Hmg20a Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

34 records found for search term Hmg20a

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405280601	CV3195590	single nucleotide variant	NM_001304504.2(HMG20A):c.-1G>A	HMG20A-related disorder [RCV003906833]	likely benign	15	77458407	77458407	Human		name , trait , alternate_id
405289016	CV3204924	single nucleotide variant	NM_001304504.2(HMG20A):c.54C>T (p.Asp18=)	HMG20A-related disorder [RCV003961568]	likely benign	15	77458461	77458461	Human		name , trait , alternate_id
15165698	CV726265	single nucleotide variant	NM_001304504.2(HMG20A):c.26C>T (p.Thr9Ile)	not provided [RCV000882470]	likely benign	15	77458433	77458433	Human		name
405790828	CV3266820	single nucleotide variant	NM_001304504.2(HMG20A):c.32C>T (p.Pro11Leu)	not specified [RCV004399643]	uncertain significance	15	77458439	77458439	Human		name
401774541	CV2691773	single nucleotide variant	NM_001304504.2(HMG20A):c.116G>A (p.Ser39Asn)	not specified [RCV004299225]	uncertain significance	15	77464266	77464266	Human		name
405790826	CV3266819	single nucleotide variant	NM_001304504.2(HMG20A):c.176A>G (p.Gln59Arg)	not specified [RCV004399642]	uncertain significance	15	77464326	77464326	Human		name
597791201	CV3682768	single nucleotide variant	NM_001304504.2(HMG20A):c.188G>A (p.Ser63Asn)	not specified [RCV004933427]	likely benign	15	77464338	77464338	Human		name
597791216	CV3682773	single nucleotide variant	NM_001304504.2(HMG20A):c.265A>G (p.Lys89Glu)	not specified [RCV004933432]	uncertain significance	15	77467122	77467122	Human		name
597791219	CV3682774	single nucleotide variant	NM_001304504.2(HMG20A):c.172G>A (p.Gly58Ser)	not specified [RCV004933433]	uncertain significance	15	77464322	77464322	Human		name
597791227	CV3682777	single nucleotide variant	NM_001304504.2(HMG20A):c.112T>C (p.Tyr38His)	not specified [RCV004933436]	uncertain significance	15	77464262	77464262	Human		name
155980482	CV2223032	single nucleotide variant	NM_001304504.2(HMG20A):c.865C>T (p.Arg289Trp)	not specified [RCV004103614]	uncertain significance	15	77478468	77478468	Human		name
156306997	CV2252798	single nucleotide variant	NM_001304504.2(HMG20A):c.925A>G (p.Thr309Ala)	not specified [RCV004118637]	uncertain significance	15	77479196	77479196	Human		name
155995748	CV2259193	single nucleotide variant	NM_001304504.2(HMG20A):c.769G>A (p.Val257Met)	not specified [RCV004120430]	uncertain significance	15	77478372	77478372	Human		name
155901500	CV2274525	single nucleotide variant	NM_001304504.2(HMG20A):c.680A>G (p.Asn227Ser)	not specified [RCV004138934]	uncertain significance	15	77477619	77477619	Human		name
155986012	CV2282482	single nucleotide variant	NM_001304504.2(HMG20A):c.889G>A (p.Ala297Thr)	not specified [RCV004133278]	uncertain significance	15	77478492	77478492	Human		name
156082975	CV2301211	single nucleotide variant	NM_001304504.2(HMG20A):c.871G>A (p.Val291Met)	not specified [RCV004160115]	uncertain significance	15	77478474	77478474	Human		name
156104376	CV2386960	single nucleotide variant	NM_001304504.2(HMG20A):c.827G>C (p.Ser276Thr)	not specified [RCV004233585]	uncertain significance	15	77478430	77478430	Human		name
401770556	CV2707278	single nucleotide variant	NM_001304504.2(HMG20A):c.638G>A (p.Arg213Gln)	not specified [RCV004312684]	uncertain significance	15	77477577	77477577	Human		name
401891052	CV2768960	single nucleotide variant	NM_001304504.2(HMG20A):c.335G>A (p.Arg112Gln)	not specified [RCV004347054]	uncertain significance	15	77467192	77467192	Human		name
401872711	CV2793146	single nucleotide variant	NM_001304504.2(HMG20A):c.983C>A (p.Pro328His)	not specified [RCV004360455]	uncertain significance	15	77479254	77479254	Human		name
405790831	CV3266821	single nucleotide variant	NM_001304504.2(HMG20A):c.484C>T (p.Arg162Cys)	not specified [RCV004399644]	uncertain significance	15	77470943	77470943	Human		name
405790834	CV3266822	single nucleotide variant	NM_001304504.2(HMG20A):c.538A>C (p.Ser180Arg)	not specified [RCV004399645]	uncertain significance	15	77470997	77470997	Human		name
405790837	CV3266823	single nucleotide variant	NM_001304504.2(HMG20A):c.556C>T (p.Arg186Cys)	not specified [RCV004399646]	uncertain significance	15	77471015	77471015	Human		name
407527638	CV3433633	single nucleotide variant	NM_001304504.2(HMG20A):c.598G>A (p.Ala200Thr)	not specified [RCV004632860]	uncertain significance	15	77471797	77471797	Human		name
407527641	CV3433634	single nucleotide variant	NM_001304504.2(HMG20A):c.555C>G (p.Asp185Glu)	not specified [RCV004632861]	uncertain significance	15	77471014	77471014	Human		name
407527644	CV3433635	single nucleotide variant	NM_001304504.2(HMG20A):c.637C>T (p.Arg213Trp)	not specified [RCV004632862]	uncertain significance	15	77477576	77477576	Human		name
597791207	CV3682770	single nucleotide variant	NM_001304504.2(HMG20A):c.932A>G (p.Asp311Gly)	not specified [RCV004933429]	uncertain significance	15	77479203	77479203	Human		name
597791210	CV3682771	single nucleotide variant	NM_001304504.2(HMG20A):c.593G>A (p.Arg198Gln)	not specified [RCV004933430]	uncertain significance	15	77471792	77471792	Human		name
597791212	CV3682772	single nucleotide variant	NM_001304504.2(HMG20A):c.730A>G (p.Met244Val)	not specified [RCV004933431]	uncertain significance	15	77478333	77478333	Human		name
597791224	CV3682776	single nucleotide variant	NM_001304504.2(HMG20A):c.892A>G (p.Ser298Gly)	not specified [RCV004933435]	uncertain significance	15	77478495	77478495	Human		name
598190303	CV3975361	single nucleotide variant	NM_001304504.2(HMG20A):c.302A>G (p.Asn101Ser)	not specified [RCV005354112]	uncertain significance	15	77467159	77467159	Human		name
598248607	CV3975362	single nucleotide variant	NM_001304504.2(HMG20A):c.709C>T (p.Arg237Cys)	not specified [RCV005345468]	uncertain significance	15	77478312	77478312	Human		name
156146944	CV2357973	single nucleotide variant	NM_001304504.2(HMG20A):c.1040G>A (p.Arg347His)	not specified [RCV004209753]	uncertain significance	15	77479311	77479311	Human		name
597791222	CV3682775	single nucleotide variant	NM_001304504.2(HMG20A):c.1022T>C (p.Val341Ala)	not specified [RCV004933434]	uncertain significance	15	77479293	77479293	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