Dusp23 Variant Search Result - Rat Genome Database

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27 records found for search term Dusp23

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156336326	CV2333656	single nucleotide variant	NM_001319658.2(DUSP23):c.13C>T (p.Pro5Ser)	not specified [RCV004192496]	uncertain significance	1	159781113	159781113	Human		name
407490343	CV3431116	single nucleotide variant	NM_001319658.2(DUSP23):c.20A>C (p.Asn7Thr)	not specified [RCV004620160]	uncertain significance	1	159781120	159781120	Human		name
405735142	CV3241260	single nucleotide variant	NM_001319658.2(DUSP23):c.34C>A (p.Leu12Ile)	not specified [RCV004379694]	uncertain significance	1	159781134	159781134	Human		name
156386456	CV2228220	single nucleotide variant	NM_001319658.2(DUSP23):c.166C>G (p.Leu56Val)	not specified [RCV004097954]	uncertain significance	1	159781266	159781266	Human		name
156334522	CV2263313	single nucleotide variant	NM_001319658.2(DUSP23):c.296T>G (p.Phe99Cys)	not specified [RCV004133589]	uncertain significance	1	159782181	159782181	Human		name
156220842	CV2392310	single nucleotide variant	NM_001319658.2(DUSP23):c.100C>G (p.Leu34Val)	not specified [RCV004243911]	uncertain significance	1	159781200	159781200	Human		name
329377597	CV2449834	single nucleotide variant	NM_001319658.2(DUSP23):c.199T>C (p.Cys67Arg)	not specified [RCV004268930]	uncertain significance	1	159781299	159781299	Human		name
329377600	CV2449835	single nucleotide variant	NM_001319658.2(DUSP23):c.200G>T (p.Cys67Phe)	not specified [RCV004268931]	uncertain significance	1	159781300	159781300	Human		name
329393750	CV2449836	single nucleotide variant	NM_001319658.2(DUSP23):c.202C>T (p.Pro68Ser)	not specified [RCV004268932]	uncertain significance	1	159781302	159781302	Human		name
329394473	CV2469889	single nucleotide variant	NM_001319658.2(DUSP23):c.177C>A (p.His59Gln)	not specified [RCV004285359]	uncertain significance	1	159781277	159781277	Human		name
401772578	CV2687741	single nucleotide variant	NM_001319658.2(DUSP23):c.176A>T (p.His59Leu)	not specified [RCV004302729]	uncertain significance	1	159781276	159781276	Human		name
407490332	CV3431112	single nucleotide variant	NM_001319658.2(DUSP23):c.154A>G (p.Ser52Gly)	not specified [RCV004620156]	uncertain significance	1	159781254	159781254	Human		name
407490335	CV3431113	single nucleotide variant	NM_001319658.2(DUSP23):c.107T>A (p.Val36Glu)	not specified [RCV004620157]	uncertain significance	1	159781207	159781207	Human		name
407490337	CV3431114	single nucleotide variant	NM_001319658.2(DUSP23):c.177C>G (p.His59Gln)	not specified [RCV004620158]	uncertain significance	1	159781277	159781277	Human		name
407490340	CV3431115	single nucleotide variant	NM_001319658.2(DUSP23):c.203C>T (p.Pro68Leu)	not specified [RCV004620159]	uncertain significance	1	159781303	159781303	Human		name
597735253	CV3670187	single nucleotide variant	NM_001319658.2(DUSP23):c.260G>T (p.Arg87Leu)	not specified [RCV004920436]	uncertain significance	1	159781360	159781360	Human		name
597802485	CV3670189	single nucleotide variant	NM_001319658.2(DUSP23):c.254A>G (p.Asn85Ser)	not specified [RCV004906708]	uncertain significance	1	159781354	159781354	Human		name
597735259	CV3670191	single nucleotide variant	NM_001319658.2(DUSP23):c.259C>T (p.Arg87Trp)	not specified [RCV004920437]	uncertain significance	1	159781359	159781359	Human		name
597802491	CV3670193	single nucleotide variant	NM_001319658.2(DUSP23):c.239T>G (p.Ile80Ser)	not specified [RCV004906711]	uncertain significance	1	159781339	159781339	Human		name
598267176	CV3957535	single nucleotide variant	NM_001319658.2(DUSP23):c.275G>A (p.Gly92Glu)	not specified [RCV005326833]	uncertain significance	1	159782160	159782160	Human		name
598267180	CV3957536	single nucleotide variant	NM_001319658.2(DUSP23):c.163G>A (p.Gly55Ser)	not specified [RCV005326834]	uncertain significance	1	159781263	159781263	Human		name
156134230	CV2196013	single nucleotide variant	NM_001319658.2(DUSP23):c.437A>G (p.Tyr146Cys)	not specified [RCV004072256]	uncertain significance	1	159782322	159782322	Human		name
155996206	CV2375908	single nucleotide variant	NM_001319658.2(DUSP23):c.341G>A (p.Arg114Gln)	not specified [RCV004217748]	uncertain significance	1	159782226	159782226	Human		name
405735133	CV3241261	single nucleotide variant	NM_001319658.2(DUSP23):c.364A>G (p.Ile122Val)	not specified [RCV004379695]	uncertain significance	1	159782249	159782249	Human		name
405735120	CV3241262	single nucleotide variant	NM_001319658.2(DUSP23):c.386G>C (p.Arg129Pro)	not specified [RCV004379696]	uncertain significance	1	159782271	159782271	Human		name
597802483	CV3670188	single nucleotide variant	NM_001319658.2(DUSP23):c.311C>T (p.Thr104Ile)	not specified [RCV004906707]	uncertain significance	1	159782196	159782196	Human		name
597802487	CV3670190	single nucleotide variant	NM_001319658.2(DUSP23):c.344G>T (p.Gly115Val)	not specified [RCV004906709]	uncertain significance	1	159782229	159782229	Human		name

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