Rgs21 Variant Search Result - Rat Genome Database

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17 records found for search term Rgs21

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8575380	CV109727	single nucleotide variant	NM_001039152.3(RGS21):c.255+827A>G	Lung cancer [RCV000090252]	uncertain significance	1	192353040	192353040	Human		name
8575379	CV109726	single nucleotide variant	NM_001039152.3(RGS21):c.-61+7455T>A	Lung cancer [RCV000090251]	uncertain significance	1	192324560	192324560	Human		name
8575381	CV109728	single nucleotide variant	NM_001039152.3(RGS21):c.255+2528T>A	Lung cancer [RCV000090253]	uncertain significance	1	192354741	192354741	Human		name
8624832	CV79947	single nucleotide variant	NM_001039152.3(RGS21):c.150C>T (p.Phe50=)	Malignant melanoma [RCV000060023]	not provided	1	192352108	192352108	Human		name
405715736	CV3309225	single nucleotide variant	NM_001039152.3(RGS21):c.38C>T (p.Ala13Val)	not specified [RCV004449164]	uncertain significance	1	192347339	192347339	Human		name
598189049	CV3902567	single nucleotide variant	NM_001039152.3(RGS21):c.44C>T (p.Thr15Ile)	not specified [RCV005266661]	uncertain significance	1	192347345	192347345	Human		name
598189058	CV3902568	single nucleotide variant	NM_001039152.3(RGS21):c.34A>T (p.Thr12Ser)	not specified [RCV005266662]	uncertain significance	1	192347335	192347335	Human		name
156284307	CV2349012	single nucleotide variant	NM_001039152.3(RGS21):c.148T>C (p.Phe50Leu)	not specified [RCV004203438]	uncertain significance	1	192352106	192352106	Human		name
401779004	CV2702012	single nucleotide variant	NM_001039152.3(RGS21):c.140A>G (p.Asn47Ser)	not specified [RCV004320600]	uncertain significance	1	192352098	192352098	Human		name
405715729	CV3309224	single nucleotide variant	NM_001039152.3(RGS21):c.146A>C (p.Glu49Ala)	not specified [RCV004449163]	uncertain significance	1	192352104	192352104	Human		name
597775809	CV3586360	single nucleotide variant	NM_001039152.3(RGS21):c.219T>G (p.Ile73Met)	not specified [RCV004852352]	uncertain significance	1	192352177	192352177	Human		name
597775813	CV3586361	single nucleotide variant	NM_001039152.3(RGS21):c.166G>T (p.Asp56Tyr)	not specified [RCV004852353]	uncertain significance	1	192352124	192352124	Human		name
597788092	CV3586363	single nucleotide variant	NM_001039152.3(RGS21):c.171T>A (p.Phe57Leu)	not specified [RCV004855407]	uncertain significance	1	192352129	192352129	Human		name
597788096	CV3586364	single nucleotide variant	NM_001039152.3(RGS21):c.248C>G (p.Pro83Arg)	not specified [RCV004855408]	uncertain significance	1	192352206	192352206	Human		name
598189034	CV3902565	single nucleotide variant	NM_001039152.3(RGS21):c.161G>A (p.Cys54Tyr)	not specified [RCV005266659]	uncertain significance	1	192352119	192352119	Human		name
598189041	CV3902566	single nucleotide variant	NM_001039152.3(RGS21):c.248C>T (p.Pro83Leu)	not specified [RCV005266660]	uncertain significance	1	192352206	192352206	Human		name
156240564	CV2213663	single nucleotide variant	NM_001039152.3(RGS21):c.410T>C (p.Val137Ala)	not specified [RCV004089740]	uncertain significance	1	192366075	192366075	Human		name