Rasgrp4 Variant Search Result - Rat Genome Database

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66 records found for search term Rasgrp4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156376261	CV2210516	single nucleotide variant	NM_170604.3(RASGRP4):c.44C>T (p.Thr15Ile)	not specified [RCV004089644]	uncertain significance	19	38422133	38422133	Human		name
156083806	CV2249221	single nucleotide variant	NM_170604.3(RASGRP4):c.46G>A (p.Gly16Arg)	not specified [RCV004118261]	uncertain significance	19	38422131	38422131	Human		name
407466990	CV3468617	single nucleotide variant	NM_170604.3(RASGRP4):c.62G>A (p.Arg21Gln)	not specified [RCV004660607]	uncertain significance	19	38422115	38422115	Human		name
156395387	CV2329166	single nucleotide variant	NM_170604.3(RASGRP4):c.295G>A (p.Ala99Thr)	not specified [RCV004173921]	uncertain significance	19	38421114	38421114	Human		name
401727696	CV2678414	single nucleotide variant	NM_170604.3(RASGRP4):c.289G>A (p.Asp97Asn)	not specified [RCV004292439]	uncertain significance	19	38421120	38421120	Human		name
405660069	CV3312418	single nucleotide variant	NM_170604.3(RASGRP4):c.109C>T (p.Arg37Trp)	not specified [RCV004438738]	uncertain significance	19	38422068	38422068	Human		name
405660078	CV3312421	single nucleotide variant	NM_170604.3(RASGRP4):c.143T>C (p.Leu48Pro)	not specified [RCV004438741]	uncertain significance	19	38422034	38422034	Human		name
407500887	CV3468618	single nucleotide variant	NM_170604.3(RASGRP4):c.281C>T (p.Pro94Leu)	not specified [RCV004669650]	uncertain significance	19	38421128	38421128	Human		name
407500893	CV3468622	single nucleotide variant	NM_170604.3(RASGRP4):c.200A>T (p.Gln67Leu)	not specified [RCV004669651]	uncertain significance	19	38421977	38421977	Human		name
15192331	CV704959	single nucleotide variant	NM_170604.3(RASGRP4):c.1662C>T (p.Cys554=)	not provided [RCV000955038]	benign	19	38412690	38412690	Human		name
156175133	CV2299522	single nucleotide variant	NM_170604.3(RASGRP4):c.832G>A (p.Ala278Thr)	not specified [RCV004154866]	uncertain significance	19	38418396	38418396	Human		name
156194601	CV2309452	single nucleotide variant	NM_170604.3(RASGRP4):c.437T>C (p.Ile146Thr)	not specified [RCV004158861]	uncertain significance	19	38420203	38420203	Human		name
156155915	CV2388822	single nucleotide variant	NM_170604.3(RASGRP4):c.530G>C (p.Gly177Ala)	not specified [RCV004239673]	uncertain significance	19	38419993	38419993	Human		name
329369811	CV2461233	single nucleotide variant	NM_170604.3(RASGRP4):c.607G>C (p.Gly203Arg)	not specified [RCV004267420]	uncertain significance	19	38419916	38419916	Human		name
401728589	CV2672981	single nucleotide variant	NM_170604.3(RASGRP4):c.536C>T (p.Pro179Leu)	not specified [RCV004283980]	uncertain significance	19	38419987	38419987	Human		name
401897786	CV2772913	single nucleotide variant	NM_170604.3(RASGRP4):c.906C>G (p.Ile302Met)	not specified [RCV004357684]	uncertain significance	19	38417100	38417100	Human		name
405660096	CV3312427	single nucleotide variant	NM_170604.3(RASGRP4):c.592G>A (p.Asp198Asn)	not specified [RCV004438747]	uncertain significance	19	38419931	38419931	Human		name
405660099	CV3312428	single nucleotide variant	NM_170604.3(RASGRP4):c.704G>A (p.Arg235Gln)	not specified [RCV004438748]	uncertain significance	19	38418524	38418524	Human		name
407466994	CV3468619	single nucleotide variant	NM_170604.3(RASGRP4):c.419C>T (p.Pro140Leu)	not specified [RCV004660608]	uncertain significance	19	38420221	38420221	Human		name
407467003	CV3468621	single nucleotide variant	NM_170604.3(RASGRP4):c.703C>G (p.Arg235Gly)	not specified [RCV004660610]	uncertain significance	19	38418525	38418525	Human		name
407467007	CV3468623	single nucleotide variant	NM_170604.3(RASGRP4):c.815A>G (p.Asp272Gly)	not specified [RCV004660611]	uncertain significance	19	38418413	38418413	Human		name
407467011	CV3468624	single nucleotide variant	NM_170604.3(RASGRP4):c.431A>G (p.Glu144Gly)	not specified [RCV004660612]	uncertain significance	19	38420209	38420209	Human		name
597784154	CV3593157	single nucleotide variant	NM_170604.3(RASGRP4):c.643C>T (p.Arg215Trp)	not specified [RCV004854410]	uncertain significance	19	38419880	38419880	Human		name
597706731	CV3593161	single nucleotide variant	NM_170604.3(RASGRP4):c.328A>T (p.Thr110Ser)	not specified [RCV004860534]	uncertain significance	19	38420957	38420957	Human		name
597706768	CV3593165	single nucleotide variant	NM_170604.3(RASGRP4):c.400G>A (p.Glu134Lys)	not specified [RCV004860538]	uncertain significance	19	38420240	38420240	Human		name
597706776	CV3593166	single nucleotide variant	NM_170604.3(RASGRP4):c.529G>A (p.Gly177Ser)	not specified [RCV004860539]	uncertain significance	19	38419994	38419994	Human		name
597784163	CV3593168	single nucleotide variant	NM_170604.3(RASGRP4):c.846C>G (p.His282Gln)	not specified [RCV004854412]	uncertain significance	19	38417160	38417160	Human		name
597706798	CV3593169	single nucleotide variant	NM_170604.3(RASGRP4):c.411C>A (p.His137Gln)	not specified [RCV004860541]	uncertain significance	19	38420229	38420229	Human		name
598184840	CV3902215	single nucleotide variant	NM_170604.3(RASGRP4):c.680G>A (p.Ser227Asn)	not specified [RCV005265818]	uncertain significance	19	38418548	38418548	Human		name
598184873	CV3902220	single nucleotide variant	NM_170604.3(RASGRP4):c.730G>A (p.Val244Ile)	not specified [RCV005265823]	uncertain significance	19	38418498	38418498	Human		name
156329114	CV2213768	single nucleotide variant	NM_170604.3(RASGRP4):c.1882T>C (p.Ser628Pro)	not specified [RCV004089833]	uncertain significance	19	38410969	38410969	Human		name
156301913	CV2258576	single nucleotide variant	NM_170604.3(RASGRP4):c.1810G>A (p.Gly604Arg)	not specified [RCV004116052]	uncertain significance	19	38411157	38411157	Human		name
156264535	CV2282668	single nucleotide variant	NM_170604.3(RASGRP4):c.2014G>C (p.Asp672His)	not specified [RCV004135217]	uncertain significance	19	38410048	38410048	Human		name
156258328	CV2304856	single nucleotide variant	NM_170604.3(RASGRP4):c.1012C>T (p.Arg338Cys)	not specified [RCV004168779]	uncertain significance	19	38415066	38415066	Human		name
156054041	CV2326479	single nucleotide variant	NM_170604.3(RASGRP4):c.1154G>A (p.Arg385Gln)	not specified [RCV004183040]	uncertain significance	19	38414924	38414924	Human		name
156181163	CV2338101	single nucleotide variant	NM_170604.3(RASGRP4):c.1912C>T (p.Arg638Cys)	not specified [RCV004184136]	uncertain significance	19	38410939	38410939	Human		name
156134109	CV2361966	single nucleotide variant	NM_170604.3(RASGRP4):c.1528C>T (p.Arg510Cys)	not specified [RCV004207733]	uncertain significance	19	38412938	38412938	Human		name
156402708	CV2371457	single nucleotide variant	NM_170604.3(RASGRP4):c.1694C>T (p.Thr565Ile)	not specified [RCV004216715]	uncertain significance	19	38411368	38411368	Human		name
329377712	CV2436010	single nucleotide variant	NM_170604.3(RASGRP4):c.1448G>A (p.Arg483Gln)	not specified [RCV004255230]	uncertain significance	19	38413018	38413018	Human		name
329400070	CV2440478	single nucleotide variant	NM_170604.3(RASGRP4):c.1795G>A (p.Asp599Asn)	not specified [RCV004256407]	uncertain significance	19	38411172	38411172	Human		name
329396767	CV2455777	single nucleotide variant	NM_170604.3(RASGRP4):c.1009C>T (p.Arg337Cys)	not specified [RCV004279069]	uncertain significance	19	38415069	38415069	Human		name
401745116	CV2681193	single nucleotide variant	NM_170604.3(RASGRP4):c.1201G>A (p.Ala401Thr)	not specified [RCV004289335]	uncertain significance	19	38414877	38414877	Human		name
401731466	CV2693818	single nucleotide variant	NM_170604.3(RASGRP4):c.1099G>A (p.Asp367Asn)	not specified [RCV004300130]	uncertain significance	19	38414979	38414979	Human		name
401773573	CV2709382	single nucleotide variant	NM_170604.3(RASGRP4):c.1000G>A (p.Ala334Thr)	not specified [RCV004316522]	uncertain significance	19	38415078	38415078	Human		name
405660064	CV3312416	single nucleotide variant	NM_170604.3(RASGRP4):c.1003C>T (p.Arg335Cys)	not specified [RCV004438736]	likely benign	19	38415075	38415075	Human		name
405660066	CV3312417	single nucleotide variant	NM_170604.3(RASGRP4):c.1013G>A (p.Arg338His)	not specified [RCV004438737]	uncertain significance	19	38415065	38415065	Human		name
405660072	CV3312419	single nucleotide variant	NM_170604.3(RASGRP4):c.1225C>T (p.Leu409Phe)	not specified [RCV004438739]	uncertain significance	19	38414853	38414853	Human		name
405660075	CV3312420	single nucleotide variant	NM_170604.3(RASGRP4):c.1291C>T (p.Pro431Ser)	not specified [RCV004438740]	uncertain significance	19	38413414	38413414	Human		name
405660081	CV3312422	single nucleotide variant	NM_170604.3(RASGRP4):c.1490A>G (p.Asn497Ser)	not specified [RCV004438742]	uncertain significance	19	38412976	38412976	Human		name
405660084	CV3312423	single nucleotide variant	NM_170604.3(RASGRP4):c.1743C>A (p.His581Gln)	not specified [RCV004438743]	uncertain significance	19	38411224	38411224	Human		name
405660087	CV3312424	single nucleotide variant	NM_170604.3(RASGRP4):c.1766A>G (p.Glu589Gly)	not specified [RCV004438744]	uncertain significance	19	38411201	38411201	Human		name
405660093	CV3312426	single nucleotide variant	NM_170604.3(RASGRP4):c.1883C>T (p.Ser628Phe)	not specified [RCV004438746]	uncertain significance	19	38410968	38410968	Human		name
597784150	CV3593155	single nucleotide variant	NM_170604.3(RASGRP4):c.1030G>A (p.Ala344Thr)	not specified [RCV004854409]	likely benign	19	38415048	38415048	Human		name
597706705	CV3593156	single nucleotide variant	NM_170604.3(RASGRP4):c.1579C>T (p.Arg527Trp)	not specified [RCV004860531]	uncertain significance	19	38412773	38412773	Human		name
597706714	CV3593158	single nucleotide variant	NM_170604.3(RASGRP4):c.1715G>A (p.Arg572Gln)	not specified [RCV004860532]	uncertain significance	19	38411347	38411347	Human		name
597706719	CV3593159	single nucleotide variant	NM_170604.3(RASGRP4):c.1328A>G (p.Asn443Ser)	not specified [RCV004860533]	uncertain significance	19	38413281	38413281	Human		name
597784158	CV3593160	single nucleotide variant	NM_170604.3(RASGRP4):c.1114G>A (p.Gly372Ser)	not specified [RCV004854411]	uncertain significance	19	38414964	38414964	Human		name
597706740	CV3593162	single nucleotide variant	NM_170604.3(RASGRP4):c.1478G>A (p.Arg493Gln)	not specified [RCV004860535]	uncertain significance	19	38412988	38412988	Human		name
597706749	CV3593163	single nucleotide variant	NM_170604.3(RASGRP4):c.1588G>A (p.Ala530Thr)	not specified [RCV004860536]	uncertain significance	19	38412764	38412764	Human		name
597706788	CV3593167	single nucleotide variant	NM_170604.3(RASGRP4):c.1243C>T (p.Leu415Phe)	not specified [RCV004860540]	uncertain significance	19	38413462	38413462	Human		name
598184826	CV3902213	single nucleotide variant	NM_170604.3(RASGRP4):c.1877C>T (p.Thr626Met)	not specified [RCV005265816]	uncertain significance	19	38410974	38410974	Human		name
598184834	CV3902214	single nucleotide variant	NM_170604.3(RASGRP4):c.1886T>G (p.Leu629Arg)	not specified [RCV005265817]	uncertain significance	19	38410965	38410965	Human		name
598184853	CV3902217	single nucleotide variant	NM_170604.3(RASGRP4):c.1841A>G (p.His614Arg)	not specified [RCV005265820]	uncertain significance	19	38411126	38411126	Human		name
598184860	CV3902218	single nucleotide variant	NM_170604.3(RASGRP4):c.1546T>G (p.Phe516Val)	not specified [RCV005265821]	uncertain significance	19	38412806	38412806	Human		name
598184865	CV3902219	single nucleotide variant	NM_170604.3(RASGRP4):c.1846A>T (p.Ser616Cys)	not specified [RCV005265822]	uncertain significance	19	38411121	38411121	Human		name
15189901	CV704960	single nucleotide variant	NM_170604.3(RASGRP4):c.1003C>G (p.Arg335Gly)	not provided [RCV000954316]	benign	19	38415075	38415075	Human		name

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