Hrh3 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

32 records found for search term Hrh3

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329390097	CV2441265	single nucleotide variant	NM_007232.3(HRH3):c.20A>T (p.Asp7Val)	not specified [RCV004263997]	uncertain significance	20	62219951	62219951	Human		name
15163325	CV705585	single nucleotide variant	NM_007232.3(HRH3):c.246C>T (p.Leu82=)	not provided [RCV000948059]	benign	20	62219725	62219725	Human		name
156133402	CV2382944	single nucleotide variant	NM_007232.3(HRH3):c.65C>T (p.Ala22Val)	not specified [RCV004217536]	uncertain significance	20	62219906	62219906	Human		name
401930501	CV2824556	single nucleotide variant	NM_007232.3(HRH3):c.306C>T (p.Phe102=)	not provided [RCV003440474]	likely benign	20	62218602	62218602	Human		name
401944634	CV2840404	single nucleotide variant	NM_007232.3(HRH3):c.798C>T (p.His266=)	not provided [RCV003457337]	likely benign	20	62216546	62216546	Human		name
15128238	CV717092	single nucleotide variant	NM_007232.3(HRH3):c.1215G>A (p.Ser405=)	not provided [RCV000964047]	benign\|likely benign	20	62216129	62216129	Human		name
15156498	CV717093	single nucleotide variant	NM_007232.3(HRH3):c.1032C>T (p.Phe344=)	not provided [RCV000969123]	benign	20	62216312	62216312	Human		name
156114868	CV2208951	single nucleotide variant	NM_007232.3(HRH3):c.602C>T (p.Thr201Met)	not specified [RCV004085299]	uncertain significance	20	62216742	62216742	Human		name
156148801	CV2212948	single nucleotide variant	NM_007232.3(HRH3):c.857C>A (p.Ala286Asp)	not specified [RCV004091573]	uncertain significance	20	62216487	62216487	Human		name
156065971	CV2270745	single nucleotide variant	NM_007232.3(HRH3):c.710G>A (p.Arg237Gln)	not specified [RCV004131805]	uncertain significance	20	62216634	62216634	Human		name
156307223	CV2335403	single nucleotide variant	NM_007232.3(HRH3):c.982G>T (p.Ala328Ser)	not specified [RCV004186957]	uncertain significance	20	62216362	62216362	Human		name
156305286	CV2369425	single nucleotide variant	NM_007232.3(HRH3):c.874G>A (p.Gly292Arg)	not specified [RCV004210370]	uncertain significance	20	62216470	62216470	Human		name
329385736	CV2432205	single nucleotide variant	NM_007232.3(HRH3):c.739G>A (p.Glu247Lys)	not specified [RCV004251137]	uncertain significance	20	62216605	62216605	Human		name
329389474	CV2445142	single nucleotide variant	NM_007232.3(HRH3):c.922G>A (p.Gly308Ser)	not specified [RCV004263785]	uncertain significance	20	62216422	62216422	Human		name
329395330	CV2458275	single nucleotide variant	NM_007232.3(HRH3):c.851C>T (p.Ala284Val)	not specified [RCV004265925]	uncertain significance	20	62216493	62216493	Human		name
401735377	CV2706769	single nucleotide variant	NM_007232.3(HRH3):c.935G>A (p.Arg312Lys)	not specified [RCV004319328]	uncertain significance	20	62216409	62216409	Human		name
401743881	CV2726213	single nucleotide variant	NM_007232.3(HRH3):c.914C>T (p.Ser305Phe)	not specified [RCV004326681]	uncertain significance	20	62216430	62216430	Human		name
401883324	CV2757863	single nucleotide variant	NM_007232.3(HRH3):c.706G>T (p.Ala236Ser)	not specified [RCV004337005]	uncertain significance	20	62216638	62216638	Human		name
405798735	CV3274003	single nucleotide variant	NM_007232.3(HRH3):c.446C>T (p.Thr149Met)	not specified [RCV004402328]	uncertain significance	20	62216898	62216898	Human		name
405798738	CV3274004	single nucleotide variant	NM_007232.3(HRH3):c.694C>T (p.Arg232Trp)	not specified [RCV004402329]	uncertain significance	20	62216650	62216650	Human		name
405798741	CV3274005	single nucleotide variant	NM_007232.3(HRH3):c.731C>T (p.Pro244Leu)	not specified [RCV004402330]	uncertain significance	20	62216613	62216613	Human		name
405798744	CV3274006	single nucleotide variant	NM_007232.3(HRH3):c.770G>C (p.Gly257Ala)	not specified [RCV004402331]	uncertain significance	20	62216574	62216574	Human		name
405798747	CV3274007	single nucleotide variant	NM_007232.3(HRH3):c.911C>T (p.Thr304Ile)	not specified [RCV004402332]	uncertain significance	20	62216433	62216433	Human		name
407510834	CV3433935	single nucleotide variant	NM_007232.3(HRH3):c.640G>A (p.Val214Ile)	not specified [RCV004626262]	uncertain significance	20	62216704	62216704	Human		name
407528351	CV3433936	single nucleotide variant	NM_007232.3(HRH3):c.460C>T (p.Arg154Trp)	not specified [RCV004633121]	uncertain significance	20	62216884	62216884	Human		name
598192884	CV3971982	single nucleotide variant	NM_007232.3(HRH3):c.410C>A (p.Thr137Asn)	not specified [RCV005354542]	uncertain significance	20	62218498	62218498	Human		name
598192888	CV3971983	single nucleotide variant	NM_007232.3(HRH3):c.661A>G (p.Ile221Val)	not specified [RCV005354543]	uncertain significance	20	62216683	62216683	Human		name
156361331	CV2269218	single nucleotide variant	NM_007232.3(HRH3):c.1006C>T (p.Arg336Cys)	not specified [RCV004130371]	uncertain significance	20	62216338	62216338	Human		name
405798733	CV3274002	single nucleotide variant	NM_007232.3(HRH3):c.1154A>G (p.His385Arg)	not specified [RCV004402327]	uncertain significance	20	62216190	62216190	Human		name
598192873	CV3971980	single nucleotide variant	NM_007232.3(HRH3):c.1147G>A (p.Ala383Thr)	not specified [RCV005354540]	uncertain significance	20	62216197	62216197	Human		name
598192896	CV3971984	single nucleotide variant	NM_007232.3(HRH3):c.1258C>T (p.Arg420Cys)	not specified [RCV005354544]	uncertain significance	20	62216086	62216086	Human		name
8637422	CV92648	single nucleotide variant	NM_007232.2(HRH3):c.1183G>A (p.Glu395Lys)	Malignant melanoma [RCV000072746]	not provided	20	62216161	62216161	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