Olfm1 Variant Search Result - Rat Genome Database

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22 records found for search term Olfm1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401904750	CV2823578	deletion	NM_006334.4(OLFM1):c.96+1247del	not provided [RCV003430384]	benign	9	135077049	135077049	Human		name
401940586	CV2840722	microsatellite	NM_006334.4(OLFM1):c.96+1349CA[8]	not provided [RCV003457577]	likely benign	9	135077151	135077152	Human		name
8626684	CV81828	single nucleotide variant	NM_014279.4(OLFM1):c.653C>T (p.Pro218Leu)	Malignant melanoma [RCV000061906]	not provided	9	135106779	135106779	Human		name
15159164	CV700884	single nucleotide variant	NM_001282611.2(OLFM1):c.717C>T (p.Val239=)	not provided [RCV000947218]	benign	9	135106789	135106789	Human		name
15138007	CV711852	single nucleotide variant	NM_001282611.2(OLFM1):c.762C>T (p.Leu254=)	not provided [RCV000965715]	benign	9	135106834	135106834	Human		name
15162082	CV711853	single nucleotide variant	NM_001282611.2(OLFM1):c.942G>A (p.Lys314=)	not provided [RCV000970206]	benign	9	135119662	135119662	Human		name
597660715	CV3573756	single nucleotide variant	NM_001282611.2(OLFM1):c.173A>G (p.Glu58Gly)	not specified [RCV004834933]	uncertain significance	9	135090217	135090217	Human		name
597733732	CV3573757	single nucleotide variant	NM_001282611.2(OLFM1):c.208G>A (p.Glu70Lys)	not specified [RCV004843216]	uncertain significance	9	135090252	135090252	Human		name
156033114	CV2236157	single nucleotide variant	NM_001282611.2(OLFM1):c.878G>A (p.Arg293His)	not specified [RCV004114298]	uncertain significance	9	135119598	135119598	Human		name
405750456	CV3370408	single nucleotide variant	NM_001282611.2(OLFM1):c.322A>T (p.Ile108Leu)	not specified [RCV004499073]	uncertain significance	9	135095885	135095885	Human		name
405750462	CV3370409	single nucleotide variant	NM_001282611.2(OLFM1):c.722C>A (p.Thr241Asn)	not specified [RCV004499074]	uncertain significance	9	135106794	135106794	Human		name
405750471	CV3370410	single nucleotide variant	NM_001282611.2(OLFM1):c.996G>T (p.Lys332Asn)	not specified [RCV004499075]	uncertain significance	9	135119716	135119716	Human		name
407527362	CV3469737	single nucleotide variant	NM_001282611.2(OLFM1):c.874C>T (p.His292Tyr)	not specified [RCV004655144]	uncertain significance	9	135119594	135119594	Human		name
407527278	CV3469738	single nucleotide variant	NM_001282611.2(OLFM1):c.823C>T (p.Arg275Cys)	not specified [RCV004655145]	uncertain significance	9	135119543	135119543	Human		name
407505494	CV3469739	single nucleotide variant	NM_001282611.2(OLFM1):c.477T>G (p.Asp159Glu)	not specified [RCV004646137]	uncertain significance	9	135098306	135098306	Human		name
597733724	CV3573755	single nucleotide variant	NM_001282611.2(OLFM1):c.364G>A (p.Val122Met)	not specified [RCV004843215]	uncertain significance	9	135095927	135095927	Human		name
155920070	CV2209871	single nucleotide variant	NM_001282611.2(OLFM1):c.1435G>A (p.Val479Ile)	not specified [RCV004076329]	uncertain significance	9	135120155	135120155	Human		name
156124653	CV2350118	single nucleotide variant	NM_001282611.2(OLFM1):c.1000C>T (p.Arg334Cys)	not specified [RCV004200040]	uncertain significance	9	135119720	135119720	Human		name
401898237	CV2790984	single nucleotide variant	NM_001282611.2(OLFM1):c.1292A>G (p.Asn431Ser)	not specified [RCV004354606]	uncertain significance	9	135120012	135120012	Human		name
405751167	CV3370411	single nucleotide variant	NM_001282611.2(OLFM1):c.1001G>A (p.Arg334His)	not specified [RCV004499076]	uncertain significance	9	135119721	135119721	Human		name
407527262	CV3469740	single nucleotide variant	NM_001282611.2(OLFM1):c.1259G>C (p.Gly420Ala)	not specified [RCV004655146]	uncertain significance	9	135119979	135119979	Human		name
597733718	CV3573754	single nucleotide variant	NM_001282611.2(OLFM1):c.1204G>A (p.Ala402Thr)	not specified [RCV004843214]	uncertain significance	9	135119924	135119924	Human		name

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