Htr3a Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

65 records found for search term Htr3a

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15180329	CV737732	single nucleotide variant	NM_000869.6(HTR3A):c.-7G>T	not provided [RCV000907327]	benign	11	113975319	113975319	Human		name
15163467	CV744674	single nucleotide variant	NM_000869.6(HTR3A):c.374+9C>T	not provided [RCV000903779]	benign	11	113981321	113981321	Human		name
15184882	CV730726	single nucleotide variant	NM_000869.6(HTR3A):c.374+10G>A	not provided [RCV000886547]	likely benign	11	113981322	113981322	Human		name
329379296	CV2456189	single nucleotide variant	NM_000869.6(HTR3A):c.80G>A (p.Arg27Gln)	not provided [RCV004696395]\|not specified [RCV004273378]	uncertain significance	11	113977783	113977783	Human		name
401934060	CV2809862	single nucleotide variant	NM_000869.6(HTR3A):c.408C>T (p.Tyr136=)	not provided [RCV003410919]	likely benign	11	113983153	113983153	Human		name
597783176	CV3686149	single nucleotide variant	NM_000869.6(HTR3A):c.71G>T (p.Arg24Met)	not specified [RCV004931325]	uncertain significance	11	113977774	113977774	Human		name
598205986	CV3968415	single nucleotide variant	NM_000869.6(HTR3A):c.78C>A (p.Ser26Arg)	not specified [RCV005337698]	uncertain significance	11	113977781	113977781	Human		name
15159971	CV701565	single nucleotide variant	NM_000869.6(HTR3A):c.783C>T (p.Ile261=)	not provided [RCV000947387]	benign	11	113986595	113986595	Human		name
15159978	CV701566	single nucleotide variant	NM_000869.6(HTR3A):c.813C>T (p.Gly271=)	not provided [RCV000947388]	benign	11	113986625	113986625	Human		name
156139896	CV2212126	single nucleotide variant	NM_000869.6(HTR3A):c.167G>T (p.Arg56Met)	not specified [RCV004089026]	uncertain significance	11	113977870	113977870	Human		name
156255144	CV2358955	single nucleotide variant	NM_000869.6(HTR3A):c.260G>C (p.Arg87Pro)	not specified [RCV004212285]	uncertain significance	11	113979273	113979273	Human		name
401763707	CV2725266	single nucleotide variant	NM_000869.6(HTR3A):c.176C>T (p.Thr59Ile)	not specified [RCV004319934]	uncertain significance	11	113977879	113977879	Human		name
401867628	CV2780687	single nucleotide variant	NM_000869.6(HTR3A):c.216C>A (p.Asn72Lys)	not specified [RCV004352029]	uncertain significance	11	113977919	113977919	Human		name
401898968	CV2792168	single nucleotide variant	NM_000869.6(HTR3A):c.132C>A (p.Asn44Lys)	not specified [RCV004361378]	uncertain significance	11	113977835	113977835	Human		name
401909736	CV2809863	single nucleotide variant	NM_000869.6(HTR3A):c.1029G>C (p.Leu343=)	not provided [RCV003398137]	likely benign	11	113986937	113986937	Human		name
404979782	CV2850262	deletion	NM_000869.6(HTR3A):c.681del (p.Tyr228fs)	not provided [RCV003487911]	uncertain significance	11	113986151	113986151	Human		name
405804190	CV3270621	single nucleotide variant	NM_000869.6(HTR3A):c.136A>G (p.Arg46Gly)	not specified [RCV004404870]	uncertain significance	11	113977839	113977839	Human		name
15117549	CV712609	single nucleotide variant	NM_000869.6(HTR3A):c.1341C>T (p.Ser447=)	not provided [RCV000962224]	benign	11	113989667	113989667	Human		name
15186215	CV768208	single nucleotide variant	NM_000869.6(HTR3A):c.1197G>A (p.Arg399=)	not provided [RCV000931289]	likely benign	11	113989523	113989523	Human		name
156071684	CV2201282	single nucleotide variant	NM_000869.6(HTR3A):c.430G>A (p.Glu144Lys)	not specified [RCV004077416]	uncertain significance	11	113983175	113983175	Human		name
156005062	CV2281434	single nucleotide variant	NM_000869.6(HTR3A):c.799C>A (p.Pro267Thr)	not specified [RCV004153764]	uncertain significance	11	113986611	113986611	Human		name
156198339	CV2293673	single nucleotide variant	NM_000869.6(HTR3A):c.568T>C (p.Trp190Arg)	not specified [RCV004153176]	uncertain significance	11	113986038	113986038	Human		name
156298344	CV2310614	single nucleotide variant	NM_000869.6(HTR3A):c.518T>G (p.Leu173Arg)	not specified [RCV004157277]	uncertain significance	11	113983263	113983263	Human		name
156156668	CV2314397	single nucleotide variant	NM_000869.6(HTR3A):c.937A>G (p.Met313Val)	not specified [RCV004168516]	uncertain significance	11	113986845	113986845	Human		name
156151744	CV2318823	single nucleotide variant	NM_000869.6(HTR3A):c.376G>A (p.Val126Met)	not specified [RCV004175735]	uncertain significance	11	113983121	113983121	Human		name
156014950	CV2360195	single nucleotide variant	NM_000869.6(HTR3A):c.887C>T (p.Pro296Leu)	not specified [RCV004215457]	uncertain significance	11	113986699	113986699	Human		name
401746443	CV2678839	single nucleotide variant	NM_000869.6(HTR3A):c.964G>A (p.Glu322Lys)	not specified [RCV004292818]	uncertain significance	11	113986872	113986872	Human		name
401754477	CV2681406	single nucleotide variant	NM_000869.6(HTR3A):c.419G>A (p.Arg140Gln)	not specified [RCV004291951]	likely benign	11	113983164	113983164	Human		name
401743354	CV2684683	single nucleotide variant	NM_000869.6(HTR3A):c.646C>T (p.Pro216Ser)	not specified [RCV004293778]	uncertain significance	11	113986116	113986116	Human		name
401731167	CV2693641	single nucleotide variant	NM_000869.6(HTR3A):c.409G>T (p.Val137Leu)	not specified [RCV004297978]	uncertain significance	11	113983154	113983154	Human		name
401782326	CV2719288	single nucleotide variant	NM_000869.6(HTR3A):c.776T>C (p.Met259Thr)	not specified [RCV004324927]	uncertain significance	11	113986588	113986588	Human		name
401891402	CV2770510	single nucleotide variant	NM_000869.6(HTR3A):c.386G>A (p.Gly129Glu)	not specified [RCV004358142]	uncertain significance	11	113983131	113983131	Human		name
405804192	CV3270622	single nucleotide variant	NM_000869.6(HTR3A):c.424C>A (p.Gln142Lys)	not specified [RCV004404871]	uncertain significance	11	113983169	113983169	Human		name
405804194	CV3270623	single nucleotide variant	NM_000869.6(HTR3A):c.470G>A (p.Cys157Tyr)	not specified [RCV004404872]	uncertain significance	11	113983215	113983215	Human		name
405804196	CV3270624	single nucleotide variant	NM_000869.6(HTR3A):c.689C>G (p.Ala230Gly)	not specified [RCV004404873]	uncertain significance	11	113986159	113986159	Human		name
405804198	CV3270625	single nucleotide variant	NM_000869.6(HTR3A):c.719G>A (p.Arg240Gln)	not specified [RCV004404874]	uncertain significance	11	113986531	113986531	Human		name
405804200	CV3270626	single nucleotide variant	NM_000869.6(HTR3A):c.896C>T (p.Ala299Val)	not specified [RCV004404875]	uncertain significance	11	113986708	113986708	Human		name
407510940	CV3444217	single nucleotide variant	NM_000869.6(HTR3A):c.383T>C (p.Val128Ala)	not specified [RCV004626299]	uncertain significance	11	113983128	113983128	Human		name
407465250	CV3444219	single nucleotide variant	NM_000869.6(HTR3A):c.908C>G (p.Pro303Arg)	not specified [RCV004635318]	uncertain significance	11	113986720	113986720	Human		name
597783172	CV3686150	single nucleotide variant	NM_000869.6(HTR3A):c.638G>T (p.Gly213Val)	not specified [RCV004931326]	uncertain significance	11	113986108	113986108	Human		name
597783164	CV3686152	single nucleotide variant	NM_000869.6(HTR3A):c.650A>G (p.Tyr217Cys)	not specified [RCV004931328]	uncertain significance	11	113986120	113986120	Human		name
597783160	CV3686153	single nucleotide variant	NM_000869.6(HTR3A):c.512G>C (p.Cys171Ser)	not specified [RCV004931329]	uncertain significance	11	113983257	113983257	Human		name
597783156	CV3686154	single nucleotide variant	NM_000869.6(HTR3A):c.335C>T (p.Thr112Met)	not specified [RCV004931330]	uncertain significance	11	113981273	113981273	Human		name
597783154	CV3686155	single nucleotide variant	NM_000869.6(HTR3A):c.559A>T (p.Ile187Phe)	not specified [RCV004931331]	uncertain significance	11	113986029	113986029	Human		name
598256498	CV3968411	single nucleotide variant	NM_000869.6(HTR3A):c.624G>C (p.Glu208Asp)	not specified [RCV005346810]	uncertain significance	11	113986094	113986094	Human		name
598256503	CV3968412	single nucleotide variant	NM_000869.6(HTR3A):c.658G>A (p.Glu220Lys)	not specified [RCV005346811]	uncertain significance	11	113986128	113986128	Human		name
598205981	CV3968414	single nucleotide variant	NM_000869.6(HTR3A):c.910C>T (p.Leu304Phe)	not specified [RCV005337697]	uncertain significance	11	113986722	113986722	Human		name
15138173	CV768207	single nucleotide variant	NM_000869.6(HTR3A):c.655C>T (p.Arg219Trp)	not provided [RCV000943354]	likely benign	11	113986125	113986125	Human		name
156051879	CV2336695	single nucleotide variant	NM_000869.6(HTR3A):c.1432G>A (p.Ala478Thr)	not specified [RCV004196935]	uncertain significance	11	113989758	113989758	Human		name
155927013	CV2345320	single nucleotide variant	NM_000869.6(HTR3A):c.1030C>T (p.Arg344Cys)	not specified [RCV004198100]	uncertain significance	11	113986938	113986938	Human		name
156247672	CV2396927	single nucleotide variant	NM_000869.6(HTR3A):c.1247G>A (p.Cys416Tyr)	not specified [RCV004234043]	uncertain significance	11	113989573	113989573	Human		name
329393134	CV2449513	single nucleotide variant	NM_000869.6(HTR3A):c.1357C>G (p.Leu453Val)	not specified [RCV004268451]	uncertain significance	11	113989683	113989683	Human		name
329353393	CV2469202	single nucleotide variant	NM_000869.6(HTR3A):c.1106C>T (p.Thr369Ile)	not specified [RCV004280552]	uncertain significance	11	113987014	113987014	Human		name
401782421	CV2686831	single nucleotide variant	NM_000869.6(HTR3A):c.1015G>A (p.Val339Met)	not specified [RCV004302011]	uncertain significance	11	113986923	113986923	Human		name
401740845	CV2702663	single nucleotide variant	NM_000869.6(HTR3A):c.1010A>G (p.Gln337Arg)	not specified [RCV004318927]	uncertain significance	11	113986918	113986918	Human		name
401898368	CV2787823	single nucleotide variant	NM_000869.6(HTR3A):c.1217C>G (p.Pro406Arg)	not specified [RCV004358508]	uncertain significance	11	113989543	113989543	Human		name
405804185	CV3270618	single nucleotide variant	NM_000869.6(HTR3A):c.1108T>C (p.Ser370Pro)	not specified [RCV004404867]	uncertain significance	11	113987016	113987016	Human		name
405804187	CV3270619	single nucleotide variant	NM_000869.6(HTR3A):c.1342G>A (p.Val448Met)	not specified [RCV004404868]	uncertain significance	11	113989668	113989668	Human		name
407465240	CV3444216	single nucleotide variant	NM_000869.6(HTR3A):c.1330C>T (p.Arg444Cys)	not specified [RCV004635316]	uncertain significance	11	113989656	113989656	Human		name
407465244	CV3444218	single nucleotide variant	NM_000869.6(HTR3A):c.1183G>A (p.Glu395Lys)	not specified [RCV004635317]	uncertain significance	11	113989509	113989509	Human		name
597783181	CV3686147	single nucleotide variant	NM_000869.6(HTR3A):c.1054G>A (p.Ala352Thr)	not specified [RCV004931323]	uncertain significance	11	113986962	113986962	Human		name
597783177	CV3686148	single nucleotide variant	NM_000869.6(HTR3A):c.1177G>A (p.Asp393Asn)	not specified [RCV004931324]	uncertain significance	11	113989503	113989503	Human		name
597783168	CV3686151	single nucleotide variant	NM_000869.6(HTR3A):c.1037T>G (p.Leu346Arg)	not specified [RCV004931327]	uncertain significance	11	113986945	113986945	Human		name
598256508	CV3968413	single nucleotide variant	NM_000869.6(HTR3A):c.1026G>T (p.Trp342Cys)	not specified [RCV005346812]	uncertain significance	11	113986934	113986934	Human		name
15194564	CV724197	single nucleotide variant	NM_000869.6(HTR3A):c.1226G>A (p.Arg409Gln)	not provided [RCV000889257]	benign	11	113989552	113989552	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