Htr4 Variant Search Result - Rat Genome Database

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35 records found for search term Htr4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
243053622	CV2404695	single nucleotide variant	NM_000870.7(HTR4):c.26+354C>A	Squamous cell carcinoma [RCV003129722]	benign	5	148636635	148636635	Human	2	name
243053425	CV2404592	single nucleotide variant	NM_000870.7(HTR4):c.26+7221G>A	Lung adenocarcinoma [RCV003129619]	likely benign	5	148629768	148629768	Human	2	name
243053592	CV2404587	single nucleotide variant	NM_000870.7(HTR4):c.1076+211C>A	Lung adenocarcinoma [RCV003129614]	uncertain significance	5	148509245	148509245	Human	2	name
15114336	CV709717	single nucleotide variant	NM_000870.7(HTR4):c.1077-996A>G	not provided [RCV000961657]	benign	5	148484289	148484289	Human		name
156033387	CV2275116	single nucleotide variant	NM_000870.7(HTR4):c.1077-1060T>C	not specified [RCV004136921]	uncertain significance	5	148484353	148484353	Human		name
597783248	CV3686197	single nucleotide variant	NM_000870.7(HTR4):c.1077-1030G>C	not specified [RCV004931371]	uncertain significance	5	148484323	148484323	Human		name
8631475	CV86679	single nucleotide variant	NM_001040172.2(HTR4):c.507+2230G>A	Malignant melanoma [RCV000066770]	not provided	5	148520963	148520963	Human		name
405779716	CV3270688	single nucleotide variant	NM_000870.7(HTR4):c.95T>C (p.Met32Thr)	not specified [RCV004397417]	uncertain significance	5	148550194	148550194	Human		name
407465310	CV3444235	single nucleotide variant	NM_000870.7(HTR4):c.83C>T (p.Thr28Met)	not specified [RCV004635333]	uncertain significance	5	148550206	148550206	Human		name
15156243	CV721289	single nucleotide variant	NM_000870.7(HTR4):c.43G>A (p.Gly15Arg)	not provided [RCV000880587]	likely benign	5	148550246	148550246	Human		name
155924498	CV2220329	single nucleotide variant	NM_000870.7(HTR4):c.205G>A (p.Val69Ile)	not specified [RCV004095750]	uncertain significance	5	148548816	148548816	Human		name
597783252	CV3686198	single nucleotide variant	NM_000870.7(HTR4):c.286C>T (p.Arg96Trp)	not specified [RCV004931372]	uncertain significance	5	148548735	148548735	Human		name
15184324	CV709718	single nucleotide variant	NM_000870.7(HTR4):c.1068T>C (p.His356=)	not provided [RCV000975085]	benign	5	148509464	148509464	Human		name
156195568	CV2223439	single nucleotide variant	NM_000870.7(HTR4):c.644T>A (p.Ile215Asn)	not specified [RCV004106016]	uncertain significance	5	148509888	148509888	Human		name
156341976	CV2225980	single nucleotide variant	NM_000870.7(HTR4):c.962G>A (p.Arg321His)	not specified [RCV004105143]	uncertain significance	5	148509570	148509570	Human		name
156075464	CV2291413	single nucleotide variant	NM_000870.7(HTR4):c.531G>C (p.Gln177His)	not specified [RCV004155750]	uncertain significance	5	148510001	148510001	Human		name
156102339	CV2313558	single nucleotide variant	NM_000870.7(HTR4):c.578C>T (p.Ala193Val)	not specified [RCV004163849]	uncertain significance	5	148509954	148509954	Human		name
155977213	CV2338722	single nucleotide variant	NM_000870.7(HTR4):c.709G>A (p.Glu237Lys)	not specified [RCV004182295]	uncertain significance	5	148509823	148509823	Human		name
401729953	CV2683874	single nucleotide variant	NM_000870.7(HTR4):c.749G>A (p.Arg250His)	not specified [RCV004284597]	uncertain significance	5	148509783	148509783	Human		name
401763984	CV2717186	single nucleotide variant	NM_000870.7(HTR4):c.641G>A (p.Arg214His)	not specified [RCV004324048]	uncertain significance	5	148509891	148509891	Human		name
405779681	CV3270683	single nucleotide variant	NM_000870.7(HTR4):c.409C>A (p.Arg137Ser)	not specified [RCV004397411]	uncertain significance	5	148523291	148523291	Human		name
405779693	CV3270684	single nucleotide variant	NM_000870.7(HTR4):c.593T>C (p.Val198Ala)	not specified [RCV004397413]	uncertain significance	5	148509939	148509939	Human		name
405779704	CV3270686	single nucleotide variant	NM_000870.7(HTR4):c.740G>A (p.Ser247Asn)	not specified [RCV004397415]	uncertain significance	5	148509792	148509792	Human		name
405779709	CV3270687	single nucleotide variant	NM_000870.7(HTR4):c.945G>C (p.Leu315Phe)	not specified [RCV004397416]	uncertain significance	5	148509587	148509587	Human		name
407465306	CV3444234	single nucleotide variant	NM_000870.7(HTR4):c.624G>A (p.Met208Ile)	not specified [RCV004635332]	uncertain significance	5	148509908	148509908	Human		name
407510946	CV3444236	single nucleotide variant	NM_000870.7(HTR4):c.787A>G (p.Ile263Val)	not specified [RCV004626301]	uncertain significance	5	148509745	148509745	Human		name
597783256	CV3686199	single nucleotide variant	NM_000870.7(HTR4):c.527A>G (p.Asn176Ser)	not specified [RCV004931373]	uncertain significance	5	148510005	148510005	Human		name
598256620	CV3968441	single nucleotide variant	NM_000870.7(HTR4):c.684G>A (p.Met228Ile)	not specified [RCV005346833]	uncertain significance	5	148509848	148509848	Human		name
8631474	CV86678	single nucleotide variant	NM_000870.7(HTR4):c.518G>A (p.Arg173Lys)	not specified [RCV004397412]	uncertain significance\|not provided	5	148510014	148510014	Human		name
155984253	CV2367894	single nucleotide variant	NM_000870.7(HTR4):c.1129A>C (p.Thr377Pro)	not specified [RCV004222995]	uncertain significance	5	148483241	148483241	Human		name
401773399	CV2709287	single nucleotide variant	NM_000870.7(HTR4):c.1084G>A (p.Val362Met)	not specified [RCV004316443]	uncertain significance	5	148483286	148483286	Human		name
405779866	CV3270681	single nucleotide variant	NM_000870.7(HTR4):c.1067A>G (p.His356Arg)	not specified [RCV004397409]	uncertain significance	5	148509465	148509465	Human		name
405779675	CV3270682	single nucleotide variant	NM_000870.7(HTR4):c.1090T>C (p.Cys364Arg)	not specified [RCV004397410]	uncertain significance	5	148483280	148483280	Human		name
597783260	CV3686200	single nucleotide variant	NM_000870.7(HTR4):c.1136C>T (p.Pro379Leu)	not specified [RCV004931374]	uncertain significance	5	148483234	148483234	Human		name
15196926	CV698903	single nucleotide variant	NM_000870.7(HTR4):c.1115G>A (p.Cys372Tyr)	not provided [RCV000956322]	benign	5	148483255	148483255	Human		name

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