Elk1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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33 records found for search term Elk1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401926904	CV2821623	single nucleotide variant	NM_001114123.3(ELK1):c.642C>T (p.Gly214=)	not provided [RCV003438208]	likely benign	X	47638907	47638907	Human		name
401926905	CV2821624	single nucleotide variant	NM_001114123.3(ELK1):c.576C>G (p.Pro192=)	not provided [RCV003438209]	likely benign	X	47638973	47638973	Human		name
15167266	CV729618	single nucleotide variant	NM_001114123.3(ELK1):c.672C>A (p.Pro224=)	not provided [RCV000882811]	benign	X	47638165	47638165	Human		name
15166657	CV758518	single nucleotide variant	NM_001114123.3(ELK1):c.993G>A (p.Pro331=)	not provided [RCV000926918]	likely benign	X	47637844	47637844	Human		name
401926903	CV2821622	single nucleotide variant	NM_001114123.3(ELK1):c.1041T>C (p.Ala347=)	not provided [RCV003438207]	likely benign	X	47637796	47637796	Human		name
597746910	CV3670915	single nucleotide variant	NM_001114123.3(ELK1):c.146G>A (p.Arg49His)	not specified [RCV004922794]	uncertain significance	X	47641296	47641296	Human		name
15128496	CV717801	single nucleotide variant	NM_001114123.3(ELK1):c.1254C>T (p.Pro418=)	not provided [RCV000964093]	benign	X	47636862	47636862	Human		name
15187672	CV729617	single nucleotide variant	NM_001114123.3(ELK1):c.1158G>A (p.Ala386=)	not provided [RCV000887318]	benign	X	47637043	47637043	Human		name
21070651	CV798312	deletion	NM_001114123.3(ELK1):c.779del (p.Ala260fs)	not provided [RCV000999411]	uncertain significance	X	47638058	47638058	Human		name
151351325	CV1323837	single nucleotide variant	NM_001114123.3(ELK1):c.548G>A (p.Ser183Asn)	not provided [RCV001810383]	benign	X	47639001	47639001	Human		name
151663219	CV1331000	single nucleotide variant	NM_001114123.3(ELK1):c.775G>T (p.Val259Phe)	not provided [RCV001825173]	not provided	X	47638062	47638062	Human		name
156276058	CV2290797	single nucleotide variant	NM_001114123.3(ELK1):c.472C>T (p.Leu158Phe)	not specified [RCV004149301]	uncertain significance	X	47639077	47639077	Human		name
156286558	CV2327246	single nucleotide variant	NM_001114123.3(ELK1):c.357A>G (p.Ile119Met)	not specified [RCV004174698]	uncertain significance	X	47639192	47639192	Human		name
156304302	CV2359587	single nucleotide variant	NM_001114123.3(ELK1):c.628G>T (p.Ala210Ser)	not specified [RCV004214887]	uncertain significance	X	47638921	47638921	Human		name
155909996	CV2369617	single nucleotide variant	NM_001114123.3(ELK1):c.506C>T (p.Pro169Leu)	not specified [RCV004215028]	uncertain significance	X	47639043	47639043	Human		name
401748040	CV2687668	single nucleotide variant	NM_001114123.3(ELK1):c.640G>A (p.Gly214Ser)	not specified [RCV004300879]	uncertain significance	X	47638909	47638909	Human		name
401720374	CV2705857	single nucleotide variant	NM_001114123.3(ELK1):c.538G>A (p.Val180Met)	not specified [RCV004320472]	uncertain significance	X	47639011	47639011	Human		name
401864843	CV2778081	single nucleotide variant	NM_001114123.3(ELK1):c.830C>T (p.Pro277Leu)	not specified [RCV004348029]	uncertain significance	X	47638007	47638007	Human		name
405738534	CV3238925	single nucleotide variant	NM_001114123.3(ELK1):c.407G>T (p.Gly136Val)	not specified [RCV004380194]	uncertain significance	X	47639142	47639142	Human		name
407506589	CV3438274	single nucleotide variant	NM_001114123.3(ELK1):c.991C>T (p.Pro331Ser)	not specified [RCV004624744]	uncertain significance	X	47637846	47637846	Human		name
407506592	CV3438275	single nucleotide variant	NM_001114123.3(ELK1):c.361G>A (p.Ala121Thr)	not specified [RCV004624745]	uncertain significance	X	47639188	47639188	Human		name
407506595	CV3438276	single nucleotide variant	NM_001114123.3(ELK1):c.761A>C (p.Lys254Thr)	not specified [RCV004624746]	uncertain significance	X	47638076	47638076	Human		name
597666212	CV3670910	single nucleotide variant	NM_001114123.3(ELK1):c.299C>T (p.Pro100Leu)	not specified [RCV004912522]	uncertain significance	X	47639250	47639250	Human		name
597746896	CV3670911	single nucleotide variant	NM_001114123.3(ELK1):c.544C>T (p.Pro182Ser)	not specified [RCV004922791]	uncertain significance	X	47639005	47639005	Human		name
597666219	CV3670912	single nucleotide variant	NM_001114123.3(ELK1):c.578C>G (p.Pro193Arg)	not specified [RCV004912523]	uncertain significance	X	47638971	47638971	Human		name
597746901	CV3670913	single nucleotide variant	NM_001114123.3(ELK1):c.574C>A (p.Pro192Thr)	not specified [RCV004922792]	uncertain significance	X	47638975	47638975	Human		name
598190751	CV3957721	single nucleotide variant	NM_001114123.3(ELK1):c.836A>G (p.Gln279Arg)	not specified [RCV005334740]	uncertain significance	X	47638001	47638001	Human		name
598190759	CV3957722	single nucleotide variant	NM_001114123.3(ELK1):c.908C>G (p.Ser303Cys)	not specified [RCV005334741]	uncertain significance	X	47637929	47637929	Human		name
598190765	CV3957723	single nucleotide variant	NM_001114123.3(ELK1):c.653A>G (p.Gln218Arg)	not specified [RCV005334742]	uncertain significance	X	47638896	47638896	Human		name
15115117	CV717802	single nucleotide variant	NM_001114123.3(ELK1):c.430G>A (p.Gly144Ser)	not provided [RCV000961794]	benign	X	47639119	47639119	Human		name
15187676	CV729619	single nucleotide variant	NM_001114123.3(ELK1):c.514C>G (p.Pro172Ala)	not provided [RCV000887319]	benign	X	47639035	47639035	Human		name
405738527	CV3238924	single nucleotide variant	NM_001114123.3(ELK1):c.1031G>C (p.Gly344Ala)	not specified [RCV004380193]	uncertain significance	X	47637806	47637806	Human		name
597746906	CV3670914	single nucleotide variant	NM_001114123.3(ELK1):c.1049C>T (p.Pro350Leu)	not specified [RCV004922793]	uncertain significance	X	47637788	47637788	Human		name

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