Emp1 Variant Search Result - Rat Genome Database

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18 records found for search term Emp1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401905979	CV2810222	single nucleotide variant	NM_001423.3(EMP1):c.316+126T>C	not provided [RCV003396247]	likely benign	12	13213947	13213947	Human		name
401929273	CV2810221	single nucleotide variant	NM_001423.3(EMP1):c.33C>T (p.Val11=)	not provided [RCV003390181]	likely benign	12	13211543	13211543	Human		name
329387775	CV2446792	single nucleotide variant	NM_001423.3(EMP1):c.46G>C (p.Val16Leu)	not specified [RCV004257653]	uncertain significance	12	13211556	13211556	Human		name
401882783	CV2778581	single nucleotide variant	NM_001423.3(EMP1):c.263C>T (p.Thr88Ile)	not specified [RCV004344232]	uncertain significance	12	13213768	13213768	Human		name
405755870	CV3245036	single nucleotide variant	NM_001423.3(EMP1):c.156C>G (p.Ser52Arg)	not specified [RCV004382668]	uncertain significance	12	13213556	13213556	Human		name
405755876	CV3245037	single nucleotide variant	NM_001423.3(EMP1):c.205A>T (p.Ile69Phe)	not specified [RCV004382669]	uncertain significance	12	13213710	13213710	Human		name
407507106	CV3435005	single nucleotide variant	NM_001423.3(EMP1):c.229A>G (p.Ile77Val)	not specified [RCV004624980]	uncertain significance	12	13213734	13213734	Human		name
156380198	CV2218078	single nucleotide variant	NM_001423.3(EMP1):c.367C>T (p.Arg123Cys)	not specified [RCV004086513]	uncertain significance	12	13214584	13214584	Human		name
156197331	CV2367312	single nucleotide variant	NM_001423.3(EMP1):c.377C>T (p.Thr126Met)	not specified [RCV004208817]	uncertain significance	12	13214594	13214594	Human		name
401738416	CV2714450	single nucleotide variant	NM_001423.3(EMP1):c.401A>G (p.Tyr134Cys)	not specified [RCV004317977]	uncertain significance	12	13214618	13214618	Human		name
401878532	CV2776322	single nucleotide variant	NM_001423.3(EMP1):c.328C>G (p.Leu110Val)	not specified [RCV004355464]	uncertain significance	12	13214545	13214545	Human		name
405755886	CV3245038	single nucleotide variant	NM_001423.3(EMP1):c.377C>A (p.Thr126Lys)	not specified [RCV004382670]	uncertain significance	12	13214594	13214594	Human		name
405755893	CV3245039	single nucleotide variant	NM_001423.3(EMP1):c.381G>T (p.Gln127His)	not specified [RCV004382671]	uncertain significance	12	13214598	13214598	Human		name
597685832	CV3667878	single nucleotide variant	NM_001423.3(EMP1):c.445G>A (p.Val149Ile)	not specified [RCV004914799]	likely benign	12	13214662	13214662	Human		name
598192907	CV3958066	single nucleotide variant	NM_001423.3(EMP1):c.409G>A (p.Gly137Ser)	not specified [RCV005335085]	uncertain significance	12	13214626	13214626	Human		name
598192913	CV3958067	single nucleotide variant	NM_001423.3(EMP1):c.424T>A (p.Cys142Ser)	not specified [RCV005335086]	uncertain significance	12	13214641	13214641	Human		name
598192919	CV3958068	single nucleotide variant	NM_001423.3(EMP1):c.431G>C (p.Ser144Thr)	not specified [RCV005335087]	uncertain significance	12	13214648	13214648	Human		name
598192924	CV3958069	single nucleotide variant	NM_001423.3(EMP1):c.332T>C (p.Val111Ala)	not specified [RCV005335088]	uncertain significance	12	13214549	13214549	Human		name