Rasgrp3 Variant Search Result - Rat Genome Database

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56 records found for search term Rasgrp3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
11345120	CV237595	single nucleotide variant	NM_170672.3(RASGRP3):c.-261+9727G>T	Lip and oral cavity carcinoma [RCV000225002]	pathogenic\|association	2	33457670	33457670	Human	1	name
407466985	CV3468615	single nucleotide variant	NM_001139488.2(RASGRP3):c.16C>T (p.Leu6Phe)	not specified [RCV004660606]	uncertain significance	2	33515152	33515152	Human		name
15170657	CV747614	single nucleotide variant	NM_001139488.2(RASGRP3):c.231C>T (p.Phe77=)	not provided [RCV000927744]	likely benign	2	33520009	33520009	Human		name
401911076	CV2815680	single nucleotide variant	NM_001139488.2(RASGRP3):c.903C>A (p.Ile301=)	not provided [RCV003425575]	likely benign	2	33527232	33527232	Human		name
15137325	CV708261	single nucleotide variant	NM_001139488.2(RASGRP3):c.417C>T (p.Ser139=)	not provided [RCV000965601]	benign	2	33522003	33522003	Human		name
156143914	CV2208682	single nucleotide variant	NM_001139488.2(RASGRP3):c.179G>A (p.Arg60Gln)	not specified [RCV004091192]	likely benign	2	33519957	33519957	Human		name
329369925	CV2424983	single nucleotide variant	NM_001139488.2(RASGRP3):c.174G>A (p.Met58Ile)	not specified [RCV004250645]	uncertain significance	2	33519952	33519952	Human		name
405660041	CV3312408	single nucleotide variant	NM_001139488.2(RASGRP3):c.169T>G (p.Cys57Gly)	not specified [RCV004438728]	uncertain significance	2	33516640	33516640	Human		name
15128658	CV763208	single nucleotide variant	NM_001139488.2(RASGRP3):c.1503C>T (p.Thr501=)	not provided [RCV000941753]	likely benign	2	33549712	33549712	Human		name
156132953	CV2216640	single nucleotide variant	NM_001139488.2(RASGRP3):c.891C>G (p.Phe297Leu)	not specified [RCV004083097]	uncertain significance	2	33527220	33527220	Human		name
156119340	CV2228887	single nucleotide variant	NM_001139488.2(RASGRP3):c.387G>A (p.Met129Ile)	not specified [RCV004095118]	uncertain significance	2	33521973	33521973	Human		name
156218532	CV2253960	single nucleotide variant	NM_001139488.2(RASGRP3):c.680A>G (p.Asn227Ser)	not specified [RCV004127634]	uncertain significance	2	33524042	33524042	Human		name
156272439	CV2277511	single nucleotide variant	NM_001139488.2(RASGRP3):c.866A>G (p.Lys289Arg)	not specified [RCV004145203]	uncertain significance	2	33527195	33527195	Human		name
156178205	CV2298277	single nucleotide variant	NM_001139488.2(RASGRP3):c.685G>A (p.Ala229Thr)	not specified [RCV004160191]	uncertain significance	2	33524047	33524047	Human		name
156152383	CV2307627	single nucleotide variant	NM_001139488.2(RASGRP3):c.856A>C (p.Asn286His)	not specified [RCV004168046]	uncertain significance	2	33527185	33527185	Human		name
155962520	CV2308159	single nucleotide variant	NM_001139488.2(RASGRP3):c.764G>A (p.Arg255His)	not specified [RCV004164668]	uncertain significance	2	33524505	33524505	Human		name
155901541	CV2345826	single nucleotide variant	NM_001139488.2(RASGRP3):c.877G>A (p.Asp293Asn)	not specified [RCV004198872]	uncertain significance	2	33527206	33527206	Human		name
156032270	CV2376474	single nucleotide variant	NM_001139488.2(RASGRP3):c.857A>G (p.Asn286Ser)	not specified [RCV004220650]	uncertain significance	2	33527186	33527186	Human		name
405660055	CV3312413	single nucleotide variant	NM_001139488.2(RASGRP3):c.349C>T (p.Leu117Phe)	not specified [RCV004438733]	uncertain significance	2	33520665	33520665	Human		name
405660058	CV3312414	single nucleotide variant	NM_001139488.2(RASGRP3):c.676A>G (p.Ile226Val)	not specified [RCV004438734]	uncertain significance	2	33524038	33524038	Human		name
407500883	CV3468616	single nucleotide variant	NM_001139488.2(RASGRP3):c.755C>A (p.Ser252Tyr)	not specified [RCV004669649]	uncertain significance	2	33524496	33524496	Human		name
597706663	CV3593148	single nucleotide variant	NM_001139488.2(RASGRP3):c.343G>A (p.Val115Ile)	not specified [RCV004860527]	likely benign	2	33520659	33520659	Human		name
597784136	CV3593150	single nucleotide variant	NM_001139488.2(RASGRP3):c.457C>T (p.Pro153Ser)	not specified [RCV004854406]	uncertain significance	2	33522043	33522043	Human		name
598184790	CV3902206	single nucleotide variant	NM_001139488.2(RASGRP3):c.419A>G (p.Lys140Arg)	not specified [RCV005265810]	uncertain significance	2	33522005	33522005	Human		name
598184802	CV3902208	single nucleotide variant	NM_001139488.2(RASGRP3):c.730G>A (p.Val244Met)	not specified [RCV005265812]	uncertain significance	2	33524471	33524471	Human		name
598184820	CV3902211	single nucleotide variant	NM_001139488.2(RASGRP3):c.902T>C (p.Ile301Thr)	not specified [RCV005265815]	uncertain significance	2	33527231	33527231	Human		name
156086168	CV2205710	single nucleotide variant	NM_001139488.2(RASGRP3):c.1694C>G (p.Ser565Trp)	not specified [RCV004075771]	uncertain significance	2	33558325	33558325	Human		name
156142616	CV2257374	single nucleotide variant	NM_001139488.2(RASGRP3):c.1244C>A (p.Thr415Lys)	not specified [RCV004125463]	uncertain significance	2	33539176	33539176	Human		name
155969841	CV2335513	single nucleotide variant	NM_001139488.2(RASGRP3):c.1295A>G (p.Tyr432Cys)	not specified [RCV004191681]	uncertain significance	2	33543528	33543528	Human		name
155970737	CV2338094	single nucleotide variant	NM_001139488.2(RASGRP3):c.1646G>A (p.Arg549Gln)	not specified [RCV004186131]	uncertain significance	2	33558277	33558277	Human		name
329368876	CV2424682	single nucleotide variant	NM_001139488.2(RASGRP3):c.2005C>T (p.Arg669Trp)	not specified [RCV004248579]	uncertain significance	2	33558971	33558971	Human		name
329378652	CV2463682	single nucleotide variant	NM_001139488.2(RASGRP3):c.1951G>T (p.Ala651Ser)	not specified [RCV004279257]	uncertain significance	2	33558917	33558917	Human		name
329387582	CV2470844	single nucleotide variant	NM_001139488.2(RASGRP3):c.1721T>C (p.Phe574Ser)	not specified [RCV004276053]	uncertain significance	2	33558687	33558687	Human		name
401726541	CV2695715	single nucleotide variant	NM_001139488.2(RASGRP3):c.1795C>T (p.Arg599Cys)	not specified [RCV004299517]	uncertain significance	2	33558761	33558761	Human		name
401718734	CV2704777	single nucleotide variant	NM_001139488.2(RASGRP3):c.1931C>T (p.Ala644Val)	not specified [RCV004307372]	uncertain significance	2	33558897	33558897	Human		name
401890981	CV2768879	single nucleotide variant	NM_001139488.2(RASGRP3):c.1592A>G (p.Asn531Ser)	not specified [RCV004346988]	uncertain significance	2	33558223	33558223	Human		name
401881327	CV2789573	single nucleotide variant	NM_001139488.2(RASGRP3):c.1111G>C (p.Asp371His)	not specified [RCV004360178]	uncertain significance	2	33534350	33534350	Human		name
405660032	CV3312405	single nucleotide variant	NM_001139488.2(RASGRP3):c.1366G>A (p.Asp456Asn)	not specified [RCV004438725]	uncertain significance	2	33543599	33543599	Human		name
405660035	CV3312406	single nucleotide variant	NM_001139488.2(RASGRP3):c.1457A>G (p.His486Arg)	not specified [RCV004438726]	uncertain significance	2	33549666	33549666	Human		name
405660038	CV3312407	single nucleotide variant	NM_001139488.2(RASGRP3):c.1500G>T (p.Met500Ile)	not specified [RCV004438727]	uncertain significance	2	33549709	33549709	Human		name
405660046	CV3312410	single nucleotide variant	NM_001139488.2(RASGRP3):c.1780G>A (p.Val594Ile)	not specified [RCV004438730]	uncertain significance	2	33558746	33558746	Human		name
405660048	CV3312411	single nucleotide variant	NM_001139488.2(RASGRP3):c.1792T>C (p.Ser598Pro)	not specified [RCV004438731]	uncertain significance	2	33558758	33558758	Human		name
405660052	CV3312412	single nucleotide variant	NM_001139488.2(RASGRP3):c.1982A>G (p.His661Arg)	not specified [RCV004438732]	uncertain significance	2	33558948	33558948	Human		name
597784132	CV3593147	single nucleotide variant	NM_001139488.2(RASGRP3):c.2006G>A (p.Arg669Gln)	not specified [RCV004854405]	uncertain significance	2	33558972	33558972	Human		name
597706674	CV3593149	single nucleotide variant	NM_001139488.2(RASGRP3):c.1144C>G (p.Pro382Ala)	not specified [RCV004860528]	uncertain significance	2	33534383	33534383	Human		name
597706686	CV3593151	single nucleotide variant	NM_001139488.2(RASGRP3):c.1073A>T (p.Asn358Ile)	not specified [RCV004860529]	uncertain significance	2	33527402	33527402	Human		name
597784146	CV3593154	single nucleotide variant	NM_001139488.2(RASGRP3):c.1642G>A (p.Ala548Thr)	not specified [RCV004854408]	uncertain significance	2	33558273	33558273	Human		name
598184765	CV3902202	single nucleotide variant	NM_001139488.2(RASGRP3):c.1079T>C (p.Leu360Pro)	not specified [RCV005265806]	uncertain significance	2	33527408	33527408	Human		name
598184770	CV3902203	single nucleotide variant	NM_001139488.2(RASGRP3):c.1487A>G (p.Asn496Ser)	not specified [RCV005265807]	uncertain significance	2	33549696	33549696	Human		name
598184778	CV3902204	single nucleotide variant	NM_001139488.2(RASGRP3):c.1649C>T (p.Ala550Val)	not specified [RCV005265808]	uncertain significance	2	33558280	33558280	Human		name
598184784	CV3902205	single nucleotide variant	NM_001139488.2(RASGRP3):c.1606T>C (p.Cys536Arg)	not specified [RCV005265809]	uncertain significance	2	33558237	33558237	Human		name
598184796	CV3902207	single nucleotide variant	NM_001139488.2(RASGRP3):c.1552A>C (p.Ile518Leu)	not specified [RCV005265811]	uncertain significance	2	33555540	33555540	Human		name
598184809	CV3902209	single nucleotide variant	NM_001139488.2(RASGRP3):c.1670A>G (p.His557Arg)	not specified [RCV005265813]	uncertain significance	2	33558301	33558301	Human		name
598184814	CV3902210	single nucleotide variant	NM_001139488.2(RASGRP3):c.1517C>T (p.Thr506Ile)	not specified [RCV005265814]	uncertain significance	2	33549726	33549726	Human		name
598203579	CV3902212	single nucleotide variant	NM_001139488.2(RASGRP3):c.1634G>A (p.Arg545Lys)	not specified [RCV005269398]	uncertain significance	2	33558265	33558265	Human		name
8630338	CV85493	single nucleotide variant	NM_001139488.1(RASGRP3):c.1241C>T (p.Pro414Leu)	Malignant melanoma [RCV000065576]	not provided	2	33539173	33539173	Human		name

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