Wfdc10a Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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11 records found for search term Wfdc10a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156400881	CV2217362	single nucleotide variant	NM_080753.3(WFDC10A):c.13A>G (p.Thr5Ala)	Inborn genetic diseases [RCV002656719]	likely benign	20	45629826	45629826	Human	1	name
156267294	CV2329665	single nucleotide variant	NM_080753.3(WFDC10A):c.78G>C (p.Lys26Asn)	not specified [RCV004180777]	uncertain significance	20	45629891	45629891	Human		name
329360570	CV2439508	single nucleotide variant	NM_080753.3(WFDC10A):c.73G>A (p.Asp25Asn)	not specified [RCV004262447]	uncertain significance	20	45629886	45629886	Human		name
329401084	CV2446098	single nucleotide variant	NM_080753.3(WFDC10A):c.81G>C (p.Lys27Asn)	not specified [RCV004270654]	uncertain significance	20	45629894	45629894	Human		name
401758752	CV2705110	single nucleotide variant	NM_080753.3(WFDC10A):c.55G>T (p.Ala19Ser)	not specified [RCV004310014]	uncertain significance	20	45629868	45629868	Human		name
156326516	CV2205780	single nucleotide variant	NM_080753.3(WFDC10A):c.185C>A (p.Ala62Glu)	not specified [RCV004599443]	uncertain significance	20	45630963	45630963	Human		name
155976255	CV2266277	single nucleotide variant	NM_080753.3(WFDC10A):c.193A>G (p.Ile65Val)	not specified [RCV004129110]	uncertain significance	20	45630971	45630971	Human		name
329352429	CV2453009	single nucleotide variant	NM_080753.3(WFDC10A):c.155A>T (p.His52Leu)	not specified [RCV004277629]	uncertain significance	20	45630933	45630933	Human		name
405807809	CV3356632	single nucleotide variant	NM_080753.3(WFDC10A):c.119T>A (p.Val40Asp)	not specified [RCV004480892]	uncertain significance	20	45630897	45630897	Human		name
407487896	CV3490021	single nucleotide variant	NM_080753.3(WFDC10A):c.117A>C (p.Lys39Asn)	not specified [RCV004678436]	uncertain significance	20	45630895	45630895	Human		name
597792217	CV3630182	single nucleotide variant	NM_080753.3(WFDC10A):c.199T>C (p.Cys67Arg)	not specified [RCV004876920]	uncertain significance	20	45630977	45630977	Human		name