Rps20 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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291 records found for search term Rps20

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150449560	CV1215124	single nucleotide variant	NM_001023.4(RPS20):c.-6A>G	Lynch syndrome [RCV005369924]\|not provided [RCV001611714]\|not specified [RCV004596476]	benign	8	56074389	56074389	Human	1	name
405008969	CV2853146	single nucleotide variant	NM_001023.4(RPS20):c.-3G>T	not specified [RCV003494340]	uncertain significance	8	56074386	56074386	Human		name
126908137	CV1045610	single nucleotide variant	NM_001023.4(RPS20):c.3+5G>A	not provided [RCV001367629]	uncertain significance	8	56074376	56074376	Human		name
127310857	CV1155994	single nucleotide variant	NM_001023.4(RPS20):c.4-3T>C	Diamond-Blackfan anemia [RCV005361641]\|not provided [RCV001518424]\|not specified [RCV002465880]	benign	8	56074162	56074162	Human	2	name
151781374	CV1422104	single nucleotide variant	NM_001023.4(RPS20):c.4-8A>G	not provided [RCV001972112]	likely benign\|uncertain significance	8	56074167	56074167	Human		name
151802395	CV1442396	single nucleotide variant	NM_001023.4(RPS20):c.4-4A>G	not provided [RCV002011694]	uncertain significance	8	56074163	56074163	Human		name
152064855	CV1535883	single nucleotide variant	NM_001023.4(RPS20):c.3+7C>T	not provided [RCV002168498]	likely benign	8	56074374	56074374	Human		name
153002263	CV1685470	single nucleotide variant	NM_001023.4(RPS20):c.-90G>T	not provided [RCV002259456]	likely benign	8	56074473	56074473	Human		name
155799397	CV1859793	deletion	NM_001023.4(RPS20):c.*21del	not specified [RCV002466037]	benign	8	56073069	56073069	Human		name
155799408	CV1859798	single nucleotide variant	NM_001023.4(RPS20):c.-33A>T	not specified [RCV002466042]	likely benign	8	56074416	56074416	Human		name
401798295	CV2741360	single nucleotide variant	NM_001023.4(RPS20):c.-44C>T	not specified [RCV003322523]	likely benign	8	56074427	56074427	Human		name
407481221	CV3415245	single nucleotide variant	NM_001023.4(RPS20):c.-22A>G	not specified [RCV004595960]	likely benign	8	56074405	56074405	Human		name
598125478	CV3881626	single nucleotide variant	NM_001023.4(RPS20):c.*21G>A	not specified [RCV005232532]	likely benign	8	56073069	56073069	Human		name
14709453	CV651993	single nucleotide variant	NM_001023.4(RPS20):c.4-3T>A	not provided [RCV000812058]\|not specified [RCV005268775]	likely benign\|uncertain significance	8	56074162	56074162	Human		name
26886648	CV851205	single nucleotide variant	NM_001023.4(RPS20):c.3+9G>T	not provided [RCV001055237]	likely benign\|uncertain significance	8	56074372	56074372	Human		name
150485820	CV1223079	single nucleotide variant	NM_001023.4(RPS20):c.4-11T>C	Familial colorectal cancer type X [RCV005361686]\|not provided [RCV001617792]\|not specified [RCV002465896]	benign	8	56074170	56074170	Human	1	name
150460284	CV1231316	single nucleotide variant	NM_001023.4(RPS20):c.4-90G>A	not provided [RCV001640880]	benign	8	56074249	56074249	Human		name
150444948	CV1249493	single nucleotide variant	NM_001023.4(RPS20):c.-117G>C	not provided [RCV001666926]	benign	8	56074500	56074500	Human		name
150472667	CV1252282	single nucleotide variant	NM_001023.4(RPS20):c.4-19T>C	not provided [RCV001671483]	benign	8	56074178	56074178	Human		name
150468569	CV1267953	single nucleotide variant	NM_001023.3(RPS20):c.*236G>C	not provided [RCV001694816]	benign	8	56072854	56072854	Human		name
150465504	CV1277250	single nucleotide variant	NM_001023.4(RPS20):c.3+57C>G	not provided [RCV001710544]	benign	8	56074324	56074324	Human		name
152027905	CV1607539	single nucleotide variant	NM_001023.4(RPS20):c.4-15T>C	not provided [RCV002105053]	likely benign	8	56074174	56074174	Human		name
152157492	CV1630565	single nucleotide variant	NM_001023.4(RPS20):c.3+13T>G	not provided [RCV002122625]	benign	8	56074368	56074368	Human		name
152047984	CV1654101	single nucleotide variant	NM_001023.4(RPS20):c.4-16A>G	not provided [RCV002088778]\|not specified [RCV004596516]	likely benign	8	56074175	56074175	Human		name
152104433	CV1658596	single nucleotide variant	NM_001023.4(RPS20):c.3+11A>G	not provided [RCV002152208]	likely benign	8	56074370	56074370	Human		name
155799404	CV1859796	single nucleotide variant	NM_001023.4(RPS20):c.4-40A>G	not specified [RCV002466040]	benign	8	56074199	56074199	Human		name
155799405	CV1859797	single nucleotide variant	NM_001023.4(RPS20):c.3+21G>A	not specified [RCV002466041]	likely benign	8	56074360	56074360	Human		name
156413610	CV1901011	single nucleotide variant	NM_001023.4(RPS20):c.4-14G>A	not provided [RCV002588215]	likely benign	8	56074173	56074173	Human		name
156109862	CV2121097	single nucleotide variant	NM_001023.4(RPS20):c.4-10C>A	not provided [RCV002953066]	likely benign	8	56074169	56074169	Human		name
401798152	CV2741356	single nucleotide variant	NM_001023.4(RPS20):c.4-45A>G	not specified [RCV003322519]	likely benign	8	56074204	56074204	Human		name
405008958	CV2853145	single nucleotide variant	NM_001023.4(RPS20):c.4-39T>A	not specified [RCV003494339]	likely benign	8	56074198	56074198	Human		name
405226840	CV2892289	duplication	NM_001023.4(RPS20):c.4-17dup	not provided [RCV003554704]	likely benign	8	56074175	56074176	Human		name
405231412	CV2895772	single nucleotide variant	NM_001023.4(RPS20):c.3+15G>A	not provided [RCV003555585]	likely benign	8	56074366	56074366	Human		name
405128928	CV3054446	single nucleotide variant	NM_001023.4(RPS20):c.4-12A>G	not provided [RCV003724646]	likely benign	8	56074171	56074171	Human		name
405272622	CV3201321	single nucleotide variant	NM_001023.4(RPS20):c.3+10C>A	RPS20-related disorder [RCV003901385]	likely benign	8	56074371	56074371	Human		name , trait , alternate_id
598125481	CV3881629	single nucleotide variant	NM_001023.4(RPS20):c.3+29C>T	not specified [RCV005232535]	likely benign	8	56074352	56074352	Human		name
151793248	CV1511237	single nucleotide variant	NM_001023.4(RPS20):c.177+1G>A	not provided [RCV001990271]	uncertain significance	8	56073694	56073694	Human		name
152087606	CV1594728	single nucleotide variant	NM_001023.4(RPS20):c.104-7C>T	not provided [RCV002113619]	likely benign	8	56073775	56073775	Human		name
152081427	CV1645077	single nucleotide variant	NM_001023.4(RPS20):c.104-6C>T	not provided [RCV002149362]	likely benign	8	56073774	56073774	Human		name
156294960	CV1884206	single nucleotide variant	NM_001023.4(RPS20):c.103+8C>T	not provided [RCV003087653]	likely benign	8	56074052	56074052	Human		name
156030239	CV1923188	single nucleotide variant	NM_001023.4(RPS20):c.178-3C>T	not provided [RCV002637127]	uncertain significance	8	56073275	56073275	Human		name
156026586	CV2078145	single nucleotide variant	NM_001023.4(RPS20):c.177+2T>C	not provided [RCV002866866]	uncertain significance	8	56073693	56073693	Human		name
156256936	CV2090086	single nucleotide variant	NM_001023.4(RPS20):c.177+4A>G	not provided [RCV002877134]	uncertain significance	8	56073691	56073691	Human		name
405240274	CV2882705	single nucleotide variant	NM_001023.4(RPS20):c.103+9A>G	not provided [RCV003557186]	likely benign	8	56074051	56074051	Human		name
597962763	CV3841083	single nucleotide variant	NM_001023.4(RPS20):c.104-6C>A	not provided [RCV005193376]	likely benign	8	56073774	56073774	Human		name
616938888	CV4015162	single nucleotide variant	NM_001023.4(RPS20):c.178-2A>C	Hereditary cancer-predisposing syndrome [RCV005412178]	likely pathogenic	8	56073274	56073274	Human	1	name
14711915	CV651983	single nucleotide variant	NM_001023.4(RPS20):c.103+5G>A	not provided [RCV000819256]	uncertain significance	8	56074055	56074055	Human		name
15161828	CV744316	single nucleotide variant	NM_001023.4(RPS20):c.178-7G>T	not provided [RCV000903426]	likely benign	8	56073279	56073279	Human		name
26916426	CV851696	single nucleotide variant	NM_001023.4(RPS20):c.178-3C>A	not provided [RCV001040381]	uncertain significance	8	56073275	56073275	Human		name
38483887	CV940109	single nucleotide variant	NM_001023.4(RPS20):c.177+6G>A	not provided [RCV001207820]	uncertain significance	8	56073689	56073689	Human		name
38494727	CV960654	single nucleotide variant	NM_001023.4(RPS20):c.103+3C>T	not provided [RCV001241492]\|not specified [RCV005269014]	uncertain significance	8	56074057	56074057	Human		name
150496054	CV1225229	single nucleotide variant	NM_001023.4(RPS20):c.177+76G>C	not provided [RCV001619707]	benign	8	56073619	56073619	Human		name
150443853	CV1249334	single nucleotide variant	NM_001023.4(RPS20):c.104-90T>C	not provided [RCV001666766]	benign	8	56073858	56073858	Human		name
150444171	CV1266492	single nucleotide variant	NM_001146227.3(RPS20):c.*35G>A	not provided [RCV001690928]\|not specified [RCV003321867]	benign	8	56069703	56069703	Human		name
150494454	CV1267355	single nucleotide variant	NM_001023.4(RPS20):c.103+88G>C	not provided [RCV001688383]	benign	8	56073972	56073972	Human		name
150535096	CV1311773	single nucleotide variant	NM_001146227.3(RPS20):c.*14C>T	Lynch syndrome [RCV005361721]\|not provided [RCV001779583]\|not specified [RCV002465904]	benign\|likely benign	8	56069724	56069724	Human	1	name
152110259	CV1519494	duplication	NM_001023.4(RPS20):c.177+19dup	not provided [RCV002152958]\|not specified [RCV002465924]	benign	8	56073675	56073676	Human		name
152072653	CV1549450	single nucleotide variant	NM_001023.4(RPS20):c.103+19C>A	not provided [RCV002091801]	likely benign	8	56074041	56074041	Human		name
152164230	CV1560541	single nucleotide variant	NM_001023.4(RPS20):c.177+19G>A	not provided [RCV002160207]	benign	8	56073676	56073676	Human		name
152121185	CV1562458	single nucleotide variant	NM_001023.4(RPS20):c.103+19C>G	not provided [RCV002098172]	likely benign	8	56074041	56074041	Human		name
152027173	CV1562527	single nucleotide variant	NM_001023.4(RPS20):c.178-12C>G	not provided [RCV002104804]	likely benign	8	56073284	56073284	Human		name
152148445	CV1566270	single nucleotide variant	NM_001023.4(RPS20):c.103+12C>T	not provided [RCV002139157]	likely benign	8	56074048	56074048	Human		name
152112531	CV1573333	single nucleotide variant	NM_001023.4(RPS20):c.178-17T>G	not provided [RCV002215689]	likely benign	8	56073289	56073289	Human		name
152094947	CV1599448	single nucleotide variant	NM_001023.4(RPS20):c.178-18C>A	not provided [RCV002094712]	likely benign	8	56073290	56073290	Human		name
152137096	CV1625464	single nucleotide variant	NM_001023.4(RPS20):c.103+14T>A	not provided [RCV002137688]	likely benign	8	56074046	56074046	Human		name
152169258	CV1636973	single nucleotide variant	NM_001023.4(RPS20):c.177+12C>T	not provided [RCV002182731]\|not specified [RCV003321900]	likely benign	8	56073683	56073683	Human		name
152117186	CV1645899	single nucleotide variant	NM_001023.4(RPS20):c.177+14G>T	not provided [RCV002175089]	likely benign	8	56073681	56073681	Human		name
156294267	CV1926674	single nucleotide variant	NM_001023.4(RPS20):c.178-19C>T	not provided [RCV002628942]	likely benign	8	56073291	56073291	Human		name
156282927	CV1929572	single nucleotide variant	NM_001023.4(RPS20):c.177+18G>A	not provided [RCV002628495]	uncertain significance	8	56073677	56073677	Human		name
401798285	CV2741347	single nucleotide variant	NM_001023.4(RPS20):c.177+14G>A	not specified [RCV003322510]	likely benign	8	56073681	56073681	Human		name
401798289	CV2741352	single nucleotide variant	NM_001023.4(RPS20):c.104-16C>T	not provided [RCV005061269]\|not specified [RCV003322515]	likely benign	8	56073784	56073784	Human		name
405008918	CV2853143	single nucleotide variant	NM_001023.4(RPS20):c.103+22G>T	not specified [RCV003494337]	likely benign	8	56074038	56074038	Human		name
405008931	CV2853144	single nucleotide variant	NM_001023.4(RPS20):c.103+20G>A	not specified [RCV003494338]	likely benign	8	56074040	56074040	Human		name
405227821	CV2889006	deletion	NM_001023.4(RPS20):c.104-11del	not provided [RCV003554853]	likely benign	8	56073779	56073779	Human		name
405128630	CV2893377	single nucleotide variant	NM_001023.4(RPS20):c.178-14G>A	not provided [RCV003559821]	likely benign	8	56073286	56073286	Human		name
405216922	CV2897226	single nucleotide variant	NM_001023.4(RPS20):c.178-14G>C	not provided [RCV003567898]	likely benign	8	56073286	56073286	Human		name
405203112	CV3052842	single nucleotide variant	NM_001023.4(RPS20):c.103+13G>C	not provided [RCV003730988]	likely benign	8	56074047	56074047	Human		name
405138418	CV3155074	deletion	NM_001023.4(RPS20):c.177+19del	not provided [RCV003855312]	benign	8	56073676	56073676	Human		name
407477230	CV3415240	single nucleotide variant	NM_001146227.3(RPS20):c.*34A>C	not specified [RCV004595955]	uncertain significance	8	56069704	56069704	Human		name
407481463	CV3415243	single nucleotide variant	NM_001023.4(RPS20):c.177+37T>C	not specified [RCV004595958]	likely benign	8	56073658	56073658	Human		name
597968983	CV3791179	single nucleotide variant	NM_001023.4(RPS20):c.178-13T>C	not provided [RCV005141211]	likely benign	8	56073285	56073285	Human		name
597971429	CV3802574	single nucleotide variant	NM_001023.4(RPS20):c.178-18C>T	not provided [RCV005142172]	likely benign	8	56073290	56073290	Human		name
597931919	CV3837939	single nucleotide variant	NM_001023.4(RPS20):c.103+16A>G	not provided [RCV005185908]	likely benign	8	56074044	56074044	Human		name
597867488	CV3838709	single nucleotide variant	NM_001023.4(RPS20):c.177+13G>A	not provided [RCV005176005]	likely benign	8	56073682	56073682	Human		name
597918710	CV3842469	single nucleotide variant	NM_001023.4(RPS20):c.177+12C>A	not provided [RCV005183954]	likely benign	8	56073683	56073683	Human		name
598121899	CV3881622	single nucleotide variant	NM_001146227.3(RPS20):c.*25T>A	not specified [RCV005232528]	likely benign	8	56069713	56069713	Human		name
598203804	CV3896533	single nucleotide variant	NM_001023.4(RPS20):c.178-12C>T	Diamond-Blackfan anemia [RCV005356761]	likely benign	8	56073284	56073284	Human	2	name
150472371	CV1272477	single nucleotide variant	NM_001023.4(RPS20):c.177+180A>G	not provided [RCV001695533]	benign	8	56073515	56073515	Human		name
150484929	CV1273835	single nucleotide variant	NM_001023.4(RPS20):c.178-181G>C	not provided [RCV001698607]	benign	8	56073453	56073453	Human		name
402479303	CV2853141	single nucleotide variant	NM_001146227.3(RPS20):c.*35+8T>A	not specified [RCV003494335]	likely benign	8	56069695	56069695	Human		name
407477243	CV3415241	single nucleotide variant	NM_001146227.3(RPS20):c.334-9G>C	not specified [RCV004595956]	likely benign	8	56069842	56069842	Human		name
155794748	CV1859792	single nucleotide variant	NM_001146227.3(RPS20):c.334-32C>G	not specified [RCV002466036]	likely benign	8	56069865	56069865	Human		name
401795773	CV2741330	deletion	NM_001146227.3(RPS20):c.334-22del	not specified [RCV003322493]	likely benign	8	56069855	56069855	Human		name
405124561	CV2889560	deletion	NM_001023.4(RPS20):c.3+11_3+20del	not provided [RCV003559441]	uncertain significance	8	56074361	56074370	Human		name
598121901	CV3881625	single nucleotide variant	NM_001146227.3(RPS20):c.334-45T>C	not specified [RCV005232531]	likely benign	8	56069878	56069878	Human		name
150509232	CV1214248	single nucleotide variant	NM_001146227.3(RPS20):c.*35+247T>C	not provided [RCV001596769]	benign	8	56069456	56069456	Human		name
150432321	CV1236721	single nucleotide variant	NM_001146227.3(RPS20):c.*35+178G>C	not provided [RCV001642126]	benign	8	56069525	56069525	Human		name
150449373	CV1260813	single nucleotide variant	NM_001146227.3(RPS20):c.334-187G>A	not provided [RCV001680482]	benign	8	56070020	56070020	Human		name
150484262	CV1263139	single nucleotide variant	NM_001146227.3(RPS20):c.*35+220C>T	not provided [RCV001686539]	benign	8	56069483	56069483	Human		name
155727140	CV1822442	single nucleotide variant	NM_001023.4(RPS20):c.6T>A (p.Ala2=)	not specified [RCV004055132]	likely benign	8	56074157	56074157	Human		name
156060077	CV2034485	deletion	NM_001023.4(RPS20):c.178-9_178-8del	not provided [RCV002736808]\|not specified [RCV003321957]	likely benign	8	56073280	56073281	Human		name
156321017	CV2101001	single nucleotide variant	NM_001023.4(RPS20):c.9T>C (p.Phe3=)	not provided [RCV002899291]\|not specified [RCV004661492]	likely benign	8	56074154	56074154	Human		name
401924019	CV2821094	single nucleotide variant	NM_001023.4(RPS20):c.6T>C (p.Ala2=)	not provided [RCV003435501]\|not specified [RCV004857980]	likely benign	8	56074157	56074157	Human		name
597931124	CV3789430	duplication	NM_001023.4(RPS20):c.173_177+165dup	not provided [RCV005131711]	uncertain significance	8	56073529	56073530	Human		name
127293914	CV1118711	single nucleotide variant	NM_001023.4(RPS20):c.21A>G (p.Gly7=)	not provided [RCV001452124]\|not specified [RCV004038506]	likely benign	8	56074142	56074142	Human		name
152046929	CV1556331	single nucleotide variant	NM_001023.4(RPS20):c.18C>T (p.Thr6=)	not provided [RCV002207030]\|not specified [RCV004045606]	likely benign	8	56074145	56074145	Human		name
152083150	CV1655063	single nucleotide variant	NM_001023.4(RPS20):c.21A>C (p.Gly7=)	not provided [RCV002113032]\|not specified [RCV004045883]	likely benign	8	56074142	56074142	Human		name
155720564	CV1835803	single nucleotide variant	NM_001023.4(RPS20):c.12G>A (p.Lys4=)	not specified [RCV004058250]	likely benign	8	56074151	56074151	Human		name
155719591	CV1837392	single nucleotide variant	NM_001023.4(RPS20):c.15T>C (p.Asp5=)	not specified [RCV004057418]	likely benign	8	56074148	56074148	Human		name
155733555	CV1842648	single nucleotide variant	NM_001023.4(RPS20):c.18C>G (p.Thr6=)	not provided [RCV005097823]\|not specified [RCV004060761]	likely benign	8	56074145	56074145	Human		name
155686481	CV1852594	single nucleotide variant	NM_001023.4(RPS20):c.27A>G (p.Thr9=)	not specified [RCV004062250]	likely benign	8	56074136	56074136	Human		name
329352592	CV2463778	single nucleotide variant	NM_001023.4(RPS20):c.24A>G (p.Lys8=)	not specified [RCV004279609]	likely benign	8	56074139	56074139	Human		name
151867648	CV1348608	single nucleotide variant	NM_001023.4(RPS20):c.5C>T (p.Ala2Val)	Hereditary nonpolyposis colon cancer [RCV003470994]\|not provided [RCV001924805]\|not specified [RCV004041321]	uncertain significance	8	56074158	56074158	Human	1	name
151828125	CV1438045	single nucleotide variant	NM_001023.4(RPS20):c.3G>A (p.Met1Ile)	not provided [RCV001920223]	uncertain significance	8	56074381	56074381	Human		name
152067075	CV1566743	single nucleotide variant	NM_001023.4(RPS20):c.93C>T (p.Ser31=)	not provided [RCV002091065]\|not specified [RCV004045776]	likely benign	8	56074070	56074070	Human		name
152138000	CV1652485	single nucleotide variant	NM_001023.4(RPS20):c.78C>T (p.Ser26=)	not provided [RCV002083776]\|not specified [RCV004045739]	likely benign	8	56074085	56074085	Human		name
152103189	CV1656769	single nucleotide variant	NM_001023.4(RPS20):c.70C>T (p.Leu24=)	not provided [RCV002115615]\|not specified [RCV004046273]	likely benign	8	56074093	56074093	Human		name
155716061	CV1785082	single nucleotide variant	NM_001023.4(RPS20):c.30C>G (p.Pro10=)	not provided [RCV003560940]\|not specified [RCV004048330]	likely benign	8	56074133	56074133	Human		name
155716085	CV1785089	single nucleotide variant	NM_001023.4(RPS20):c.30C>T (p.Pro10=)	not provided [RCV003099197]\|not specified [RCV003493932]	likely benign	8	56074133	56074133	Human		name
155696910	CV1793907	single nucleotide variant	NM_001023.4(RPS20):c.39G>A (p.Pro13=)	not specified [RCV004050576]	likely benign	8	56074124	56074124	Human		name
155710265	CV1811617	single nucleotide variant	NM_001023.4(RPS20):c.63A>G (p.Arg21=)	not specified [RCV004053936]	likely benign	8	56074100	56074100	Human		name
155726991	CV1822370	single nucleotide variant	NM_001023.4(RPS20):c.69C>T (p.Thr23=)	not specified [RCV004055105]	likely benign	8	56074094	56074094	Human		name
155728901	CV1822694	single nucleotide variant	NM_001023.4(RPS20):c.72A>T (p.Leu24=)	not specified [RCV004055861]	likely benign	8	56074091	56074091	Human		name
155744707	CV1824354	single nucleotide variant	NM_001023.4(RPS20):c.84C>T (p.Asn28=)	RPS20-related disorder [RCV005397403]\|not specified [RCV004056194]	likely benign	8	56074079	56074079	Human		name , trait , alternate_id
155690852	CV1825058	single nucleotide variant	NM_001023.4(RPS20):c.93C>G (p.Ser31=)	not specified [RCV004055734]	likely benign	8	56074070	56074070	Human		name
155730995	CV1825872	single nucleotide variant	NM_001023.4(RPS20):c.99A>G (p.Glu33=)	not specified [RCV004057755]	likely benign	8	56074064	56074064	Human		name
156261903	CV2030161	single nucleotide variant	NM_001023.4(RPS20):c.54C>T (p.His18=)	not provided [RCV002746339]	likely benign	8	56074109	56074109	Human		name
329392111	CV2470391	single nucleotide variant	NM_001023.4(RPS20):c.66C>T (p.Ile22=)	not specified [RCV004273427]	likely benign	8	56074097	56074097	Human		name
401765045	CV2733458	single nucleotide variant	NM_001023.4(RPS20):c.69C>G (p.Thr23=)	not specified [RCV004330386]	likely benign	8	56074094	56074094	Human		name
401867968	CV2787263	single nucleotide variant	NM_001023.4(RPS20):c.87A>T (p.Val29=)	not specified [RCV004366232]	likely benign	8	56074076	56074076	Human		name
401947442	CV2833476	single nucleotide variant	NM_001023.4(RPS20):c.5C>G (p.Ala2Gly)	Hereditary nonpolyposis colon cancer [RCV003466263]	uncertain significance	8	56074158	56074158	Human	1	name
405701464	CV3392171	single nucleotide variant	NM_001023.4(RPS20):c.94T>C (p.Leu32=)	not specified [RCV004521050]	likely benign	8	56074069	56074069	Human		name
598125480	CV3881628	single nucleotide variant	NM_001023.4(RPS20):c.30C>A (p.Pro10=)	not specified [RCV005232534]	likely benign	8	56074133	56074133	Human		name
598220270	CV3903007	single nucleotide variant	NM_001023.4(RPS20):c.75A>C (p.Thr25=)	not specified [RCV005272446]	likely benign	8	56074088	56074088	Human		name
598220295	CV3903011	single nucleotide variant	NM_001023.4(RPS20):c.48A>G (p.Ala16=)	not specified [RCV005272450]	likely benign	8	56074115	56074115	Human		name
15102651	CV723153	single nucleotide variant	NM_001023.4(RPS20):c.87A>G (p.Val29=)	not provided [RCV000892521]\|not specified [RCV004028421]	likely benign	8	56074076	56074076	Human		name
126761155	CV992885	single nucleotide variant	NM_001023.4(RPS20):c.81C>T (p.Arg27=)	not provided [RCV001300008]\|not specified [RCV004036158]	likely benign\|uncertain significance	8	56074082	56074082	Human		name
127273245	CV1097152	single nucleotide variant	NM_001023.4(RPS20):c.117G>A (p.Leu39=)	not provided [RCV001442463]\|not specified [RCV004038404]	likely benign	8	56073755	56073755	Human		name
127336020	CV1118710	single nucleotide variant	NM_001023.4(RPS20):c.144C>T (p.Leu48=)	not provided [RCV001474708]\|not specified [RCV004037154]	likely benign	8	56073728	56073728	Human		name
127307135	CV1155992	single nucleotide variant	NM_001023.4(RPS20):c.271T>C (p.Leu91=)	not provided [RCV001516945]\|not specified [RCV004037940]	benign\|likely benign	8	56073179	56073179	Human		name
127291770	CV1155993	single nucleotide variant	NM_001023.4(RPS20):c.195A>G (p.Thr65=)	not provided [RCV001510547]	benign	8	56073255	56073255	Human		name
151757565	CV1459773	single nucleotide variant	NM_001023.4(RPS20):c.177G>A (p.Lys59=)	not provided [RCV001986905]	uncertain significance	8	56073695	56073695	Human		name
152046277	CV1519591	single nucleotide variant	NM_001023.4(RPS20):c.282T>G (p.Pro94=)	not provided [RCV002145115]\|not specified [RCV004046381]	likely benign	8	56073168	56073168	Human		name
152158138	CV1564344	single nucleotide variant	NM_001023.4(RPS20):c.270C>T (p.Asp90=)	not provided [RCV002140461]\|not specified [RCV003321909]	likely benign	8	56073180	56073180	Human		name
152030068	CV1565981	single nucleotide variant	NM_001023.4(RPS20):c.192T>C (p.Thr64=)	not provided [RCV002086020]\|not specified [RCV004045759]	likely benign	8	56073258	56073258	Human		name
152138325	CV1570877	single nucleotide variant	NM_001023.4(RPS20):c.138G>A (p.Lys46=)	not provided [RCV002120016]\|not specified [RCV004046297]	likely benign	8	56073734	56073734	Human		name
152129264	CV1584273	single nucleotide variant	NM_001023.4(RPS20):c.219T>G (p.Gly73=)	not provided [RCV002082640]\|not specified [RCV004044954]	likely benign	8	56073231	56073231	Human		name
152083805	CV1624032	single nucleotide variant	NM_001023.4(RPS20):c.105G>A (p.Val35=)	not provided [RCV002149655]\|not specified [RCV004046340]	likely benign	8	56073767	56073767	Human		name
155666618	CV1793172	single nucleotide variant	NM_001023.4(RPS20):c.114C>T (p.Asp38=)	not specified [RCV004049305]	likely benign	8	56073758	56073758	Human		name
155682593	CV1804404	single nucleotide variant	NM_001023.4(RPS20):c.121A>C (p.Arg41=)	not specified [RCV004053469]	likely benign	8	56073751	56073751	Human		name
155732623	CV1826460	single nucleotide variant	NM_001023.4(RPS20):c.102G>A (p.Lys34=)	not provided [RCV003738239]\|not specified [RCV004058824]	likely benign\|uncertain significance	8	56074061	56074061	Human		name
155689153	CV1826647	single nucleotide variant	NM_001023.4(RPS20):c.141T>C (p.Asn47=)	not specified [RCV004057236]	likely benign	8	56073731	56073731	Human		name
155709798	CV1830893	single nucleotide variant	NM_001023.4(RPS20):c.163C>A (p.Arg55=)	not specified [RCV004058129]	likely benign	8	56073709	56073709	Human		name
155745494	CV1831320	single nucleotide variant	NM_001023.4(RPS20):c.171T>A (p.Pro57=)	not specified [RCV004060616]	likely benign	8	56073701	56073701	Human		name
155732701	CV1834081	single nucleotide variant	NM_001023.4(RPS20):c.162T>G (p.Val54=)	not specified [RCV004058072]	likely benign	8	56073710	56073710	Human		name
155743385	CV1839393	single nucleotide variant	NM_001023.4(RPS20):c.183G>A (p.Leu61=)	not provided [RCV005097784]\|not specified [RCV004059973]	likely benign	8	56073267	56073267	Human		name
155669599	CV1842182	single nucleotide variant	NM_001023.4(RPS20):c.261A>G (p.Arg87=)	not provided [RCV003574965]\|not specified [RCV004062957]	likely benign	8	56073189	56073189	Human		name
155733453	CV1842623	single nucleotide variant	NM_001023.4(RPS20):c.189C>T (p.Ile63=)	not specified [RCV004060751]	likely benign	8	56073261	56073261	Human		name
155695520	CV1844646	single nucleotide variant	NM_001023.4(RPS20):c.225G>A (p.Lys75=)	not provided [RCV003101177]\|not specified [RCV004061944]	likely benign	8	56073225	56073225	Human		name
155748129	CV1846834	single nucleotide variant	NM_001023.4(RPS20):c.210T>C (p.Cys70=)	not specified [RCV004060363]	likely benign	8	56073240	56073240	Human		name
155726361	CV1848580	single nucleotide variant	NM_001023.4(RPS20):c.255C>T (p.His85=)	not specified [RCV004062218]	likely benign	8	56073195	56073195	Human		name
155683884	CV1849477	single nucleotide variant	NM_001023.4(RPS20):c.198A>G (p.Arg66=)	not specified [RCV004061667]	likely benign	8	56073252	56073252	Human		name
155706197	CV1850753	single nucleotide variant	NM_001023.4(RPS20):c.228G>C (p.Thr76=)	not specified [RCV004062568]	likely benign	8	56073222	56073222	Human		name
155724505	CV1851728	single nucleotide variant	NM_001023.4(RPS20):c.252T>A (p.Ile84=)	not specified [RCV004062118]	likely benign	8	56073198	56073198	Human		name
155686462	CV1852585	single nucleotide variant	NM_001023.4(RPS20):c.279T>C (p.Ser93=)	not specified [RCV004062247]	likely benign	8	56073171	56073171	Human		name
155666146	CV1855524	single nucleotide variant	NM_001023.4(RPS20):c.285T>G (p.Ser95=)	not specified [RCV004062447]	likely benign	8	56073165	56073165	Human		name
155674915	CV1855850	single nucleotide variant	NM_001023.4(RPS20):c.288G>A (p.Glu96=)	not specified [RCV004063059]	likely benign	8	56073162	56073162	Human		name
155689722	CV1856522	single nucleotide variant	NM_001023.4(RPS20):c.297G>A (p.Lys99=)	not provided [RCV003561047]\|not specified [RCV004065419]	likely benign	8	56073153	56073153	Human		name
329384533	CV2428954	single nucleotide variant	NM_001023.4(RPS20):c.222T>C (p.Ser74=)	RPS20-related disorder [RCV005399273]\|not specified [RCV004247481]	likely benign	8	56073228	56073228	Human		name , trait , alternate_id
329352529	CV2453154	single nucleotide variant	NM_001023.4(RPS20):c.126C>T (p.Gly42=)	not provided [RCV005101332]\|not specified [RCV004279534]	likely benign	8	56073746	56073746	Human		name
401774924	CV2728315	single nucleotide variant	NM_001023.4(RPS20):c.276C>T (p.His92=)	not specified [RCV004326096]	likely benign	8	56073174	56073174	Human		name
401867963	CV2787262	single nucleotide variant	NM_001023.4(RPS20):c.144C>G (p.Leu48=)	not specified [RCV004366231]	likely benign	8	56073728	56073728	Human		name
405226570	CV2892598	single nucleotide variant	NM_001023.4(RPS20):c.16A>T (p.Thr6Ser)	not provided [RCV003554767]	uncertain significance	8	56074147	56074147	Human		name
405153398	CV2894061	single nucleotide variant	NM_001023.4(RPS20):c.184A>C (p.Arg62=)	not provided [RCV003561883]\|not specified [RCV005273732]	likely benign	8	56073266	56073266	Human		name
405701437	CV3392167	single nucleotide variant	NM_001023.4(RPS20):c.123A>G (p.Arg41=)	not specified [RCV004521046]	likely benign	8	56073749	56073749	Human		name
405701455	CV3392170	single nucleotide variant	NM_001023.4(RPS20):c.285T>C (p.Ser95=)	not specified [RCV004521049]	likely benign	8	56073165	56073165	Human		name
407488029	CV3476197	single nucleotide variant	NM_001023.4(RPS20):c.17C>T (p.Thr6Ile)	not specified [RCV004665793]	uncertain significance	8	56074146	56074146	Human		name
407513777	CV3476201	single nucleotide variant	NM_001023.4(RPS20):c.135A>G (p.Glu45=)	not specified [RCV004674243]	likely benign	8	56073737	56073737	Human		name
597786024	CV3594350	single nucleotide variant	NM_001023.4(RPS20):c.174C>A (p.Thr58=)	not specified [RCV004854899]	likely benign	8	56073698	56073698	Human		name
597709902	CV3594352	single nucleotide variant	NM_001023.4(RPS20):c.115T>C (p.Leu39=)	not specified [RCV004860894]	likely benign	8	56073757	56073757	Human		name
598220257	CV3903005	single nucleotide variant	NM_001023.4(RPS20):c.258G>A (p.Lys86=)	not specified [RCV005272444]	likely benign	8	56073192	56073192	Human		name
598220275	CV3903008	single nucleotide variant	NM_001023.4(RPS20):c.273G>A (p.Leu91=)	not specified [RCV005272447]	likely benign	8	56073177	56073177	Human		name
15191254	CV736721	single nucleotide variant	NM_001023.4(RPS20):c.228G>A (p.Thr76=)	Familial colorectal cancer type X [RCV005367623]\|not provided [RCV000910192]\|not specified [RCV002465810]	benign\|likely benign	8	56073222	56073222	Human	1	name
15129154	CV736722	single nucleotide variant	NM_001023.4(RPS20):c.150G>A (p.Val50=)	Diamond-Blackfan anemia [RCV005359649]\|not provided [RCV000897393]\|not specified [RCV002465808]	likely benign	8	56073722	56073722	Human	2	name
15185701	CV766864	single nucleotide variant	NM_001023.4(RPS20):c.174C>T (p.Thr58=)	not provided [RCV000931134]\|not specified [RCV004659262]	likely benign	8	56073698	56073698	Human		name
26894243	CV834918	single nucleotide variant	NM_001023.4(RPS20):c.26C>T (p.Thr9Ile)	Hereditary nonpolyposis colon cancer [RCV004570266]\|not provided [RCV001063332]\|not specified [RCV004030490]	uncertain significance	8	56074137	56074137	Human	1	name
26885944	CV834919	single nucleotide variant	NM_001023.4(RPS20):c.11A>G (p.Lys4Arg)	not provided [RCV001054358]	uncertain significance	8	56074152	56074152	Human		name
126921330	CV1045609	single nucleotide variant	NM_001023.4(RPS20):c.43G>A (p.Val15Met)	not provided [RCV001374331]\|not specified [RCV004037610]	uncertain significance	8	56074120	56074120	Human		name
127270036	CV1097151	single nucleotide variant	NM_001023.4(RPS20):c.348T>C (p.Ile116=)	not provided [RCV001441290]\|not specified [RCV004038393]	likely benign	8	56073102	56073102	Human		name
151831448	CV1343638	single nucleotide variant	NM_001023.4(RPS20):c.31G>A (p.Val11Met)	not provided [RCV001920530]\|not specified [RCV004043323]	uncertain significance	8	56074132	56074132	Human		name
151848900	CV1358465	single nucleotide variant	NM_001023.4(RPS20):c.28C>G (p.Pro10Ala)	not provided [RCV001937086]	uncertain significance	8	56074135	56074135	Human		name
155715900	CV1785040	single nucleotide variant	NM_001023.4(RPS20):c.309C>T (p.Ser103=)	not specified [RCV004048317]	likely benign	8	56073141	56073141	Human		name
155729566	CV1786271	single nucleotide variant	NM_001023.4(RPS20):c.354T>C (p.Asp118=)	not specified [RCV004049100]	likely benign	8	56073096	56073096	Human		name
155676418	CV1796134	single nucleotide variant	NM_001023.4(RPS20):c.35A>G (p.Glu12Gly)	not specified [RCV004049206]	uncertain significance	8	56074128	56074128	Human		name
155707845	CV1798741	single nucleotide variant	NM_001023.4(RPS20):c.46G>A (p.Ala16Thr)	not specified [RCV004052001]	uncertain significance	8	56074117	56074117	Human		name
155737149	CV1805326	single nucleotide variant	NM_001023.4(RPS20):c.47C>T (p.Ala16Val)	not specified [RCV004052156]	uncertain significance	8	56074116	56074116	Human		name
155715476	CV1812236	single nucleotide variant	NM_001023.4(RPS20):c.68C>T (p.Thr23Ile)	not specified [RCV004052941]	uncertain significance	8	56074095	56074095	Human		name
155698583	CV1855093	single nucleotide variant	NM_001023.4(RPS20):c.306T>C (p.Thr102=)	not provided [RCV005098413]\|not specified [RCV004066435]	likely benign	8	56073144	56073144	Human		name
155698618	CV1855100	single nucleotide variant	NM_001023.4(RPS20):c.306T>G (p.Thr102=)	not specified [RCV004066437]	likely benign	8	56073144	56073144	Human		name
155667876	CV1856060	single nucleotide variant	NM_001023.4(RPS20):c.300G>A (p.Gln100=)	not specified [RCV004065503]	likely benign	8	56073150	56073150	Human		name
156378976	CV1876788	single nucleotide variant	NM_001023.4(RPS20):c.49A>G (p.Ile17Val)	not provided [RCV003066998]	uncertain significance	8	56074114	56074114	Human		name
156274130	CV1880489	single nucleotide variant	NM_001023.4(RPS20):c.357T>C (p.Ala119=)	not provided [RCV003060826]	likely benign	8	56073093	56073093	Human		name
10408145	CV205411	duplication	NM_001023.4(RPS20):c.147dup (p.Val50fs)	not provided [RCV000190884]\|not specified [RCV004020304]	uncertain significance	8	56073724	56073725	Human		name
155957853	CV2066495	single nucleotide variant	NM_001023.4(RPS20):c.73A>C (p.Thr25Pro)	not provided [RCV002816618]	uncertain significance	8	56074090	56074090	Human		name
401774921	CV2728314	single nucleotide variant	NM_001023.4(RPS20):c.84C>A (p.Asn28Lys)	not specified [RCV004326095]	uncertain significance	8	56074079	56074079	Human		name
401765042	CV2733456	single nucleotide variant	NM_001023.4(RPS20):c.91T>C (p.Ser31Pro)	not specified [RCV004330384]	uncertain significance	8	56074072	56074072	Human		name
401947448	CV2833479	single nucleotide variant	NM_001023.4(RPS20):c.29C>T (p.Pro10Leu)	Hereditary nonpolyposis colon cancer [RCV003466266]\|not specified [RCV005273702]	uncertain significance	8	56074134	56074134	Human	1	name
405125604	CV2886487	single nucleotide variant	NM_001023.4(RPS20):c.92C>T (p.Ser31Phe)	not provided [RCV003559539]\|not specified [RCV004369223]	uncertain significance	8	56074071	56074071	Human		name
405220749	CV3032204	single nucleotide variant	NM_001023.4(RPS20):c.38C>A (p.Pro13Gln)	not provided [RCV003709933]	uncertain significance	8	56074125	56074125	Human		name
405215276	CV3075376	single nucleotide variant	NM_001023.4(RPS20):c.71T>C (p.Leu24Pro)	not provided [RCV003732551]	uncertain significance	8	56074092	56074092	Human		name
407513769	CV3476196	single nucleotide variant	NM_001023.4(RPS20):c.46G>T (p.Ala16Ser)	not specified [RCV004674240]	uncertain significance	8	56074117	56074117	Human		name
407513774	CV3476199	single nucleotide variant	NM_001023.4(RPS20):c.345C>T (p.Thr115=)	not specified [RCV004674242]	likely benign	8	56073105	56073105	Human		name
597786009	CV3594346	single nucleotide variant	NM_001023.4(RPS20):c.67A>C (p.Thr23Pro)	not specified [RCV004854896]	uncertain significance	8	56074096	56074096	Human		name
597830382	CV3735391	indel	NM_001023.4(RPS20):c.3+11_3+13delinsGGG	Diamond-Blackfan anemia [RCV005055308]	uncertain significance	8	56074368	56074370	Human		name
597951156	CV3765338	single nucleotide variant	NM_001023.4(RPS20):c.52C>A (p.His18Asn)	not provided [RCV005120982]	uncertain significance	8	56074111	56074111	Human		name
597909596	CV3850010	single nucleotide variant	NM_001023.4(RPS20):c.36G>T (p.Glu12Asp)	not provided [RCV005203358]	uncertain significance	8	56074127	56074127	Human		name
598125479	CV3881627	single nucleotide variant	NM_001023.4(RPS20):c.98A>T (p.Glu33Val)	not specified [RCV005232533]	uncertain significance	8	56074065	56074065	Human		name
598220289	CV3903010	single nucleotide variant	NM_001023.4(RPS20):c.34G>A (p.Glu12Lys)	not specified [RCV005272449]	uncertain significance	8	56074129	56074129	Human		name
15194347	CV723152	single nucleotide variant	NM_001023.4(RPS20):c.333G>A (p.Glu111=)	RPS20-related disorder [RCV005392510]\|not provided [RCV000889198]\|not specified [RCV004028385]	likely benign	8	56073117	56073117	Human		name , trait , alternate_id
15200936	CV766863	single nucleotide variant	NM_001023.4(RPS20):c.351A>G (p.Ala117=)	not provided [RCV000935521]\|not specified [RCV004029625]	likely benign	8	56073099	56073099	Human		name
38499977	CV955468	duplication	NM_001023.4(RPS20):c.257dup (p.Arg87fs)	not provided [RCV001245340]	uncertain significance	8	56073192	56073193	Human		name
126754881	CV1008107	single nucleotide variant	NM_001023.4(RPS20):c.158C>A (p.Pro53Gln)	Hereditary nonpolyposis colon cancer [RCV004570797]\|not provided [RCV001327610]	uncertain significance	8	56073714	56073714	Human	1	name
127254512	CV1097153	indel	NM_001023.4(RPS20):c.103+7_103+8delinsTT	not provided [RCV001437262]	likely benign	8	56074052	56074053	Human		name
151750474	CV1359086	single nucleotide variant	NM_001023.4(RPS20):c.173C>G (p.Thr58Ser)	not provided [RCV001969139]	uncertain significance	8	56073699	56073699	Human		name
151782422	CV1369823	single nucleotide variant	NM_001023.4(RPS20):c.280C>T (p.Pro94Ser)	not provided [RCV001930565]	uncertain significance	8	56073170	56073170	Human		name
151860342	CV1374049	single nucleotide variant	NM_001023.4(RPS20):c.275A>G (p.His92Arg)	not provided [RCV001938459]\|not specified [RCV004043585]	uncertain significance	8	56073175	56073175	Human		name
151750133	CV1377775	single nucleotide variant	NM_001023.4(RPS20):c.131A>G (p.Lys44Arg)	not provided [RCV002043205]\|not specified [RCV004046694]	uncertain significance	8	56073741	56073741	Human		name
155723571	CV1804583	single nucleotide variant	NM_001023.4(RPS20):c.101A>C (p.Lys34Thr)	not specified [RCV004054359]	uncertain significance	8	56074062	56074062	Human		name
155672597	CV1809198	single nucleotide variant	NM_001023.4(RPS20):c.118A>G (p.Ile40Val)	not specified [RCV004050298]	uncertain significance	8	56073754	56073754	Human		name
155675464	CV1818517	single nucleotide variant	NM_001023.4(RPS20):c.122G>A (p.Arg41Lys)	not provided [RCV003098359]\|not specified [RCV004052767]	uncertain significance	8	56073750	56073750	Human		name
155718032	CV1827680	single nucleotide variant	NM_001023.4(RPS20):c.158C>T (p.Pro53Leu)	not provided [RCV003561015]\|not specified [RCV004057350]	uncertain significance	8	56073714	56073714	Human		name
155713435	CV1828143	single nucleotide variant	NM_001023.4(RPS20):c.166A>C (p.Met56Leu)	not specified [RCV004059818]	uncertain significance	8	56073706	56073706	Human		name
155720848	CV1834498	single nucleotide variant	NM_001023.4(RPS20):c.170C>T (p.Pro57Leu)	not specified [RCV004060564]	uncertain significance	8	56073702	56073702	Human		name
155699457	CV1836529	single nucleotide variant	NM_001023.4(RPS20):c.143T>C (p.Leu48Pro)	not specified [RCV004057855]	uncertain significance	8	56073729	56073729	Human		name
155678131	CV1845221	single nucleotide variant	NM_001023.4(RPS20):c.109G>A (p.Ala37Thr)	not specified [RCV004063930]	uncertain significance	8	56073763	56073763	Human		name
155712933	CV1845482	single nucleotide variant	NM_001023.4(RPS20):c.248G>T (p.Arg83Ile)	not specified [RCV004063992]	uncertain significance	8	56073202	56073202	Human		name
155671662	CV1845904	single nucleotide variant	NM_001023.4(RPS20):c.260G>A (p.Arg87Gln)	Hereditary nonpolyposis colon cancer [RCV004571153]\|not provided [RCV005098214]\|not specified [RCV004062923]	uncertain significance	8	56073190	56073190	Human	1	name
155691709	CV1848857	single nucleotide variant	NM_001023.4(RPS20):c.257A>C (p.Lys86Thr)	not specified [RCV004062800]	uncertain significance	8	56073193	56073193	Human		name
155691714	CV1848858	single nucleotide variant	NM_001023.4(RPS20):c.257A>G (p.Lys86Arg)	not specified [RCV004062801]	uncertain significance	8	56073193	56073193	Human		name
155704461	CV1849083	single nucleotide variant	NM_001023.4(RPS20):c.269A>G (p.Asp90Gly)	not specified [RCV004063677]	uncertain significance	8	56073181	56073181	Human		name
155685722	CV1850292	single nucleotide variant	NM_001023.4(RPS20):c.107G>A (p.Cys36Tyr)	not specified [RCV004060357]	uncertain significance	8	56073765	56073765	Human		name
401774918	CV2728313	single nucleotide variant	NM_001023.4(RPS20):c.182T>G (p.Leu61Trp)	not specified [RCV004326094]	uncertain significance	8	56073268	56073268	Human		name
401798273	CV2741337	single nucleotide variant	NM_001023.4(RPS20):c.266T>C (p.Ile89Thr)	not provided [RCV005061268]\|not specified [RCV003322500]	uncertain significance	8	56073184	56073184	Human		name
401867972	CV2787264	single nucleotide variant	NM_001023.4(RPS20):c.191C>A (p.Thr64Asn)	not specified [RCV004366233]	uncertain significance	8	56073259	56073259	Human		name
401947444	CV2833477	single nucleotide variant	NM_001023.4(RPS20):c.163C>G (p.Arg55Gly)	Hereditary nonpolyposis colon cancer [RCV003466264]	uncertain significance	8	56073709	56073709	Human	1	name
401947446	CV2833478	single nucleotide variant	NM_001023.4(RPS20):c.133G>A (p.Glu45Lys)	Hereditary nonpolyposis colon cancer [RCV003466265]	uncertain significance	8	56073739	56073739	Human	1	name
402479311	CV2853142	deletion	NM_001146227.3(RPS20):c.334-25_334-22del	not specified [RCV003494336]	likely benign	8	56069855	56069858	Human		name
405163813	CV2895522	single nucleotide variant	NM_001023.4(RPS20):c.193A>G (p.Thr65Ala)	not provided [RCV003562533]	uncertain significance	8	56073257	56073257	Human		name
405231846	CV2895812	single nucleotide variant	NM_001023.4(RPS20):c.157C>T (p.Pro53Ser)	not provided [RCV003555595]\|not specified [RCV004661696]	uncertain significance	8	56073715	56073715	Human		name
402479911	CV2991011	single nucleotide variant	NM_001023.4(RPS20):c.286G>T (p.Glu96Ter)	not provided [RCV003686489]	uncertain significance	8	56073164	56073164	Human		name
405025570	CV3079091	single nucleotide variant	NM_001023.4(RPS20):c.239T>A (p.Phe80Tyr)	not provided [RCV003738759]	uncertain significance	8	56073211	56073211	Human		name
405701448	CV3392169	single nucleotide variant	NM_001023.4(RPS20):c.243G>C (p.Gln81His)	not specified [RCV004521048]	uncertain significance	8	56073207	56073207	Human		name
405871333	CV3399365	single nucleotide variant	NM_001023.4(RPS20):c.236G>A (p.Arg79His)	Hereditary nonpolyposis colon cancer [RCV004574796]	uncertain significance	8	56073214	56073214	Human	1	name
405871334	CV3399366	single nucleotide variant	NM_001023.4(RPS20):c.110C>G (p.Ala37Gly)	Hereditary nonpolyposis colon cancer [RCV004574797]\|not specified [RCV005274044]	uncertain significance	8	56073762	56073762	Human	1	name
407481325	CV3415244	single nucleotide variant	NM_001023.4(RPS20):c.119T>G (p.Ile40Arg)	not specified [RCV004595959]	uncertain significance	8	56073753	56073753	Human		name
407488033	CV3476200	single nucleotide variant	NM_001023.4(RPS20):c.157C>G (p.Pro53Ala)	not specified [RCV004665794]	uncertain significance	8	56073715	56073715	Human		name
407488038	CV3476203	single nucleotide variant	NM_001023.4(RPS20):c.236G>T (p.Arg79Leu)	not specified [RCV004665795]	uncertain significance	8	56073214	56073214	Human		name
597709896	CV3594349	single nucleotide variant	NM_001023.4(RPS20):c.235C>A (p.Arg79Ser)	not specified [RCV004860893]	uncertain significance	8	56073215	56073215	Human		name
597786259	CV3594351	single nucleotide variant	NM_001023.4(RPS20):c.173C>T (p.Thr58Ile)	not specified [RCV004854900]	uncertain significance	8	56073699	56073699	Human		name
597947882	CV3771779	duplication	NM_001023.4(RPS20):c.334dup (p.Val112fs)	not provided [RCV005120305]	uncertain significance	8	56073115	56073116	Human		name
597871744	CV3835747	single nucleotide variant	NM_001023.4(RPS20):c.227C>T (p.Thr76Met)	not provided [RCV005176738]	uncertain significance	8	56073223	56073223	Human		name
597907565	CV3853595	single nucleotide variant	NM_001023.4(RPS20):c.128C>G (p.Ala43Gly)	not provided [RCV005203075]	uncertain significance	8	56073744	56073744	Human		name
597866727	CV3861257	single nucleotide variant	NM_001023.4(RPS20):c.104T>C (p.Val35Ala)	not provided [RCV005196605]	uncertain significance	8	56073768	56073768	Human		name
598220301	CV3903012	single nucleotide variant	NM_001023.4(RPS20):c.142C>T (p.Leu48Phe)	not specified [RCV005272451]	uncertain significance	8	56073730	56073730	Human		name
14708263	CV637301	single nucleotide variant	NM_001023.4(RPS20):c.154G>A (p.Gly52Arg)	not provided [RCV000809089]	uncertain significance	8	56073718	56073718	Human		name
26920382	CV834917	single nucleotide variant	NM_001023.4(RPS20):c.226A>T (p.Thr76Ser)	not provided [RCV001047460]	uncertain significance	8	56073224	56073224	Human		name
8633046	CV88260	single nucleotide variant	NM_001023.4(RPS20):c.191C>T (p.Thr64Ile)	Familial colorectal cancer type X [RCV005358241]\|not provided [RCV005183665]	uncertain significance\|not provided	8	56073259	56073259	Human	1	name
40888234	CV969273	single nucleotide variant	NM_001023.4(RPS20):c.251T>G (p.Ile84Ser)	Diamond-Blackfan anemia [RCV001267810]	pathogenic	8	56073199	56073199	Human	2	name
40888235	CV969274	single nucleotide variant	NM_001023.4(RPS20):c.251T>A (p.Ile84Asn)	Diamond-Blackfan anemia [RCV001267811]	pathogenic	8	56073199	56073199	Human	2	name
155715312	CV1784910	single nucleotide variant	NM_001023.4(RPS20):c.308C>A (p.Ser103Tyr)	not specified [RCV004048287]	uncertain significance	8	56073142	56073142	Human		name
155799399	CV1859794	single nucleotide variant	NM_001023.4(RPS20):c.356C>G (p.Ala119Gly)	not provided [RCV002571395]\|not specified [RCV002466038]	uncertain significance	8	56073094	56073094	Human		name
401765043	CV2733457	deletion	NM_001023.4(RPS20):c.32_33del (p.Val11fs)	not specified [RCV004330385]	uncertain significance	8	56074130	56074131	Human		name
405008603	CV2926919	single nucleotide variant	NM_001023.4(RPS20):c.333G>T (p.Glu111Asp)	not provided [RCV003576540]	uncertain significance	8	56073117	56073117	Human		name
597786014	CV3594347	single nucleotide variant	NM_001023.4(RPS20):c.346A>G (p.Ile116Val)	not specified [RCV004854897]	uncertain significance	8	56073104	56073104	Human		name
597786020	CV3594348	single nucleotide variant	NM_001023.4(RPS20):c.353A>G (p.Asp118Gly)	not specified [RCV004854898]	uncertain significance	8	56073097	56073097	Human		name
597889134	CV3856021	single nucleotide variant	NM_001023.4(RPS20):c.298C>T (p.Gln100Ter)	not provided [RCV005200266]	uncertain significance	8	56073152	56073152	Human		name
598220282	CV3903009	single nucleotide variant	NM_001023.4(RPS20):c.355G>T (p.Ala119Ser)	not specified [RCV005272448]	uncertain significance	8	56073095	56073095	Human		name
126763860	CV1008108	insertion	NM_001023.4(RPS20):c.25_26insTA (p.Thr9fs)	not provided [RCV001319412]	uncertain significance	8	56074137	56074138	Human		name
155738022	CV1831863	deletion	NM_001023.4(RPS20):c.181_182del (p.Leu61fs)	not specified [RCV004059321]	uncertain significance	8	56073268	56073269	Human		name
405701441	CV3392168	microsatellite	NM_001023.4(RPS20):c.143_144del (p.Leu48fs)	not specified [RCV004521047]	uncertain significance	8	56073728	56073729	Human		name
407513780	CV3476202	microsatellite	NM_001023.4(RPS20):c.136_140del (p.Lys46fs)	not specified [RCV004674244]	uncertain significance	8	56073732	56073736	Human		name
597830198	CV3746618	deletion	NM_001023.4(RPS20):c.137_140del (p.Lys46fs)	not provided [RCV005061904]	uncertain significance	8	56073732	56073735	Human		name
126912305	CV1037871	single nucleotide variant	NM_001146227.3(RPS20):c.410C>T (p.Pro137Leu)	not provided [RCV001356380]	uncertain significance	8	56069757	56069757	Human		name
150497579	CV1219429	single nucleotide variant	NM_001146227.3(RPS20):c.343T>C (p.Ser115Pro)	Familial colorectal cancer type X [RCV005361685]\|not provided [RCV001620098]\|not specified [RCV002465895]	benign	8	56069824	56069824	Human	1	name
401795772	CV2741328	single nucleotide variant	NM_001146227.3(RPS20):c.350A>T (p.Asp117Val)	not specified [RCV003322491]	uncertain significance	8	56069817	56069817	Human		name
405275177	CV3209111	single nucleotide variant	NM_001146227.3(RPS20):c.421C>G (p.Pro141Ala)	RPS20-related disorder [RCV003934509]	likely benign	8	56069746	56069746	Human		name , trait , alternate_id
598121900	CV3881624	single nucleotide variant	NM_001146227.3(RPS20):c.418T>C (p.Cys140Arg)	not specified [RCV005232530]	uncertain significance	8	56069749	56069749	Human		name
598122257	CV3888679	single nucleotide variant	NM_001146227.3(RPS20):c.419G>C (p.Cys140Ser)	not provided [RCV005244853]	uncertain significance	8	56069748	56069748	Human		name
14706202	CV637302	deletion	NM_001023.4(RPS20):c.138_140del (p.Lys46del)	not provided [RCV000803228]	uncertain significance	8	56073732	56073734	Human		name
38481100	CV934371	deletion	NM_001023.4(RPS20):c.283_285del (p.Ser95del)	not provided [RCV001206688]	uncertain significance	8	56073165	56073167	Human		name
156385913	CV1893920	deletion	NM_001023.4(RPS20):c.141_146del (p.Asn47_Leu48del)	not provided [RCV003093683]	uncertain significance	8	56073726	56073731	Human		name

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