Dcaf12l2 Variant Search Result - Rat Genome Database

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41 records found for search term Dcaf12l2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156052590	CV2246301	single nucleotide variant	NM_001013628.3(DCAF12L2):c.49G>A (p.Glu17Lys)	not specified [RCV004107747]	uncertain significance	X	126165876	126165876	Human		name
598252299	CV3963536	single nucleotide variant	NM_001013628.3(DCAF12L2):c.91G>T (p.Ala31Ser)	not specified [RCV005323223]	uncertain significance	X	126165834	126165834	Human		name
156071988	CV2255011	single nucleotide variant	NM_001013628.3(DCAF12L2):c.155T>C (p.Val52Ala)	not specified [RCV004117234]	uncertain significance	X	126165770	126165770	Human		name
155914389	CV2341989	single nucleotide variant	NM_001013628.3(DCAF12L2):c.229G>C (p.Gly77Arg)	not specified [RCV004184930]	uncertain significance	X	126165696	126165696	Human		name
156155364	CV2388779	single nucleotide variant	NM_001013628.3(DCAF12L2):c.139A>C (p.Thr47Pro)	not specified [RCV004239637]	uncertain significance	X	126165786	126165786	Human		name
597800659	CV3651895	single nucleotide variant	NM_001013628.3(DCAF12L2):c.199G>C (p.Gly67Arg)	not specified [RCV004905800]	uncertain significance	X	126165726	126165726	Human		name
597800669	CV3651900	single nucleotide variant	NM_001013628.3(DCAF12L2):c.191G>T (p.Gly64Val)	not specified [RCV004905805]	uncertain significance	X	126165734	126165734	Human		name
598252310	CV3963538	single nucleotide variant	NM_001013628.3(DCAF12L2):c.218G>A (p.Gly73Asp)	not specified [RCV005323225]	uncertain significance	X	126165707	126165707	Human		name
155916485	CV2197450	single nucleotide variant	NM_001013628.3(DCAF12L2):c.392C>T (p.Thr131Met)	not specified [RCV004081185]	uncertain significance	X	126165533	126165533	Human		name
156188716	CV2205840	single nucleotide variant	NM_001013628.3(DCAF12L2):c.630C>A (p.Ser210Arg)	not specified [RCV004076237]	uncertain significance	X	126165295	126165295	Human		name
156077959	CV2230324	single nucleotide variant	NM_001013628.3(DCAF12L2):c.404T>G (p.Leu135Arg)	not specified [RCV004099931]	uncertain significance	X	126165521	126165521	Human		name
156122283	CV2241072	single nucleotide variant	NM_001013628.3(DCAF12L2):c.530A>G (p.Tyr177Cys)	not specified [RCV004104113]	uncertain significance	X	126165395	126165395	Human		name
155905843	CV2303193	single nucleotide variant	NM_001013628.3(DCAF12L2):c.368T>C (p.Val123Ala)	not specified [RCV004156955]	uncertain significance	X	126165557	126165557	Human		name
329380668	CV2464285	single nucleotide variant	NM_001013628.3(DCAF12L2):c.968T>G (p.Val323Gly)	not specified [RCV004276244]	uncertain significance	X	126164957	126164957	Human		name
401758889	CV2705223	single nucleotide variant	NM_001013628.3(DCAF12L2):c.707A>T (p.Glu236Val)	not specified [RCV004311925]	uncertain significance	X	126165218	126165218	Human		name
401929563	CV2823951	single nucleotide variant	NM_001013628.3(DCAF12L2):c.809T>G (p.Phe270Cys)	not provided [RCV003439783]\|not specified [RCV004364666]	likely benign\|uncertain significance	X	126165116	126165116	Human		name
401929566	CV2826970	single nucleotide variant	NM_001013628.3(DCAF12L2):c.811A>G (p.Ser271Gly)	not provided [RCV003439782]\|not specified [RCV004364665]	likely benign\|uncertain significance	X	126165114	126165114	Human		name
405689852	CV3246516	single nucleotide variant	NM_001013628.3(DCAF12L2):c.376C>G (p.Gln126Glu)	not specified [RCV004373086]	uncertain significance	X	126165549	126165549	Human		name
405689862	CV3246518	single nucleotide variant	NM_001013628.3(DCAF12L2):c.549C>G (p.Asp183Glu)	not specified [RCV004373088]	uncertain significance	X	126165376	126165376	Human		name
405689867	CV3246519	single nucleotide variant	NM_001013628.3(DCAF12L2):c.629G>C (p.Ser210Thr)	not specified [RCV004373089]	uncertain significance	X	126165296	126165296	Human		name
405689872	CV3246520	single nucleotide variant	NM_001013628.3(DCAF12L2):c.700C>T (p.His234Tyr)	not specified [RCV004373090]	uncertain significance	X	126165225	126165225	Human		name
405689877	CV3246521	single nucleotide variant	NM_001013628.3(DCAF12L2):c.984C>G (p.His328Gln)	not specified [RCV004373091]	uncertain significance	X	126164941	126164941	Human		name
405689884	CV3246522	single nucleotide variant	NM_001013628.3(DCAF12L2):c.988T>A (p.Ser330Thr)	not specified [RCV004373092]	uncertain significance	X	126164937	126164937	Human		name
407457818	CV3430201	single nucleotide variant	NM_001013628.3(DCAF12L2):c.727G>T (p.Ala243Ser)	not specified [RCV004611302]	uncertain significance	X	126165198	126165198	Human		name
407457822	CV3430202	single nucleotide variant	NM_001013628.3(DCAF12L2):c.928G>A (p.Val310Met)	not specified [RCV004611303]	uncertain significance	X	126164997	126164997	Human		name
597800661	CV3651896	single nucleotide variant	NM_001013628.3(DCAF12L2):c.779C>G (p.Pro260Arg)	not specified [RCV004905801]	uncertain significance	X	126165146	126165146	Human		name
597800663	CV3651897	single nucleotide variant	NM_001013628.3(DCAF12L2):c.565G>A (p.Asp189Asn)	not specified [RCV004905802]	uncertain significance	X	126165360	126165360	Human		name
597800665	CV3651898	single nucleotide variant	NM_001013628.3(DCAF12L2):c.997G>A (p.Asp333Asn)	not specified [RCV004905803]	uncertain significance	X	126164928	126164928	Human		name
598252292	CV3963534	single nucleotide variant	NM_001013628.3(DCAF12L2):c.629G>T (p.Ser210Ile)	not specified [RCV005323222]	uncertain significance	X	126165296	126165296	Human		name
598160511	CV3963535	single nucleotide variant	NM_001013628.3(DCAF12L2):c.892C>G (p.Leu298Val)	not specified [RCV005328789]	uncertain significance	X	126165033	126165033	Human		name
598252304	CV3963537	single nucleotide variant	NM_001013628.3(DCAF12L2):c.436G>A (p.Ala146Thr)	not specified [RCV005323224]	uncertain significance	X	126165489	126165489	Human		name
598252322	CV3963540	single nucleotide variant	NM_001013628.3(DCAF12L2):c.529T>C (p.Tyr177His)	not specified [RCV005323227]	uncertain significance	X	126165396	126165396	Human		name
8628716	CV83860	single nucleotide variant	NM_001013628.2(DCAF12L2):c.662G>A (p.Arg221Gln)	Malignant melanoma [RCV000063941]	not provided	X	126165263	126165263	Human		name
155915413	CV2274152	single nucleotide variant	NM_001013628.3(DCAF12L2):c.1381C>G (p.Leu461Val)	not specified [RCV004134788]	uncertain significance	X	126164544	126164544	Human		name
156271071	CV2290256	single nucleotide variant	NM_001013628.3(DCAF12L2):c.1139A>G (p.Gln380Arg)	not specified [RCV004152905]	uncertain significance	X	126164786	126164786	Human		name
156047562	CV2319173	single nucleotide variant	NM_001013628.3(DCAF12L2):c.1045G>A (p.Gly349Ser)	not specified [RCV004178235]	uncertain significance	X	126164880	126164880	Human		name
405689840	CV3246514	single nucleotide variant	NM_001013628.3(DCAF12L2):c.1184C>T (p.Pro395Leu)	not specified [RCV004373084]	uncertain significance	X	126164741	126164741	Human		name
405689845	CV3246515	single nucleotide variant	NM_001013628.3(DCAF12L2):c.1237C>A (p.Gln413Lys)	not specified [RCV004373085]	uncertain significance	X	126164688	126164688	Human		name
407457815	CV3430200	single nucleotide variant	NM_001013628.3(DCAF12L2):c.1286A>G (p.Asn429Ser)	not specified [RCV004611301]	uncertain significance	X	126164639	126164639	Human		name
597800667	CV3651899	single nucleotide variant	NM_001013628.3(DCAF12L2):c.1234A>C (p.Asn412His)	not specified [RCV004905804]	uncertain significance	X	126164691	126164691	Human		name
8628715	CV83859	single nucleotide variant	NM_001013628.2(DCAF12L2):c.1144T>C (p.Phe382Leu)	Malignant melanoma [RCV000063940]	not provided	X	126164781	126164781	Human		name

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