Gmps Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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42 records found for search term Gmps

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15196275	CV777229	single nucleotide variant	NM_003875.3(GMPS):c.27+9G>T	not provided [RCV000956149]	benign	3	155870906	155870906	Human		name
15202867	CV777384	single nucleotide variant	NM_003875.3(GMPS):c.209+5A>G	not provided [RCV000958079]	benign	3	155893704	155893704	Human		name
405767952	CV3262026	single nucleotide variant	NM_003875.3(GMPS):c.25A>C (p.Lys9Gln)	not specified [RCV004395415]	uncertain significance	3	155870895	155870895	Human		name
401876827	CV2793248	single nucleotide variant	NM_003875.3(GMPS):c.74A>T (p.Glu25Val)	not specified [RCV004362078]	uncertain significance	3	155893564	155893564	Human		name
597730187	CV3678164	single nucleotide variant	NM_003875.3(GMPS):c.71A>G (p.Tyr24Cys)	not specified [RCV004919793]	uncertain significance	3	155893561	155893561	Human		name
15155224	CV720272	single nucleotide variant	NM_003875.3(GMPS):c.708G>A (p.Thr236=)	not provided [RCV000880375]	benign	3	155910873	155910873	Human		name
155901029	CV2275306	single nucleotide variant	NM_003875.3(GMPS):c.217A>G (p.Ile73Val)	not specified [RCV004137078]	uncertain significance	3	155897934	155897934	Human		name
155995121	CV2375785	single nucleotide variant	NM_003875.3(GMPS):c.208C>T (p.Arg70Cys)	not specified [RCV004224371]	uncertain significance	3	155893698	155893698	Human		name
15196278	CV697909	single nucleotide variant	NM_003875.3(GMPS):c.1779T>C (p.Phe593=)	not provided [RCV000956150]	benign	3	155935018	155935018	Human		name
15151767	CV748087	single nucleotide variant	NM_003875.3(GMPS):c.1017C>T (p.Ile339=)	not provided [RCV000923742]	benign	3	155914549	155914549	Human		name
156378678	CV2207780	single nucleotide variant	NM_003875.3(GMPS):c.863A>G (p.Lys288Arg)	not specified [RCV004084217]	uncertain significance	3	155911256	155911256	Human		name
156204473	CV2297793	single nucleotide variant	NM_003875.3(GMPS):c.977C>T (p.Thr326Met)	not specified [RCV004157747]	uncertain significance	3	155914509	155914509	Human		name
329357372	CV2427691	single nucleotide variant	NM_003875.3(GMPS):c.583C>T (p.Leu195Phe)	not specified [RCV004252477]	uncertain significance	3	155910748	155910748	Human		name
401778427	CV2709113	single nucleotide variant	NM_003875.3(GMPS):c.524C>A (p.Ala175Glu)	not specified [RCV004314444]	uncertain significance	3	155906261	155906261	Human		name
401761746	CV2726889	single nucleotide variant	NM_003875.3(GMPS):c.403A>G (p.Asn135Asp)	not specified [RCV004323180]	uncertain significance	3	155903941	155903941	Human		name
401888130	CV2791266	single nucleotide variant	NM_003875.3(GMPS):c.653C>T (p.Thr218Ile)	not specified [RCV004356896]	uncertain significance	3	155910818	155910818	Human		name
405767964	CV3262028	single nucleotide variant	NM_003875.3(GMPS):c.505C>T (p.Arg169Cys)	not specified [RCV004395417]	uncertain significance	3	155906242	155906242	Human		name
407519946	CV3443544	single nucleotide variant	NM_003875.3(GMPS):c.872G>A (p.Gly291Glu)	not specified [RCV004629858]	uncertain significance	3	155911265	155911265	Human		name
597788614	CV3678166	single nucleotide variant	NM_003875.3(GMPS):c.905C>G (p.Ser302Cys)	not specified [RCV004932724]	uncertain significance	3	155914437	155914437	Human		name
598264056	CV3974329	single nucleotide variant	NM_003875.3(GMPS):c.314A>G (p.Tyr105Cys)	not specified [RCV005348750]	uncertain significance	3	155898031	155898031	Human		name
156077769	CV2198254	single nucleotide variant	NM_003875.3(GMPS):c.1814C>T (p.Ala605Val)	not specified [RCV004079832]	uncertain significance	3	155936344	155936344	Human		name
156273960	CV2277853	single nucleotide variant	NM_003875.3(GMPS):c.1559A>G (p.Gln520Arg)	not specified [RCV004147269]	uncertain significance	3	155925365	155925365	Human		name
156345090	CV2290921	single nucleotide variant	NM_003875.3(GMPS):c.1655G>A (p.Arg552His)	not specified [RCV004151483]	uncertain significance	3	155931859	155931859	Human		name
156297134	CV2297647	single nucleotide variant	NM_003875.3(GMPS):c.1696C>T (p.Pro566Ser)	not specified [RCV004155337]	uncertain significance	3	155934935	155934935	Human		name
156107310	CV2303933	single nucleotide variant	NM_003875.3(GMPS):c.1786C>T (p.His596Tyr)	not specified [RCV004168208]	uncertain significance	3	155935025	155935025	Human		name
156267637	CV2305674	single nucleotide variant	NM_003875.3(GMPS):c.1200G>T (p.Lys400Asn)	not specified [RCV004167502]	uncertain significance	3	155916180	155916180	Human		name
156203722	CV2335018	single nucleotide variant	NM_003875.3(GMPS):c.1689A>G (p.Ile563Met)	not specified [RCV004182108]	uncertain significance	3	155934928	155934928	Human		name
156121796	CV2354282	single nucleotide variant	NM_003875.3(GMPS):c.1028C>A (p.Thr343Asn)	not specified [RCV004206703]	uncertain significance	3	155914560	155914560	Human		name
405767914	CV3262019	single nucleotide variant	NM_003875.3(GMPS):c.1373A>C (p.Asp458Ala)	not specified [RCV004395408]	uncertain significance	3	155922241	155922241	Human		name
405767919	CV3262020	single nucleotide variant	NM_003875.3(GMPS):c.1451A>G (p.Gln484Arg)	not specified [RCV004395409]	uncertain significance	3	155925257	155925257	Human		name
405767926	CV3262021	single nucleotide variant	NM_003875.3(GMPS):c.1570C>T (p.Arg524Cys)	not specified [RCV004395410]	uncertain significance	3	155931774	155931774	Human		name
405767932	CV3262022	single nucleotide variant	NM_003875.3(GMPS):c.1586T>C (p.Val529Ala)	not specified [RCV004395411]	uncertain significance	3	155931790	155931790	Human		name
405767936	CV3262023	single nucleotide variant	NM_003875.3(GMPS):c.1765C>T (p.Arg589Cys)	not specified [RCV004395412]	uncertain significance	3	155935004	155935004	Human		name
405767940	CV3262024	single nucleotide variant	NM_003875.3(GMPS):c.1778T>C (p.Phe593Ser)	not specified [RCV004395413]	uncertain significance	3	155935017	155935017	Human		name
405767946	CV3262025	single nucleotide variant	NM_003875.3(GMPS):c.1789A>G (p.Asn597Asp)	not specified [RCV004395414]	uncertain significance	3	155935028	155935028	Human		name
407519947	CV3443545	single nucleotide variant	NM_003875.3(GMPS):c.1873C>T (p.Leu625Phe)	not specified [RCV004629859]	uncertain significance	3	155936403	155936403	Human		name
597730206	CV3678167	single nucleotide variant	NM_003875.3(GMPS):c.1184C>G (p.Thr395Arg)	not specified [RCV004919795]	uncertain significance	3	155916164	155916164	Human		name
597788610	CV3678168	single nucleotide variant	NM_003875.3(GMPS):c.1643G>C (p.Arg548Thr)	not specified [RCV004932725]	uncertain significance	3	155931847	155931847	Human		name
597730214	CV3678169	single nucleotide variant	NM_003875.3(GMPS):c.1585G>A (p.Val529Met)	not specified [RCV004919796]	uncertain significance	3	155931789	155931789	Human		name
598264054	CV3974328	single nucleotide variant	NM_003875.3(GMPS):c.1244A>G (p.His415Arg)	not specified [RCV005348749]	uncertain significance	3	155919264	155919264	Human		name
15164162	CV697908	single nucleotide variant	NM_003875.3(GMPS):c.1583A>C (p.Tyr528Ser)	not provided [RCV000948270]	benign	3	155931787	155931787	Human	1	name
15164162	CV697908	single nucleotide variant	NM_003875.3(GMPS):c.1583A>C (p.Tyr528Ser)	not provided [RCV000948270]	benign	3	155931787	155931788	Human	1	name

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