Sfrp2 Variant Search Result - Rat Genome Database

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24 records found for search term Sfrp2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15196706	CV777311	single nucleotide variant	NM_003013.3(SFRP2):c.584-4A>T	not provided [RCV000956262]	benign	4	153781759	153781759	Human		name
407489881	CV3484014	single nucleotide variant	NM_003013.3(SFRP2):c.11G>A (p.Gly4Asp)	not specified [RCV004666179]	uncertain significance	4	153788825	153788825	Human		name
15196710	CV698398	single nucleotide variant	NM_003013.3(SFRP2):c.246G>A (p.Leu82=)	not provided [RCV000956263]	benign	4	153788590	153788590	Human		name
156074172	CV2247769	single nucleotide variant	NM_003013.3(SFRP2):c.79C>G (p.Leu27Val)	not specified [RCV004121239]	uncertain significance	4	153788757	153788757	Human		name
329361748	CV2468271	single nucleotide variant	NM_003013.3(SFRP2):c.47A>G (p.His16Arg)	not specified [RCV004275833]	uncertain significance	4	153788789	153788789	Human		name
405763891	CV3321498	single nucleotide variant	NM_003013.3(SFRP2):c.91C>G (p.Pro31Ala)	not specified [RCV004455790]	uncertain significance	4	153788745	153788745	Human		name
407489894	CV3484017	single nucleotide variant	NM_003013.3(SFRP2):c.51C>G (p.Cys17Trp)	not specified [RCV004666181]	uncertain significance	4	153788785	153788785	Human		name
15185898	CV764359	single nucleotide variant	NM_003013.3(SFRP2):c.675C>T (p.Asn225=)	not provided [RCV000931192]	likely benign	4	153781664	153781664	Human		name
155926525	CV2230636	single nucleotide variant	NM_003013.3(SFRP2):c.205A>G (p.Met69Val)	not specified [RCV004097590]	uncertain significance	4	153788631	153788631	Human		name
407492617	CV3484015	single nucleotide variant	NM_003013.3(SFRP2):c.194G>T (p.Gly65Val)	not specified [RCV004667204]	uncertain significance	4	153788642	153788642	Human		name
407489887	CV3484016	single nucleotide variant	NM_003013.3(SFRP2):c.220G>C (p.Glu74Gln)	not specified [RCV004666180]	uncertain significance	4	153788616	153788616	Human		name
11040236	CV223618	single nucleotide variant	NM_003013.3(SFRP2):c.626A>G (p.Asp209Gly)	Anophthalmia-microphthalmia syndrome [RCV000207374]\|not specified [RCV005278538]	pathogenic\|likely benign\|uncertain significance	4	153781713	153781713	Human	1	name
156267940	CV2275585	single nucleotide variant	NM_003013.3(SFRP2):c.607A>T (p.Ile203Leu)	not specified [RCV004137221]	uncertain significance	4	153781732	153781732	Human		name
156338445	CV2370647	single nucleotide variant	NM_003013.3(SFRP2):c.544G>T (p.Asp182Tyr)	not specified [RCV004215968]	uncertain significance	4	153785903	153785903	Human		name
401745319	CV2698513	single nucleotide variant	NM_003013.3(SFRP2):c.539A>G (p.Asp180Gly)	not specified [RCV004299011]	uncertain significance	4	153785908	153785908	Human		name
401719121	CV2731189	single nucleotide variant	NM_003013.3(SFRP2):c.772C>G (p.Leu258Val)	not specified [RCV004332672]	uncertain significance	4	153781567	153781567	Human		name
405763872	CV3321495	single nucleotide variant	NM_003013.3(SFRP2):c.331A>C (p.Ile111Leu)	not specified [RCV004455787]	uncertain significance	4	153788505	153788505	Human		name
405763879	CV3321496	single nucleotide variant	NM_003013.3(SFRP2):c.799G>A (p.Glu267Lys)	not specified [RCV004455788]	uncertain significance	4	153781540	153781540	Human		name
405763885	CV3321497	single nucleotide variant	NM_003013.3(SFRP2):c.872G>A (p.Arg291His)	not specified [RCV004455789]	uncertain significance	4	153781467	153781467	Human		name
407489899	CV3484018	single nucleotide variant	NM_003013.3(SFRP2):c.754G>A (p.Asp252Asn)	not specified [RCV004666182]	uncertain significance	4	153781585	153781585	Human		name
407489905	CV3484019	single nucleotide variant	NM_003013.3(SFRP2):c.578A>G (p.Asp193Gly)	not specified [RCV004666183]	uncertain significance	4	153785869	153785869	Human		name
598198523	CV3921135	single nucleotide variant	NM_003013.3(SFRP2):c.550G>A (p.Asp184Asn)	not specified [RCV005268260]	uncertain significance	4	153785897	153785897	Human		name
598166364	CV3921136	single nucleotide variant	NM_003013.3(SFRP2):c.376G>T (p.Ala126Ser)	not specified [RCV005283657]	uncertain significance	4	153788460	153788460	Human		name
598166371	CV3921137	single nucleotide variant	NM_003013.3(SFRP2):c.419T>C (p.Leu140Pro)	not specified [RCV005283658]	uncertain significance	4	153788417	153788417	Human		name

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