Ets1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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27 records found for search term Ets1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150439060	CV1266720	single nucleotide variant	NM_001143820.2(ETS1):c.*1736A>G	not provided [RCV001690155]	benign	11	128460625	128460625	Human	6	name
8652712	CV129287	single nucleotide variant	NM_001143820.1(ETS1):c.862+1864A>T	Lung cancer [RCV000109774]	uncertain significance	11	128482959	128482959	Human		name
15107024	CV712707	single nucleotide variant	NM_001143820.2(ETS1):c.36C>T (p.Pro12=)	not provided [RCV000960201]	benign	11	128573095	128573095	Human		name
15105633	CV712706	single nucleotide variant	NM_001143820.2(ETS1):c.103C>A (p.Arg35=)	not provided [RCV000959923]	benign	11	128556402	128556402	Human		name
15202376	CV701654	single nucleotide variant	NM_001143820.2(ETS1):c.600G>A (p.Ser200=)	not provided [RCV000957897]	benign	11	128486082	128486082	Human		name
15189650	CV724299	single nucleotide variant	NM_001143820.2(ETS1):c.921C>T (p.Arg307=)	not provided [RCV000887879]	benign	11	128480393	128480393	Human		name
151349646	CV1324438	single nucleotide variant	NM_001143820.2(ETS1):c.103C>T (p.Arg35Ter)	ETS1-related disorder [RCV001808883]	likely pathogenic	11	128556402	128556402	Human		name , trait , alternate_id
597692183	CV3665217	single nucleotide variant	NM_001143820.2(ETS1):c.296G>T (p.Gly99Val)	not specified [RCV004915450]	uncertain significance	11	128490495	128490495	Human		name
598193661	CV3958380	single nucleotide variant	NM_001143820.2(ETS1):c.1434C>T (p.Asp478=)	not specified [RCV005335230]	likely benign	11	128462385	128462385	Human		name
10449856	CV215427	single nucleotide variant	NM_001143820.2(ETS1):c.617A>G (p.Tyr206Cys)	ETS1-related disorder [RCV004553106]\|not specified [RCV000203016]	likely benign\|uncertain significance	11	128485068	128485068	Human		name , trait , alternate_id
156193420	CV2296968	single nucleotide variant	NM_001143820.2(ETS1):c.808A>G (p.Ile270Val)	not specified [RCV004150900]	uncertain significance	11	128484877	128484877	Human		name
156103647	CV2386916	single nucleotide variant	NM_001143820.2(ETS1):c.859C>T (p.Arg287Cys)	not specified [RCV004233547]	uncertain significance	11	128484826	128484826	Human		name
401725427	CV2697407	single nucleotide variant	NM_001143820.2(ETS1):c.665C>T (p.Pro222Leu)	not specified [RCV004304157]	uncertain significance	11	128485020	128485020	Human		name
401892094	CV2775932	single nucleotide variant	NM_001143820.2(ETS1):c.650C>T (p.Ser217Leu)	not specified [RCV004344957]	uncertain significance	11	128485035	128485035	Human		name
405758897	CV3256053	single nucleotide variant	NM_001143820.2(ETS1):c.752C>T (p.Ser251Leu)	not specified [RCV004383118]	uncertain significance	11	128484933	128484933	Human		name
405758904	CV3256054	single nucleotide variant	NM_001143820.2(ETS1):c.823G>A (p.Val275Ile)	not specified [RCV004383119]	uncertain significance	11	128484862	128484862	Human		name
407499211	CV3438404	single nucleotide variant	NM_001143820.2(ETS1):c.871G>A (p.Gly291Arg)	not specified [RCV004622724]	uncertain significance	11	128480443	128480443	Human		name
407499219	CV3438406	single nucleotide variant	NM_001143820.2(ETS1):c.432G>A (p.Met144Ile)	not specified [RCV004622726]	uncertain significance	11	128489393	128489393	Human		name
407499224	CV3438407	single nucleotide variant	NM_001143820.2(ETS1):c.860G>T (p.Arg287Leu)	not specified [RCV004622727]	uncertain significance	11	128484825	128484825	Human		name
597692161	CV3665215	single nucleotide variant	NM_001143820.2(ETS1):c.340C>T (p.Arg114Trp)	not specified [RCV004915448]	uncertain significance	11	128489485	128489485	Human		name
597692171	CV3665216	single nucleotide variant	NM_001143820.2(ETS1):c.341G>A (p.Arg114Gln)	not specified [RCV004915449]	uncertain significance	11	128489484	128489484	Human		name
598193668	CV3958381	single nucleotide variant	NM_001143820.2(ETS1):c.580C>T (p.Pro194Ser)	not specified [RCV005335231]	uncertain significance	11	128486102	128486102	Human		name
15107362	CV712705	single nucleotide variant	NM_001143820.2(ETS1):c.451G>A (p.Ala151Thr)	not provided [RCV000960275]	likely benign	11	128489374	128489374	Human		name
156146274	CV2265113	single nucleotide variant	NM_001143820.2(ETS1):c.1013C>T (p.Ala338Val)	not specified [RCV004126249]	uncertain significance	11	128480301	128480301	Human		name
329396751	CV2455761	single nucleotide variant	NM_001143820.2(ETS1):c.1423G>A (p.Ala475Thr)	not specified [RCV004279055]	uncertain significance	11	128462396	128462396	Human		name
407499215	CV3438405	single nucleotide variant	NM_001143820.2(ETS1):c.1304G>A (p.Arg435His)	not specified [RCV004622725]	uncertain significance	11	128462515	128462515	Human		name
14689884	CV615873	indel	NM_001143820.2(ETS1):c.1044_1049delinsTT (p.Lys349fs)	11q partial monosomy syndrome [RCV000770888]	pathogenic	11	128480265	128480270	Human		name

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