Hexim1 Variant Search Result - Rat Genome Database

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22 records found for search term Hexim1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405776760	CV3273925	single nucleotide variant	NM_006460.3(HEXIM1):c.13T>C (p.Phe5Leu)	not specified [RCV004396900]	likely benign	17	45149203	45149203	Human		name
15163277	CV727222	single nucleotide variant	NM_006460.3(HEXIM1):c.108G>C (p.Ala36=)	not provided [RCV000881935]	benign	17	45149298	45149298	Human		name
598177244	CV3978684	single nucleotide variant	NM_006460.3(HEXIM1):c.41A>G (p.Gln14Arg)	not specified [RCV005351799]	uncertain significance	17	45149231	45149231	Human		name
156064015	CV2200051	single nucleotide variant	NM_006460.3(HEXIM1):c.173G>A (p.Arg58His)	not specified [RCV004074205]	uncertain significance	17	45149363	45149363	Human		name
156272256	CV2333910	single nucleotide variant	NM_006460.3(HEXIM1):c.239C>A (p.Pro80Gln)	not specified [RCV004183445]	uncertain significance	17	45149429	45149429	Human		name
155969668	CV2337979	single nucleotide variant	NM_006460.3(HEXIM1):c.173G>T (p.Arg58Leu)	not specified [RCV004186023]	uncertain significance	17	45149363	45149363	Human		name
329357205	CV2457517	single nucleotide variant	NM_006460.3(HEXIM1):c.166G>C (p.Gly56Arg)	not specified [RCV004267327]	uncertain significance	17	45149356	45149356	Human		name
401873924	CV2757777	single nucleotide variant	NM_006460.3(HEXIM1):c.112G>A (p.Glu38Lys)	not specified [RCV004336924]	uncertain significance	17	45149302	45149302	Human		name
405776753	CV3273924	single nucleotide variant	NM_006460.3(HEXIM1):c.100C>G (p.Pro34Ala)	not specified [RCV004396899]	uncertain significance	17	45149290	45149290	Human		name
405776764	CV3273926	single nucleotide variant	NM_006460.3(HEXIM1):c.289T>G (p.Ser97Ala)	not specified [RCV004396901]	uncertain significance	17	45149479	45149479	Human		name
407522045	CV3437202	single nucleotide variant	NM_006460.3(HEXIM1):c.194G>A (p.Gly65Glu)	not specified [RCV004630515]	uncertain significance	17	45149384	45149384	Human		name
598177252	CV3978685	single nucleotide variant	NM_006460.3(HEXIM1):c.249C>G (p.Ser83Arg)	not specified [RCV005351800]	uncertain significance	17	45149439	45149439	Human		name
329402213	CV2454054	single nucleotide variant	NM_006460.3(HEXIM1):c.502T>C (p.Tyr168His)	not specified [RCV004271701]	uncertain significance	17	45149692	45149692	Human		name
401736318	CV2682990	single nucleotide variant	NM_006460.3(HEXIM1):c.374C>T (p.Ser125Phe)	not specified [RCV004283777]	uncertain significance	17	45149564	45149564	Human		name
401723897	CV2725077	single nucleotide variant	NM_006460.3(HEXIM1):c.298G>A (p.Gly100Ser)	not specified [RCV004319828]	uncertain significance	17	45149488	45149488	Human		name
405776778	CV3273928	single nucleotide variant	NM_006460.3(HEXIM1):c.556G>T (p.Ala186Ser)	not specified [RCV004396903]	uncertain significance	17	45149746	45149746	Human		name
407522052	CV3437200	single nucleotide variant	NM_006460.3(HEXIM1):c.533T>G (p.Phe178Cys)	not specified [RCV004630513]	uncertain significance	17	45149723	45149723	Human		name
407522048	CV3437201	single nucleotide variant	NM_006460.3(HEXIM1):c.368A>C (p.His123Pro)	not specified [RCV004630514]	uncertain significance	17	45149558	45149558	Human		name
597761220	CV3685658	single nucleotide variant	NM_006460.3(HEXIM1):c.736G>C (p.Gly246Arg)	not specified [RCV004925859]	uncertain significance	17	45149926	45149926	Human		name
598177238	CV3978683	single nucleotide variant	NM_006460.3(HEXIM1):c.944T>C (p.Leu315Pro)	not specified [RCV005351798]	uncertain significance	17	45150134	45150134	Human		name
156160969	CV2323405	single nucleotide variant	NM_006460.3(HEXIM1):c.1040G>A (p.Arg347Gln)	not specified [RCV004171800]	uncertain significance	17	45150230	45150230	Human		name
597761223	CV3685659	single nucleotide variant	NM_006460.3(HEXIM1):c.1034T>G (p.Leu345Arg)	not specified [RCV004925860]	uncertain significance	17	45150224	45150224	Human		name

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