Rpl10 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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104 records found for search term Rpl10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401929909	CV2824370	single nucleotide variant	NM_006013.5(RPL10):c.*1G>A	not provided [RCV003440047]	likely benign	X	154400855	154400855	Human		name
21075230	CV798224	single nucleotide variant	NM_006013.5(RPL10):c.-4C>T	not provided [RCV000996070]	uncertain significance	X	154398516	154398516	Human		name
405259718	CV3195190	single nucleotide variant	NM_006013.5(RPL10):c.*87C>G	RPL10-related disorder [RCV003894386]	uncertain significance	X	154400941	154400941	Human		name , trait , alternate_id
405854349	CV3392994	single nucleotide variant	NM_006013.5(RPL10):c.*78C>T	not specified [RCV004527151]	uncertain significance	X	154400932	154400932	Human		name
8660547	CV135608	single nucleotide variant	NM_006013.5(RPL10):c.23+9T>A	not provided [RCV004713296]\|not specified [RCV000118190]	benign\|likely benign\|conflicting interpretations of pathogenicity	X	154398551	154398551	Human		name
401929911	CV2824371	single nucleotide variant	NM_006013.5(RPL10):c.*163C>T	not provided [RCV003440048]	likely benign	X	154401017	154401017	Human		name
405264252	CV3185288	single nucleotide variant	NM_006013.5(RPL10):c.24-8C>G	not provided [RCV003885852]	uncertain significance	X	154399330	154399330	Human		name
596946837	CV3548670	single nucleotide variant	NM_006013.5(RPL10):c.*156A>G	not provided [RCV004810498]	uncertain significance	X	154401010	154401010	Human		name
598159774	CV3897156	single nucleotide variant	NM_006013.5(RPL10):c.*111C>G	not provided [RCV005368130]	uncertain significance	X	154400965	154400965	Human		name
126740763	CV1018953	single nucleotide variant	NM_006013.5(RPL10):c.191-5C>T	Intellectual disability, X-linked, syndromic, 35 [RCV001329520]	uncertain significance	X	154399798	154399798	Human	1	name
150336899	CV1166436	single nucleotide variant	NM_006013.5(RPL10):c.190+7C>T	not provided [RCV001532224]	uncertain significance	X	154399601	154399601	Human		name
151233755	CV1318588	single nucleotide variant	NM_006013.5(RPL10):c.-24+3G>A	Intellectual disability, X-linked, syndromic, 35 [RCV001794916]\|not provided [RCV004714342]	benign	X	154398397	154398397	Human	1	name
152981809	CV1677100	single nucleotide variant	NM_006013.5(RPL10):c.24-13C>T	not specified [RCV002248169]	uncertain significance	X	154399325	154399325	Human		name
153305755	CV1687754	duplication	NM_006013.5(RPL10):c.190+4dup	not provided [RCV002263575]	likely benign	X	154399596	154399597	Human		name
155798223	CV1863508	single nucleotide variant	NM_006013.5(RPL10):c.-24+2T>G	not provided [RCV002473403]	uncertain significance	X	154398396	154398396	Human		name
401912418	CV2802865	single nucleotide variant	NM_006013.5(RPL10):c.329+6C>G	RPL10-related disorder [RCV003399844]	uncertain significance	X	154399947	154399947	Human		name , trait , alternate_id
13462865	CV438580	single nucleotide variant	NM_006013.5(RPL10):c.492+4T>A	not provided [RCV000514973]	uncertain significance	X	154400630	154400630	Human		name
15110412	CV776791	single nucleotide variant	NM_006013.5(RPL10):c.24-10T>C	not provided [RCV000938546]	likely benign	X	154399328	154399328	Human		name
15137167	CV776895	single nucleotide variant	NM_006013.5(RPL10):c.330-7A>G	not provided [RCV000943194]	likely benign	X	154400457	154400457	Human		name
153000197	CV1682911	single nucleotide variant	NM_006013.5(RPL10):c.191-10C>T	See cases [RCV002252921]	uncertain significance	X	154399793	154399793	Human		name
616934249	CV4012239	single nucleotide variant	NM_006013.5(RPL10):c.329+12C>A	not specified [RCV005409273]	likely benign	X	154399953	154399953	Human		name
408381980	CV3526663	deletion	NM_006013.5(RPL10):c.71_72del	not provided [RCV004771976]	uncertain significance	X	154400924	154400925	Human		name
8642242	CV101226	single nucleotide variant	NM_006013.5(RPL10):c.605= (p.Ser202=)	Inborn genetic diseases [RCV002311629]\|not provided [RCV004713245]\|not specified [RCV000081344]	benign\|conflicting interpretations of pathogenicity\|conflicting data from submitters	X	154400814	154400814	Human	1	name
13211966	CV426436	single nucleotide variant	NM_006013.5(RPL10):c.8G>A (p.Arg3His)	not provided [RCV000498157]	likely pathogenic	X	154398527	154398527	Human		name
9693294	CV178024	single nucleotide variant	NM_006013.5(RPL10):c.291C>T (p.Ile97=)	Inborn genetic diseases [RCV002313001]\|not provided [RCV000153857]	likely benign\|uncertain significance	X	154399903	154399903	Human	1	name
155724386	CV1851711	single nucleotide variant	NM_006013.5(RPL10):c.252C>T (p.Gly84=)	Inborn genetic diseases [RCV002433131]	likely benign	X	154399864	154399864	Human	1	name
617151236	CV4021815	single nucleotide variant	NM_006013.5(RPL10):c.207A>C (p.Arg69=)	not provided [RCV005426776]	likely benign	X	154399819	154399819	Human		name
13829461	CV581034	single nucleotide variant	NM_006013.5(RPL10):c.264G>A (p.Arg88=)	Inborn genetic diseases [RCV002315312]	likely benign	X	154399876	154399876	Human	1	name
401873368	CV2776553	single nucleotide variant	NM_006013.5(RPL10):c.42C>A (p.Asn14Lys)	Inborn genetic diseases [RCV003361995]	likely benign	X	154399356	154399356	Human	1	name
13830140	CV580717	single nucleotide variant	NM_006013.5(RPL10):c.633C>T (p.Ala211=)	Inborn genetic diseases [RCV002316757]\|not provided [RCV000912214]	benign	X	154400842	154400842	Human	1	name
15104702	CV758389	single nucleotide variant	NM_006013.5(RPL10):c.630G>A (p.Arg210=)	not provided [RCV000915401]	likely benign	X	154400839	154400839	Human		name
150554685	CV1304407	single nucleotide variant	NM_006013.5(RPL10):c.121G>A (p.Ala41Thr)	not provided [RCV001771377]	uncertain significance	X	154399525	154399525	Human		name
152032118	CV1671100	single nucleotide variant	NM_006013.5(RPL10):c.218A>C (p.Asn73Thr)	Intellectual disability, X-linked, syndromic, 35 [RCV002226637]	uncertain significance	X	154399830	154399830	Human	1	name
156385502	CV2227946	single nucleotide variant	NM_006013.5(RPL10):c.224A>T (p.Tyr75Phe)	Inborn genetic diseases [RCV002723454]	uncertain significance	X	154399836	154399836	Human	1	name
405003777	CV3184498	single nucleotide variant	NM_006013.5(RPL10):c.214G>A (p.Ala72Thr)	Autism, susceptibility to, X-linked 5 [RCV003883287]	uncertain significance	X	154399826	154399826	Human	1	name
408365464	CV3499938	single nucleotide variant	NM_006013.5(RPL10):c.218A>G (p.Asn73Ser)	Intellectual disability, X-linked, syndromic, 35 [RCV004796882]\|not provided [RCV004721980]	uncertain significance	X	154399830	154399830	Human	1	name
408377212	CV3501544	single nucleotide variant	NM_006013.5(RPL10):c.283C>T (p.His95Tyr)	not provided [RCV004727602]	likely pathogenic	X	154399895	154399895	Human		name
408391938	CV3523508	single nucleotide variant	NM_006013.5(RPL10):c.142C>T (p.Leu48Phe)	not provided [RCV004770882]	uncertain significance	X	154399546	154399546	Human		name
13207651	CV423403	single nucleotide variant	NM_006013.5(RPL10):c.232A>G (p.Lys78Glu)	Intellectual disability, X-linked, syndromic, 35 [RCV000494720]\|not provided [RCV001575333]	pathogenic\|conflicting interpretations of pathogenicity	X	154399844	154399844	Human	1	name
13207650	CV423405	single nucleotide variant	NM_006013.5(RPL10):c.191C>T (p.Ala64Val)	Intellectual disability, X-linked, syndromic, 35 [RCV000494719]	pathogenic	X	154399803	154399803	Human	1	name
21075231	CV798225	single nucleotide variant	NM_006013.5(RPL10):c.251G>A (p.Gly84Asp)	not provided [RCV000996071]	uncertain significance	X	154399863	154399863	Human		name
38461919	CV919990	single nucleotide variant	NM_006013.5(RPL10):c.236G>C (p.Ser79Thr)	Intellectual disability, X-linked, syndromic, 35 [RCV001198026]\|not provided [RCV001773450]	uncertain significance	X	154399848	154399848	Human	1	name
126730565	CV1022156	single nucleotide variant	NM_006013.5(RPL10):c.347G>A (p.Arg116Gln)	Intellectual disability, X-linked, syndromic, 35 [RCV001333474]\|not provided [RCV004789530]	uncertain significance	X	154400481	154400481	Human	1	name
150465500	CV1201086	single nucleotide variant	NM_006013.5(RPL10):c.482G>A (p.Gly161Asp)	not provided [RCV001587566]	likely pathogenic	X	154400616	154400616	Human		name
150461177	CV1205872	single nucleotide variant	NM_006013.5(RPL10):c.484C>T (p.Arg162Cys)	not provided [RCV001586829]\|not specified [RCV003317516]	uncertain significance	X	154400618	154400618	Human		name
150549424	CV1299443	single nucleotide variant	NM_006013.5(RPL10):c.467A>C (p.Lys156Thr)	not provided [RCV001752369]	uncertain significance	X	154400601	154400601	Human		name
152979974	CV1678322	single nucleotide variant	NM_006013.5(RPL10):c.628C>T (p.Arg210Trp)	not specified [RCV002246827]	benign	X	154400837	154400837	Human		name
155682840	CV1801128	single nucleotide variant	NM_006013.5(RPL10):c.629G>A (p.Arg210Gln)	Inborn genetic diseases [RCV002353949]	benign	X	154400838	154400838	Human	1	name
155798151	CV1859619	single nucleotide variant	NM_006013.5(RPL10):c.535G>A (p.Asp179Asn)	Intellectual disability, X-linked, syndromic, 35 [RCV002465412]	uncertain significance	X	154400744	154400744	Human	1	name
10053040	CV195697	single nucleotide variant	NM_006013.4(RPL10):c.639C>G (p.His213Gln)	not provided [RCV000179911]	uncertain significance	X	154400848	154400848	Human		name
155989985	CV2276406	single nucleotide variant	NM_006013.5(RPL10):c.561A>C (p.Glu187Asp)	Inborn genetic diseases [RCV002864419]	uncertain significance	X	154400770	154400770	Human	1	name
596938436	CV3401393	single nucleotide variant	NM_006013.5(RPL10):c.452C>T (p.Ala151Val)	Intellectual disability, X-linked, syndromic, 35 [RCV004808543]	pathogenic	X	154400586	154400586	Human	1	name
596946287	CV3550552	single nucleotide variant	NM_006013.5(RPL10):c.550A>T (p.Met184Leu)	not provided [RCV004819090]	uncertain significance	X	154400759	154400759	Human		name
597925509	CV3863473	single nucleotide variant	NM_006013.5(RPL10):c.406A>G (p.Met136Val)	not provided [RCV005205798]	uncertain significance	X	154400540	154400540	Human		name
8568050	CV38945	single nucleotide variant	NM_006013.5(RPL10):c.616C>A (p.Leu206Met)	Autism, susceptibility to, X-linked 5 [RCV000022883]	risk factor	X	154400825	154400825	Human	1	name
8568051	CV38946	single nucleotide variant	NM_006013.5(RPL10):c.639C>G (p.His213Gln)	Autism, susceptibility to, X-linked 5 [RCV000022884]\|not provided [RCV000179911]	risk factor\|uncertain significance	X	154400848	154400848	Human	1	name
13207649	CV423404	single nucleotide variant	NM_006013.5(RPL10):c.481G>A (p.Gly161Ser)	Intellectual disability, X-linked, syndromic, 35 [RCV000494718]	pathogenic	X	154400615	154400615	Human	1	name
15163754	CV706162	single nucleotide variant	NM_006013.5(RPL10):c.605G>A (p.Ser202Asn)	not provided [RCV000948166]	benign	X	154400814	154400814	Human		name
25321569	CV806438	single nucleotide variant	NM_006013.5(RPL10):c.565C>T (p.Arg189Trp)	Intellectual disability, X-linked, syndromic, 35 [RCV001009624]	likely pathogenic	X	154400774	154400774	Human	1	name
38597356	CV965239	single nucleotide variant	NM_006013.5(RPL10):c.578A>G (p.Asp193Gly)	Intellectual disability, X-linked, syndromic, 35 [RCV001254603]\|not provided [RCV004769978]	uncertain significance	X	154400787	154400787	Human	1	name
40887265	CV974338	single nucleotide variant	NM_006013.5(RPL10):c.479C>G (p.Pro160Arg)	Inborn genetic diseases [RCV001266758]	uncertain significance	X	154400613	154400613	Human	1	name
598218399	CV3906321	single nucleotide variant	NM_080746.3(RPL10L):c.7C>T (p.Arg3Cys)	not specified [RCV005272304]	uncertain significance	14	46651730	46651730	Human		name
155999934	CV2287326	single nucleotide variant	NM_080746.3(RPL10L):c.10C>G (p.Arg4Gly)	not specified [RCV004146949]	uncertain significance	14	46651727	46651727	Human		name
401893222	CV2766247	single nucleotide variant	NM_007104.5(RPL10A):c.16T>C (p.Ser6Pro)	not specified [RCV004340682]	uncertain significance	6	35468809	35468809	Human		name
405721121	CV3320078	single nucleotide variant	NM_080746.3(RPL10L):c.10C>T (p.Arg4Cys)	not specified [RCV004449830]	uncertain significance	14	46651727	46651727	Human		name
9687114	CV171547	single nucleotide variant	NM_080746.3(RPL10L):c.94C>T (p.Arg32Cys)	Prostate cancer [RCV000149333]\|not specified [RCV004019791]	uncertain significance	14	46651643	46651643	Human	2	name
329401339	CV2442191	single nucleotide variant	NM_080746.3(RPL10L):c.37A>C (p.Lys13Gln)	not specified [RCV004264686]	uncertain significance	14	46651700	46651700	Human		name
401730704	CV2686669	single nucleotide variant	NM_007104.5(RPL10A):c.74G>A (p.Arg25His)	not specified [RCV004300081]	uncertain significance	6	35468867	35468867	Human		name
401735405	CV2687575	single nucleotide variant	NM_080746.3(RPL10L):c.43A>C (p.Lys15Gln)	not specified [RCV004300799]	uncertain significance	14	46651694	46651694	Human		name
405867056	CV2842567	single nucleotide variant	NM_080746.3(RPL10L):c.399A>G (p.Gln133=)	EBV-positive nodal T- and NK-cell lymphoma [RCV004557924]	likely benign	14	46651338	46651338	Human		name
597709219	CV3594159	single nucleotide variant	NM_007104.5(RPL10A):c.68G>A (p.Arg23His)	not specified [RCV004860811]	uncertain significance	6	35468861	35468861	Human		name
598218412	CV3906323	single nucleotide variant	NM_080746.3(RPL10L):c.52C>T (p.Pro18Ser)	not specified [RCV005272306]	uncertain significance	14	46651685	46651685	Human		name
155974958	CV2235796	single nucleotide variant	NM_080746.3(RPL10L):c.268C>T (p.Arg90Trp)	not specified [RCV004111919]	uncertain significance	14	46651469	46651469	Human		name
156355208	CV2324435	single nucleotide variant	NM_080746.3(RPL10L):c.154A>G (p.Met52Val)	not specified [RCV004178923]	uncertain significance	14	46651583	46651583	Human		name
156049924	CV2367402	single nucleotide variant	NM_080746.3(RPL10L):c.168A>C (p.Glu56Asp)	not specified [RCV004209304]	uncertain significance	14	46651569	46651569	Human		name
156090103	CV2392154	single nucleotide variant	NM_080746.3(RPL10L):c.292C>T (p.Arg98Cys)	not specified [RCV004238046]	uncertain significance	14	46651445	46651445	Human		name
329371655	CV2432042	single nucleotide variant	NM_007104.5(RPL10A):c.191C>G (p.Ser64Cys)	not specified [RCV004249193]	uncertain significance	6	35469410	35469410	Human		name
329382710	CV2445427	single nucleotide variant	NM_080746.3(RPL10L):c.102T>G (p.Phe34Leu)	not specified [RCV004257490]	uncertain significance	14	46651635	46651635	Human		name
329359387	CV2450990	single nucleotide variant	NM_080746.3(RPL10L):c.182C>G (p.Ser61Cys)	not specified [RCV004267871]	uncertain significance	14	46651555	46651555	Human		name
405867057	CV2842568	single nucleotide variant	NM_080746.3(RPL10L):c.293G>A (p.Arg98His)	EBV-positive nodal T- and NK-cell lymphoma [RCV004557925]	likely benign	14	46651444	46651444	Human		name
405721132	CV3320079	single nucleotide variant	NM_080746.3(RPL10L):c.157G>A (p.Val53Met)	not specified [RCV004449831]	uncertain significance	14	46651580	46651580	Human		name
597709225	CV3594160	single nucleotide variant	NM_080746.3(RPL10L):c.221A>G (p.Lys74Arg)	not specified [RCV004860812]	uncertain significance	14	46651516	46651516	Human		name
597785710	CV3594163	single nucleotide variant	NM_080746.3(RPL10L):c.269G>A (p.Arg90Gln)	not specified [RCV004854799]	uncertain significance	14	46651468	46651468	Human		name
598218404	CV3906322	single nucleotide variant	NM_080746.3(RPL10L):c.263G>A (p.Arg88Gln)	not specified [RCV005272305]	uncertain significance	14	46651474	46651474	Human		name
26902897	CV858296	single nucleotide variant	NM_080746.3(RPL10L):c.257A>C (p.His86Pro)	Spermatogenesis maturation arrest [RCV001089644]\|Spermatogenic failure 63 [RCV001806022]	pathogenic\|likely pathogenic	14	46651480	46651480	Human	3	name
127261664	CV1087374	single nucleotide variant	NM_080746.3(RPL10L):c.501C>G (p.Ile167Met)	Intellectual developmental disorder with dysmorphic facies and ptosis [RCV001420561]	uncertain significance	14	46651236	46651236	Human	1	name
155917624	CV2199020	single nucleotide variant	NM_080746.3(RPL10L):c.502T>A (p.Ser168Thr)	not specified [RCV004080426]	uncertain significance	14	46651235	46651235	Human		name
156070260	CV2232368	single nucleotide variant	NM_080746.3(RPL10L):c.490A>G (p.Lys164Glu)	not specified [RCV004099002]	uncertain significance	14	46651247	46651247	Human		name
156050531	CV2237795	single nucleotide variant	NM_080746.3(RPL10L):c.629G>A (p.Arg210Gln)	not specified [RCV004109039]	uncertain significance	14	46651108	46651108	Human		name
156139963	CV2246956	single nucleotide variant	NM_080746.3(RPL10L):c.386T>C (p.Val129Ala)	not specified [RCV004112746]	uncertain significance	14	46651351	46651351	Human		name
156107911	CV2304081	single nucleotide variant	NM_080746.3(RPL10L):c.568C>T (p.Leu190Phe)	not specified [RCV004170124]	uncertain significance	14	46651169	46651169	Human		name
155905508	CV2349785	single nucleotide variant	NM_080746.3(RPL10L):c.551T>C (p.Met184Thr)	not specified [RCV004204197]	uncertain significance	14	46651186	46651186	Human		name
156044000	CV2381591	single nucleotide variant	NM_080746.3(RPL10L):c.383G>A (p.Arg128Gln)	not specified [RCV004232067]	uncertain significance	14	46651354	46651354	Human		name
156051690	CV2391262	single nucleotide variant	NM_080746.3(RPL10L):c.314G>T (p.Cys105Phe)	not specified [RCV004237270]	uncertain significance	14	46651423	46651423	Human		name
329398545	CV2471123	single nucleotide variant	NM_080746.3(RPL10L):c.302A>G (p.Lys101Arg)	not specified [RCV004278376]	uncertain significance	14	46651435	46651435	Human		name
401736013	CV2689235	single nucleotide variant	NM_080746.3(RPL10L):c.482G>T (p.Gly161Val)	not specified [RCV004306080]	uncertain significance	14	46651255	46651255	Human		name
401735741	CV2695389	single nucleotide variant	NM_080746.3(RPL10L):c.451G>T (p.Ala151Ser)	not specified [RCV004305594]	uncertain significance	14	46651286	46651286	Human		name
405721113	CV3320077	single nucleotide variant	NM_007104.5(RPL10A):c.604C>T (p.Arg202Trp)	not specified [RCV004449829]	uncertain significance	6	35470700	35470700	Human		name
405721140	CV3320080	single nucleotide variant	NM_080746.3(RPL10L):c.577G>A (p.Asp193Asn)	not specified [RCV004449832]	uncertain significance	14	46651160	46651160	Human		name
405721148	CV3320081	single nucleotide variant	NM_080746.3(RPL10L):c.628C>T (p.Arg210Trp)	not specified [RCV004449833]	uncertain significance	14	46651109	46651109	Human		name
407513691	CV3476081	single nucleotide variant	NM_080746.3(RPL10L):c.446T>C (p.Ile149Thr)	not specified [RCV004674211]	uncertain significance	14	46651291	46651291	Human		name
597709232	CV3594161	single nucleotide variant	NM_080746.3(RPL10L):c.497A>G (p.His166Arg)	not specified [RCV004860813]	uncertain significance	14	46651240	46651240	Human		name
598218393	CV3906320	single nucleotide variant	NM_080746.3(RPL10L):c.553G>A (p.Val185Met)	not specified [RCV005272303]	uncertain significance	14	46651184	46651184	Human		name
8635221	CV90443	single nucleotide variant	NM_080746.2(RPL10L):c.448G>A (p.Glu150Lys)	Malignant melanoma [RCV000070541]	not provided	14	46651289	46651289	Human		name

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