Pcdhga12 Variant Search Result - Rat Genome Database

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80 records found for search term Pcdhga12

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597737849	CV3575290	single nucleotide variant	NM_003735.3(PCDHGA12):c.86C>T (p.Thr29Ile)	not specified [RCV004844021]	uncertain significance	5	141430845	141430845	Human		name
156209854	CV2370165	single nucleotide variant	NM_003735.3(PCDHGA12):c.152A>C (p.Asp51Ala)	not specified [RCV004211047]	uncertain significance	5	141430911	141430911	Human		name
401882235	CV2774750	single nucleotide variant	NM_003735.3(PCDHGA12):c.191T>G (p.Val64Gly)	not specified [RCV004343850]	uncertain significance	5	141430950	141430950	Human		name
401883527	CV2785687	single nucleotide variant	NM_003735.3(PCDHGA12):c.1869G>A (p.Thr623=)	not specified [RCV004364951]	likely benign	5	141432628	141432628	Human		name
401917966	CV2825356	single nucleotide variant	NM_003735.3(PCDHGA12):c.1110T>C (p.Asn370=)	not provided [RCV003429856]	likely benign	5	141431869	141431869	Human		name
401917969	CV2825357	single nucleotide variant	NM_003735.3(PCDHGA12):c.1656G>A (p.Val552=)	not provided [RCV003429857]	likely benign	5	141432415	141432415	Human		name
597737880	CV3575298	single nucleotide variant	NM_003735.3(PCDHGA12):c.151G>A (p.Asp51Asn)	not specified [RCV004844027]	uncertain significance	5	141430910	141430910	Human		name
155955468	CV2274460	single nucleotide variant	NM_003735.3(PCDHGA12):c.376A>G (p.Ile126Val)	not specified [RCV004136821]	uncertain significance	5	141431135	141431135	Human		name
156089365	CV2344405	single nucleotide variant	NM_003735.3(PCDHGA12):c.664C>A (p.Arg222Ser)	not specified [RCV004195155]	uncertain significance	5	141431423	141431423	Human		name
156388793	CV2376076	single nucleotide variant	NM_003735.3(PCDHGA12):c.356T>C (p.Val119Ala)	not specified [RCV004220312]	uncertain significance	5	141431115	141431115	Human		name
156202992	CV2399658	single nucleotide variant	NM_003735.3(PCDHGA12):c.605G>T (p.Arg202Leu)	not specified [RCV004245478]	uncertain significance	5	141431364	141431364	Human		name
329352113	CV2452047	single nucleotide variant	NM_003735.3(PCDHGA12):c.698T>C (p.Leu233Pro)	not specified [RCV004278777]	uncertain significance	5	141431457	141431457	Human		name
401747644	CV2688971	single nucleotide variant	NM_003735.3(PCDHGA12):c.714C>G (p.Asn238Lys)	not specified [RCV004305757]	uncertain significance	5	141431473	141431473	Human		name
401863076	CV2755842	single nucleotide variant	NM_003735.3(PCDHGA12):c.503A>G (p.Gln168Arg)	not specified [RCV004342211]	uncertain significance	5	141431262	141431262	Human		name
401863721	CV2773227	single nucleotide variant	NM_003735.3(PCDHGA12):c.408T>G (p.Ser136Arg)	not specified [RCV004353908]	uncertain significance	5	141431167	141431167	Human		name
405744286	CV3368167	single nucleotide variant	NM_003735.3(PCDHGA12):c.329T>C (p.Met110Thr)	not specified [RCV004498234]	uncertain significance	5	141431088	141431088	Human		name
405744298	CV3368168	single nucleotide variant	NM_003735.3(PCDHGA12):c.469G>C (p.Ala157Pro)	not specified [RCV004498235]	uncertain significance	5	141431228	141431228	Human		name
405744305	CV3368169	single nucleotide variant	NM_003735.3(PCDHGA12):c.616G>T (p.Ala206Ser)	not specified [RCV004498236]	uncertain significance	5	141431375	141431375	Human		name
405744311	CV3368170	single nucleotide variant	NM_003735.3(PCDHGA12):c.657C>G (p.Asp219Glu)	not specified [RCV004498237]	uncertain significance	5	141431416	141431416	Human		name
405744322	CV3368171	single nucleotide variant	NM_003735.3(PCDHGA12):c.821A>G (p.Asn274Ser)	not specified [RCV004498238]	uncertain significance	5	141431580	141431580	Human		name
405744330	CV3368172	single nucleotide variant	NM_003735.3(PCDHGA12):c.913G>A (p.Gly305Arg)	not specified [RCV004498239]	uncertain significance	5	141431672	141431672	Human		name
405744341	CV3368173	single nucleotide variant	NM_003735.3(PCDHGA12):c.985G>A (p.Ala329Thr)	not specified [RCV004498240]	uncertain significance	5	141431744	141431744	Human		name
407483141	CV3463227	single nucleotide variant	NM_003735.3(PCDHGA12):c.778C>A (p.Gln260Lys)	not specified [RCV004653244]	uncertain significance	5	141431537	141431537	Human		name
407484458	CV3463229	single nucleotide variant	NM_003735.3(PCDHGA12):c.941T>C (p.Phe314Ser)	not specified [RCV004659470]	uncertain significance	5	141431700	141431700	Human		name
597737870	CV3575294	single nucleotide variant	NM_003735.3(PCDHGA12):c.701A>T (p.Asp234Val)	not specified [RCV004844025]	uncertain significance	5	141431460	141431460	Human		name
597737885	CV3575299	single nucleotide variant	NM_003735.3(PCDHGA12):c.691A>G (p.Met231Val)	not specified [RCV004844028]	uncertain significance	5	141431450	141431450	Human		name
598270210	CV3996261	single nucleotide variant	NM_003735.3(PCDHGA12):c.718C>A (p.Pro240Thr)	not specified [RCV005388981]	uncertain significance	5	141431477	141431477	Human		name
156075855	CV2198127	single nucleotide variant	NM_003735.3(PCDHGA12):c.1922G>A (p.Ser641Asn)	not specified [RCV004079720]	uncertain significance	5	141432681	141432681	Human		name
156317131	CV2203914	single nucleotide variant	NM_003735.3(PCDHGA12):c.1942G>A (p.Asp648Asn)	not specified [RCV004069965]	uncertain significance	5	141432701	141432701	Human		name
155977029	CV2218668	single nucleotide variant	NM_003735.3(PCDHGA12):c.1883C>T (p.Thr628Met)	not specified [RCV004090918]	uncertain significance	5	141432642	141432642	Human		name
156120451	CV2233687	single nucleotide variant	NM_003735.3(PCDHGA12):c.1436C>T (p.Pro479Leu)	not specified [RCV004100135]	uncertain significance	5	141432195	141432195	Human		name
155996157	CV2250429	single nucleotide variant	NM_003735.3(PCDHGA12):c.2293A>C (p.Lys765Gln)	not specified [RCV004127300]	uncertain significance	5	141433052	141433052	Human		name
156112796	CV2267556	single nucleotide variant	NM_003735.3(PCDHGA12):c.1012C>G (p.Leu338Val)	not specified [RCV004135972]	uncertain significance	5	141431771	141431771	Human		name
156032899	CV2275060	single nucleotide variant	NM_003735.3(PCDHGA12):c.1607A>T (p.Asp536Val)	not specified [RCV004136880]	uncertain significance	5	141432366	141432366	Human		name
156259227	CV2277812	single nucleotide variant	NM_003735.3(PCDHGA12):c.1888C>G (p.Arg630Gly)	not specified [RCV004147234]	uncertain significance	5	141432647	141432647	Human		name
156083536	CV2343042	single nucleotide variant	NM_003735.3(PCDHGA12):c.1132G>A (p.Glu378Lys)	not specified [RCV004192641]	uncertain significance	5	141431891	141431891	Human		name
156196872	CV2367272	single nucleotide variant	NM_003735.3(PCDHGA12):c.2057C>A (p.Thr686Asn)	not specified [RCV004215692]	uncertain significance	5	141432816	141432816	Human		name
155929916	CV2389265	single nucleotide variant	NM_003735.3(PCDHGA12):c.1781T>A (p.Val594Glu)	not specified [RCV004235582]	uncertain significance	5	141432540	141432540	Human		name
156246021	CV2396754	single nucleotide variant	NM_003735.3(PCDHGA12):c.1802A>C (p.Asn601Thr)	not specified [RCV004233902]	uncertain significance	5	141432561	141432561	Human		name
329367113	CV2442106	single nucleotide variant	NM_003735.3(PCDHGA12):c.1924C>T (p.Leu642Phe)	not specified [RCV004264303]	uncertain significance	5	141432683	141432683	Human		name
329380099	CV2444187	single nucleotide variant	NM_003735.3(PCDHGA12):c.1523A>C (p.Asn508Thr)	not specified [RCV004260919]	uncertain significance	5	141432282	141432282	Human		name
329358224	CV2450226	single nucleotide variant	NM_003735.3(PCDHGA12):c.1036G>A (p.Glu346Lys)	not specified [RCV004271332]	uncertain significance	5	141431795	141431795	Human		name
329360517	CV2458805	single nucleotide variant	NM_003735.3(PCDHGA12):c.1062C>G (p.Ser354Arg)	not specified [RCV004270231]	uncertain significance	5	141431821	141431821	Human		name
401741448	CV2680410	single nucleotide variant	NM_003735.3(PCDHGA12):c.1585C>G (p.Gln529Glu)	not specified [RCV004288651]	uncertain significance	5	141432344	141432344	Human		name
401720370	CV2705856	single nucleotide variant	NM_003735.3(PCDHGA12):c.1436C>A (p.Pro479His)	not specified [RCV004320471]	uncertain significance	5	141432195	141432195	Human		name
401749469	CV2710754	single nucleotide variant	NM_003735.3(PCDHGA12):c.2041C>G (p.Pro681Ala)	not specified [RCV004308690]	uncertain significance	5	141432800	141432800	Human		name
401723616	CV2724966	single nucleotide variant	NM_003735.3(PCDHGA12):c.1448A>G (p.Glu483Gly)	not specified [RCV004319730]	uncertain significance	5	141432207	141432207	Human		name
401898238	CV2790985	single nucleotide variant	NM_003735.3(PCDHGA12):c.1825C>T (p.Leu609Phe)	not specified [RCV004354607]	uncertain significance	5	141432584	141432584	Human		name
405744250	CV3368162	single nucleotide variant	NM_003735.3(PCDHGA12):c.1268C>G (p.Thr423Ser)	not specified [RCV004498229]	uncertain significance	5	141432027	141432027	Human		name
405744265	CV3368164	single nucleotide variant	NM_003735.3(PCDHGA12):c.1396C>T (p.Pro466Ser)	not specified [RCV004498231]	uncertain significance	5	141432155	141432155	Human		name
405744269	CV3368165	single nucleotide variant	NM_003735.3(PCDHGA12):c.1702C>T (p.Pro568Ser)	not specified [RCV004498232]	uncertain significance	5	141432461	141432461	Human		name
405744279	CV3368166	single nucleotide variant	NM_003735.3(PCDHGA12):c.1948G>A (p.Gly650Ser)	not specified [RCV004498233]	uncertain significance	5	141432707	141432707	Human		name
407483120	CV3463225	single nucleotide variant	NM_003735.3(PCDHGA12):c.1488C>G (p.Ile496Met)	not specified [RCV004653242]	uncertain significance	5	141432247	141432247	Human		name
407483129	CV3463226	single nucleotide variant	NM_003735.3(PCDHGA12):c.1567G>C (p.Glu523Gln)	not specified [RCV004653243]	uncertain significance	5	141432326	141432326	Human		name
407483150	CV3463228	single nucleotide variant	NM_003735.3(PCDHGA12):c.1174T>G (p.Phe392Val)	not specified [RCV004653245]	uncertain significance	5	141431933	141431933	Human		name
407483160	CV3463230	single nucleotide variant	NM_003735.3(PCDHGA12):c.2093C>G (p.Ala698Gly)	not specified [RCV004653246]	uncertain significance	5	141432852	141432852	Human		name
597737827	CV3575286	single nucleotide variant	NM_003735.3(PCDHGA12):c.1523A>G (p.Asn508Ser)	not specified [RCV004844017]	uncertain significance	5	141432282	141432282	Human		name
597737832	CV3575287	single nucleotide variant	NM_003735.3(PCDHGA12):c.1886C>A (p.Ala629Glu)	not specified [RCV004844018]	uncertain significance	5	141432645	141432645	Human		name
597737836	CV3575288	single nucleotide variant	NM_003735.3(PCDHGA12):c.1444G>A (p.Glu482Lys)	not specified [RCV004844019]	uncertain significance	5	141432203	141432203	Human		name
597737840	CV3575289	single nucleotide variant	NM_003735.3(PCDHGA12):c.2032C>T (p.Leu678Phe)	not specified [RCV004844020]	uncertain significance	5	141432791	141432791	Human		name
597737854	CV3575291	single nucleotide variant	NM_003735.3(PCDHGA12):c.2383G>T (p.Gly795Cys)	not specified [RCV004844022]	uncertain significance	5	141433142	141433142	Human		name
597737859	CV3575292	single nucleotide variant	NM_003735.3(PCDHGA12):c.1432G>C (p.Asp478His)	not specified [RCV004844023]	uncertain significance	5	141432191	141432191	Human		name
597737863	CV3575293	single nucleotide variant	NM_003735.3(PCDHGA12):c.2300A>G (p.His767Arg)	not specified [RCV004844024]	uncertain significance	5	141433059	141433059	Human		name
597737875	CV3575295	single nucleotide variant	NM_003735.3(PCDHGA12):c.1279C>T (p.Arg427Trp)	not specified [RCV004844026]	uncertain significance	5	141432038	141432038	Human		name
597756405	CV3575296	single nucleotide variant	NM_003735.3(PCDHGA12):c.1023C>G (p.Asn341Lys)	not specified [RCV004848116]	uncertain significance	5	141431782	141431782	Human		name
597756410	CV3575297	single nucleotide variant	NM_003735.3(PCDHGA12):c.1973T>G (p.Val658Gly)	not specified [RCV004848117]	uncertain significance	5	141432732	141432732	Human		name
597737892	CV3575300	single nucleotide variant	NM_003735.3(PCDHGA12):c.1871G>A (p.Gly624Asp)	not specified [RCV004844029]	uncertain significance	5	141432630	141432630	Human		name
597737898	CV3575301	single nucleotide variant	NM_003735.3(PCDHGA12):c.1786A>G (p.Arg596Gly)	not specified [RCV004844030]	uncertain significance	5	141432545	141432545	Human		name
598270167	CV3996252	single nucleotide variant	NM_003735.3(PCDHGA12):c.2351G>A (p.Ser784Asn)	not specified [RCV005388974]	uncertain significance	5	141433110	141433110	Human		name
598270174	CV3996253	single nucleotide variant	NM_003735.3(PCDHGA12):c.2269G>T (p.Val757Phe)	not specified [RCV005388975]	uncertain significance	5	141433028	141433028	Human		name
598270180	CV3996254	single nucleotide variant	NM_003735.3(PCDHGA12):c.1571A>G (p.Gln524Arg)	not specified [RCV005388976]	uncertain significance	5	141432330	141432330	Human		name
598195623	CV3996255	single nucleotide variant	NM_003735.3(PCDHGA12):c.1608C>A (p.Asp536Glu)	not specified [RCV005397563]	uncertain significance	5	141432367	141432367	Human		name
598270185	CV3996256	single nucleotide variant	NM_003735.3(PCDHGA12):c.2310C>G (p.Phe770Leu)	not specified [RCV005388977]	likely benign	5	141433069	141433069	Human		name
598270193	CV3996257	single nucleotide variant	NM_003735.3(PCDHGA12):c.2253G>C (p.Gln751His)	not specified [RCV005388978]	uncertain significance	5	141433012	141433012	Human		name
598195630	CV3996258	single nucleotide variant	NM_003735.3(PCDHGA12):c.1156A>G (p.Ile386Val)	not specified [RCV005397564]	uncertain significance	5	141431915	141431915	Human		name
598270199	CV3996259	single nucleotide variant	NM_003735.3(PCDHGA12):c.2227G>T (p.Val743Leu)	not specified [RCV005388979]	uncertain significance	5	141432986	141432986	Human		name
598195637	CV3996262	single nucleotide variant	NM_003735.3(PCDHGA12):c.1133A>G (p.Glu378Gly)	not specified [RCV005397565]	uncertain significance	5	141431892	141431892	Human		name
598270215	CV3996263	single nucleotide variant	NM_003735.3(PCDHGA12):c.1060A>C (p.Ser354Arg)	not specified [RCV005388982]	uncertain significance	5	141431819	141431819	Human		name
598270220	CV3996264	single nucleotide variant	NM_003735.3(PCDHGA12):c.1738C>G (p.Arg580Gly)	not specified [RCV005388983]	uncertain significance	5	141432497	141432497	Human		name
8657749	CV81086	single nucleotide variant	NM_003735.2(PCDHGA12):c.1619C>T (p.Pro540Leu)	Malignant melanoma [RCV000061164]	not provided	5	141432378	141432378	Human		name

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