Mrpl21 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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20 records found for search term Mrpl21

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407525182	CV3450318	single nucleotide variant	NM_181514.2(MRPL21):c.50G>C (p.Cys17Ser)	not specified [RCV004631645]	uncertain significance	11	68903761	68903761	Human		name
407474451	CV3450319	single nucleotide variant	NM_181514.2(MRPL21):c.79C>T (p.Pro27Ser)	not specified [RCV004638157]	uncertain significance	11	68903732	68903732	Human		name
156044698	CV2237748	single nucleotide variant	NM_181514.2(MRPL21):c.149A>G (p.Tyr50Cys)	not specified [RCV004100527]	uncertain significance	11	68898010	68898010	Human		name
156097563	CV2253197	single nucleotide variant	NM_181514.2(MRPL21):c.223C>G (p.His75Asp)	not specified [RCV004122749]	uncertain significance	11	68897936	68897936	Human		name
156369060	CV2263257	single nucleotide variant	NM_181514.2(MRPL21):c.175C>T (p.Pro59Ser)	not specified [RCV004131756]	uncertain significance	11	68897984	68897984	Human		name
156000926	CV2391825	single nucleotide variant	NM_181514.2(MRPL21):c.125A>G (p.Gln42Arg)	not specified [RCV004235704]	uncertain significance	11	68900569	68900569	Human		name
329361898	CV2437780	single nucleotide variant	NM_181514.2(MRPL21):c.205C>G (p.Pro69Ala)	not specified [RCV004261080]	uncertain significance	11	68897954	68897954	Human		name
401730770	CV2686708	single nucleotide variant	NM_181514.2(MRPL21):c.245A>T (p.Lys82Met)	not specified [RCV004300115]	uncertain significance	11	68896666	68896666	Human		name
401886816	CV2776760	single nucleotide variant	NM_181514.2(MRPL21):c.112A>G (p.Arg38Gly)	not specified [RCV004357911]	uncertain significance	11	68900582	68900582	Human		name
405785394	CV3374285	single nucleotide variant	NM_181514.2(MRPL21):c.137A>G (p.Tyr46Cys)	not specified [RCV004504498]	uncertain significance	11	68900557	68900557	Human		name
405784908	CV3374296	single nucleotide variant	NM_181514.2(MRPL21):c.216G>T (p.Glu72Asp)	not specified [RCV004504509]	uncertain significance	11	68897943	68897943	Human		name
597633639	CV3561115	single nucleotide variant	NM_181514.2(MRPL21):c.268G>T (p.Gly90Trp)	not specified [RCV004830837]	uncertain significance	11	68896643	68896643	Human		name
597633653	CV3561117	single nucleotide variant	NM_181514.2(MRPL21):c.101C>T (p.Ser34Phe)	not specified [RCV004830839]	uncertain significance	11	68900593	68900593	Human		name
156133733	CV2216885	single nucleotide variant	NM_181514.2(MRPL21):c.386G>A (p.Arg129Gln)	not specified [RCV004083300]	uncertain significance	11	68896525	68896525	Human		name
329384708	CV2435179	single nucleotide variant	NM_181514.2(MRPL21):c.368C>T (p.Ala123Val)	not specified [RCV004252816]	uncertain significance	11	68896543	68896543	Human		name
401719021	CV2679388	single nucleotide variant	NM_181514.2(MRPL21):c.581G>A (p.Arg194Gln)	not specified [RCV004285917]	uncertain significance	11	68891368	68891368	Human		name
401735239	CV2690824	single nucleotide variant	NM_181514.2(MRPL21):c.584T>G (p.Ile195Arg)	not specified [RCV004298532]	uncertain significance	11	68891365	68891365	Human		name
597633647	CV3561116	single nucleotide variant	NM_181514.2(MRPL21):c.518G>A (p.Arg173Lys)	not specified [RCV004830838]	likely benign	11	68892925	68892925	Human		name
597637879	CV3561118	single nucleotide variant	NM_181514.2(MRPL21):c.540C>A (p.Phe180Leu)	not specified [RCV004824817]	uncertain significance	11	68892903	68892903	Human		name
598178839	CV3982858	single nucleotide variant	NM_181514.2(MRPL21):c.310C>T (p.Arg104Cys)	not specified [RCV005371832]	uncertain significance	11	68896601	68896601	Human		name

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