Defb10 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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43 records found for search term Defb10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405668674	CV3240147	single nucleotide variant	NM_152250.1(DEFB105A):c.200G>T	not specified [RCV004368199]	uncertain significance	8	7822045	7822045	Human		name
155921725	CV2208577	single nucleotide variant	NM_152250.3(DEFB105A):c.11T>A (p.Ile4Asn)	not specified [RCV004091101]	likely benign	8	7823828	7823828	Human		name
156113308	CV2228679	single nucleotide variant	NM_080389.3(DEFB104A):c.50A>G (p.Asp17Gly)	not specified [RCV004092898]	uncertain significance	8	7836534	7836534	Human		name
155919831	CV2279484	single nucleotide variant	NM_152251.4(DEFB106A):c.91G>C (p.Gly31Arg)	not specified [RCV004142008]	uncertain significance	8	7828846	7828846	Human		name
155940187	CV2294039	single nucleotide variant	NM_152251.4(DEFB106A):c.59C>G (p.Ala20Gly)	not specified [RCV004149426]	likely benign	8	7828814	7828814	Human		name
155929863	CV2353990	single nucleotide variant	NM_080389.3(DEFB104A):c.67G>C (p.Glu23Gln)	not specified [RCV004204425]	uncertain significance	8	7841042	7841042	Human		name
405668661	CV3240145	single nucleotide variant	NM_080389.3(DEFB104A):c.78G>C (p.Leu26Phe)	not specified [RCV004368197]	uncertain significance	8	7841053	7841053	Human		name
407465681	CV3426749	single nucleotide variant	NM_152250.3(DEFB105A):c.79G>A (p.Ala27Thr)	not specified [RCV004613770]	uncertain significance	8	7823415	7823415	Human		name
597640687	CV3658534	single nucleotide variant	NM_152250.3(DEFB105A):c.85C>T (p.Leu29Phe)	not specified [RCV004908981]	uncertain significance	8	7823409	7823409	Human		name
597640682	CV3658535	single nucleotide variant	NM_152251.4(DEFB106A):c.59C>T (p.Ala20Val)	not specified [RCV004908982]	uncertain significance	8	7828814	7828814	Human		name
598223028	CV3893952	single nucleotide variant	NM_001040704.2(DEFB106B):c.27C>T (p.Ala9=)	not provided [RCV005257195]	likely benign	8	7486356	7486356	Human		name
15158547	CV700667	single nucleotide variant	NM_080389.3(DEFB104A):c.28A>G (p.Ile10Val)	not provided [RCV000947093]	benign	8	7836512	7836512	Human		name
156380761	CV2208385	single nucleotide variant	NM_152251.4(DEFB106A):c.188T>G (p.Ile63Ser)	not specified [RCV004088815]	likely benign	8	7828943	7828943	Human		name
156342362	CV2222223	single nucleotide variant	NM_080389.3(DEFB104A):c.124C>T (p.Arg42Cys)	not specified [RCV004105251]	uncertain significance	8	7841099	7841099	Human		name
155998429	CV2373289	single nucleotide variant	NM_152250.3(DEFB105A):c.110C>T (p.Ser37Leu)	not specified [RCV004220001]	uncertain significance	8	7823384	7823384	Human		name
156064532	CV2375993	single nucleotide variant	NM_080389.3(DEFB104A):c.137A>G (p.Tyr46Cys)	not specified [RCV004218198]	uncertain significance	8	7841112	7841112	Human		name
329385163	CV2431359	single nucleotide variant	NM_080389.3(DEFB104A):c.112C>T (p.Arg38Trp)	not specified [RCV004252910]	uncertain significance	8	7841087	7841087	Human		name
401735296	CV2687545	single nucleotide variant	NM_152251.4(DEFB106A):c.167C>G (p.Thr56Ser)	not specified [RCV004300774]	uncertain significance	8	7828922	7828922	Human		name
401756253	CV2733914	single nucleotide variant	NM_152251.4(DEFB106A):c.148T>G (p.Ser50Ala)	not specified [RCV004330477]	uncertain significance	8	7828903	7828903	Human		name
407465685	CV3426750	single nucleotide variant	NM_152251.4(DEFB106A):c.182G>A (p.Gly61Glu)	not specified [RCV004613771]	likely benign	8	7828937	7828937	Human		name
597640693	CV3658533	single nucleotide variant	NM_080389.3(DEFB104A):c.215C>A (p.Pro72His)	not specified [RCV004908980]	likely benign	8	7841190	7841190	Human		name
597640677	CV3658536	single nucleotide variant	NM_152251.4(DEFB106A):c.161G>A (p.Cys54Tyr)	not specified [RCV004908983]	uncertain significance	8	7828916	7828916	Human		name
597640670	CV3658537	single nucleotide variant	NM_152251.4(DEFB106A):c.191T>C (p.Ile64Thr)	not specified [RCV004908984]	likely benign	8	7828946	7828946	Human		name
598223663	CV3956518	single nucleotide variant	NM_152251.4(DEFB106A):c.136C>G (p.Leu46Val)	not specified [RCV005318109]	uncertain significance	8	7828891	7828891	Human		name
15158542	CV700666	single nucleotide variant	NM_001037668.1(DEFB107A):c.25G>T (p.Val9Phe)	not provided [RCV000947092]	benign	8	7815604	7815604	Human		name
156208199	CV2382465	single nucleotide variant	NM_001002035.2(DEFB108B):c.88C>T (p.Arg30Cys)	not specified [RCV004230799]	uncertain significance	11	71837428	71837428	Human		name
156208686	CV2382537	single nucleotide variant	NM_001040704.2(DEFB106B):c.88A>C (p.Lys30Gln)	not specified [RCV004232869]	uncertain significance	8	7482714	7482714	Human		name
329365595	CV2440917	single nucleotide variant	NM_001002035.2(DEFB108B):c.92C>G (p.Pro31Arg)	not specified [RCV004261307]	uncertain significance	11	71837432	71837432	Human		name
405668684	CV3240149	single nucleotide variant	NM_001040704.2(DEFB106B):c.77G>A (p.Cys26Tyr)	not specified [RCV004368201]	uncertain significance	8	7482725	7482725	Human		name
597640665	CV3658538	single nucleotide variant	NM_001002035.2(DEFB108B):c.45C>A (p.Ser15Arg)	not specified [RCV004908985]	uncertain significance	11	71833244	71833244	Human		name
598223670	CV3956519	single nucleotide variant	NM_001040704.2(DEFB106B):c.63T>G (p.Phe21Leu)	not specified [RCV005318110]	uncertain significance	8	7482739	7482739	Human		name
156316044	CV2192998	single nucleotide variant	NM_001040702.1(DEFB104B):c.106C>T (p.Arg36Cys)	not specified [RCV004069550]	likely benign	8	7470469	7470469	Human		name
156323604	CV2201769	single nucleotide variant	NM_001040702.1(DEFB104B):c.113G>A (p.Arg38Gln)	not specified [RCV004082211]	likely benign	8	7470462	7470462	Human		name
155990194	CV2259778	single nucleotide variant	NM_001040705.2(DEFB107B):c.104A>G (p.Lys35Arg)	not specified [RCV004116783]	uncertain significance	8	7509114	7509114	Human		name
155920554	CV2279615	single nucleotide variant	NM_001040702.1(DEFB104B):c.101C>T (p.Thr34Ile)	not specified [RCV004142115]	uncertain significance	8	7470474	7470474	Human		name
156164469	CV2319712	single nucleotide variant	NM_001002035.2(DEFB108B):c.116G>A (p.Cys39Tyr)	not specified [RCV004187250]	uncertain significance	11	71837456	71837456	Human		name
401751935	CV2672626	single nucleotide variant	NM_001040703.3(DEFB105B):c.214C>G (p.Leu72Val)	not specified [RCV004287652]	uncertain significance	8	7489528	7489528	Human		name
405668668	CV3240146	single nucleotide variant	NM_001040702.1(DEFB104B):c.215C>G (p.Pro72Arg)	not specified [RCV004368198]	uncertain significance	8	7470360	7470360	Human		name
405668680	CV3240148	single nucleotide variant	NM_001040703.3(DEFB105B):c.200G>T (p.Cys67Phe)	not specified [RCV004368200]	uncertain significance	8	7489514	7489514	Human		name
405668689	CV3240150	single nucleotide variant	NM_001002035.2(DEFB108B):c.188C>A (p.Pro63Gln)	not specified [RCV004368202]	uncertain significance	11	71837528	71837528	Human		name
405668694	CV3240151	single nucleotide variant	NM_001002035.2(DEFB108B):c.203C>G (p.Thr68Ser)	not specified [RCV004368203]	uncertain significance	11	71837543	71837543	Human		name
598223676	CV3956520	single nucleotide variant	NM_001040704.2(DEFB106B):c.143A>G (p.Gln48Arg)	not specified [RCV005318111]	uncertain significance	8	7482659	7482659	Human		name
15159840	CV701969	single nucleotide variant	NM_001002035.2(DEFB108B):c.158A>G (p.Gln53Arg)	not provided [RCV000947359]	benign	11	71837498	71837498	Human		name

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