Fahd2a Variant Search Result - Rat Genome Database

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37 records found for search term Fahd2a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401912220	CV2812086	single nucleotide variant	NM_016044.3(FAHD2A):c.195G>A (p.Thr65=)	not provided [RCV003427112]	likely benign	2	95405753	95405753	Human		name
401912221	CV2812087	single nucleotide variant	NM_016044.3(FAHD2A):c.213G>A (p.Glu71=)	not provided [RCV003427113]	likely benign	2	95405771	95405771	Human		name
405724518	CV3249639	single nucleotide variant	NM_016044.3(FAHD2A):c.19A>G (p.Arg7Gly)	not specified [RCV004378459]	uncertain significance	2	95405577	95405577	Human		name
155953124	CV2264308	single nucleotide variant	NM_016044.3(FAHD2A):c.76G>T (p.Asp26Tyr)	not specified [RCV004138228]	uncertain significance	2	95405634	95405634	Human		name
598223555	CV3965692	single nucleotide variant	NM_016044.3(FAHD2A):c.44A>G (p.Gln15Arg)	not specified [RCV005341172]	uncertain significance	2	95405602	95405602	Human		name
156275744	CV2202787	single nucleotide variant	NM_016044.3(FAHD2A):c.108C>G (p.His36Gln)	not specified [RCV004083024]	uncertain significance	2	95405666	95405666	Human		name
156109197	CV2211149	single nucleotide variant	NM_016044.3(FAHD2A):c.199A>G (p.Thr67Ala)	not specified [RCV004088319]	uncertain significance	2	95405757	95405757	Human		name
155969537	CV2213350	single nucleotide variant	NM_016044.3(FAHD2A):c.296T>G (p.Leu99Arg)	not specified [RCV004085553]	uncertain significance	2	95406991	95406991	Human		name
156259397	CV2304953	single nucleotide variant	NM_016044.3(FAHD2A):c.277C>T (p.Arg93Trp)	not specified [RCV004168855]	uncertain significance	2	95406972	95406972	Human		name
401720896	CV2702180	single nucleotide variant	NM_016044.3(FAHD2A):c.148G>A (p.Gly50Arg)	not specified [RCV004314530]	uncertain significance	2	95405706	95405706	Human		name
405724511	CV3249638	single nucleotide variant	NM_016044.3(FAHD2A):c.152G>A (p.Gly51Glu)	not specified [RCV004378458]	uncertain significance	2	95405710	95405710	Human		name
405724527	CV3249640	single nucleotide variant	NM_016044.3(FAHD2A):c.224C>G (p.Ala75Gly)	not specified [RCV004378460]	uncertain significance	2	95405782	95405782	Human		name
405724536	CV3249641	single nucleotide variant	NM_016044.3(FAHD2A):c.268G>C (p.Val90Leu)	not specified [RCV004378461]	uncertain significance	2	95406963	95406963	Human		name
598223562	CV3965693	single nucleotide variant	NM_016044.3(FAHD2A):c.278G>A (p.Arg93Gln)	not specified [RCV005341173]	uncertain significance	2	95406973	95406973	Human		name
156172200	CV2194209	single nucleotide variant	NM_016044.3(FAHD2A):c.370G>A (p.Val124Met)	not specified [RCV004079335]	uncertain significance	2	95407065	95407065	Human		name
156397362	CV2200359	single nucleotide variant	NM_016044.3(FAHD2A):c.371T>A (p.Val124Glu)	not specified [RCV004076686]	uncertain significance	2	95407066	95407066	Human		name
156384224	CV2231024	single nucleotide variant	NM_016044.3(FAHD2A):c.398T>C (p.Phe133Ser)	not specified [RCV004092474]	uncertain significance	2	95407093	95407093	Human		name
156294363	CV2293184	single nucleotide variant	NM_016044.3(FAHD2A):c.705C>G (p.Ile235Met)	not specified [RCV004150697]	uncertain significance	2	95412453	95412453	Human		name
155924378	CV2358140	single nucleotide variant	NM_016044.3(FAHD2A):c.580C>T (p.Arg194Cys)	not specified [RCV004211946]	uncertain significance	2	95410921	95410921	Human		name
155996337	CV2393171	single nucleotide variant	NM_016044.3(FAHD2A):c.317A>C (p.Asp106Ala)	not specified [RCV004226647]	uncertain significance	2	95407012	95407012	Human		name
329399885	CV2444330	single nucleotide variant	NM_016044.3(FAHD2A):c.823A>G (p.Ile275Val)	not specified [RCV004263085]	uncertain significance	2	95412705	95412705	Human		name
401719256	CV2679470	single nucleotide variant	NM_016044.3(FAHD2A):c.686A>T (p.Asp229Val)	not specified [RCV004287779]	uncertain significance	2	95412434	95412434	Human		name
401742862	CV2715337	single nucleotide variant	NM_016044.3(FAHD2A):c.340A>G (p.Asn114Asp)	not specified [RCV004324670]	uncertain significance	2	95407035	95407035	Human		name
401885018	CV2786649	single nucleotide variant	NM_016044.3(FAHD2A):c.412A>G (p.Ser138Gly)	not specified [RCV004363782]	uncertain significance	2	95407107	95407107	Human		name
405724545	CV3249642	single nucleotide variant	NM_016044.3(FAHD2A):c.328T>C (p.Cys110Arg)	not specified [RCV004378462]	uncertain significance	2	95407023	95407023	Human		name
405724553	CV3249643	single nucleotide variant	NM_016044.3(FAHD2A):c.383A>G (p.Lys128Arg)	not specified [RCV004378463]	uncertain significance	2	95407078	95407078	Human		name
405724561	CV3249644	single nucleotide variant	NM_016044.3(FAHD2A):c.467T>G (p.Val156Gly)	not specified [RCV004378464]	uncertain significance	2	95410531	95410531	Human		name
405724576	CV3249646	single nucleotide variant	NM_016044.3(FAHD2A):c.841C>A (p.Pro281Thr)	not specified [RCV004378466]	uncertain significance	2	95412723	95412723	Human		name
407507698	CV3435371	single nucleotide variant	NM_016044.3(FAHD2A):c.302C>T (p.Pro101Leu)	not specified [RCV004625176]	uncertain significance	2	95406997	95406997	Human		name
407507700	CV3435372	single nucleotide variant	NM_016044.3(FAHD2A):c.571G>A (p.Val191Met)	not specified [RCV004625177]	uncertain significance	2	95410912	95410912	Human		name
407507703	CV3435373	single nucleotide variant	NM_016044.3(FAHD2A):c.839C>T (p.Pro280Leu)	not specified [RCV004625178]	uncertain significance	2	95412721	95412721	Human		name
597718707	CV3671807	single nucleotide variant	NM_016044.3(FAHD2A):c.487G>T (p.Ala163Ser)	not specified [RCV004918553]	uncertain significance	2	95410551	95410551	Human		name
597718717	CV3671808	single nucleotide variant	NM_016044.3(FAHD2A):c.503A>G (p.Lys168Arg)	not specified [RCV004918554]	uncertain significance	2	95410567	95410567	Human		name
597718726	CV3671809	single nucleotide variant	NM_016044.3(FAHD2A):c.682G>A (p.Ala228Thr)	not specified [RCV004918555]	uncertain significance	2	95411023	95411023	Human		name
598223548	CV3965691	single nucleotide variant	NM_016044.3(FAHD2A):c.530A>G (p.Asp177Gly)	not specified [RCV005341171]	uncertain significance	2	95410871	95410871	Human		name
598223578	CV3965695	single nucleotide variant	NM_016044.3(FAHD2A):c.308C>T (p.Thr103Ile)	not specified [RCV005341175]	uncertain significance	2	95407003	95407003	Human		name
598223586	CV3965696	single nucleotide variant	NM_016044.3(FAHD2A):c.311G>A (p.Arg104Gln)	not specified [RCV005341176]	uncertain significance	2	95407006	95407006	Human		name

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