Rras Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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410 records found for search term Rras

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
151236255	CV1319711	single nucleotide variant	NM_006270.5(RRAS):c.-5G>A	not specified [RCV001797916]	uncertain significance	19	49640103	49640103	Human		name
329955336	CV2671280	single nucleotide variant	NM_006270.5(RRAS):c.*5G>A	RRAS-related disorder [RCV003928971]\|not specified [RCV003236556]	likely benign\|uncertain significance	19	49635571	49635571	Human		name , trait , alternate_id
34896253	CV917300	single nucleotide variant	NM_006270.5(RRAS):c.*4A>G	RRAS-related disorder [RCV003928778]\|not provided [RCV001683750]\|not specified [RCV001193593]	benign	19	49635572	49635572	Human		name , trait , alternate_id
152034814	CV1669583	single nucleotide variant	NM_006270.5(RRAS):c.*230C>T	not provided [RCV002223574]	uncertain significance	19	49635346	49635346	Human		name
126760355	CV1034416	single nucleotide variant	NM_006270.5(RRAS):c.241+6G>A	Noonan syndrome [RCV001340385]	uncertain significance	19	49637037	49637037	Human	1	name
127239198	CV1084906	single nucleotide variant	NM_006270.5(RRAS):c.241+9G>A	Noonan syndrome [RCV001397485]	likely benign	19	49637034	49637034	Human	1	name
127276577	CV1106654	single nucleotide variant	NM_006270.5(RRAS):c.453+7G>A	Noonan syndrome [RCV001443860]	likely benign	19	49636612	49636612	Human	1	name
127276736	CV1106655	single nucleotide variant	NM_006270.5(RRAS):c.242-8C>T	Noonan syndrome [RCV001443973]	likely benign	19	49636934	49636934	Human	1	name
127328096	CV1148997	single nucleotide variant	NM_006270.5(RRAS):c.154-5G>A	Noonan syndrome [RCV001486613]\|not provided [RCV001773755]	likely benign	19	49637135	49637135	Human	1	name
151351869	CV1322079	single nucleotide variant	NM_006270.5(RRAS):c.573-4A>C	not specified [RCV001806701]	uncertain significance	19	49635664	49635664	Human		name
151351879	CV1322085	deletion	NM_006270.5(RRAS):c.344+6del	not specified [RCV001806707]	uncertain significance	19	49636818	49636818	Human		name
151888783	CV1402312	single nucleotide variant	NM_006270.5(RRAS):c.153+3A>G	Noonan syndrome [RCV001942658]	uncertain significance	19	49639943	49639943	Human	1	name
151772184	CV1427561	single nucleotide variant	NM_006270.5(RRAS):c.453+4C>T	Noonan syndrome [RCV001915089]	uncertain significance	19	49636615	49636615	Human	1	name
151866709	CV1447458	single nucleotide variant	NM_006270.5(RRAS):c.241+6G>C	Noonan syndrome [RCV001924695]	uncertain significance	19	49637037	49637037	Human	1	name
151747025	CV1478513	single nucleotide variant	NM_006270.5(RRAS):c.453+5G>A	Noonan syndrome [RCV002022945]\|RRAS-related disorder [RCV003893079]	likely benign\|uncertain significance	19	49636614	49636614	Human	1	name , trait , alternate_id
152081675	CV1607852	single nucleotide variant	NM_006270.5(RRAS):c.454-7C>T	Noonan syndrome [RCV002193100]	likely benign	19	49635859	49635859	Human	1	name
156166426	CV1929995	single nucleotide variant	NM_006270.5(RRAS):c.242-8C>G	Noonan syndrome [RCV002624566]	likely benign	19	49636934	49636934	Human	1	name
156441517	CV1944179	single nucleotide variant	NM_006270.5(RRAS):c.572+3G>A	Noonan syndrome [RCV003111844]	uncertain significance	19	49635731	49635731	Human	1	name
155948866	CV2104599	single nucleotide variant	NM_006270.5(RRAS):c.454-4C>T	Noonan syndrome [RCV002904946]\|RRAS-related disorder [RCV004754903]\|not specified [RCV005239541]	benign\|likely benign	19	49635856	49635856	Human	1	name , trait , alternate_id
156090589	CV2172824	single nucleotide variant	NM_006270.5(RRAS):c.572+5G>A	Noonan syndrome [RCV003054345]	uncertain significance	19	49635729	49635729	Human	1	name
405029851	CV2892384	single nucleotide variant	NM_006270.5(RRAS):c.154-6C>T	Noonan syndrome [RCV003529264]	likely benign	19	49637136	49637136	Human	1	name
402478943	CV3046625	single nucleotide variant	NM_006270.5(RRAS):c.345-5C>T	Noonan syndrome [RCV003642477]	likely benign	19	49636732	49636732	Human	1	name
597894849	CV3781810	single nucleotide variant	NM_006270.5(RRAS):c.242-4G>A	Noonan syndrome [RCV005126238]	likely benign	19	49636930	49636930	Human	1	name
13465072	CV468971	single nucleotide variant	NM_006270.5(RRAS):c.154-4C>G	Noonan syndrome [RCV000545294]\|not provided [RCV001541535]\|not specified [RCV001264470]	benign\|likely benign	19	49637134	49637134	Human	1	name
13465597	CV471085	single nucleotide variant	NM_006270.5(RRAS):c.454-9T>C	Noonan syndrome [RCV000547715]\|not provided [RCV001755809]	likely benign	19	49635861	49635861	Human	1	name
13801856	CV570929	single nucleotide variant	NM_006270.5(RRAS):c.454-6C>T	Noonan syndrome [RCV000699125]	likely benign\|uncertain significance	19	49635858	49635858	Human	1	name
15119043	CV695833	single nucleotide variant	NM_006270.5(RRAS):c.345-4G>A	Noonan syndrome [RCV000873816]\|not specified [RCV002265907]	benign\|likely benign	19	49636731	49636731	Human	1	name
15101720	CV776751	single nucleotide variant	NM_006270.5(RRAS):c.454-9T>A	Noonan syndrome [RCV001464025]\|RRAS-related disorder [RCV003970605]\|not provided [RCV004704345]	likely benign	19	49635861	49635861	Human	1	name , trait , alternate_id
26922327	CV851823	single nucleotide variant	NM_006270.5(RRAS):c.241+5G>A	Noonan syndrome [RCV001061868]	uncertain significance	19	49637038	49637038	Human	1	name
34896246	CV917557	single nucleotide variant	NM_006270.5(RRAS):c.345-2A>C	not specified [RCV001193588]	uncertain significance	19	49636729	49636729	Human		name
127231694	CV1087555	single nucleotide variant	NM_006270.5(RRAS):c.454-19G>A	Noonan syndrome [RCV002070262]\|not specified [RCV001420789]	likely benign\|uncertain significance	19	49635871	49635871	Human	1	name
150447305	CV1250809	single nucleotide variant	NM_006270.5(RRAS):c.454-19G>C	not provided [RCV001667314]	benign	19	49635871	49635871	Human		name
150466041	CV1277338	single nucleotide variant	NM_006270.5(RRAS):c.242-26G>A	not provided [RCV001710633]	benign	19	49636952	49636952	Human		name
150482903	CV1280089	single nucleotide variant	NM_006270.5(RRAS):c.241+54G>T	not provided [RCV001715098]	benign	19	49636989	49636989	Human		name
151663019	CV1330889	single nucleotide variant	NM_006270.5(RRAS):c.344+17G>A	Noonan syndrome [RCV003642980]\|not specified [RCV001825066]	benign\|likely benign	19	49636807	49636807	Human	1	name
151820725	CV1390930	single nucleotide variant	NM_006270.5(RRAS):c.153+17C>A	Noonan syndrome [RCV001992743]	likely benign\|uncertain significance	19	49639929	49639929	Human	1	name
151747445	CV1485351	single nucleotide variant	NM_006270.5(RRAS):c.573-16T>A	Noonan syndrome [RCV002006475]	uncertain significance	19	49635676	49635676	Human	1	name
152056191	CV1522996	single nucleotide variant	NM_006270.5(RRAS):c.573-19C>G	Noonan syndrome [RCV002167464]	likely benign	19	49635679	49635679	Human	1	name
152036987	CV1532194	single nucleotide variant	NM_006270.5(RRAS):c.573-13C>T	Noonan syndrome [RCV002125499]	likely benign	19	49635673	49635673	Human	1	name
152093694	CV1584939	single nucleotide variant	NM_006270.5(RRAS):c.345-19C>G	Noonan syndrome [RCV002114418]	likely benign	19	49636746	49636746	Human	1	name
152131950	CV1585001	single nucleotide variant	NM_006270.5(RRAS):c.572+20T>G	Noonan syndrome [RCV002082981]	likely benign	19	49635714	49635714	Human	1	name
152164329	CV1619821	single nucleotide variant	NM_006270.5(RRAS):c.453+18T>C	Noonan syndrome [RCV002181516]	likely benign	19	49636601	49636601	Human	1	name
152088548	CV1655691	single nucleotide variant	NM_006270.5(RRAS):c.241+13A>G	Noonan syndrome [RCV002193985]	likely benign	19	49637030	49637030	Human	1	name
152984265	CV1675218	deletion	NM_006270.5(RRAS):c.153+13del	not specified [RCV002238621]	likely benign\|uncertain significance	19	49639933	49639933	Human		name
156045566	CV1999227	duplication	NM_006270.5(RRAS):c.454-10dup	Noonan syndrome [RCV002659194]	benign	19	49635861	49635862	Human	1	name
156060823	CV2034529	single nucleotide variant	NM_006270.5(RRAS):c.153+10C>A	Noonan syndrome [RCV002736832]	likely benign	19	49639936	49639936	Human	1	name
156051452	CV2091451	single nucleotide variant	NM_006270.5(RRAS):c.573-15G>A	Noonan syndrome [RCV002886177]	likely benign	19	49635675	49635675	Human	1	name
156141384	CV2116829	single nucleotide variant	NM_006270.5(RRAS):c.345-14G>A	Noonan syndrome [RCV002914921]	uncertain significance	19	49636741	49636741	Human	1	name
156285890	CV2134134	single nucleotide variant	NM_006270.5(RRAS):c.453+17T>C	Noonan syndrome [RCV003009767]	likely benign	19	49636602	49636602	Human	1	name
156160052	CV2191740	single nucleotide variant	NM_006270.5(RRAS):c.572+13C>A	Noonan syndrome [RCV003040673]	likely benign	19	49635721	49635721	Human	1	name
401919270	CV2794831	single nucleotide variant	NM_006270.5(RRAS):c.454-13C>T	Noonan syndrome [RCV003528466]\|not specified [RCV003388506]	likely benign	19	49635865	49635865	Human	1	name
405026899	CV2869329	single nucleotide variant	NM_006270.5(RRAS):c.454-20C>T	Noonan syndrome [RCV003529063]	likely benign	19	49635872	49635872	Human	1	name
405033942	CV2911661	single nucleotide variant	NM_006270.5(RRAS):c.154-10A>T	Noonan syndrome [RCV003529668]	likely benign	19	49637140	49637140	Human	1	name
405015161	CV2916323	single nucleotide variant	NM_006270.5(RRAS):c.454-11C>G	Noonan syndrome [RCV003527657]	likely benign	19	49635863	49635863	Human	1	name
402486106	CV2955318	single nucleotide variant	NM_006270.5(RRAS):c.241+17T>C	Noonan syndrome [RCV003643324]	likely benign	19	49637026	49637026	Human	1	name
402489702	CV2973124	deletion	NM_006270.5(RRAS):c.573-16del	Noonan syndrome [RCV003643699]	likely benign	19	49635676	49635676	Human	1	name
402482197	CV3075841	single nucleotide variant	NM_006270.5(RRAS):c.241+20A>G	Noonan syndrome [RCV003642839]	likely benign	19	49637023	49637023	Human	1	name
405120209	CV3131457	single nucleotide variant	NM_006270.5(RRAS):c.153+18G>A	Noonan syndrome [RCV003837321]	likely benign	19	49639928	49639928	Human	1	name
596920806	CV3534224	single nucleotide variant	NM_006270.5(RRAS):c.345-11T>C	not specified [RCV004783443]	likely benign	19	49636738	49636738	Human		name
597865072	CV3767163	single nucleotide variant	NM_006270.5(RRAS):c.573-15G>C	Noonan syndrome [RCV005106685]	likely benign	19	49635675	49635675	Human	1	name
597961725	CV3795240	single nucleotide variant	NM_006270.5(RRAS):c.344+19G>C	Noonan syndrome [RCV005138932]	likely benign	19	49636805	49636805	Human	1	name
597971523	CV3802586	deletion	NM_006270.5(RRAS):c.242-17del	Noonan syndrome [RCV005142184]	likely benign	19	49636943	49636943	Human	1	name
597851841	CV3805607	single nucleotide variant	NM_006270.5(RRAS):c.345-15C>T	Noonan syndrome [RCV005145537]	likely benign	19	49636742	49636742	Human	1	name
597896830	CV3834651	single nucleotide variant	NM_006270.5(RRAS):c.454-12C>T	Noonan syndrome [RCV005180562]	likely benign	19	49635864	49635864	Human	1	name
597886715	CV3855201	single nucleotide variant	NM_006270.5(RRAS):c.572+10G>A	Noonan syndrome [RCV005199846]	likely benign	19	49635724	49635724	Human	1	name
13521828	CV487951	single nucleotide variant	NM_006270.5(RRAS):c.454-10C>G	Noonan syndrome [RCV001518555]\|not provided [RCV000590550]	benign	19	49635862	49635862	Human	1	name
13519895	CV487954	single nucleotide variant	NM_006270.5(RRAS):c.344+13G>A	Noonan syndrome [RCV002061984]\|not provided [RCV000586770]\|not specified [RCV001700163]	benign	19	49636811	49636811	Human	1	name
13520333	CV488002	single nucleotide variant	NM_006270.5(RRAS):c.573-12G>A	Noonan syndrome [RCV002061986]\|not provided [RCV000587608]	benign\|likely benign	19	49635672	49635672	Human	1	name
13520094	CV488004	single nucleotide variant	NM_006270.5(RRAS):c.453+20C>T	Noonan syndrome [RCV002061985]\|not provided [RCV000587129]	benign\|likely benign	19	49636599	49636599	Human	1	name
150441187	CV1265519	single nucleotide variant	NM_006270.5(RRAS):c.154-262G>A	not provided [RCV001679222]	benign	19	49637392	49637392	Human		name
150467781	CV1269289	single nucleotide variant	NM_006270.5(RRAS):c.154-169C>T	not provided [RCV001694697]	benign	19	49637299	49637299	Human		name
150476375	CV1271326	single nucleotide variant	NM_006270.5(RRAS):c.154-102T>G	not provided [RCV001696149]	benign	19	49637232	49637232	Human		name
150536026	CV1309099	duplication	NM_006270.5(RRAS):c.154-171dup	not provided [RCV001759306]	likely benign	19	49637300	49637301	Human		name
150536083	CV1309120	single nucleotide variant	NM_006270.5(RRAS):c.453+145A>G	not provided [RCV001759327]	likely benign	19	49636474	49636474	Human		name
155727073	CV1822412	single nucleotide variant	NM_006270.5(RRAS):c.6C>T (p.Ser2=)	not specified [RCV004055127]	likely benign	19	49640093	49640093	Human		name
38464021	CV960924	deletion	NM_006270.5(RRAS):c.344+6_344+7del	Noonan syndrome [RCV001247330]\|not specified [RCV001844277]	benign\|uncertain significance	19	49636817	49636818	Human	1	name
401717996	CV2728398	single nucleotide variant	NM_006270.5(RRAS):c.12G>A (p.Gly4=)	not specified [RCV004333421]	likely benign	19	49640087	49640087	Human		name
127303138	CV1128047	single nucleotide variant	NM_006270.5(RRAS):c.69C>T (p.Asp23=)	Noonan syndrome [RCV001454639]\|not specified [RCV004038535]	likely benign	19	49640030	49640030	Human	1	name
150534548	CV1308466	deletion	NM_006270.5(RRAS):c.454-44_454-43del	not provided [RCV001757510]	likely benign	19	49635895	49635896	Human		name
151806122	CV1359589	single nucleotide variant	NM_006270.5(RRAS):c.2T>A (p.Met1Lys)	Noonan syndrome [RCV002028540]	uncertain significance	19	49640097	49640097	Human	1	name
151745744	CV1401106	single nucleotide variant	NM_006270.5(RRAS):c.81C>T (p.Ser27=)	Noonan syndrome [RCV002022797]\|RRAS-related disorder [RCV003402044]\|not provided [RCV005225555]\|not specified [RCV004046073]	likely benign\|uncertain significance	19	49640018	49640018	Human	1	name , trait , alternate_id
151713546	CV1451079	single nucleotide variant	NM_006270.5(RRAS):c.30G>C (p.Gly10=)	Noonan syndrome [RCV002002465]	likely benign	19	49640069	49640069	Human	1	name
152166037	CV1524244	deletion	NM_006270.5(RRAS):c.345-19_345-18del	Noonan syndrome [RCV002141840]	likely benign	19	49636745	49636746	Human	1	name
152176083	CV1562289	single nucleotide variant	NM_006270.5(RRAS):c.42C>T (p.Pro14=)	Noonan syndrome [RCV002164223]	likely benign	19	49640057	49640057	Human	1	name
152109358	CV1563861	single nucleotide variant	NM_006270.5(RRAS):c.66G>A (p.Gly22=)	Noonan syndrome [RCV002174133]	likely benign	19	49640033	49640033	Human	1	name
152094262	CV1565725	single nucleotide variant	NM_006270.5(RRAS):c.43C>A (p.Arg15=)	Noonan syndrome [RCV002150990]\|RRAS-related disorder [RCV003951257]\|not specified [RCV004046997]	likely benign	19	49640056	49640056	Human	1	name , trait , alternate_id
152117215	CV1566501	single nucleotide variant	NM_006270.5(RRAS):c.75G>C (p.Pro25=)	Noonan syndrome [RCV002153805]	likely benign	19	49640024	49640024	Human	1	name
155716122	CV1785099	single nucleotide variant	NM_006270.5(RRAS):c.30G>A (p.Gly10=)	not specified [RCV004048334]	likely benign	19	49640069	49640069	Human		name
155674316	CV1810122	single nucleotide variant	NM_006270.5(RRAS):c.54A>G (p.Gly18=)	not specified [RCV004053155]	likely benign	19	49640045	49640045	Human		name
155704459	CV1810691	single nucleotide variant	NM_006270.5(RRAS):c.57T>G (p.Pro19=)	not specified [RCV004054114]	likely benign	19	49640042	49640042	Human		name
155705496	CV1811225	single nucleotide variant	NM_006270.5(RRAS):c.60G>A (p.Gly20=)	not specified [RCV004052728]	likely benign	19	49640039	49640039	Human		name
155699072	CV1813337	single nucleotide variant	NM_006270.5(RRAS):c.75G>A (p.Pro25=)	not specified [RCV004056441]	likely benign	19	49640024	49640024	Human		name
156352433	CV1870257	deletion	NM_006270.5(RRAS):c.242-12_242-11del	Noonan syndrome [RCV003064963]	likely benign	19	49636937	49636938	Human	1	name
156312752	CV1874567	single nucleotide variant	NM_006270.5(RRAS):c.1A>T (p.Met1Leu)	Noonan syndrome [RCV003062552]	uncertain significance	19	49640098	49640098	Human	1	name
156369176	CV2021177	single nucleotide variant	NM_006270.5(RRAS):c.1A>G (p.Met1Val)	Noonan syndrome [RCV002721396]	uncertain significance	19	49640098	49640098	Human	1	name
401908477	CV2801349	single nucleotide variant	NM_006270.5(RRAS):c.9C>G (p.Ser3Arg)	RRAS-related disorder [RCV003397590]	uncertain significance	19	49640090	49640090	Human		name , trait , alternate_id
405293183	CV3207264	single nucleotide variant	NM_006270.5(RRAS):c.39G>T (p.Arg13=)	RRAS-related disorder [RCV003931660]	likely benign	19	49640060	49640060	Human		name , trait , alternate_id
405272630	CV3210102	single nucleotide variant	NM_006270.5(RRAS):c.54A>C (p.Gly18=)	RRAS-related disorder [RCV003914351]	likely benign	19	49640045	49640045	Human		name , trait , alternate_id
405273258	CV3210364	single nucleotide variant	NM_006270.5(RRAS):c.57T>C (p.Pro19=)	RRAS-related disorder [RCV003914588]	likely benign	19	49640042	49640042	Human		name , trait , alternate_id
405273280	CV3210382	single nucleotide variant	NM_006270.5(RRAS):c.60G>C (p.Gly20=)	RRAS-related disorder [RCV003914603]	likely benign	19	49640039	49640039	Human		name , trait , alternate_id
405723593	CV3381251	single nucleotide variant	NM_006270.5(RRAS):c.51G>T (p.Gly17=)	Noonan syndrome [RCV005100542]\|not specified [RCV004524172]	likely benign	19	49640048	49640048	Human	1	name
597953771	CV3795616	single nucleotide variant	NM_006270.5(RRAS):c.1A>C (p.Met1Leu)	Noonan syndrome [RCV005136626]	uncertain significance	19	49640098	49640098	Human	1	name
597874142	CV3816798	microsatellite	NM_006270.5(RRAS):c.453+16_453+17del	Noonan syndrome [RCV005148851]	likely benign	19	49636602	49636603	Human		name
597914308	CV3833913	single nucleotide variant	NM_006270.5(RRAS):c.2T>G (p.Met1Arg)	Noonan syndrome [RCV005183272]	uncertain significance	19	49640097	49640097	Human	1	name
597943429	CV3847674	single nucleotide variant	NM_006270.5(RRAS):c.99G>A (p.Val33=)	Noonan syndrome [RCV005188402]	likely benign	19	49640000	49640000	Human	1	name
617153234	CV4018630	deletion	NM_006270.5(RRAS):c.153+12_153+21del	not specified [RCV005418892]	likely benign	19	49639925	49639934	Human		name
13615422	CV533228	single nucleotide variant	NM_006270.5(RRAS):c.37C>A (p.Arg13=)	Noonan syndrome [RCV000632775]	likely benign	19	49640062	49640062	Human	1	name
15144297	CV694478	single nucleotide variant	NM_006270.5(RRAS):c.54A>T (p.Gly18=)	Noonan syndrome [RCV000878196]\|not provided [RCV001720267]\|not specified [RCV001193591]	benign\|likely benign	19	49640045	49640045	Human	1	name
26887203	CV847858	single nucleotide variant	NM_006270.5(RRAS):c.94C>T (p.Leu32=)	Noonan syndrome [RCV001044726]\|RRAS-related disorder [RCV003938413]\|not specified [RCV004031369]	likely benign\|uncertain significance	19	49640005	49640005	Human	1	name , trait , alternate_id
151724439	CV1514933	duplication	NM_006270.5(RRAS):c.74dup (p.Pro26fs)	Noonan syndrome [RCV001983506]	uncertain significance	19	49640024	49640025	Human	1	name
152163383	CV1561346	single nucleotide variant	NM_006270.5(RRAS):c.291C>T (p.Tyr97=)	Noonan syndrome [RCV002104220]\|not specified [RCV005266191]	likely benign	19	49636877	49636877	Human	1	name
152137087	CV1603673	single nucleotide variant	NM_006270.5(RRAS):c.102C>T (p.Val34=)	Noonan syndrome [RCV002218865]	likely benign	19	49639997	49639997	Human	1	name
155732641	CV1834064	single nucleotide variant	NM_006270.5(RRAS):c.162C>T (p.Phe54=)	Noonan syndrome [RCV003121006]\|not specified [RCV004058066]	likely benign	19	49637122	49637122	Human	1	name
155720845	CV1840585	single nucleotide variant	NM_006270.5(RRAS):c.216G>A (p.Val72=)	not specified [RCV004061102]	likely benign	19	49637068	49637068	Human		name
155714733	CV1849255	single nucleotide variant	NM_006270.5(RRAS):c.270C>T (p.Phe90=)	Noonan syndrome [RCV003643023]\|not specified [RCV004063719]	likely benign	19	49636898	49636898	Human	1	name
155724381	CV1851709	single nucleotide variant	NM_006270.5(RRAS):c.252C>T (p.Thr84=)	Noonan syndrome [RCV003101926]\|not specified [RCV004062113]	likely benign	19	49636916	49636916	Human	1	name
155678916	CV1854084	single nucleotide variant	NM_006270.5(RRAS):c.273G>T (p.Gly91=)	not specified [RCV004064073]	likely benign	19	49636895	49636895	Human		name
156419047	CV1929271	single nucleotide variant	NM_006270.5(RRAS):c.288G>A (p.Gln96=)	Noonan syndrome [RCV002612260]	likely benign	19	49636880	49636880	Human	1	name
401717991	CV2728397	single nucleotide variant	NM_006270.5(RRAS):c.13G>A (p.Ala5Thr)	not specified [RCV004333420]	uncertain significance	19	49640086	49640086	Human		name
405723567	CV3381248	single nucleotide variant	NM_006270.5(RRAS):c.14C>G (p.Ala5Gly)	not specified [RCV004524169]	uncertain significance	19	49640085	49640085	Human		name
405723579	CV3381249	single nucleotide variant	NM_006270.5(RRAS):c.17C>T (p.Ala6Val)	not specified [RCV004524170]	uncertain significance	19	49640082	49640082	Human		name
597963705	CV3837730	single nucleotide variant	NM_006270.5(RRAS):c.198C>T (p.Tyr66=)	Noonan syndrome [RCV005193712]	likely benign	19	49637086	49637086	Human	1	name
13498505	CV469940	single nucleotide variant	NM_006270.5(RRAS):c.243C>T (p.Ile81=)	Noonan syndrome [RCV000529197]\|not specified [RCV002469185]	benign\|likely benign	19	49636925	49636925	Human	1	name
13468806	CV469944	single nucleotide variant	NM_006270.5(RRAS):c.201G>A (p.Thr67=)	Noonan syndrome [RCV000559966]\|not specified [RCV004023773]	likely benign	19	49637083	49637083	Human	1	name
13615438	CV533226	single nucleotide variant	NM_006270.5(RRAS):c.231C>A (p.Ala77=)	Noonan syndrome [RCV000632783]\|not specified [RCV004025418]	likely benign	19	49637053	49637053	Human	1	name
13615440	CV533652	single nucleotide variant	NM_006270.5(RRAS):c.174C>T (p.Tyr58=)	Noonan syndrome [RCV000632784]\|not provided [RCV001756048]\|not specified [RCV001264567]	benign\|likely benign	19	49637110	49637110	Human	1	name
15141183	CV694477	single nucleotide variant	NM_006270.5(RRAS):c.255G>A (p.Ala85=)	Noonan syndrome [RCV000877627]\|RRAS-related disorder [RCV003955760]\|not specified [RCV001527016]	benign\|likely benign	19	49636913	49636913	Human	1	name , trait , alternate_id
26886410	CV847859	single nucleotide variant	NM_006270.5(RRAS):c.11G>C (p.Gly4Ala)	Noonan syndrome [RCV001044204]\|not specified [RCV004031348]	uncertain significance	19	49640088	49640088	Human	1	name
42723993	CV984002	single nucleotide variant	NM_006270.5(RRAS):c.10G>T (p.Gly4Trp)	Noonan syndrome [RCV001863160]\|not specified [RCV001290633]	uncertain significance	19	49640089	49640089	Human	1	name
127234904	CV1084903	single nucleotide variant	NM_006270.5(RRAS):c.492C>T (p.His164=)	Noonan syndrome [RCV001396518]	likely benign	19	49635814	49635814	Human	1	name
127282030	CV1084904	single nucleotide variant	NM_006270.5(RRAS):c.351C>T (p.Asn117=)	Noonan syndrome [RCV001410849]	likely benign	19	49636721	49636721	Human	1	name
127273243	CV1084905	single nucleotide variant	NM_006270.5(RRAS):c.324C>T (p.Phe108=)	Noonan syndrome [RCV001405960]\|not specified [RCV004656586]	likely benign	19	49636844	49636844	Human	1	name
127255493	CV1106652	single nucleotide variant	NM_006270.5(RRAS):c.543G>A (p.Glu181=)	Noonan syndrome [RCV001426597]\|not specified [RCV004038239]	likely benign	19	49635763	49635763	Human	1	name
127245299	CV1106653	single nucleotide variant	NM_006270.5(RRAS):c.534C>T (p.Asn178=)	Noonan syndrome [RCV001424281]	likely benign	19	49635772	49635772	Human	1	name
127336587	CV1128045	single nucleotide variant	NM_006270.5(RRAS):c.495C>T (p.His165=)	Noonan syndrome [RCV001475069]\|RRAS-related disorder [RCV004754763]\|not provided [RCV003426131]\|not specified [RCV004656606]	likely benign	19	49635811	49635811	Human	1	name , trait , alternate_id
127309974	CV1128046	single nucleotide variant	NM_006270.5(RRAS):c.408C>G (p.Pro136=)	Noonan syndrome [RCV001463757]	likely benign	19	49636664	49636664	Human	1	name
127288608	CV1148996	single nucleotide variant	NM_006270.5(RRAS):c.540C>T (p.Asp180=)	Noonan syndrome [RCV001495311]\|not specified [RCV004037351]	likely benign	19	49635766	49635766	Human	1	name
151854061	CV1370819	single nucleotide variant	NM_006270.5(RRAS):c.98T>C (p.Val33Ala)	Noonan syndrome [RCV001904467]	uncertain significance	19	49640001	49640001	Human	1	name
151879614	CV1395631	single nucleotide variant	NM_006270.5(RRAS):c.363G>A (p.Lys121=)	Noonan syndrome [RCV001999363]\|not specified [RCV004045935]	likely benign	19	49636709	49636709	Human	1	name
151767980	CV1434150	single nucleotide variant	NM_006270.5(RRAS):c.38G>A (p.Arg13Gln)	Noonan syndrome [RCV001874161]\|not specified [RCV004847838]	uncertain significance	19	49640061	49640061	Human	1	name
151874110	CV1493489	single nucleotide variant	NM_006270.5(RRAS):c.53G>A (p.Gly18Glu)	Noonan syndrome [RCV001906853]	uncertain significance	19	49640046	49640046	Human	1	name
151770540	CV1502481	single nucleotide variant	NM_006270.5(RRAS):c.29G>C (p.Gly10Ala)	Noonan syndrome [RCV001896294]	uncertain significance	19	49640070	49640070	Human	1	name
151728538	CV1515736	single nucleotide variant	NM_006270.5(RRAS):c.70C>T (p.Pro24Ser)	Noonan syndrome [RCV001983958]	uncertain significance	19	49640029	49640029	Human	1	name
152109980	CV1617590	single nucleotide variant	NM_006270.5(RRAS):c.624G>A (p.Lys208=)	Noonan syndrome [RCV002116424]\|not specified [RCV004700654]	likely benign	19	49635609	49635609	Human	1	name
152097080	CV1628013	single nucleotide variant	NM_006270.5(RRAS):c.652C>T (p.Leu218=)	Noonan syndrome [RCV002195063]\|not specified [RCV004045563]	likely benign	19	49635581	49635581	Human	1	name
152133607	CV1651972	single nucleotide variant	NM_006270.5(RRAS):c.516G>A (p.Ser172=)	Noonan syndrome [RCV002199651]\|RRAS-related disorder [RCV003941330]\|not specified [RCV004045548]	likely benign	19	49635790	49635790	Human	1	name , trait , alternate_id
152173625	CV1655643	single nucleotide variant	NM_006270.5(RRAS):c.645C>T (p.Cys215=)	Noonan syndrome [RCV002184237]\|RRAS-related disorder [RCV003916364]\|not specified [RCV004047115]	likely benign	19	49635588	49635588	Human	1	name , trait , alternate_id
155749531	CV1773911	single nucleotide variant	NM_006270.5(RRAS):c.77C>T (p.Pro26Leu)	Noonan syndrome [RCV002304748]	uncertain significance	19	49640022	49640022	Human	1	name
155726389	CV1791062	single nucleotide variant	NM_006270.5(RRAS):c.420C>T (p.Val140=)	Noonan syndrome [RCV005096510]\|not specified [RCV004051897]	likely benign	19	49636652	49636652	Human	1	name
155703282	CV1791497	single nucleotide variant	NM_006270.5(RRAS):c.441G>A (p.Glu147=)	not specified [RCV004050671]	likely benign	19	49636631	49636631	Human		name
155695579	CV1793862	single nucleotide variant	NM_006270.5(RRAS):c.399C>T (p.Asp133=)	not provided [RCV004703269]\|not specified [RCV004050566]	likely benign	19	49636673	49636673	Human		name
155682862	CV1801146	single nucleotide variant	NM_006270.5(RRAS):c.62C>T (p.Pro21Leu)	not specified [RCV004053804]	uncertain significance	19	49640037	49640037	Human		name
155673043	CV1801215	single nucleotide variant	NM_006270.5(RRAS):c.630C>T (p.Gly210=)	Noonan syndrome [RCV003098198]\|RRAS-related disorder [RCV003896143]\|not specified [RCV004053822]	likely benign	19	49635603	49635603	Human	1	name , trait , alternate_id
155745892	CV1803053	single nucleotide variant	NM_006270.5(RRAS):c.53G>T (p.Gly18Val)	not specified [RCV004053023]	uncertain significance	19	49640046	49640046	Human		name
155721978	CV1805625	single nucleotide variant	NM_006270.5(RRAS):c.483C>T (p.Gly161=)	not specified [RCV004052215]	likely benign	19	49635823	49635823	Human		name
155679892	CV1807085	single nucleotide variant	NM_006270.5(RRAS):c.585A>G (p.Glu195=)	not specified [RCV004054197]	likely benign	19	49635648	49635648	Human		name
155711379	CV1807855	single nucleotide variant	NM_006270.5(RRAS):c.642C>T (p.Pro214=)	Noonan syndrome [RCV003103296]\|not specified [RCV004053977]	likely benign	19	49635591	49635591	Human	1	name
155740373	CV1809361	single nucleotide variant	NM_006270.5(RRAS):c.498G>A (p.Val166=)	Noonan syndrome [RCV003096552]\|not specified [RCV004050333]	likely benign\|uncertain significance	19	49635808	49635808	Human	1	name
155715434	CV1812222	single nucleotide variant	NM_006270.5(RRAS):c.68A>C (p.Asp23Ala)	not specified [RCV004052939]	uncertain significance	19	49640031	49640031	Human		name
155699074	CV1824533	single nucleotide variant	NM_006270.5(RRAS):c.88C>G (p.His30Asp)	not specified [RCV004054848]	uncertain significance	19	49640011	49640011	Human		name
155698513	CV1855076	single nucleotide variant	NM_006270.5(RRAS):c.306C>T (p.His102=)	Noonan syndrome [RCV003528402]\|not specified [RCV004066433]	likely benign	19	49636862	49636862	Human	1	name
155799099	CV1862333	single nucleotide variant	NM_006270.5(RRAS):c.43C>T (p.Arg15Trp)	Noonan syndrome [RCV002471738]	uncertain significance	19	49640056	49640056	Human	1	name
156161035	CV1925345	single nucleotide variant	NM_006270.5(RRAS):c.50G>T (p.Gly17Val)	Noonan syndrome [RCV002664248]	uncertain significance	19	49640049	49640049	Human	1	name
156127666	CV2031401	single nucleotide variant	NM_006270.5(RRAS):c.480C>T (p.Phe160=)	Noonan syndrome [RCV002740444]\|not specified [RCV004067718]	likely benign	19	49635826	49635826	Human	1	name
156048950	CV2059970	single nucleotide variant	NM_006270.5(RRAS):c.44G>A (p.Arg15Gln)	Noonan syndrome [RCV002796699]	uncertain significance	19	49640055	49640055	Human	1	name
156165693	CV2090876	single nucleotide variant	NM_006270.5(RRAS):c.44G>C (p.Arg15Pro)	Noonan syndrome [RCV002872825]	uncertain significance	19	49640055	49640055	Human	1	name
156314864	CV2120275	single nucleotide variant	NM_006270.5(RRAS):c.84G>C (p.Glu28Asp)	Noonan syndrome [RCV002962835]	uncertain significance	19	49640015	49640015	Human	1	name
329369279	CV2429176	single nucleotide variant	NM_006270.5(RRAS):c.507T>C (p.Phe169=)	not specified [RCV004247605]	likely benign	19	49635799	49635799	Human		name
401717987	CV2728395	single nucleotide variant	NM_006270.5(RRAS):c.375G>A (p.Gln125=)	not specified [RCV004333418]	likely benign	19	49636697	49636697	Human		name
401717989	CV2728396	single nucleotide variant	NM_006270.5(RRAS):c.95T>A (p.Leu32Gln)	not specified [RCV004333419]	uncertain significance	19	49640004	49640004	Human		name
405028812	CV2881988	single nucleotide variant	NM_006270.5(RRAS):c.609C>T (p.Pro203=)	Noonan syndrome [RCV003529242]\|RRAS-related disorder [RCV003901169]	likely benign	19	49635624	49635624	Human	1	name , trait , alternate_id
405030513	CV2883215	single nucleotide variant	NM_006270.5(RRAS):c.567T>C (p.Ala189=)	Noonan syndrome [RCV003529386]\|not specified [RCV004661690]	likely benign	19	49635739	49635739	Human	1	name
405030296	CV2889832	single nucleotide variant	NM_006270.5(RRAS):c.516G>T (p.Ser172=)	Noonan syndrome [RCV003529369]	likely benign	19	49635790	49635790	Human	1	name
402490172	CV2976886	single nucleotide variant	NM_006270.5(RRAS):c.28G>A (p.Gly10Arg)	Noonan syndrome [RCV003643747]\|not specified [RCV004857988]	uncertain significance	19	49640071	49640071	Human	1	name
405060019	CV3129410	single nucleotide variant	NM_006270.5(RRAS):c.576A>G (p.Lys192=)	Noonan syndrome [RCV003832679]	uncertain significance	19	49635657	49635657	Human	1	name
402478734	CV3174345	deletion	NM_006270.5(RRAS):c.262del (p.Glu88fs)	Noonan syndrome [RCV003875692]	uncertain significance	19	49636906	49636906	Human	1	name
405723615	CV3381254	single nucleotide variant	NM_006270.5(RRAS):c.79A>T (p.Ser27Cys)	not specified [RCV004524175]	uncertain significance	19	49640020	49640020	Human		name
405723627	CV3381255	single nucleotide variant	NM_006270.5(RRAS):c.82G>A (p.Glu28Lys)	not specified [RCV004524176]	uncertain significance	19	49640017	49640017	Human		name
407488441	CV3476301	single nucleotide variant	NM_006270.5(RRAS):c.579C>T (p.Tyr193=)	not specified [RCV004665867]	likely benign	19	49635654	49635654	Human		name
408365778	CV3509790	single nucleotide variant	NM_006270.5(RRAS):c.372G>T (p.Thr124=)	RRAS-related disorder [RCV004755253]	likely benign	19	49636700	49636700	Human		name , trait , alternate_id
597786479	CV3604467	single nucleotide variant	NM_006270.5(RRAS):c.345T>C (p.Ser115=)	not specified [RCV004854990]	likely benign	19	49636727	49636727	Human		name
597710459	CV3604469	single nucleotide variant	NM_006270.5(RRAS):c.411T>C (p.Val137=)	not specified [RCV004860959]	likely benign	19	49636661	49636661	Human		name
597832403	CV3751368	single nucleotide variant	NM_006270.5(RRAS):c.43C>G (p.Arg15Gly)	Noonan syndrome [RCV005084914]	uncertain significance	19	49640056	49640056	Human	1	name
597860225	CV3770059	single nucleotide variant	NM_006270.5(RRAS):c.92A>G (p.Lys31Arg)	Noonan syndrome [RCV005105911]	uncertain significance	19	49640007	49640007	Human	1	name
597955147	CV3787036	single nucleotide variant	NM_006270.5(RRAS):c.53G>C (p.Gly18Ala)	Noonan syndrome [RCV005121920]	uncertain significance	19	49640046	49640046	Human	1	name
597888141	CV3787690	single nucleotide variant	NM_006270.5(RRAS):c.393C>T (p.Asp131=)	Noonan syndrome [RCV005125257]	likely benign	19	49636679	49636679	Human	1	name
597974705	CV3798522	single nucleotide variant	NM_006270.5(RRAS):c.465A>C (p.Ser155=)	Noonan syndrome [RCV005144110]	likely benign	19	49635841	49635841	Human	1	name
597921117	CV3852110	single nucleotide variant	NM_006270.5(RRAS):c.360C>T (p.Gly120=)	Noonan syndrome [RCV005205090]	likely benign	19	49636712	49636712	Human	1	name
597872916	CV3859172	single nucleotide variant	NM_006270.5(RRAS):c.64G>A (p.Gly22Arg)	Noonan syndrome [RCV005197761]	uncertain significance	19	49640035	49640035	Human	1	name
13504193	CV468963	single nucleotide variant	NM_006270.5(RRAS):c.408C>T (p.Pro136=)	Noonan syndrome [RCV001084941]\|not provided [RCV000588533]\|not specified [RCV004023775]	benign\|likely benign	19	49636664	49636664	Human	1	name
13503692	CV469932	single nucleotide variant	NM_006270.5(RRAS):c.600G>A (p.Pro200=)	Noonan syndrome [RCV000557852]\|RRAS-related disorder [RCV003942742]\|not specified [RCV001174704]	benign\|likely benign	19	49635633	49635633	Human	1	name , trait , alternate_id
13464795	CV469937	single nucleotide variant	NM_006270.5(RRAS):c.379C>T (p.Leu127=)	Noonan syndrome [RCV001079480]\|RRAS-related disorder [RCV003925593]\|not provided [RCV000588817]\|not specified [RCV004023774]	benign\|likely benign	19	49636693	49636693	Human	1	name , trait , alternate_id
13521667	CV487955	single nucleotide variant	NM_006270.5(RRAS):c.333C>T (p.Asn111=)	Noonan syndrome [RCV001518485]\|not provided [RCV000589712]\|not specified [RCV001195552]	benign	19	49636835	49636835	Human	1	name
13615426	CV533227	single nucleotide variant	NM_006270.5(RRAS):c.64G>T (p.Gly22Trp)	Noonan syndrome [RCV000632777]\|not provided [RCV003411498]	uncertain significance	19	49640035	49640035	Human	1	name
13801829	CV573235	single nucleotide variant	NM_006270.5(RRAS):c.49G>T (p.Gly17Trp)	Noonan syndrome [RCV000697940]\|not specified [RCV001824868]	conflicting interpretations of pathogenicity\|uncertain significance	19	49640050	49640050	Human	1	name
14699570	CV624660	single nucleotide variant	NM_006270.5(RRAS):c.61C>T (p.Pro21Ser)	Noonan syndrome [RCV001352311]\|not provided [RCV000788980]	uncertain significance	19	49640038	49640038	Human	1	name
14719059	CV648254	single nucleotide variant	NM_006270.5(RRAS):c.74C>T (p.Pro25Leu)	Noonan syndrome [RCV000796007]\|not specified [RCV001280656]	likely benign\|uncertain significance	19	49640025	49640025	Human	1	name
15133796	CV694475	single nucleotide variant	NM_006270.5(RRAS):c.516G>C (p.Ser172=)	Noonan syndrome [RCV000876369]\|not provided [RCV001090747]\|not specified [RCV001193589]	benign\|likely benign	19	49635790	49635790	Human	1	name
15148043	CV694476	single nucleotide variant	NM_006270.5(RRAS):c.396C>T (p.Arg132=)	Noonan syndrome [RCV001423780]\|RRAS-related disorder [RCV003895397]\|not specified [RCV004027918]	benign\|likely benign	19	49636676	49636676	Human	1	name , trait , alternate_id
15188226	CV705168	single nucleotide variant	NM_006270.5(RRAS):c.372G>A (p.Thr124=)	Noonan syndrome [RCV000953819]\|not specified [RCV001328444]	benign\|likely benign	19	49636700	49636700	Human	1	name
15125598	CV772808	single nucleotide variant	NM_006270.5(RRAS):c.438G>T (p.Leu146=)	Noonan syndrome [RCV001399350]	likely benign	19	49636634	49636634	Human	1	name
126757690	CV998711	single nucleotide variant	NM_006270.5(RRAS):c.67G>A (p.Asp23Asn)	Noonan syndrome [RCV001308499]	uncertain significance	19	49640032	49640032	Human	1	name
150451721	CV1207261	deletion	NM_006270.5(RRAS):c.423del (p.Asn142fs)	not specified [RCV001582391]	uncertain significance	19	49636649	49636649	Human		name
151852139	CV1360911	single nucleotide variant	NM_006270.5(RRAS):c.233G>A (p.Arg78Gln)	Noonan syndrome [RCV001904239]	uncertain significance	19	49637051	49637051	Human	1	name
151817978	CV1390472	single nucleotide variant	NM_006270.5(RRAS):c.200C>T (p.Thr67Met)	Noonan syndrome [RCV001954468]\|not specified [RCV004847866]	uncertain significance	19	49637084	49637084	Human	1	name
151859101	CV1403466	single nucleotide variant	NM_006270.5(RRAS):c.227C>T (p.Pro76Leu)	Noonan syndrome [RCV001979892]	uncertain significance	19	49637057	49637057	Human	1	name
151730948	CV1421236	single nucleotide variant	NM_006270.5(RRAS):c.163G>A (p.Val55Met)	Noonan syndrome [RCV001892244]	uncertain significance	19	49637121	49637121	Human	1	name
151862267	CV1457957	single nucleotide variant	NM_006270.5(RRAS):c.296G>A (p.Arg99His)	Noonan syndrome [RCV001938704]	uncertain significance	19	49636872	49636872	Human	1	name
151782822	CV1486928	single nucleotide variant	NM_006270.5(RRAS):c.232C>T (p.Arg78Trp)	Noonan syndrome [RCV001916038]\|not specified [RCV004042726]	uncertain significance	19	49637052	49637052	Human	1	name
151834537	CV1505093	single nucleotide variant	NM_006270.5(RRAS):c.115G>T (p.Gly39Cys)	Noonan syndrome [RCV001976991]	uncertain significance	19	49639984	49639984	Human	1	name
155672912	CV1801188	single nucleotide variant	NM_006270.5(RRAS):c.121G>A (p.Gly41Ser)	not specified [RCV004053817]	uncertain significance	19	49639978	49639978	Human		name
155690601	CV1850723	single nucleotide variant	NM_006270.5(RRAS):c.220G>A (p.Gly74Ser)	not specified [RCV004061762]	uncertain significance	19	49637064	49637064	Human		name
155725781	CV1851977	single nucleotide variant	NM_006270.5(RRAS):c.254C>T (p.Ala85Val)	Noonan syndrome [RCV005098194]\|not specified [RCV004062187]	uncertain significance	19	49636914	49636914	Human	1	name
156320195	CV1872990	single nucleotide variant	NM_006270.5(RRAS):c.209G>A (p.Cys70Tyr)	Noonan syndrome [RCV003063009]\|not specified [RCV004070343]	uncertain significance	19	49637075	49637075	Human	1	name
156345583	CV1995173	single nucleotide variant	NM_006270.5(RRAS):c.295C>T (p.Arg99Cys)	Noonan syndrome [RCV002650555]\|not specified [RCV004066774]	uncertain significance	19	49636873	49636873	Human	1	name
156005248	CV2064761	single nucleotide variant	NM_006270.5(RRAS):c.292A>G (p.Met98Val)	Noonan syndrome [RCV002843597]	uncertain significance	19	49636876	49636876	Human	1	name
329368075	CV2429174	single nucleotide variant	NM_006270.5(RRAS):c.275C>T (p.Ala92Val)	not specified [RCV004247603]	uncertain significance	19	49636893	49636893	Human		name
401942596	CV2839683	single nucleotide variant	NM_006270.5(RRAS):c.259C>G (p.Gln87Glu)	not provided [RCV003456601]	uncertain significance	19	49636909	49636909	Human		name
405021886	CV2861686	single nucleotide variant	NM_006270.5(RRAS):c.182C>A (p.Thr61Asn)	Noonan syndrome [RCV003528575]	uncertain significance	19	49637102	49637102	Human	1	name
405026792	CV2872825	single nucleotide variant	NM_006270.5(RRAS):c.274G>A (p.Ala92Thr)	Noonan syndrome [RCV003529055]	uncertain significance	19	49636894	49636894	Human	1	name
405031227	CV2890849	single nucleotide variant	NM_006270.5(RRAS):c.289T>C (p.Tyr97His)	Noonan syndrome [RCV003529444]	uncertain significance	19	49636879	49636879	Human	1	name
402482097	CV3078718	single nucleotide variant	NM_006270.5(RRAS):c.253G>A (p.Ala85Thr)	Noonan syndrome [RCV003642830]	uncertain significance	19	49636915	49636915	Human	1	name
407488428	CV3476299	single nucleotide variant	NM_006270.5(RRAS):c.211A>C (p.Ser71Arg)	not specified [RCV004665865]	uncertain significance	19	49637073	49637073	Human		name
597837196	CV3761460	single nucleotide variant	NM_006270.5(RRAS):c.124A>G (p.Lys42Glu)	Noonan syndrome [RCV005085831]	uncertain significance	19	49639975	49639975	Human	1	name
597854756	CV3806184	single nucleotide variant	NM_006270.5(RRAS):c.286C>T (p.Gln96Ter)	Noonan syndrome [RCV005145926]	uncertain significance	19	49636882	49636882	Human	1	name
597870459	CV3835531	single nucleotide variant	NM_006270.5(RRAS):c.295C>A (p.Arg99Ser)	Noonan syndrome [RCV005176523]	uncertain significance	19	49636873	49636873	Human	1	name
598220745	CV3903135	single nucleotide variant	NM_006270.5(RRAS):c.131C>T (p.Ala44Val)	not specified [RCV005272574]	uncertain significance	19	49639968	49639968	Human		name
598220752	CV3903136	single nucleotide variant	NM_006270.5(RRAS):c.193T>G (p.Ser65Ala)	not specified [RCV005272575]	uncertain significance	19	49637091	49637091	Human		name
13615429	CV533126	single nucleotide variant	NM_006270.5(RRAS):c.145T>C (p.Phe49Leu)	Noonan syndrome [RCV000632778]\|RRAS-related disorder [RCV003905693]\|not provided [RCV001756047]\|not specified [RCV001174601]	likely benign\|uncertain significance	19	49639954	49639954	Human	1	name , trait , alternate_id
13801928	CV570935	single nucleotide variant	NM_006270.5(RRAS):c.158A>T (p.Tyr53Phe)	Noonan syndrome [RCV000702591]\|not specified [RCV004026600]	uncertain significance	19	49637126	49637126	Human	1	name
13801765	CV573234	single nucleotide variant	NM_006270.5(RRAS):c.167C>G (p.Ser56Cys)	Noonan syndrome [RCV000695645]\|RRAS-related disorder [RCV005392302]\|not specified [RCV003403613]	uncertain significance	19	49637117	49637117	Human	1	name , trait , alternate_id
13801823	CV575007	single nucleotide variant	NM_006270.5(RRAS):c.175G>C (p.Asp59His)	Noonan syndrome [RCV000697539]\|not specified [RCV004026408]	uncertain significance	19	49637109	49637109	Human	1	name
26917877	CV847857	single nucleotide variant	NM_006270.5(RRAS):c.147C>A (p.Phe49Leu)	Noonan syndrome [RCV001057323]	uncertain significance	19	49639952	49639952	Human	1	name
38469858	CV921491	single nucleotide variant	NM_006270.5(RRAS):c.229G>A (p.Ala77Thr)	Noonan syndrome [RCV001397494]\|not provided [RCV003490112]\|not specified [RCV001201213]	benign\|likely benign\|uncertain significance	19	49637055	49637055	Human	1	name
126739810	CV1013844	single nucleotide variant	NM_006270.5(RRAS):c.572G>T (p.Arg191Leu)	Noonan syndrome [RCV001325108]	uncertain significance	19	49635734	49635734	Human	1	name
126737845	CV1013845	single nucleotide variant	NM_006270.5(RRAS):c.533A>G (p.Asn178Ser)	Noonan syndrome [RCV001314034]\|not specified [RCV004671334]	uncertain significance	19	49635773	49635773	Human	1	name
126762258	CV1013846	single nucleotide variant	NM_006270.5(RRAS):c.448C>T (p.Arg150Cys)	Noonan syndrome [RCV001318882]\|not specified [RCV005271151]	uncertain significance	19	49636624	49636624	Human	1	name
126768061	CV1034415	single nucleotide variant	NM_006270.5(RRAS):c.496G>A (p.Val166Met)	Noonan syndrome [RCV001343124]\|not specified [RCV001797834]	uncertain significance	19	49635810	49635810	Human	1	name
126924617	CV1051414	single nucleotide variant	NM_006270.5(RRAS):c.553C>A (p.Gln185Lys)	Noonan syndrome [RCV001367235]	uncertain significance	19	49635753	49635753	Human	1	name
126920131	CV1051415	single nucleotide variant	NM_006270.5(RRAS):c.371C>G (p.Thr124Arg)	Noonan syndrome [RCV001362696]	uncertain significance	19	49636701	49636701	Human	1	name
150529072	CV1288643	duplication	NM_006270.5(RRAS):c.38_54dup (p.Pro19fs)	not provided [RCV001727111]	uncertain significance	19	49640044	49640045	Human		name
150534914	CV1311687	single nucleotide variant	NM_006270.5(RRAS):c.325G>A (p.Ala109Thr)	Noonan syndrome [RCV002541105]\|not specified [RCV001779497]	uncertain significance	19	49636843	49636843	Human	1	name
151821181	CV1338440	single nucleotide variant	NM_006270.5(RRAS):c.487T>C (p.Ser163Pro)	Noonan syndrome [RCV001900900]\|not specified [RCV004041523]	uncertain significance	19	49635819	49635819	Human	1	name
151824308	CV1350865	single nucleotide variant	NM_006270.5(RRAS):c.481G>A (p.Gly161Ser)	Noonan syndrome [RCV001919875]\|not provided [RCV004693899]	uncertain significance	19	49635825	49635825	Human	1	name
151856333	CV1387555	single nucleotide variant	NM_006270.5(RRAS):c.356T>G (p.Val119Gly)	Noonan syndrome [RCV001996583]	uncertain significance	19	49636716	49636716	Human	1	name
151729456	CV1388819	single nucleotide variant	NM_006270.5(RRAS):c.541G>C (p.Glu181Gln)	Noonan syndrome [RCV001966954]	uncertain significance	19	49635765	49635765	Human	1	name
151893086	CV1411930	single nucleotide variant	NM_006270.5(RRAS):c.646G>A (p.Val216Ile)	Noonan syndrome [RCV001944747]\|not specified [RCV004040358]	uncertain significance	19	49635587	49635587	Human	1	name
151826817	CV1414883	single nucleotide variant	NM_006270.5(RRAS):c.412G>T (p.Val138Leu)	Noonan syndrome [RCV001920101]	uncertain significance	19	49636660	49636660	Human	1	name
151783803	CV1435141	single nucleotide variant	NM_006270.5(RRAS):c.382C>T (p.Arg128Trp)	Noonan syndrome [RCV001916121]	uncertain significance	19	49636690	49636690	Human	1	name
151847588	CV1439692	single nucleotide variant	NM_006270.5(RRAS):c.535G>A (p.Val179Met)	Noonan syndrome [RCV002016138]	uncertain significance	19	49635771	49635771	Human	1	name
151774591	CV1440096	single nucleotide variant	NM_006270.5(RRAS):c.461G>A (p.Arg154Gln)	Noonan syndrome [RCV001874776]\|not specified [RCV004040565]	uncertain significance	19	49635845	49635845	Human	1	name
151833553	CV1446643	single nucleotide variant	NM_006270.5(RRAS):c.449G>C (p.Arg150Pro)	Noonan syndrome [RCV002031038]	uncertain significance	19	49636623	49636623	Human	1	name
151866116	CV1484484	single nucleotide variant	NM_006270.5(RRAS):c.422G>C (p.Gly141Ala)	Noonan syndrome [RCV001959848]\|not specified [RCV004671542]	uncertain significance	19	49636650	49636650	Human	1	name
151727727	CV1488545	single nucleotide variant	NM_006270.5(RRAS):c.527G>A (p.Arg176His)	Noonan syndrome [RCV001966793]\|not specified [RCV004042176]	uncertain significance	19	49635779	49635779	Human	1	name
151879864	CV1506368	single nucleotide variant	NM_006270.5(RRAS):c.560T>C (p.Val187Ala)	Noonan syndrome [RCV001886313]	uncertain significance	19	49635746	49635746	Human	1	name
155742472	CV1777279	single nucleotide variant	NM_006270.5(RRAS):c.475G>C (p.Ala159Pro)	Noonan syndrome [RCV002302916]	uncertain significance	19	49635831	49635831	Human	1	name
155721972	CV1789914	single nucleotide variant	NM_006270.5(RRAS):c.383G>A (p.Arg128Gln)	not specified [RCV004048187]	uncertain significance	19	49636689	49636689	Human		name
155695089	CV1797041	single nucleotide variant	NM_006270.5(RRAS):c.395G>A (p.Arg132His)	Noonan syndrome [RCV003094460]\|not specified [RCV004050479]	uncertain significance	19	49636677	49636677	Human	1	name
155739486	CV1801741	single nucleotide variant	NM_006270.5(RRAS):c.463T>C (p.Ser155Pro)	not specified [RCV004051559]	uncertain significance	19	49635843	49635843	Human		name
155732849	CV1801908	single nucleotide variant	NM_006270.5(RRAS):c.484G>A (p.Ala162Thr)	Noonan syndrome [RCV003642998]\|not specified [RCV004050094]	uncertain significance	19	49635822	49635822	Human	1	name
155665308	CV1804063	single nucleotide variant	NM_006270.5(RRAS):c.620G>A (p.Arg207Lys)	not specified [RCV004053395]	uncertain significance	19	49635613	49635613	Human		name
156393194	CV1876077	single nucleotide variant	NM_006270.5(RRAS):c.493C>G (p.His165Asp)	Noonan syndrome [RCV003068258]	uncertain significance	19	49635813	49635813	Human	1	name
156380568	CV1927511	single nucleotide variant	NM_006270.5(RRAS):c.337C>T (p.Arg113Trp)	Noonan syndrome [RCV002634232]	uncertain significance	19	49636831	49636831	Human	1	name
156410317	CV1958315	single nucleotide variant	NM_006270.5(RRAS):c.454G>A (p.Val152Ile)	Noonan syndrome [RCV002587112]	uncertain significance	19	49635852	49635852	Human	1	name
156312085	CV2031635	single nucleotide variant	NM_006270.5(RRAS):c.436C>A (p.Leu146Met)	Noonan syndrome [RCV002716597]	uncertain significance	19	49636636	49636636	Human	1	name
156046045	CV2091214	single nucleotide variant	NM_006270.5(RRAS):c.610A>G (p.Ser204Gly)	Noonan syndrome [RCV002885994]	uncertain significance	19	49635623	49635623	Human	1	name
156109554	CV2108177	single nucleotide variant	NM_006270.5(RRAS):c.541G>A (p.Glu181Lys)	Noonan syndrome [RCV002927367]	uncertain significance	19	49635765	49635765	Human	1	name
156198809	CV2113821	single nucleotide variant	NM_006270.5(RRAS):c.599C>T (p.Pro200Leu)	Noonan syndrome [RCV002957303]	uncertain significance	19	49635634	49635634	Human	1	name
156043628	CV2143588	single nucleotide variant	NM_006270.5(RRAS):c.571C>T (p.Arg191Trp)	Noonan syndrome [RCV002999626]\|not specified [RCV003388140]	uncertain significance	19	49635735	49635735	Human	1	name
156303327	CV2187740	single nucleotide variant	NM_006270.5(RRAS):c.643T>C (p.Cys215Arg)	Noonan syndrome [RCV003062066]	uncertain significance	19	49635590	49635590	Human	1	name
156069983	CV2316862	single nucleotide variant	NM_006270.5(RRAS):c.349A>T (p.Asn117Tyr)	not specified [RCV004174390]	uncertain significance	19	49636723	49636723	Human		name
156175179	CV2345997	single nucleotide variant	NM_006270.5(RRAS):c.449G>A (p.Arg150His)	not specified [RCV004199029]	uncertain significance	19	49636623	49636623	Human		name
155935054	CV2372597	single nucleotide variant	NM_006270.5(RRAS):c.613G>A (p.Ala205Thr)	not specified [RCV004219388]	likely benign	19	49635620	49635620	Human		name
329383351	CV2472409	single nucleotide variant	NM_006270.5(RRAS):c.334G>T (p.Asp112Tyr)	not specified [RCV004283602]	uncertain significance	19	49636834	49636834	Human		name
401717985	CV2728394	single nucleotide variant	NM_006270.5(RRAS):c.319G>A (p.Val107Met)	Noonan syndrome [RCV003777176]\|not specified [RCV004333417]	uncertain significance	19	49636849	49636849	Human	1	name
401882613	CV2793634	single nucleotide variant	NM_006270.5(RRAS):c.571C>G (p.Arg191Gly)	Noonan syndrome [RCV005104197]\|not specified [RCV004364274]	uncertain significance	19	49635735	49635735	Human	1	name
401925199	CV2805300	single nucleotide variant	NM_006270.5(RRAS):c.355G>A (p.Val119Met)	not specified [RCV003405121]	uncertain significance	19	49636717	49636717	Human		name
402489729	CV2973133	single nucleotide variant	NM_006270.5(RRAS):c.367T>A (p.Phe123Ile)	Noonan syndrome [RCV003643702]	uncertain significance	19	49636705	49636705	Human	1	name
404998214	CV3123940	single nucleotide variant	NM_006270.5(RRAS):c.533A>C (p.Asn178Thr)	Noonan syndrome [RCV003827847]	uncertain significance	19	49635773	49635773	Human	1	name
405740189	CV3316547	single nucleotide variant	NM_006270.5(RRAS):c.412G>C (p.Val138Leu)	not specified [RCV004452258]	uncertain significance	19	49636660	49636660	Human		name
405723583	CV3381250	single nucleotide variant	NM_006270.5(RRAS):c.491A>T (p.His164Leu)	not specified [RCV004524171]	uncertain significance	19	49635815	49635815	Human		name
405723599	CV3381252	single nucleotide variant	NM_006270.5(RRAS):c.563G>C (p.Arg188Pro)	not specified [RCV004524173]	uncertain significance	19	49635743	49635743	Human		name
405723608	CV3381253	single nucleotide variant	NM_006270.5(RRAS):c.616C>T (p.Pro206Ser)	not specified [RCV004524174]	uncertain significance	19	49635617	49635617	Human		name
407488435	CV3476300	single nucleotide variant	NM_006270.5(RRAS):c.595C>A (p.Pro199Thr)	Noonan syndrome [RCV005103419]\|not specified [RCV004665866]	uncertain significance	19	49635638	49635638	Human	1	name
596921037	CV3534483	single nucleotide variant	NM_006270.5(RRAS):c.605C>T (p.Pro202Leu)	not specified [RCV004783702]	uncertain significance	19	49635628	49635628	Human		name
597786482	CV3604468	single nucleotide variant	NM_006270.5(RRAS):c.437T>G (p.Leu146Arg)	not specified [RCV004854991]	uncertain significance	19	49636635	49636635	Human		name
597786486	CV3604470	single nucleotide variant	NM_006270.5(RRAS):c.328A>C (p.Ile110Leu)	not specified [RCV004854992]	uncertain significance	19	49636840	49636840	Human		name
597786489	CV3604472	single nucleotide variant	NM_006270.5(RRAS):c.640C>T (p.Pro214Ser)	not specified [RCV004854993]	uncertain significance	19	49635593	49635593	Human		name
597710467	CV3604473	single nucleotide variant	NM_006270.5(RRAS):c.446A>G (p.Gln149Arg)	not specified [RCV004860960]	uncertain significance	19	49636626	49636626	Human		name
597830223	CV3746643	single nucleotide variant	NM_006270.5(RRAS):c.454G>C (p.Val152Leu)	Noonan syndrome [RCV005061929]	uncertain significance	19	49635852	49635852	Human	1	name
597832538	CV3760217	single nucleotide variant	NM_006270.5(RRAS):c.562C>G (p.Arg188Gly)	Noonan syndrome [RCV005084960]	uncertain significance	19	49635744	49635744	Human	1	name
597845593	CV3761588	single nucleotide variant	NM_006270.5(RRAS):c.353A>G (p.Glu118Gly)	Noonan syndrome [RCV005087188]	uncertain significance	19	49636719	49636719	Human	1	name
597946164	CV3777266	microsatellite	NM_006270.5(RRAS):c.90_91del (p.His30fs)	Noonan syndrome [RCV005119905]	uncertain significance	19	49640008	49640009	Human		name
597955681	CV3796266	single nucleotide variant	NM_006270.5(RRAS):c.403T>C (p.Phe135Leu)	Noonan syndrome [RCV005137083]	uncertain significance	19	49636669	49636669	Human	1	name
597886277	CV3800105	single nucleotide variant	NM_006270.5(RRAS):c.473C>T (p.Ser158Phe)	Noonan syndrome [RCV005150585]	uncertain significance	19	49635833	49635833	Human	1	name
597922709	CV3839843	single nucleotide variant	NM_006270.5(RRAS):c.354G>T (p.Glu118Asp)	Noonan syndrome [RCV005184582]	uncertain significance	19	49636718	49636718	Human	1	name
598122382	CV3884365	single nucleotide variant	NM_006270.5(RRAS):c.442T>C (p.Ser148Pro)	not specified [RCV005237056]	uncertain significance	19	49636630	49636630	Human		name
13468633	CV468964	single nucleotide variant	NM_006270.5(RRAS):c.397G>A (p.Asp133Asn)	Noonan syndrome [RCV001080292]\|RRAS-related disorder [RCV003915494]\|not provided [RCV000590808]\|not specified [RCV001449781]	benign\|likely benign	19	49636675	49636675	Human	10	name , trait , alternate_id
13468633	CV468964	single nucleotide variant	NM_006270.5(RRAS):c.397G>A (p.Asp133Asn)	Noonan syndrome [RCV001080292]\|RRAS-related disorder [RCV003915494]\|not provided [RCV000590808]\|not specified [RCV001449781]	benign\|likely benign	19	49636675	49636676	Human	10	name , trait , alternate_id
13615436	CV533122	single nucleotide variant	NM_006270.5(RRAS):c.362A>G (p.Lys121Arg)	Noonan syndrome [RCV000632782]\|not specified [RCV001174821]	benign\|likely benign	19	49636710	49636710	Human	1	name
13615434	CV533206	single nucleotide variant	NM_006270.5(RRAS):c.568G>C (p.Val190Leu)	Noonan syndrome [RCV000632781]\|not provided [RCV001771853]\|not specified [RCV001251387]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	19	49635738	49635738	Human	1	name
13615430	CV533211	single nucleotide variant	NM_006270.5(RRAS):c.515C>T (p.Ser172Leu)	Noonan syndrome [RCV000632779]	uncertain significance	19	49635791	49635791	Human	1	name
13615424	CV533214	single nucleotide variant	NM_006270.5(RRAS):c.409G>A (p.Val137Ile)	Noonan syndrome [RCV000632776]\|not specified [RCV001174918]	conflicting interpretations of pathogenicity\|uncertain significance	19	49636663	49636663	Human	1	name
13615432	CV533225	single nucleotide variant	NM_006270.5(RRAS):c.371C>T (p.Thr124Met)	Hereditary cancer [RCV005231202]\|Noonan syndrome [RCV000632780]\|not specified [RCV004025417]	uncertain significance	19	49636701	49636701	Human	2	name
13801513	CV572608	single nucleotide variant	NM_006270.5(RRAS):c.649C>G (p.Leu217Val)	Noonan syndrome [RCV000685059]\|not specified [RCV004857726]	uncertain significance	19	49635584	49635584	Human	1	name
13801619	CV572610	single nucleotide variant	NM_006270.5(RRAS):c.400G>A (p.Asp134Asn)	Noonan syndrome [RCV000690644]	uncertain significance	19	49636672	49636672	Human	1	name
13802013	CV573231	single nucleotide variant	NM_006270.5(RRAS):c.631G>A (p.Gly211Arg)	Noonan syndrome [RCV000706684]\|not specified [RCV002282342]	uncertain significance	19	49635602	49635602	Human	1	name
13801881	CV573233	single nucleotide variant	NM_006270.5(RRAS):c.623A>G (p.Lys208Arg)	Noonan syndrome [RCV000699964]\|not specified [RCV004026495]	uncertain significance	19	49635610	49635610	Human	1	name
13801706	CV575006	single nucleotide variant	NM_006270.5(RRAS):c.338G>A (p.Arg113Gln)	Noonan syndrome [RCV000693439]\|not specified [RCV004025155]	uncertain significance	19	49636830	49636830	Human	1	name
14714743	CV648251	single nucleotide variant	NM_006270.5(RRAS):c.572G>A (p.Arg191Gln)	Noonan syndrome [RCV000794537]\|not specified [RCV001420771]	uncertain significance	19	49635734	49635734	Human	1	name
14728067	CV648252	single nucleotide variant	NM_006270.5(RRAS):c.457C>A (p.Pro153Thr)	Noonan syndrome [RCV000799889]	uncertain significance	19	49635849	49635849	Human	1	name
14744467	CV648253	single nucleotide variant	NM_006270.5(RRAS):c.427A>T (p.Lys143Ter)	Noonan syndrome [RCV000824130]	uncertain significance	19	49636645	49636645	Human	1	name
26911409	CV847853	single nucleotide variant	NM_006270.5(RRAS):c.627G>T (p.Lys209Asn)	Noonan syndrome [RCV001052997]\|not specified [RCV001193594]	uncertain significance	19	49635606	49635606	Human	1	name
26906687	CV847854	single nucleotide variant	NM_006270.5(RRAS):c.394C>T (p.Arg132Cys)	Noonan syndrome [RCV001051854]\|not specified [RCV004031618]	uncertain significance	19	49636678	49636678	Human	1	name
26920029	CV847855	single nucleotide variant	NM_006270.5(RRAS):c.352G>A (p.Glu118Lys)	Noonan syndrome [RCV001059574]\|not specified [RCV004031888]	uncertain significance	19	49636720	49636720	Human	1	name
26894949	CV847856	single nucleotide variant	NM_006270.5(RRAS):c.307G>A (p.Gly103Ser)	Noonan syndrome [RCV001069483]	uncertain significance	19	49636861	49636861	Human	1	name
34896248	CV917301	single nucleotide variant	NM_006270.5(RRAS):c.563G>A (p.Arg188Gln)	Noonan syndrome [RCV001863059]\|RRAS-related disorder [RCV003945910]\|not specified [RCV001193590]	benign\|conflicting interpretations of pathogenicity\|uncertain significance	19	49635743	49635743	Human	1	name , trait , alternate_id
34896251	CV917302	single nucleotide variant	NM_006270.5(RRAS):c.421G>A (p.Gly141Arg)	Noonan syndrome [RCV005094027]\|not specified [RCV001193592]	uncertain significance	19	49636651	49636651	Human	1	name
38472777	CV938777	single nucleotide variant	NM_006270.5(RRAS):c.614C>T (p.Ala205Val)	Noonan syndrome [RCV001203108]\|not specified [RCV004033559]	uncertain significance	19	49635619	49635619	Human	1	name
38497634	CV958690	single nucleotide variant	NM_006270.5(RRAS):c.526C>T (p.Arg176Cys)	Noonan syndrome [RCV001243292]	uncertain significance	19	49635780	49635780	Human	1	name
40889456	CV972605	single nucleotide variant	NM_006270.5(RRAS):c.562C>T (p.Arg188Trp)	Noonan syndrome [RCV001315165]\|not specified [RCV001264469]	uncertain significance	19	49635744	49635744	Human	1	name
126762348	CV998709	single nucleotide variant	NM_006270.5(RRAS):c.598C>T (p.Pro200Ser)	Noonan syndrome [RCV001300366]	uncertain significance	19	49635635	49635635	Human	1	name
126729429	CV998710	single nucleotide variant	NM_006270.5(RRAS):c.509A>G (p.Glu170Gly)	Noonan syndrome [RCV001303565]	uncertain significance	19	49635797	49635797	Human	1	name
597917528	CV3842099	indel	NM_006270.5(RRAS):c.454-11_454-10delinsTG	Noonan syndrome [RCV005183774]	uncertain significance	19	49635862	49635863	Human		name
13531345	CV512430	microsatellite	NM_006270.5(RRAS):c.107GCG[5] (p.Gly39dup)	Inborn genetic diseases [RCV000623257]	likely pathogenic\|uncertain significance	19	49639980	49639981	Human		name
156419362	CV1932610	indel	NM_006270.5(RRAS):c.12_13delinsAA (p.Ala5Thr)	Noonan syndrome [RCV002612593]\|not specified [RCV005239686]	uncertain significance	19	49640086	49640087	Human		name
13802012	CV570923	insertion	NM_006270.5(RRAS):c.472_473insTT (p.Ser158fs)	Noonan syndrome [RCV000706443]\|not specified [RCV001269263]	benign\|uncertain significance	19	49635833	49635834	Human	1	name
150456202	CV1278467	single nucleotide variant	NM_012250.6(RRAS2):c.*124G>C	not provided [RCV001709082]	benign	11	14279213	14279213	Human		name
150506173	CV1226281	deletion	NM_012250.6(RRAS2):c.300-4del	not provided [RCV001635649]	benign	11	14294583	14294583	Human		name
150446792	CV1250717	single nucleotide variant	NM_001177314.2(RRAS2):c.-2C>T	not provided [RCV001667222]	benign	11	14364395	14364395	Human		name
152083468	CV1623882	duplication	NM_012250.6(RRAS2):c.300-4dup	not provided [RCV002149612]	benign	11	14294582	14294583	Human		name
329351646	CV2476482	single nucleotide variant	NM_012250.6(RRAS2):c.528-2A>C	not provided [RCV003222714]	uncertain significance	11	14279426	14279426	Human		name
405219721	CV2870234	single nucleotide variant	NM_012250.6(RRAS2):c.196+9A>G	not provided [RCV003553698]	uncertain significance	11	14295759	14295759	Human		name
405218197	CV2873671	single nucleotide variant	NM_012250.6(RRAS2):c.300-4T>G	not provided [RCV003553497]	likely benign	11	14294583	14294583	Human		name
597896354	CV3773510	single nucleotide variant	NM_012250.6(RRAS2):c.108+5C>T	not provided [RCV005111417]	likely benign	11	14358758	14358758	Human		name
598242700	CV3894107	single nucleotide variant	NM_001177314.2(RRAS2):c.-1C>A	not provided [RCV005257350]	likely benign	11	14364394	14364394	Human		name
150448304	CV1261949	single nucleotide variant	NM_012250.6(RRAS2):c.409-16A>T	Noonan syndrome 12 [RCV001796695]\|RASopathy [RCV004762169]\|not provided [RCV001680334]	benign	11	14281736	14281736	Human	2	name
150447388	CV1270304	duplication	NM_012250.6(RRAS2):c.408+98dup	not provided [RCV001691440]	benign	11	14294372	14294373	Human		name
152080512	CV1580036	single nucleotide variant	NM_012250.6(RRAS2):c.299+19T>C	not provided [RCV002076304]	benign	11	14294741	14294741	Human		name
156073753	CV1959570	single nucleotide variant	NM_012250.6(RRAS2):c.528-18G>T	not provided [RCV002569687]	likely benign	11	14279442	14279442	Human		name
405225597	CV2882123	single nucleotide variant	NM_012250.6(RRAS2):c.299+12A>C	not provided [RCV003554599]	likely benign	11	14294748	14294748	Human		name
597893124	CV3743921	single nucleotide variant	NM_012250.6(RRAS2):c.408+17C>T	not provided [RCV005071391]	likely benign	11	14294454	14294454	Human		name
150515715	CV1227645	single nucleotide variant	NM_012250.6(RRAS2):c.408+102G>A	not provided [RCV001638919]	benign	11	14294369	14294369	Human	1	name
150515715	CV1227645	single nucleotide variant	NM_012250.6(RRAS2):c.408+102G>A	not provided [RCV001638919]	benign	11	14294369	14294370	Human	1	name
156052353	CV2192480	single nucleotide variant	NM_012250.6(RRAS2):c.108+509A>G	not provided [RCV003036954]	uncertain significance	11	14358254	14358254	Human		name
150511635	CV1242762	single nucleotide variant	NM_001177314.2(RRAS2):c.3+5109C>T	not provided [RCV001661115]	benign	11	14359282	14359282	Human		name
156102284	CV2099325	single nucleotide variant	NM_012250.6(RRAS2):c.90C>T (p.Leu30=)	RRAS2-related disorder [RCV003943539]\|not provided [RCV002913449]	benign\|likely benign	11	14358781	14358781	Human	1	name , trait , alternate_id
155932493	CV2129247	single nucleotide variant	NM_012250.6(RRAS2):c.122C>T (p.Thr41Met)	RRAS2-related disorder [RCV003395547]\|not provided [RCV002970709]	uncertain significance	11	14295842	14295842	Human	1	name , trait , alternate_id
156042873	CV2305733	single nucleotide variant	NM_012250.6(RRAS2):c.449A>C (p.Lys150Thr)	Inborn genetic diseases [RCV002923988]\|RRAS2-related disorder [RCV003410188]	uncertain significance	11	14281680	14281680	Human	2	name , trait , alternate_id
243052438	CV2417899	single nucleotide variant	NM_012250.6(RRAS2):c.67G>A (p.Gly23Ser)	Noonan syndrome 12 [RCV003152964]\|RRAS2-related disorder [RCV003395714]\|not provided [RCV004820289]	pathogenic\|likely pathogenic\|uncertain significance	11	14358804	14358804	Human	1	name , trait , alternate_id
243057033	CV2419408	single nucleotide variant	NM_012250.6(RRAS2):c.439C>T (p.Arg147Trp)	Noonan syndrome 12 [RCV003155904]\|RRAS2-related disorder [RCV003900975]\|not provided [RCV003883964]	likely pathogenic\|uncertain significance	11	14281690	14281690	Human	1	name , trait , alternate_id
401937796	CV2797074	single nucleotide variant	NM_012250.6(RRAS2):c.330G>C (p.Gln110His)	RRAS2-related disorder [RCV003416891]	uncertain significance	11	14294549	14294549	Human		name , trait , alternate_id
401937799	CV2797078	single nucleotide variant	NM_012250.6(RRAS2):c.349C>G (p.Arg117Gly)	RRAS2-related disorder [RCV003416894]	uncertain significance	11	14294530	14294530	Human		name , trait , alternate_id
401919240	CV2798211	single nucleotide variant	NM_012250.6(RRAS2):c.32G>A (p.Gly11Asp)	RRAS2-related disorder [RCV003402232]	uncertain significance	11	14358839	14358839	Human		name , trait , alternate_id
401902807	CV2799619	single nucleotide variant	NM_012250.6(RRAS2):c.99G>T (p.Gln33His)	RRAS2-related disorder [RCV003419061]	uncertain significance	11	14358772	14358772	Human		name , trait , alternate_id
405259946	CV3190122	single nucleotide variant	NM_012250.6(RRAS2):c.258C>T (p.Gly86=)	RRAS2-related disorder [RCV003894525]	likely benign	11	14294801	14294801	Human		name , trait , alternate_id
405270257	CV3215453	single nucleotide variant	NM_012250.6(RRAS2):c.138C>T (p.Thr46=)	RRAS2-related disorder [RCV003949195]	likely benign	11	14295826	14295826	Human		name , trait , alternate_id
408380349	CV3514812	single nucleotide variant	NM_012250.6(RRAS2):c.46C>T (p.Arg16Trp)	RRAS2-related disorder [RCV004754141]	uncertain significance	11	14358825	14358825	Human		name , trait , alternate_id
15014878	CV615263	single nucleotide variant	NM_012250.6(RRAS2):c.208G>A (p.Ala70Thr)	Noonan syndrome 12 [RCV000853183]\|Noonan syndrome [RCV000852397]\|RASopathy [RCV004760768]\|RRAS2-related disorder [RCV003411705]	pathogenic\|likely pathogenic\|uncertain significance	11	14294851	14294851	Human	3	name , trait , alternate_id
617151603	CV4021766	single nucleotide variant	NM_012250.6(RRAS2):c.72C>T (p.Gly24=)	not provided [RCV005426727]	likely benign	11	14358799	14358799	Human		name
151868585	CV1516650	single nucleotide variant	NM_012250.6(RRAS2):c.195T>C (p.Asp65=)	not provided [RCV001981013]	uncertain significance	11	14295769	14295769	Human		name
152099428	CV1606544	single nucleotide variant	NM_012250.6(RRAS2):c.135A>G (p.Pro45=)	not provided [RCV002195349]	likely benign	11	14295829	14295829	Human		name
155909246	CV2131043	single nucleotide variant	NM_012250.6(RRAS2):c.210A>G (p.Ala70=)	not provided [RCV002967922]	likely benign	11	14294849	14294849	Human		name
405249527	CV3170109	single nucleotide variant	NM_012250.6(RRAS2):c.123G>A (p.Thr41=)	not provided [RCV003869738]	likely benign	11	14295841	14295841	Human		name
597859555	CV3850347	single nucleotide variant	NM_012250.6(RRAS2):c.276C>A (p.Val92=)	not provided [RCV005195680]	likely benign	11	14294783	14294783	Human		name
598159899	CV3897181	single nucleotide variant	NM_012250.6(RRAS2):c.13G>A (p.Gly5Ser)	not provided [RCV005368155]	uncertain significance	11	14358858	14358858	Human		name
150336788	CV1165987	single nucleotide variant	NM_012250.6(RRAS2):c.70G>A (p.Gly24Ser)	not provided [RCV001532152]	uncertain significance	11	14358801	14358801	Human		name
150507400	CV1244556	single nucleotide variant	NM_012250.6(RRAS2):c.98A>G (p.Gln33Arg)	not provided [RCV001658805]	uncertain significance	11	14358773	14358773	Human		name
151662853	CV1333490	single nucleotide variant	NM_012250.6(RRAS2):c.67G>T (p.Gly23Cys)	Noonan syndrome [RCV003153250]\|not provided [RCV001837682]	pathogenic\|likely pathogenic	11	14358804	14358804	Human	1	name
152147579	CV1647316	single nucleotide variant	NM_012250.6(RRAS2):c.609T>C (p.Ile203=)	not provided [RCV002201466]	likely benign	11	14279343	14279343	Human		name
152981811	CV1677102	single nucleotide variant	NM_012250.6(RRAS2):c.59T>C (p.Val20Ala)	not specified [RCV002248171]	uncertain significance	11	14358812	14358812	Human		name
153345873	CV1691491	single nucleotide variant	NM_012250.6(RRAS2):c.68G>A (p.Gly23Asp)	Noonan syndrome 12 [RCV002272974]\|not provided [RCV003232571]	pathogenic	11	14358803	14358803	Human	1	name
156373821	CV1963137	single nucleotide variant	NM_012250.6(RRAS2):c.402A>G (p.Gln134=)	not provided [RCV002582633]	likely benign	11	14294477	14294477	Human		name
156325876	CV2108557	single nucleotide variant	NM_012250.6(RRAS2):c.552T>C (p.Pro184=)	not provided [RCV002938079]	benign\|likely benign	11	14279400	14279400	Human		name
243050697	CV2403823	single nucleotide variant	NM_012250.6(RRAS2):c.71G>T (p.Gly24Val)	See cases [RCV003128494]	uncertain significance	11	14358800	14358800	Human		name
329350698	CV2421654	single nucleotide variant	NM_012250.6(RRAS2):c.71G>A (p.Gly24Asp)	Noonan syndrome 12 [RCV005254745]\|not provided [RCV003159356]	pathogenic\|likely pathogenic	11	14358800	14358800	Human	1	name
405172075	CV2961432	single nucleotide variant	NM_012250.6(RRAS2):c.606C>G (p.Val202=)	not provided [RCV003675500]	likely benign	11	14279346	14279346	Human		name
405136070	CV3130597	single nucleotide variant	NM_012250.6(RRAS2):c.453A>G (p.Val151=)	not provided [RCV003838830]	likely benign	11	14281676	14281676	Human		name
596946860	CV3548694	single nucleotide variant	NM_012250.6(RRAS2):c.519G>A (p.Arg173=)	not provided [RCV004810522]	likely benign	11	14281610	14281610	Human		name
15014877	CV615266	single nucleotide variant	NM_012250.6(RRAS2):c.68G>T (p.Gly23Val)	Noonan syndrome [RCV000852396]\|not provided [RCV003232089]	pathogenic	11	14358803	14358803	Human	1	name
150428319	CV1187692	single nucleotide variant	NM_012250.6(RRAS2):c.247A>T (p.Met83Leu)	not provided [RCV001562110]	uncertain significance	11	14294812	14294812	Human		name
151805670	CV1429932	single nucleotide variant	NM_012250.6(RRAS2):c.212G>A (p.Gly71Glu)	not provided [RCV001974311]	likely pathogenic	11	14294847	14294847	Human		name
151808609	CV1500789	single nucleotide variant	NM_012250.6(RRAS2):c.133C>G (p.Pro45Ala)	not provided [RCV001974562]	uncertain significance	11	14295831	14295831	Human		name
156190946	CV1994621	single nucleotide variant	NM_012250.6(RRAS2):c.271T>A (p.Leu91Met)	not provided [RCV002643310]	uncertain significance	11	14294788	14294788	Human		name
156033514	CV2002516	single nucleotide variant	NM_012250.6(RRAS2):c.232A>T (p.Met78Leu)	not provided [RCV002658760]	uncertain significance	11	14294827	14294827	Human		name
156246307	CV2086224	single nucleotide variant	NM_012250.6(RRAS2):c.287C>T (p.Thr96Ile)	not provided [RCV002876783]	uncertain significance	11	14294772	14294772	Human		name
156184014	CV2239098	single nucleotide variant	NM_012250.6(RRAS2):c.196A>G (p.Ile66Val)	Inborn genetic diseases [RCV002802451]	uncertain significance	11	14295768	14295768	Human	1	name
8561053	CV24486	single nucleotide variant	NM_012250.6(RRAS2):c.215A>T (p.Gln72Leu)	Noonan syndrome 12 [RCV000010054]\|Noonan syndrome [RCV000852398]\|Ovarian neoplasm [RCV001072115]	pathogenic\|other	11	14294844	14294844	Human	4	name
401903157	CV2816463	single nucleotide variant	NM_001177314.2(RRAS2):c.2T>C (p.Met1Thr)	not provided [RCV003409273]	uncertain significance	11	14364392	14364392	Human		name
405175255	CV3123006	single nucleotide variant	NM_012250.6(RRAS2):c.188G>A (p.Arg63Gln)	not provided [RCV003819404]	uncertain significance	11	14295776	14295776	Human		name
596924844	CV3536770	single nucleotide variant	NM_012250.6(RRAS2):c.139A>G (p.Ile47Val)	Noonan syndrome 12 [RCV004785764]	uncertain significance	11	14295825	14295825	Human	1	name
598220760	CV3903137	single nucleotide variant	NM_012250.6(RRAS2):c.274G>A (p.Val92Ile)	Inborn genetic diseases [RCV005272576]	uncertain significance	11	14294785	14294785	Human	1	name
151862585	CV1454180	single nucleotide variant	NM_012250.6(RRAS2):c.571C>T (p.Arg191Trp)	not provided [RCV001938746]	uncertain significance	11	14279381	14279381	Human		name
152033866	CV1610473	single nucleotide variant	NM_012250.6(RRAS2):c.412A>T (p.Thr138Ser)	not provided [RCV002125008]	benign	11	14281717	14281717	Human		name
155958941	CV1911956	single nucleotide variant	NM_012250.6(RRAS2):c.314A>G (p.Tyr105Cys)	Inborn genetic diseases [RCV002616635]\|not provided [RCV002628315]	uncertain significance	11	14294565	14294565	Human	1	name
156073077	CV2201381	single nucleotide variant	NM_012250.6(RRAS2):c.350G>A (p.Arg117His)	Inborn genetic diseases [RCV002660351]	uncertain significance	11	14294529	14294529	Human	1	name
156328925	CV2216292	single nucleotide variant	NM_012250.6(RRAS2):c.484A>G (p.Met162Val)	Inborn genetic diseases [RCV002717754]	uncertain significance	11	14281645	14281645	Human	1	name
156434484	CV2402927	single nucleotide variant	NM_012250.6(RRAS2):c.596G>C (p.Cys199Ser)	not provided [RCV003126365]	uncertain significance	11	14279356	14279356	Human		name
401798384	CV2741490	single nucleotide variant	NM_012250.6(RRAS2):c.560C>G (p.Pro187Arg)	Noonan syndrome 12 [RCV003322709]	uncertain significance	11	14279392	14279392	Human	1	name
402522815	CV2900184	single nucleotide variant	NM_012250.6(RRAS2):c.440G>A (p.Arg147Gln)	Noonan syndrome [RCV004786969]\|not provided [RCV003575991]	uncertain significance	11	14281689	14281689	Human	1	name
405176707	CV2951990	single nucleotide variant	NM_012250.6(RRAS2):c.364A>T (p.Met122Leu)	not provided [RCV003675893]	uncertain significance	11	14294515	14294515	Human		name
405123364	CV2954278	single nucleotide variant	NM_012250.6(RRAS2):c.318G>C (p.Lys106Asn)	not provided [RCV003667680]	uncertain significance	11	14294561	14294561	Human		name
405064316	CV3148462	single nucleotide variant	NM_012250.6(RRAS2):c.517C>T (p.Arg173Trp)	not provided [RCV003850418]	uncertain significance	11	14281612	14281612	Human		name
405740195	CV3316548	single nucleotide variant	NM_012250.6(RRAS2):c.581A>G (p.Lys194Arg)	Inborn genetic diseases [RCV004452259]	uncertain significance	11	14279371	14279371	Human	1	name
407506789	CV3496189	single nucleotide variant	NM_012250.6(RRAS2):c.349C>T (p.Arg117Cys)	not provided [RCV004698030]	uncertain significance	11	14294530	14294530	Human		name
408390699	CV3527687	single nucleotide variant	NM_012250.6(RRAS2):c.451G>A (p.Val151Ile)	not provided [RCV004774955]	uncertain significance	11	14281678	14281678	Human		name
596928495	CV3532934	single nucleotide variant	NM_012250.6(RRAS2):c.489T>A (p.Asn163Lys)	not provided [RCV004779033]	uncertain significance	11	14281640	14281640	Human		name
150412824	CV1191176	duplication	NM_012250.6(RRAS2):c.62_73dup (p.Gly21_Gly24dup)	not provided [RCV001567025]	likely pathogenic	11	14358797	14358798	Human		name
15014879	CV615264	duplication	NM_012250.6(RRAS2):c.70_78dup (p.Gly24_Gly26dup)	Inborn genetic diseases [RCV001265738]\|Noonan syndrome 12 [RCV000853184]\|Noonan syndrome [RCV000852399]\|not provided [RCV003117554]	pathogenic	11	14358792	14358793	Human	3	name
15014876	CV615265	duplication	NM_012250.6(RRAS2):c.65_73dup (p.Gly22_Gly24dup)	Noonan syndrome [RCV000852395]	pathogenic	11	14358797	14358798	Human	1	name

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