Ier2 Variant Search Result - Rat Genome Database

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22 records found for search term Ier2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156057217	CV2375830	single nucleotide variant	NM_004907.3(IER2):c.35C>T (p.Thr12Ile)	not specified [RCV004224410]	uncertain significance	19	13153221	13153221	Human		name
156071644	CV2328604	single nucleotide variant	NM_004907.3(IER2):c.295C>G (p.Gln99Glu)	not specified [RCV004177861]	uncertain significance	19	13153481	13153481	Human		name
155992312	CV2381449	single nucleotide variant	NM_004907.3(IER2):c.118A>C (p.Met40Leu)	not specified [RCV004229936]	uncertain significance	19	13153304	13153304	Human		name
401881970	CV2784912	single nucleotide variant	NM_004907.3(IER2):c.236C>T (p.Ser79Phe)	not specified [RCV004352688]	uncertain significance	19	13153422	13153422	Human		name
407466798	CV3444447	single nucleotide variant	NM_004907.3(IER2):c.130C>G (p.Arg44Gly)	not specified [RCV004635517]	uncertain significance	19	13153316	13153316	Human		name
597762690	CV3683114	single nucleotide variant	NM_004907.3(IER2):c.268C>T (p.His90Tyr)	not specified [RCV004926179]	uncertain significance	19	13153454	13153454	Human		name
598267605	CV3979099	single nucleotide variant	NM_004907.3(IER2):c.190G>T (p.Ala64Ser)	not specified [RCV005349545]	uncertain significance	19	13153376	13153376	Human		name
156061440	CV2239988	single nucleotide variant	NM_004907.3(IER2):c.305C>T (p.Pro102Leu)	not specified [RCV004110778]	uncertain significance	19	13153491	13153491	Human		name
156100212	CV2260236	single nucleotide variant	NM_004907.3(IER2):c.320C>A (p.Thr107Asn)	not specified [RCV004129348]	uncertain significance	19	13153506	13153506	Human		name
155917258	CV2336301	single nucleotide variant	NM_004907.3(IER2):c.415A>C (p.Lys139Gln)	not specified [RCV004192050]	uncertain significance	19	13153601	13153601	Human		name
155984820	CV2368005	single nucleotide variant	NM_004907.3(IER2):c.463G>A (p.Glu155Lys)	not specified [RCV004223092]	uncertain significance	19	13153649	13153649	Human		name
329396810	CV2455810	single nucleotide variant	NM_004907.3(IER2):c.637C>T (p.Leu213Phe)	not specified [RCV004279099]	uncertain significance	19	13153823	13153823	Human		name
405791756	CV3267331	single nucleotide variant	NM_004907.3(IER2):c.299A>G (p.Glu100Gly)	not specified [RCV004399967]	uncertain significance	19	13153485	13153485	Human		name
405791759	CV3267332	single nucleotide variant	NM_004907.3(IER2):c.320C>T (p.Thr107Ile)	not specified [RCV004399968]	uncertain significance	19	13153506	13153506	Human		name
405791761	CV3267333	single nucleotide variant	NM_004907.3(IER2):c.367C>T (p.Arg123Cys)	not specified [RCV004399969]	uncertain significance	19	13153553	13153553	Human		name
405791764	CV3267334	single nucleotide variant	NM_004907.3(IER2):c.474T>G (p.Asp158Glu)	not specified [RCV004399970]	uncertain significance	19	13153660	13153660	Human		name
405791767	CV3267335	single nucleotide variant	NM_004907.3(IER2):c.490C>G (p.Pro164Ala)	not specified [RCV004399971]	uncertain significance	19	13153676	13153676	Human		name
405791770	CV3267336	single nucleotide variant	NM_004907.3(IER2):c.623C>T (p.Pro208Leu)	not specified [RCV004399972]	uncertain significance	19	13153809	13153809	Human		name
407511029	CV3444445	single nucleotide variant	NM_004907.3(IER2):c.310G>A (p.Ala104Thr)	not specified [RCV004626329]	uncertain significance	19	13153496	13153496	Human		name
407466802	CV3444446	single nucleotide variant	NM_004907.3(IER2):c.506G>A (p.Gly169Asp)	not specified [RCV004635516]	uncertain significance	19	13153692	13153692	Human		name
407466793	CV3444448	single nucleotide variant	NM_004907.3(IER2):c.500C>T (p.Ala167Val)	not specified [RCV004635518]	uncertain significance	19	13153686	13153686	Human		name
15114113	CV716191	single nucleotide variant	NM_004907.3(IER2):c.571G>A (p.Ala191Thr)	not provided [RCV000961612]	benign	19	13153757	13153757	Human		name

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