Hrh3 Variant Search Result - Rat Genome Database

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32 records found for search term Hrh3

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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

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