Zdhhc22 Variant Search Result - Rat Genome Database

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18 records found for search term Zdhhc22

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405813003	CV3349776	single nucleotide variant	NM_174976.2(ZDHHC22):c.67T>C (p.Phe23Leu)	not specified [RCV004483629]	uncertain significance	14	77139672	77139672	Human		name
156357506	CV2254032	single nucleotide variant	NM_174976.2(ZDHHC22):c.260C>T (p.Thr87Ile)	not specified [RCV004129485]	uncertain significance	14	77139479	77139479	Human		name
156279607	CV2316773	single nucleotide variant	NM_174976.2(ZDHHC22):c.150C>A (p.His50Gln)	not specified [RCV004171991]	uncertain significance	14	77139589	77139589	Human		name
405812999	CV3349774	single nucleotide variant	NM_174976.2(ZDHHC22):c.149A>G (p.His50Arg)	not specified [RCV004483627]	uncertain significance	14	77139590	77139590	Human		name
405813001	CV3349775	single nucleotide variant	NM_174976.2(ZDHHC22):c.190A>G (p.Asn64Asp)	not specified [RCV004483628]	uncertain significance	14	77139549	77139549	Human		name
407457308	CV3492091	single nucleotide variant	NM_174976.2(ZDHHC22):c.244G>A (p.Ala82Thr)	not specified [RCV004686276]	likely benign	14	77139495	77139495	Human		name
407457312	CV3492093	single nucleotide variant	NM_174976.2(ZDHHC22):c.127C>G (p.Leu43Val)	not specified [RCV004686278]	uncertain significance	14	77139612	77139612	Human		name
598258535	CV3927004	single nucleotide variant	NM_174976.2(ZDHHC22):c.107A>C (p.Glu36Ala)	not specified [RCV005300040]	uncertain significance	14	77139632	77139632	Human		name
156068333	CV2270897	single nucleotide variant	NM_174976.2(ZDHHC22):c.422T>C (p.Met141Thr)	not specified [RCV004131937]	uncertain significance	14	77139317	77139317	Human		name
156081971	CV2292867	single nucleotide variant	NM_174976.2(ZDHHC22):c.655G>A (p.Val219Met)	not specified [RCV004148374]	uncertain significance	14	77133820	77133820	Human		name
156192943	CV2388864	single nucleotide variant	NM_174976.2(ZDHHC22):c.667G>T (p.Val223Leu)	not specified [RCV004239705]	uncertain significance	14	77133808	77133808	Human		name
405813004	CV3349777	single nucleotide variant	NM_174976.2(ZDHHC22):c.751T>C (p.Phe251Leu)	not specified [RCV004483630]	uncertain significance	14	77133724	77133724	Human		name
407457310	CV3492092	single nucleotide variant	NM_174976.2(ZDHHC22):c.344G>A (p.Gly115Asp)	not specified [RCV004686277]	uncertain significance	14	77139395	77139395	Human		name
597724757	CV3631062	single nucleotide variant	NM_174976.2(ZDHHC22):c.634C>G (p.Arg212Gly)	not specified [RCV004888197]	uncertain significance	14	77133841	77133841	Human		name
597793368	CV3631063	single nucleotide variant	NM_174976.2(ZDHHC22):c.610T>G (p.Cys204Gly)	not specified [RCV004877294]	uncertain significance	14	77133865	77133865	Human		name
598258527	CV3927001	single nucleotide variant	NM_174976.2(ZDHHC22):c.664G>C (p.Gly222Arg)	not specified [RCV005300039]	uncertain significance	14	77133811	77133811	Human		name
598198220	CV3927002	single nucleotide variant	NM_174976.2(ZDHHC22):c.740T>A (p.Leu247Gln)	not specified [RCV005313757]	uncertain significance	14	77133735	77133735	Human		name
598198229	CV3927003	single nucleotide variant	NM_174976.2(ZDHHC22):c.770G>A (p.Ser257Asn)	not specified [RCV005313758]	uncertain significance	14	77133705	77133705	Human		name