Rpl23 Variant Search Result - Rat Genome Database

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63 records found for search term Rpl23

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155937268	CV2071501	single nucleotide variant	NM_000978.4(RPL23):c.98-9C>T	not provided [RCV002839169]	likely benign	17	38852741	38852741	Human		name
156077909	CV2141876	single nucleotide variant	NM_000978.4(RPL23):c.97+8C>G	not provided [RCV002979157]	benign	17	38853014	38853014	Human		name
405123078	CV3020986	single nucleotide variant	NM_000978.4(RPL23):c.14-5C>T	not provided [RCV003700968]	likely benign	17	38853110	38853110	Human		name
405159928	CV3061786	single nucleotide variant	NM_000978.4(RPL23):c.97+6G>A	not provided [RCV003727024]	uncertain significance	17	38853016	38853016	Human		name
597879819	CV3810182	single nucleotide variant	NM_000978.4(RPL23):c.98-4G>T	not provided [RCV005149644]	likely benign	17	38852736	38852736	Human		name
156286904	CV2050223	single nucleotide variant	NM_000978.4(RPL23):c.14-10A>G	not provided [RCV002807190]	likely benign	17	38853115	38853115	Human		name
405070628	CV2940974	single nucleotide variant	NM_000978.4(RPL23):c.97+11T>G	not provided [RCV003663960]	likely benign	17	38853011	38853011	Human		name
405200389	CV3041143	single nucleotide variant	NM_000978.4(RPL23):c.98-12A>G	not provided [RCV003707331]	likely benign	17	38852744	38852744	Human		name
402481955	CV3041598	single nucleotide variant	NM_000978.4(RPL23):c.14-14C>T	not provided [RCV003712882]	likely benign	17	38853119	38853119	Human		name
597882563	CV3822959	single nucleotide variant	NM_000978.4(RPL23):c.341-5T>C	not provided [RCV005178285]	likely benign	17	38850219	38850219	Human		name
597860954	CV3826077	single nucleotide variant	NM_000978.4(RPL23):c.14-12T>C	not provided [RCV005174976]	likely benign	17	38853117	38853117	Human		name
597936030	CV3845353	single nucleotide variant	NM_000978.4(RPL23):c.340+6A>C	not provided [RCV005186666]	uncertain significance	17	38850356	38850356	Human		name
156251112	CV2029612	single nucleotide variant	NM_000978.4(RPL23):c.227-12T>C	not provided [RCV002745991]	benign	17	38850487	38850487	Human		name
405100439	CV2938137	single nucleotide variant	NM_000978.4(RPL23):c.340+17G>A	not provided [RCV003665819]	likely benign	17	38850345	38850345	Human		name
597972000	CV3829395	single nucleotide variant	NM_000978.4(RPL23):c.227-20G>A	not provided [RCV005167182]	likely benign	17	38850495	38850495	Human		name
597935337	CV3858881	single nucleotide variant	NM_000978.4(RPL23):c.340+11A>C	not provided [RCV005207351]	likely benign	17	38850351	38850351	Human		name
151356299	CV1329063	microsatellite	NM_000978.4(RPL23):c.341-30ATTTT[3]	not provided [RCV002542672]\|not specified [RCV001822652]	likely benign	17	38850225	38850229	Human		name
156132807	CV2022812	microsatellite	NM_000978.4(RPL23):c.341-30ATTTT[5]	not provided [RCV002740627]	likely benign	17	38850224	38850225	Human		name
156241480	CV2086000	microsatellite	NM_000978.4(RPL23):c.341-30ATTTT[2]	not provided [RCV002876612]	likely benign	17	38850225	38850234	Human		name
405068851	CV3031029	deletion	NM_000978.4(RPL23):c.98-18_98-16del	not provided [RCV003698197]	likely benign	17	38852748	38852750	Human		name
597926330	CV3819692	deletion	NM_000978.4(RPL23):c.227-7_227-3del	not provided [RCV005156392]	uncertain significance	17	38850478	38850482	Human		name
405223093	CV2891240	single nucleotide variant	NM_000978.4(RPL23):c.12A>G (p.Arg4=)	not provided [RCV003554222]	uncertain significance	17	38853699	38853699	Human		name
405169386	CV2951146	single nucleotide variant	NM_000978.4(RPL23):c.24G>A (p.Gly8=)	not provided [RCV003675294]	likely benign	17	38853095	38853095	Human		name
405093846	CV3045618	single nucleotide variant	NM_000978.4(RPL23):c.51C>G (p.Ser17=)	not provided [RCV003718014]	likely benign	17	38853068	38853068	Human		name
597916421	CV3814693	single nucleotide variant	NM_000978.4(RPL23):c.39A>G (p.Lys13=)	not provided [RCV005155008]	likely benign	17	38853080	38853080	Human		name
405210732	CV2867859	single nucleotide variant	NM_000978.4(RPL23):c.222A>G (p.Lys74=)	not provided [RCV003552561]	likely benign	17	38852608	38852608	Human		name
402503568	CV2879860	single nucleotide variant	NM_000978.4(RPL23):c.138G>A (p.Lys46=)	not provided [RCV003546153]	likely benign	17	38852692	38852692	Human		name
405235954	CV2976522	single nucleotide variant	NM_000978.4(RPL23):c.279C>A (p.Gly93=)	not provided [RCV003682984]	likely benign	17	38850423	38850423	Human		name
405037662	CV3067579	single nucleotide variant	NM_000978.4(RPL23):c.279C>T (p.Gly93=)	not provided [RCV003739641]	likely benign	17	38850423	38850423	Human		name
597948178	CV3800892	single nucleotide variant	NM_000978.4(RPL23):c.276T>C (p.Asp92=)	not provided [RCV005135292]	likely benign	17	38850426	38850426	Human		name
597876623	CV3825664	single nucleotide variant	NM_000978.4(RPL23):c.145C>T (p.Leu49=)	not provided [RCV005177538]	likely benign	17	38852685	38852685	Human		name
156403328	CV1908627	single nucleotide variant	NM_000978.4(RPL23):c.80A>G (p.Asn27Ser)	not provided [RCV002605875]	uncertain significance	17	38853039	38853039	Human		name
156016833	CV2121449	single nucleotide variant	NM_000978.4(RPL23):c.366A>G (p.Ala122=)	not provided [RCV002948577]	likely benign	17	38850189	38850189	Human		name
405012134	CV2933875	single nucleotide variant	NM_000978.4(RPL23):c.54G>C (p.Leu18Phe)	not provided [RCV003576824]	uncertain significance	17	38853065	38853065	Human		name
405178678	CV3027492	single nucleotide variant	NM_000978.4(RPL23):c.372G>A (p.Glu124=)	not provided [RCV003705254]	likely benign	17	38850183	38850183	Human		name
405131263	CV3163626	single nucleotide variant	NM_000978.4(RPL23):c.366A>C (p.Ala122=)	not provided [RCV003854614]	likely benign	17	38850189	38850189	Human		name
597957737	CV3800585	single nucleotide variant	NM_000978.4(RPL23):c.330C>G (p.Gly110=)	not provided [RCV005137677]	likely benign	17	38850372	38850372	Human		name
151356374	CV1329138	single nucleotide variant	NM_000978.4(RPL23):c.280G>A (p.Val94Met)	not provided [RCV002542683]\|not specified [RCV001822727]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	17	38850422	38850422	Human		name
156393327	CV2002373	single nucleotide variant	NM_000978.4(RPL23):c.115A>G (p.Ile39Val)	not provided [RCV002680984]	uncertain significance	17	38852715	38852715	Human		name
155963897	CV2308325	single nucleotide variant	NM_000978.4(RPL23):c.266G>A (p.Arg89His)	not provided [RCV003699000]\|not specified [RCV004164811]	uncertain significance	17	38850436	38850436	Human		name
402489946	CV3011653	single nucleotide variant	NM_000978.4(RPL23):c.289T>A (p.Tyr97Asn)	not provided [RCV003687438]	uncertain significance	17	38850413	38850413	Human		name
402506227	CV3039127	single nucleotide variant	NM_000978.4(RPL23):c.265C>G (p.Arg89Gly)	not provided [RCV003715226]	uncertain significance	17	38850437	38850437	Human		name
597897329	CV3834712	single nucleotide variant	NM_000978.4(RPL23):c.175G>A (p.Asp59Asn)	not provided [RCV005180623]	uncertain significance	17	38852655	38852655	Human		name
597943324	CV3847152	single nucleotide variant	NM_000978.4(RPL23):c.101C>G (p.Ala34Gly)	not provided [RCV005188072]	uncertain significance	17	38852729	38852729	Human		name
156413965	CV1901936	single nucleotide variant	NM_000978.4(RPL23):c.335T>C (p.Met112Thr)	not provided [RCV003073519]	uncertain significance	17	38850367	38850367	Human		name
155925323	CV2045085	single nucleotide variant	NM_000978.4(RPL23):c.394A>G (p.Ile132Val)	not provided [RCV002750903]\|not specified [RCV004847924]	uncertain significance	17	38850161	38850161	Human		name
405737937	CV3320111	single nucleotide variant	NM_000978.4(RPL23):c.314T>C (p.Ile105Thr)	not specified [RCV004451932]	uncertain significance	17	38850388	38850388	Human		name
597924126	CV3808602	single nucleotide variant	NM_000978.4(RPL23):c.313A>G (p.Ile105Val)	not provided [RCV005156116]	uncertain significance	17	38850389	38850389	Human		name
597885127	CV3854772	single nucleotide variant	NM_000978.4(RPL23):c.364G>A (p.Ala122Thr)	not provided [RCV005199617]	uncertain significance	17	38850191	38850191	Human		name
405737949	CV3320113	single nucleotide variant	NM_000984.6(RPL23A):c.4G>A (p.Ala2Thr)	not specified [RCV004451934]	uncertain significance	17	28720009	28720009	Human		name
156106579	CV2257288	single nucleotide variant	NM_000984.6(RPL23A):c.91G>T (p.Gly31Cys)	not specified [RCV004125396]	uncertain significance	17	28720772	28720772	Human		name
156344940	CV2382002	single nucleotide variant	NM_000984.6(RPL23A):c.34C>G (p.Pro12Ala)	not specified [RCV004225929]	uncertain significance	17	28720715	28720715	Human		name
329359761	CV2462271	single nucleotide variant	NM_000984.6(RPL23A):c.80C>T (p.Ala27Val)	not specified [RCV004266266]	uncertain significance	17	28720761	28720761	Human		name
401732405	CV2678094	single nucleotide variant	NM_000984.6(RPL23A):c.29C>T (p.Pro10Leu)	not specified [RCV004296609]	uncertain significance	17	28720710	28720710	Human		name
401892592	CV2782256	single nucleotide variant	NM_000984.6(RPL23A):c.61G>C (p.Ala21Pro)	not specified [RCV004359222]	uncertain significance	17	28720742	28720742	Human		name
598218877	CV3906341	single nucleotide variant	NM_000984.6(RPL23A):c.79G>A (p.Ala27Thr)	not specified [RCV005272324]	uncertain significance	17	28720760	28720760	Human		name
155990785	CV2384047	single nucleotide variant	NM_000984.6(RPL23A):c.122G>T (p.Arg41Leu)	not specified [RCV004225412]	uncertain significance	17	28720803	28720803	Human		name
405737944	CV3320112	single nucleotide variant	NM_000984.6(RPL23A):c.172C>G (p.Pro58Ala)	not specified [RCV004451933]	uncertain significance	17	28720853	28720853	Human		name
407513705	CV3476093	single nucleotide variant	NM_000984.6(RPL23A):c.119T>C (p.Ile40Thr)	not specified [RCV004674216]	uncertain significance	17	28720800	28720800	Human		name
407513707	CV3476094	single nucleotide variant	NM_000984.6(RPL23A):c.256G>T (p.Ala86Ser)	not specified [RCV004674217]	uncertain significance	17	28722769	28722769	Human		name
597786237	CV3594190	single nucleotide variant	NM_000984.6(RPL23A):c.124A>G (p.Thr42Ala)	not specified [RCV004854811]	uncertain significance	17	28720805	28720805	Human		name
598218892	CV3906339	single nucleotide variant	NM_000984.6(RPL23A):c.176A>C (p.Lys59Thr)	not specified [RCV005272322]	uncertain significance	17	28720857	28720857	Human		name
598218886	CV3906340	single nucleotide variant	NM_000984.6(RPL23A):c.315C>G (p.Asn105Lys)	not specified [RCV005272323]	uncertain significance	17	28722828	28722828	Human		name

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