311	Human		name
407521461	CV3437044	single nucleotide variant	NM_197978.3(HEMGN):c.1205C>T (p.Thr402Ile)	not specified [RCV004630372]	uncertain significance	9	97930190	97930190	Human		name
597760514	CV3689278	single nucleotide variant	NM_197978.3(HEMGN):c.1102C>A (p.Pro368Thr)	not specified [RCV004925719]	uncertain significance	9	97930293	97930293	Human		name
597760530	CV3689281	single nucleotide variant	NM_197978.3(HEMGN):c.1219G>T (p.Asp407Tyr)	not specified [RCV004925722]	uncertain significance	9	97930176	97930176	Human		name
598247489	CV3968135	single nucleotide variant	NM_197978.3(HEMGN):c.1034A>G (p.Glu345Gly)	not specified [RCV005345306]	uncertain significance	9	97930361	97930361	Human		name
598247497	CV3968136	single nucleotide variant	NM_197978.3(HEMGN):c.1362A>T (p.Glu454Asp)	not specified [RCV005345307]	uncertain significance	9	97927477	97927477	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