Hrh1 Variant Search Result - Rat Genome Database

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20 records found for search term Hrh1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8577819	CV112196	single nucleotide variant	NM_001098211.1(HRH1):c.-36+9418C>T	Lung cancer [RCV000092719]	uncertain significance	3	11235477	11235477	Human		name
405798712	CV3273999	single nucleotide variant	NM_001098212.2(HRH1):c.65T>C (p.Met22Thr)	not specified [RCV004402324]	uncertain significance	3	11259102	11259102	Human		name
15175735	CV708467	single nucleotide variant	NM_001098212.2(HRH1):c.57G>C (p.Lys19Asn)	not provided [RCV000973020]	benign	3	11259094	11259094	Human		name
15184874	CV733674	single nucleotide variant	NM_001098212.2(HRH1):c.42G>A (p.Met14Ile)	not provided [RCV000908376]	benign	3	11259079	11259079	Human		name
329402052	CV2453953	single nucleotide variant	NM_001098212.2(HRH1):c.163G>A (p.Glu55Lys)	not specified [RCV004271625]	uncertain significance	3	11259200	11259200	Human		name
401719626	CV2701204	single nucleotide variant	NM_001098212.2(HRH1):c.214G>A (p.Ala72Thr)	not specified [RCV004309778]	uncertain significance	3	11259251	11259251	Human		name
405798705	CV3273998	single nucleotide variant	NM_001098212.2(HRH1):c.242T>C (p.Met81Thr)	not specified [RCV004402323]	uncertain significance	3	11259279	11259279	Human		name
597773860	CV3689532	single nucleotide variant	NM_001098212.2(HRH1):c.196A>G (p.Ile66Val)	not specified [RCV004928884]	uncertain significance	3	11259233	11259233	Human		name
156048487	CV2271730	single nucleotide variant	NM_001098212.2(HRH1):c.581C>G (p.Thr194Ser)	not specified [RCV004130577]	uncertain significance	3	11259618	11259618	Human		name
329370461	CV2435613	single nucleotide variant	NM_001098212.2(HRH1):c.670C>T (p.Arg224Trp)	not specified [RCV004254862]	uncertain significance	3	11259707	11259707	Human		name
407528348	CV3433934	single nucleotide variant	NM_001098212.2(HRH1):c.983A>G (p.His328Arg)	not specified [RCV004633120]	uncertain significance	3	11260020	11260020	Human		name
597773864	CV3689531	single nucleotide variant	NM_001098212.2(HRH1):c.920T>C (p.Ile307Thr)	not specified [RCV004928883]	uncertain significance	3	11259957	11259957	Human		name
598192836	CV3971971	single nucleotide variant	NM_001098212.2(HRH1):c.380G>A (p.Arg127His)	not specified [RCV005354533]	uncertain significance	3	11259417	11259417	Human		name
598205360	CV3971972	single nucleotide variant	NM_001098212.2(HRH1):c.406C>T (p.Leu136Phe)	not specified [RCV005337599]	uncertain significance	3	11259443	11259443	Human		name
598192842	CV3971973	single nucleotide variant	NM_001098212.2(HRH1):c.737G>A (p.Gly246Glu)	not specified [RCV005354534]	uncertain significance	3	11259774	11259774	Human		name
15151634	CV720068	single nucleotide variant	NM_001098212.2(HRH1):c.977G>A (p.Arg326Gln)	not provided [RCV000879637]	benign	3	11260014	11260014	Human		name
156272281	CV2333911	single nucleotide variant	NM_001098212.2(HRH1):c.1337A>G (p.Asn446Ser)	not specified [RCV004183446]	uncertain significance	3	11260374	11260374	Human		name
401757110	CV2678237	single nucleotide variant	NM_001098212.2(HRH1):c.1067A>G (p.Gln356Arg)	not specified [RCV004289831]	uncertain significance	3	11260104	11260104	Human		name
597773857	CV3689533	single nucleotide variant	NM_001098212.2(HRH1):c.1051A>T (p.Met351Leu)	not specified [RCV004928885]	uncertain significance	3	11260088	11260088	Human		name
15187052	CV697752	single nucleotide variant	NM_001098212.2(HRH1):c.1045G>C (p.Asp349His)	not provided [RCV000953472]	benign	3	11260082	11260082	Human		name

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