Emp3 Variant Search Result - Rat Genome Database

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15 records found for search term Emp3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155926728	CV2365802	single nucleotide variant	NM_001425.3(EMP3):c.22G>A (p.Val8Ile)	not specified [RCV004214337]	uncertain significance	19	48326866	48326866	Human		name
401777238	CV2707819	single nucleotide variant	NM_001425.3(EMP3):c.50T>C (p.Ile17Thr)	not specified [RCV004309104]	uncertain significance	19	48326894	48326894	Human		name
598192940	CV3958072	single nucleotide variant	NM_001425.3(EMP3):c.98G>A (p.Gly33Glu)	not specified [RCV005335091]	uncertain significance	19	48327540	48327540	Human		name
155945296	CV2269557	single nucleotide variant	NM_001425.3(EMP3):c.208A>T (p.Met70Leu)	not specified [RCV004124659]	uncertain significance	19	48329378	48329378	Human		name
407507115	CV3435008	single nucleotide variant	NM_001425.3(EMP3):c.169G>A (p.Val57Ile)	not specified [RCV004624983]	uncertain significance	19	48327611	48327611	Human		name
597685852	CV3667880	single nucleotide variant	NM_001425.3(EMP3):c.124G>A (p.Asp42Asn)	not specified [RCV004914801]	uncertain significance	19	48327566	48327566	Human		name
598192945	CV3958073	single nucleotide variant	NM_001425.3(EMP3):c.142G>A (p.Asp48Asn)	not specified [RCV005335092]	uncertain significance	19	48327584	48327584	Human		name
156059425	CV2239334	single nucleotide variant	NM_001425.3(EMP3):c.359T>C (p.Ile120Thr)	not specified [RCV004114074]	uncertain significance	19	48330337	48330337	Human		name
156173589	CV2247611	single nucleotide variant	NM_001425.3(EMP3):c.320C>T (p.Thr107Ile)	not specified [RCV004108903]	uncertain significance	19	48329490	48329490	Human		name
329376425	CV2425133	single nucleotide variant	NM_001425.3(EMP3):c.301G>A (p.Gly101Ser)	not specified [RCV004249024]	uncertain significance	19	48329471	48329471	Human		name
405755918	CV3245043	single nucleotide variant	NM_001425.3(EMP3):c.364G>T (p.Ala122Ser)	not specified [RCV004382675]	uncertain significance	19	48330342	48330342	Human		name
405755925	CV3245044	single nucleotide variant	NM_001425.3(EMP3):c.485G>A (p.Arg162Gln)	not specified [RCV004382676]	uncertain significance	19	48330463	48330463	Human		name
407507112	CV3435007	single nucleotide variant	NM_001425.3(EMP3):c.467A>G (p.Tyr156Cys)	not specified [RCV004624982]	uncertain significance	19	48330445	48330445	Human		name
597747202	CV3667881	single nucleotide variant	NM_001425.3(EMP3):c.457G>C (p.Gly153Arg)	not specified [RCV004922879]	uncertain significance	19	48330435	48330435	Human		name
597685860	CV3667882	single nucleotide variant	NM_001425.3(EMP3):c.314T>C (p.Leu105Pro)	not specified [RCV004914802]	uncertain significance	19	48329484	48329484	Human		name