Dusp13 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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40 records found for search term Dusp13

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401904044	CV2809395	single nucleotide variant	NM_001007273.2(DUSP13B):c.-153C>G	not provided [RCV003417523]	likely benign	10	75109140	75109140	Human		name
15116372	CV712472	single nucleotide variant	NM_001007273.2(DUSP13B):c.105C>T (p.Val35=)	not provided [RCV000962022]	benign	10	75103972	75103972	Human		name
15151639	CV712471	single nucleotide variant	NM_001007273.2(DUSP13B):c.143C>T (p.Ala48Val)	not provided [RCV000968183]	benign	10	75103934	75103934	Human		name
150331654	CV1169408	single nucleotide variant	NM_001363514.2(DUSP13B):c.875G>A (p.Cys292Tyr)	not provided [RCV001536566]	benign	10	75094806	75094806	Human	3	name
156137861	CV2196298	single nucleotide variant	NM_001363514.2(DUSP13B):c.952C>T (p.Arg318Trp)	not specified [RCV004550454]	uncertain significance	10	75094729	75094729	Human		name
156400310	CV2199096	single nucleotide variant	NM_001363514.2(DUSP13B):c.482C>T (p.Pro161Leu)	not specified [RCV004550501]	uncertain significance	10	75097811	75097811	Human		name
156000864	CV2257792	single nucleotide variant	NM_001363514.2(DUSP13B):c.958C>G (p.Leu320Val)	not specified [RCV004552221]	uncertain significance	10	75094723	75094723	Human		name
156130698	CV2279854	single nucleotide variant	NM_001363514.2(DUSP13B):c.785C>G (p.Ala262Gly)	not specified [RCV004552266]	uncertain significance	10	75095592	75095592	Human		name
155995746	CV2286561	single nucleotide variant	NM_001363514.2(DUSP13B):c.628C>G (p.His210Asp)	not specified [RCV004552264]	uncertain significance	10	75095749	75095749	Human		name
156064119	CV2287067	single nucleotide variant	NM_001363514.2(DUSP13B):c.985C>T (p.Arg329Trp)	not specified [RCV004552273]	uncertain significance	10	75094696	75094696	Human		name
156269853	CV2293363	single nucleotide variant	NM_001363514.2(DUSP13B):c.826A>T (p.Met276Leu)	not specified [RCV004552289]	uncertain significance	10	75094855	75094855	Human		name
156195140	CV2297195	single nucleotide variant	NM_001363514.2(DUSP13B):c.793G>A (p.Val265Ile)	not specified [RCV004552294]	likely benign	10	75095584	75095584	Human		name
156357589	CV2318329	single nucleotide variant	NM_001363514.2(DUSP13B):c.923G>A (p.Arg308His)	not specified [RCV004552357]	uncertain significance	10	75094758	75094758	Human		name
156202202	CV2334660	single nucleotide variant	NM_001363514.2(DUSP13B):c.482C>A (p.Pro161Gln)	not specified [RCV004552378]	uncertain significance	10	75097811	75097811	Human		name
155912783	CV2341648	single nucleotide variant	NM_001363514.2(DUSP13B):c.521G>A (p.Arg174His)	not specified [RCV004552385]	uncertain significance	10	75097772	75097772	Human		name
156181421	CV2353077	single nucleotide variant	NM_001363514.2(DUSP13B):c.770G>A (p.Arg257Gln)	not specified [RCV004553873]	uncertain significance	10	75095607	75095607	Human		name
405855192	CV3394595	single nucleotide variant	NM_001363514.2(DUSP13B):c.437G>A (p.Arg146Gln)	not specified [RCV004549246]	uncertain significance	10	75097856	75097856	Human		name
405855193	CV3394596	single nucleotide variant	NM_001363514.2(DUSP13B):c.595G>C (p.Asp199His)	not specified [RCV004549247]	uncertain significance	10	75095782	75095782	Human		name
405855194	CV3394597	single nucleotide variant	NM_001363514.2(DUSP13B):c.615G>T (p.Gln205His)	not specified [RCV004549248]	uncertain significance	10	75095762	75095762	Human		name
405855195	CV3394598	single nucleotide variant	NM_001363514.2(DUSP13B):c.654G>C (p.Lys218Asn)	not specified [RCV004549249]	uncertain significance	10	75095723	75095723	Human		name
405855196	CV3394599	single nucleotide variant	NM_001363514.2(DUSP13B):c.767C>A (p.Ala256Asp)	not specified [RCV004549250]	uncertain significance	10	75095610	75095610	Human		name
405855197	CV3394600	single nucleotide variant	NM_001363514.2(DUSP13B):c.805C>T (p.Arg269Cys)	not specified [RCV004549251]	uncertain significance	10	75094876	75094876	Human		name
405855198	CV3394601	single nucleotide variant	NM_001363514.2(DUSP13B):c.806G>A (p.Arg269His)	not specified [RCV004549252]	uncertain significance	10	75094875	75094875	Human		name
405855199	CV3394602	single nucleotide variant	NM_001363514.2(DUSP13B):c.838C>T (p.Arg280Cys)	not specified [RCV004549253]	uncertain significance	10	75094843	75094843	Human		name
405855200	CV3394603	single nucleotide variant	NM_001363514.2(DUSP13B):c.860C>A (p.Ala287Asp)	not specified [RCV004549254]	uncertain significance	10	75094821	75094821	Human		name
405855201	CV3394605	single nucleotide variant	NM_001363514.2(DUSP13B):c.932G>T (p.Cys311Phe)	not specified [RCV004549256]	uncertain significance	10	75094749	75094749	Human		name
405855202	CV3394606	single nucleotide variant	NM_001363514.2(DUSP13B):c.953G>A (p.Arg318Gln)	not specified [RCV004549257]	uncertain significance	10	75094728	75094728	Human		name
405855203	CV3394607	single nucleotide variant	NM_001363514.2(DUSP13B):c.992C>T (p.Thr331Met)	not specified [RCV004549258]	uncertain significance	10	75094689	75094689	Human		name
407490289	CV3431096	single nucleotide variant	NM_001363514.2(DUSP13B):c.839G>A (p.Arg280His)	not specified [RCV004620140]	uncertain significance	10	75094842	75094842	Human		name
597802347	CV3674021	single nucleotide variant	NM_001363514.2(DUSP13B):c.547G>A (p.Asp183Asn)	not specified [RCV004906664]	likely benign	10	75097746	75097746	Human		name
597802351	CV3674023	single nucleotide variant	NM_001363514.2(DUSP13B):c.908C>T (p.Thr303Met)	not specified [RCV004906666]	uncertain significance	10	75094773	75094773	Human		name
597802403	CV3674024	single nucleotide variant	NM_001363514.2(DUSP13B):c.997C>T (p.Arg333Trp)	not specified [RCV004906667]	uncertain significance	10	75094684	75094684	Human		name
597802406	CV3674025	single nucleotide variant	NM_001363514.2(DUSP13B):c.998G>A (p.Arg333Gln)	not specified [RCV004906668]	uncertain significance	10	75094683	75094683	Human		name
597802408	CV3674026	single nucleotide variant	NM_001363514.2(DUSP13B):c.565C>T (p.Leu189Phe)	not specified [RCV004906669]	uncertain significance	10	75097728	75097728	Human		name
597735200	CV3674027	single nucleotide variant	NM_001363514.2(DUSP13B):c.685C>T (p.Arg229Cys)	not specified [RCV004920425]	uncertain significance	10	75095692	75095692	Human		name
598267067	CV3957505	single nucleotide variant	NM_001363514.2(DUSP13B):c.493G>A (p.Ala165Thr)	not specified [RCV005326803]	uncertain significance	10	75097800	75097800	Human		name
598267071	CV3957506	single nucleotide variant	NM_001363514.2(DUSP13B):c.986G>A (p.Arg329Gln)	not specified [RCV005326804]	uncertain significance	10	75094695	75094695	Human		name
598267075	CV3957507	single nucleotide variant	NM_001363514.2(DUSP13B):c.739G>A (p.Asp247Asn)	not specified [RCV005326805]	uncertain significance	10	75095638	75095638	Human		name
15116366	CV712470	single nucleotide variant	NM_001363514.2(DUSP13B):c.976C>G (p.Arg326Gly)	not provided [RCV000962021]	benign	10	75094705	75094705	Human		name
15189057	CV737598	single nucleotide variant	NM_001363514.2(DUSP13B):c.977G>A (p.Arg326Gln)	not provided [RCV000909542]	benign	10	75094704	75094704	Human		name

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