Cyp20a1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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40 records found for search term Cyp20a1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156184669	CV2292252	single nucleotide variant	NM_177538.3(CYP20A1):c.71C>A (p.Pro24Gln)	not specified [RCV004148290]	uncertain significance	2	203239133	203239133	Human		name
155928796	CV2224437	single nucleotide variant	NM_177538.3(CYP20A1):c.275A>G (p.Asn92Ser)	not specified [RCV004098040]	uncertain significance	2	203246907	203246907	Human		name
156388265	CV2231748	single nucleotide variant	NM_177538.3(CYP20A1):c.119A>C (p.Glu40Ala)	not specified [RCV004098565]	uncertain significance	2	203245892	203245892	Human		name
155907761	CV2302282	single nucleotide variant	NM_177538.3(CYP20A1):c.193T>G (p.Tyr65Asp)	not specified [RCV004161048]	uncertain significance	2	203246825	203246825	Human		name
155986064	CV2368210	single nucleotide variant	NM_177538.3(CYP20A1):c.226C>T (p.Arg76Cys)	not specified [RCV004216550]	uncertain significance	2	203246858	203246858	Human		name
329375505	CV2468644	single nucleotide variant	NM_177538.3(CYP20A1):c.168G>T (p.Glu56Asp)	not specified [RCV004278196]	uncertain significance	2	203246800	203246800	Human		name
401773138	CV2716468	single nucleotide variant	NM_177538.3(CYP20A1):c.173T>A (p.Leu58Gln)	not specified [RCV004325775]	uncertain significance	2	203246805	203246805	Human		name
405666680	CV3239546	single nucleotide variant	NM_177538.3(CYP20A1):c.183G>T (p.Leu61Phe)	not specified [RCV004367790]	uncertain significance	2	203246815	203246815	Human		name
405666686	CV3239547	single nucleotide variant	NM_177538.3(CYP20A1):c.200C>T (p.Pro67Leu)	not specified [RCV004367791]	uncertain significance	2	203246832	203246832	Human		name
156382960	CV2223720	single nucleotide variant	NM_177538.3(CYP20A1):c.364A>G (p.Met122Val)	not specified [RCV004093806]	uncertain significance	2	203252041	203252041	Human		name
156104658	CV2260592	single nucleotide variant	NM_177538.3(CYP20A1):c.926T>C (p.Val309Ala)	not specified [RCV004123362]	uncertain significance	2	203285687	203285687	Human		name
155997732	CV2287064	single nucleotide variant	NM_177538.3(CYP20A1):c.550A>C (p.Thr184Pro)	not specified [RCV004144942]	uncertain significance	2	203266631	203266631	Human		name
155910389	CV2303585	single nucleotide variant	NM_177538.3(CYP20A1):c.736A>G (p.Asn246Asp)	not specified [RCV004161671]	uncertain significance	2	203278629	203278629	Human		name
156047108	CV2390913	single nucleotide variant	NM_177538.3(CYP20A1):c.749A>G (p.His250Arg)	not specified [RCV004234927]	uncertain significance	2	203278642	203278642	Human		name
329391971	CV2470243	single nucleotide variant	NM_177538.3(CYP20A1):c.623G>C (p.Gly208Ala)	not specified [RCV004279653]	uncertain significance	2	203272692	203272692	Human		name
405666691	CV3239548	single nucleotide variant	NM_177538.3(CYP20A1):c.658C>T (p.Arg220Trp)	not specified [RCV004367792]	uncertain significance	2	203272727	203272727	Human		name
405666698	CV3239549	single nucleotide variant	NM_177538.3(CYP20A1):c.838A>G (p.Ile280Val)	not specified [RCV004367793]	uncertain significance	2	203280101	203280101	Human		name
407452328	CV3420068	single nucleotide variant	NM_177538.3(CYP20A1):c.789C>A (p.Asp263Glu)	not specified [RCV004608417]	uncertain significance	2	203278682	203278682	Human		name
407452333	CV3420070	single nucleotide variant	NM_177538.3(CYP20A1):c.998C>G (p.Thr333Ser)	not specified [RCV004608419]	uncertain significance	2	203289791	203289791	Human		name
407452335	CV3420071	single nucleotide variant	NM_177538.3(CYP20A1):c.968T>C (p.Leu323Pro)	not specified [RCV004608420]	uncertain significance	2	203285729	203285729	Human		name
597671082	CV3658123	single nucleotide variant	NM_177538.3(CYP20A1):c.659G>A (p.Arg220Gln)	not specified [RCV004913186]	uncertain significance	2	203272728	203272728	Human		name
597671101	CV3658125	single nucleotide variant	NM_177538.3(CYP20A1):c.517A>G (p.Met173Val)	not specified [RCV004913188]	uncertain significance	2	203266598	203266598	Human		name
597671119	CV3658127	single nucleotide variant	NM_177538.3(CYP20A1):c.313A>G (p.Lys105Glu)	not specified [RCV004913190]	uncertain significance	2	203251990	203251990	Human		name
597671128	CV3658128	single nucleotide variant	NM_177538.3(CYP20A1):c.992G>A (p.Cys331Tyr)	not specified [RCV004913191]	uncertain significance	2	203289785	203289785	Human		name
598237336	CV3952385	single nucleotide variant	NM_177538.3(CYP20A1):c.535A>G (p.Met179Val)	not specified [RCV005320624]	uncertain significance	2	203266616	203266616	Human		name
598237341	CV3952386	single nucleotide variant	NM_177538.3(CYP20A1):c.567G>C (p.Gln189His)	not specified [RCV005320625]	uncertain significance	2	203266648	203266648	Human		name
156070309	CV2203974	single nucleotide variant	NM_177538.3(CYP20A1):c.1042G>A (p.Asp348Asn)	not specified [RCV004070017]	uncertain significance	2	203289835	203289835	Human		name
156133832	CV2216913	single nucleotide variant	NM_177538.3(CYP20A1):c.1268T>A (p.Leu423His)	not specified [RCV004083324]	uncertain significance	2	203296787	203296787	Human		name
155954503	CV2389778	single nucleotide variant	NM_177538.3(CYP20A1):c.1106G>A (p.Gly369Asp)	not specified [RCV004236009]	uncertain significance	2	203292284	203292284	Human		name
401721577	CV2683568	single nucleotide variant	NM_177538.3(CYP20A1):c.1216A>T (p.Thr406Ser)	not specified [RCV004282499]	uncertain significance	2	203296541	203296541	Human		name
401875705	CV2766971	single nucleotide variant	NM_177538.3(CYP20A1):c.1105G>T (p.Gly369Cys)	not specified [RCV004343355]	uncertain significance	2	203292283	203292283	Human		name
401868688	CV2781911	single nucleotide variant	NM_177538.3(CYP20A1):c.1364G>C (p.Trp455Ser)	not specified [RCV004357154]	uncertain significance	2	203296883	203296883	Human		name
405666671	CV3239544	single nucleotide variant	NM_177538.3(CYP20A1):c.1310G>A (p.Gly437Glu)	not specified [RCV004367788]	uncertain significance	2	203296829	203296829	Human		name
407452326	CV3420067	single nucleotide variant	NM_177538.3(CYP20A1):c.1093C>T (p.Leu365Phe)	not specified [RCV004608416]	uncertain significance	2	203292271	203292271	Human		name
407452331	CV3420069	single nucleotide variant	NM_177538.3(CYP20A1):c.1315G>A (p.Val439Ile)	not specified [RCV004608418]	uncertain significance	2	203296834	203296834	Human		name
597671108	CV3658126	single nucleotide variant	NM_177538.3(CYP20A1):c.1323A>C (p.Glu441Asp)	not specified [RCV004913189]	uncertain significance	2	203296842	203296842	Human		name
597671136	CV3658129	single nucleotide variant	NM_177538.3(CYP20A1):c.1199C>T (p.Ser400Leu)	not specified [RCV004913192]	likely benign	2	203296524	203296524	Human		name
597671145	CV3658130	single nucleotide variant	NM_177538.3(CYP20A1):c.1069A>G (p.Ile357Val)	not specified [RCV004913193]	uncertain significance	2	203289862	203289862	Human		name
15133061	CV707948	single nucleotide variant	NM_177538.3(CYP20A1):c.1059T>G (p.Ile353Met)	not provided [RCV000964884]	benign	2	203289852	203289852	Human		name
15168999	CV707949	single nucleotide variant	NM_177538.3(CYP20A1):c.1174G>A (p.Glu392Lys)	not provided [RCV000971725]	benign	2	203296499	203296499	Human		name

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