Pcdhb1 Variant Search Result - Rat Genome Database

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885 records found for search term Pcdhb1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598269461	CV3999531	single nucleotide variant	NM_013340.4(PCDHB1):c.14G>A (p.Arg5His)	not specified [RCV005388788]	uncertain significance	5	141051484	141051484	Human		name
155966604	CV2329819	single nucleotide variant	NM_013340.4(PCDHB1):c.55A>T (p.Ile19Phe)	not specified [RCV004183281]	uncertain significance	5	141051525	141051525	Human		name
401765462	CV2712749	single nucleotide variant	NM_013340.4(PCDHB1):c.59T>C (p.Phe20Ser)	not specified [RCV004310094]	uncertain significance	5	141051529	141051529	Human		name
405741972	CV3371831	single nucleotide variant	NM_013340.4(PCDHB1):c.92T>A (p.Ile31Asn)	not specified [RCV004497904]	uncertain significance	5	141051562	141051562	Human		name
598269447	CV3999526	single nucleotide variant	NM_013340.4(PCDHB1):c.40G>A (p.Val14Met)	not specified [RCV005388785]	uncertain significance	5	141051510	141051510	Human		name
401745679	CV2729124	single nucleotide variant	NM_013340.4(PCDHB1):c.215A>G (p.Lys72Arg)	not specified [RCV004332508]	uncertain significance	5	141051685	141051685	Human		name
401897217	CV2789913	single nucleotide variant	NM_013340.4(PCDHB1):c.263A>C (p.Glu88Ala)	not specified [RCV004362293]	uncertain significance	5	141051733	141051733	Human		name
405742364	CV3371819	single nucleotide variant	NM_013340.4(PCDHB1):c.116T>C (p.Met39Thr)	not specified [RCV004497892]	uncertain significance	5	141051586	141051586	Human		name
405742348	CV3371821	single nucleotide variant	NM_013340.4(PCDHB1):c.125G>C (p.Gly42Ala)	not specified [RCV004497894]	uncertain significance	5	141051595	141051595	Human		name
598269421	CV3999520	single nucleotide variant	NM_013340.4(PCDHB1):c.268C>G (p.Leu90Val)	not specified [RCV005388779]	uncertain significance	5	141051738	141051738	Human		name
156030659	CV2202508	single nucleotide variant	NM_013340.4(PCDHB1):c.994A>G (p.Lys332Glu)	not specified [RCV004080806]	uncertain significance	5	141052464	141052464	Human		name
156194955	CV2251796	single nucleotide variant	NM_013340.4(PCDHB1):c.411G>T (p.Glu137Asp)	not specified [RCV004119787]	uncertain significance	5	141051881	141051881	Human		name
156005177	CV2281464	single nucleotide variant	NM_013340.4(PCDHB1):c.541C>T (p.His181Tyr)	not specified [RCV004153790]	uncertain significance	5	141052011	141052011	Human		name
155905980	CV2303220	single nucleotide variant	NM_013340.4(PCDHB1):c.714C>A (p.His238Gln)	not specified [RCV004156978]	uncertain significance	5	141052184	141052184	Human		name
156158147	CV2322631	single nucleotide variant	NM_013340.4(PCDHB1):c.301C>T (p.Pro101Ser)	not specified [RCV004182765]	uncertain significance	5	141051771	141051771	Human		name
156359854	CV2328320	single nucleotide variant	NM_013340.4(PCDHB1):c.779T>C (p.Leu260Ser)	not specified [RCV004175438]	uncertain significance	5	141052249	141052249	Human		name
155975906	CV2342717	single nucleotide variant	NM_013340.4(PCDHB1):c.911G>C (p.Arg304Thr)	not specified [RCV004196794]	uncertain significance	5	141052381	141052381	Human		name
401771850	CV2722968	single nucleotide variant	NM_013340.4(PCDHB1):c.967G>A (p.Asp323Asn)	not specified [RCV004327145]	uncertain significance	5	141052437	141052437	Human		name
401859994	CV2768435	single nucleotide variant	NM_013340.4(PCDHB1):c.809A>G (p.Asp270Gly)	not specified [RCV004344326]	uncertain significance	5	141052279	141052279	Human		name
401896793	CV2788789	single nucleotide variant	NM_013340.4(PCDHB1):c.382G>T (p.Asp128Tyr)	not specified [RCV004361251]	uncertain significance	5	141051852	141051852	Human		name
405741967	CV3371830	single nucleotide variant	NM_013340.4(PCDHB1):c.373G>T (p.Asp125Tyr)	not specified [RCV004497903]	uncertain significance	5	141051843	141051843	Human		name
407523434	CV3463072	single nucleotide variant	NM_013340.4(PCDHB1):c.946G>A (p.Asp316Asn)	not specified [RCV004653154]	uncertain significance	5	141052416	141052416	Human		name
407480303	CV3463075	single nucleotide variant	NM_013340.4(PCDHB1):c.407A>G (p.Lys136Arg)	not specified [RCV004664381]	uncertain significance	5	141051877	141051877	Human		name
597674953	CV3578872	single nucleotide variant	NM_013340.4(PCDHB1):c.770A>G (p.Asn257Ser)	not specified [RCV004836751]	uncertain significance	5	141052240	141052240	Human		name
597736764	CV3578879	single nucleotide variant	NM_013340.4(PCDHB1):c.353G>A (p.Arg118Gln)	not specified [RCV004843774]	uncertain significance	5	141051823	141051823	Human		name
598269411	CV3999518	single nucleotide variant	NM_013340.4(PCDHB1):c.872C>T (p.Thr291Met)	not specified [RCV005388777]	uncertain significance	5	141052342	141052342	Human		name
598269436	CV3999523	single nucleotide variant	NM_013340.4(PCDHB1):c.574G>T (p.Ala192Ser)	not specified [RCV005388782]	uncertain significance	5	141052044	141052044	Human		name
598269442	CV3999525	single nucleotide variant	NM_013340.4(PCDHB1):c.827C>T (p.Ala276Val)	not specified [RCV005388784]	uncertain significance	5	141052297	141052297	Human		name
598195419	CV3999528	single nucleotide variant	NM_013340.4(PCDHB1):c.310C>A (p.Leu104Met)	not specified [RCV005397532]	uncertain significance	5	141051780	141051780	Human		name
598195426	CV3999529	single nucleotide variant	NM_013340.4(PCDHB1):c.896G>A (p.Gly299Glu)	not specified [RCV005397533]	uncertain significance	5	141052366	141052366	Human		name
9686984	CV171394	single nucleotide variant	NM_013340.4(PCDHB1):c.1655T>C (p.Val552Ala)	Prostate cancer [RCV000149203]	uncertain significance	5	141053125	141053125	Human	2	name
156178786	CV2201614	single nucleotide variant	NM_013340.4(PCDHB1):c.2306G>A (p.Arg769His)	not specified [RCV004082079]	uncertain significance	5	141053776	141053776	Human		name
156338020	CV2224885	single nucleotide variant	NM_013340.4(PCDHB1):c.1924A>G (p.Ile642Val)	not specified [RCV004092970]	uncertain significance	5	141053394	141053394	Human		name
156334270	CV2230899	single nucleotide variant	NM_013340.4(PCDHB1):c.1195G>A (p.Gly399Arg)	not specified [RCV004092371]	likely benign	5	141052665	141052665	Human		name
156142154	CV2257232	single nucleotide variant	NM_013340.4(PCDHB1):c.1402G>A (p.Ala468Thr)	not specified [RCV004123434]	uncertain significance	5	141052872	141052872	Human		name
155961711	CV2285566	single nucleotide variant	NM_013340.4(PCDHB1):c.2059T>C (p.Ser687Pro)	not specified [RCV004141444]	uncertain significance	5	141053529	141053529	Human		name
156095753	CV2297396	single nucleotide variant	NM_013340.4(PCDHB1):c.1330G>A (p.Asp444Asn)	not specified [RCV004153339]	uncertain significance	5	141052800	141052800	Human		name
156196501	CV2306729	single nucleotide variant	NM_013340.4(PCDHB1):c.1483A>G (p.Lys495Glu)	not specified [RCV004159314]	uncertain significance	5	141052953	141052953	Human		name
156120984	CV2354220	single nucleotide variant	NM_013340.4(PCDHB1):c.1725C>A (p.Asp575Glu)	not specified [RCV004206645]	uncertain significance	5	141053195	141053195	Human		name
156347875	CV2375574	single nucleotide variant	NM_013340.4(PCDHB1):c.2138A>G (p.His713Arg)	not specified [RCV004226063]	uncertain significance	5	141053608	141053608	Human		name
329387214	CV2436265	single nucleotide variant	NM_013340.4(PCDHB1):c.1171C>A (p.Pro391Thr)	not specified [RCV004251676]	uncertain significance	5	141052641	141052641	Human		name
329354115	CV2437026	single nucleotide variant	NM_013340.4(PCDHB1):c.2426G>A (p.Gly809Asp)	not specified [RCV004260391]	uncertain significance	5	141053896	141053896	Human		name
329382668	CV2449322	single nucleotide variant	NM_013340.4(PCDHB1):c.2383T>G (p.Leu795Val)	not specified [RCV004257451]	uncertain significance	5	141053853	141053853	Human		name
329380327	CV2466559	single nucleotide variant	NM_013340.4(PCDHB1):c.1742C>T (p.Ala581Val)	not specified [RCV004274095]	uncertain significance	5	141053212	141053212	Human		name
401744136	CV2688103	single nucleotide variant	NM_013340.4(PCDHB1):c.1250G>A (p.Gly417Asp)	not specified [RCV004305160]	uncertain significance	5	141052720	141052720	Human		name
401753874	CV2716916	single nucleotide variant	NM_013340.4(PCDHB1):c.1378A>C (p.Thr460Pro)	not specified [RCV004330008]	uncertain significance	5	141052848	141052848	Human		name
401765832	CV2717884	single nucleotide variant	NM_013340.4(PCDHB1):c.2403G>C (p.Arg801Ser)	not specified [RCV004321853]	uncertain significance	5	141053873	141053873	Human		name
401896375	CV2781177	single nucleotide variant	NM_013340.4(PCDHB1):c.2443G>A (p.Asp815Asn)	not specified [RCV004352225]	uncertain significance	5	141053913	141053913	Human		name
405742373	CV3371818	single nucleotide variant	NM_013340.4(PCDHB1):c.1120C>T (p.Arg374Trp)	not specified [RCV004497891]	uncertain significance	5	141052590	141052590	Human		name
405742354	CV3371820	single nucleotide variant	NM_013340.4(PCDHB1):c.1234C>T (p.Arg412Trp)	not specified [RCV004497893]	uncertain significance	5	141052704	141052704	Human		name
405742342	CV3371822	single nucleotide variant	NM_013340.4(PCDHB1):c.1270G>C (p.Ala424Pro)	not specified [RCV004497895]	uncertain significance	5	141052740	141052740	Human		name
405742335	CV3371823	single nucleotide variant	NM_013340.4(PCDHB1):c.1412T>G (p.Ile471Ser)	not specified [RCV004497896]	uncertain significance	5	141052882	141052882	Human		name
405742100	CV3371825	single nucleotide variant	NM_013340.4(PCDHB1):c.1589T>G (p.Phe530Cys)	not specified [RCV004497898]	uncertain significance	5	141053059	141053059	Human		name
405741938	CV3371826	single nucleotide variant	NM_013340.4(PCDHB1):c.1759G>A (p.Val587Met)	not specified [RCV004497899]	uncertain significance	5	141053229	141053229	Human		name
405741946	CV3371827	single nucleotide variant	NM_013340.4(PCDHB1):c.1760T>C (p.Val587Ala)	not specified [RCV004497900]	uncertain significance	5	141053230	141053230	Human		name
405741952	CV3371828	single nucleotide variant	NM_013340.4(PCDHB1):c.2302T>G (p.Phe768Val)	not specified [RCV004497901]	uncertain significance	5	141053772	141053772	Human		name
405741957	CV3371829	single nucleotide variant	NM_013340.4(PCDHB1):c.2309T>C (p.Phe770Ser)	not specified [RCV004497902]	uncertain significance	5	141053779	141053779	Human		name
407523431	CV3463073	single nucleotide variant	NM_013340.4(PCDHB1):c.1085C>T (p.Pro362Leu)	not specified [RCV004653155]	likely benign	5	141052555	141052555	Human		name
407523428	CV3463074	single nucleotide variant	NM_013340.4(PCDHB1):c.1978A>C (p.Asn660His)	not specified [RCV004653156]	uncertain significance	5	141053448	141053448	Human		name
407523425	CV3463076	single nucleotide variant	NM_013340.4(PCDHB1):c.2405A>G (p.Asn802Ser)	not specified [RCV004653157]	uncertain significance	5	141053875	141053875	Human		name
597674965	CV3578873	single nucleotide variant	NM_013340.4(PCDHB1):c.1529G>A (p.Gly510Asp)	not specified [RCV004836752]	likely benign	5	141052999	141052999	Human		name
597674975	CV3578874	single nucleotide variant	NM_013340.4(PCDHB1):c.1414G>A (p.Gly472Ser)	not specified [RCV004836753]	uncertain significance	5	141052884	141052884	Human		name
597674988	CV3578875	single nucleotide variant	NM_013340.4(PCDHB1):c.1676G>A (p.Arg559His)	not specified [RCV004836754]	uncertain significance	5	141053146	141053146	Human		name
597756043	CV3578876	single nucleotide variant	NM_013340.4(PCDHB1):c.2090T>C (p.Ile697Thr)	not specified [RCV004848061]	uncertain significance	5	141053560	141053560	Human		name
597736753	CV3578877	single nucleotide variant	NM_013340.4(PCDHB1):c.1303G>C (p.Glu435Gln)	not specified [RCV004843772]	uncertain significance	5	141052773	141052773	Human		name
597736759	CV3578878	single nucleotide variant	NM_013340.4(PCDHB1):c.1493A>G (p.Asp498Gly)	not specified [RCV004843773]	uncertain significance	5	141052963	141052963	Human		name
597736769	CV3578880	single nucleotide variant	NM_013340.4(PCDHB1):c.1397G>T (p.Ser466Ile)	not specified [RCV004843775]	uncertain significance	5	141052867	141052867	Human		name
598269409	CV3999517	single nucleotide variant	NM_013340.4(PCDHB1):c.2247A>T (p.Leu749Phe)	not specified [RCV005388776]	uncertain significance	5	141053717	141053717	Human		name
598269416	CV3999519	single nucleotide variant	NM_013340.4(PCDHB1):c.1591G>C (p.Val531Leu)	not specified [RCV005388778]	uncertain significance	5	141053061	141053061	Human		name
598269426	CV3999521	single nucleotide variant	NM_013340.4(PCDHB1):c.2287A>G (p.Thr763Ala)	not specified [RCV005388780]	uncertain significance	5	141053757	141053757	Human		name
598269431	CV3999522	single nucleotide variant	NM_013340.4(PCDHB1):c.1960T>C (p.Ser654Pro)	not specified [RCV005388781]	uncertain significance	5	141053430	141053430	Human		name
598269452	CV3999527	single nucleotide variant	NM_013340.4(PCDHB1):c.2137C>A (p.His713Asn)	not specified [RCV005388786]	uncertain significance	5	141053607	141053607	Human		name
598269455	CV3999530	single nucleotide variant	NM_013340.4(PCDHB1):c.1705G>A (p.Gly569Ser)	not specified [RCV005388787]	uncertain significance	5	141053175	141053175	Human		name
8625937	CV81076	single nucleotide variant	NM_018931.2(PCDHB11):c.9C>T (p.Asn3=)	Malignant melanoma [RCV000061154]	not provided	5	141199783	141199783	Human		name
8625936	CV81075	single nucleotide variant	NM_018931.2(PCDHB11):c.8A>T (p.Asn3Ile)	Malignant melanoma [RCV000061153]	not provided	5	141199782	141199782	Human		name
156169478	CV2247318	single nucleotide variant	NM_020957.4(PCDHB16):c.13T>A (p.Trp5Arg)	not specified [RCV004108666]	uncertain significance	5	141182572	141182572	Human		name
401780555	CV2674078	single nucleotide variant	NM_020957.4(PCDHB16):c.23A>G (p.Asn8Ser)	not specified [RCV004295484]	likely benign	5	141182582	141182582	Human		name
405742873	CV3367940	single nucleotide variant	NM_018934.4(PCDHB14):c.17C>T (p.Ala6Val)	not specified [RCV004498007]	uncertain significance	5	141223522	141223522	Human		name
405744538	CV3367961	single nucleotide variant	NM_018935.4(PCDHB15):c.19C>A (p.Arg7Ser)	not specified [RCV004498028]	uncertain significance	5	141245597	141245597	Human		name
597737341	CV3575066	single nucleotide variant	NM_018933.4(PCDHB13):c.26G>A (p.Cys9Tyr)	not specified [RCV004843842]	uncertain significance	5	141214149	141214149	Human		name
156277760	CV2300268	single nucleotide variant	NM_018934.4(PCDHB14):c.98A>G (p.Tyr33Cys)	not specified [RCV004153228]	uncertain significance	5	141223603	141223603	Human		name
156101007	CV2313453	single nucleotide variant	NM_018932.4(PCDHB12):c.82T>C (p.Ser28Pro)	not specified [RCV004163767]	uncertain significance	5	141208989	141208989	Human		name
156395360	CV2329151	single nucleotide variant	NM_020957.4(PCDHB16):c.65G>A (p.Ser22Asn)	not specified [RCV004173908]	uncertain significance	5	141182624	141182624	Human		name
155906909	CV2357405	single nucleotide variant	NM_018930.4(PCDHB10):c.61T>G (p.Trp21Gly)	not specified [RCV004200285]	likely benign	5	141192613	141192613	Human		name
329371472	CV2458137	single nucleotide variant	NM_018931.3(PCDHB11):c.49C>G (p.Leu17Val)	not specified [RCV004271948]	uncertain significance	5	141199823	141199823	Human		name
329394796	CV2461464	single nucleotide variant	NM_018932.4(PCDHB12):c.69G>A (p.Met23Ile)	not specified [RCV004267606]	uncertain significance	5	141208976	141208976	Human		name
401744858	CV2688245	single nucleotide variant	NM_018932.4(PCDHB12):c.32T>C (p.Ile11Thr)	not specified [RCV004298929]	likely benign	5	141208939	141208939	Human		name
401726066	CV2699062	single nucleotide variant	NM_018935.4(PCDHB15):c.49C>A (p.Leu17Ile)	not specified [RCV004303577]	uncertain significance	5	141245627	141245627	Human		name
401876209	CV2777705	single nucleotide variant	NM_018935.4(PCDHB15):c.50T>A (p.Leu17His)	not specified [RCV004345542]	uncertain significance	5	141245628	141245628	Human		name
401897501	CV2787107	single nucleotide variant	NM_018930.4(PCDHB10):c.76G>A (p.Ala26Thr)	not specified [RCV004360544]	uncertain significance	5	141192628	141192628	Human		name
401915156	CV2825326	single nucleotide variant	NM_018933.4(PCDHB13):c.771G>A (p.Pro257=)	not provided [RCV003428642]	likely benign	5	141214894	141214894	Human		name
401915158	CV2825327	single nucleotide variant	NM_018934.4(PCDHB14):c.846C>T (p.Phe282=)	not provided [RCV003428643]	likely benign	5	141224351	141224351	Human		name
405744221	CV3367967	single nucleotide variant	NM_018935.4(PCDHB15):c.62T>C (p.Leu21Pro)	not specified [RCV004498034]	uncertain significance	5	141245640	141245640	Human		name
405743555	CV3367971	single nucleotide variant	NM_018935.4(PCDHB15):c.98A>G (p.Tyr33Cys)	not specified [RCV004498038]	uncertain significance	5	141245676	141245676	Human		name
405742321	CV3371881	single nucleotide variant	NM_018931.3(PCDHB11):c.64G>A (p.Gly22Arg)	not specified [RCV004497954]	uncertain significance	5	141199838	141199838	Human		name
407523242	CV3463105	single nucleotide variant	NM_018932.4(PCDHB12):c.67A>G (p.Met23Val)	not specified [RCV004653171]	uncertain significance	5	141208974	141208974	Human		name
597737051	CV3575053	single nucleotide variant	NM_018933.4(PCDHB13):c.28A>G (p.Arg10Gly)	not specified [RCV004843833]	uncertain significance	5	141214151	141214151	Human		name
597736788	CV3578885	single nucleotide variant	NM_018930.4(PCDHB10):c.53T>G (p.Phe18Cys)	not specified [RCV004843779]	uncertain significance	5	141192605	141192605	Human		name
597736851	CV3578901	single nucleotide variant	NM_018931.3(PCDHB11):c.61C>A (p.Leu21Ile)	not specified [RCV004843792]	uncertain significance	5	141199835	141199835	Human		name
597736856	CV3578902	single nucleotide variant	NM_018931.3(PCDHB11):c.52T>A (p.Phe18Ile)	not specified [RCV004843793]	uncertain significance	5	141199826	141199826	Human		name
8625935	CV81074	single nucleotide variant	NM_018930.3(PCDHB10):c.777C>T (p.Phe259=)	Malignant melanoma [RCV000061152]	not provided	5	141193329	141193329	Human		name
8631443	CV86630	single nucleotide variant	NM_018930.3(PCDHB10):c.339C>T (p.Pro113=)	Malignant melanoma [RCV000066721]	not provided	5	141192891	141192891	Human		name
8631450	CV86637	single nucleotide variant	NM_018935.3(PCDHB15):c.447G>A (p.Gly149=)	Malignant melanoma [RCV000066728]	not provided	5	141246025	141246025	Human		name
156139141	CV2202881	single nucleotide variant	NM_020957.4(PCDHB16):c.213C>G (p.Asn71Lys)	not specified [RCV004069157]	uncertain significance	5	141182772	141182772	Human		name
156335335	CV2211449	single nucleotide variant	NM_018934.4(PCDHB14):c.101C>T (p.Ser34Phe)	not specified [RCV004090676]	uncertain significance	5	141223606	141223606	Human		name
155978096	CV2214962	single nucleotide variant	NM_018934.4(PCDHB14):c.293C>A (p.Ser98Tyr)	not specified [RCV004084740]	uncertain significance	5	141223798	141223798	Human		name
156194620	CV2223357	single nucleotide variant	NM_018932.4(PCDHB12):c.129C>A (p.Ser43Arg)	not specified [RCV004105957]	uncertain significance	5	141209036	141209036	Human		name
155922219	CV2240650	single nucleotide variant	NM_018935.4(PCDHB15):c.233A>T (p.Asp78Val)	not specified [RCV004119285]	uncertain significance	5	141245811	141245811	Human		name
155914954	CV2242882	single nucleotide variant	NM_018934.4(PCDHB14):c.293C>G (p.Ser98Cys)	not specified [RCV004107473]	uncertain significance	5	141223798	141223798	Human		name
156037081	CV2243708	single nucleotide variant	NM_018932.4(PCDHB12):c.210T>A (p.Asp70Glu)	not specified [RCV004114411]	uncertain significance	5	141209117	141209117	Human		name
156281946	CV2252368	single nucleotide variant	NM_018931.3(PCDHB11):c.235A>G (p.Ile79Val)	not specified [RCV004116214]	uncertain significance	5	141200009	141200009	Human		name
156090654	CV2256523	single nucleotide variant	NM_018931.3(PCDHB11):c.164A>T (p.Lys55Met)	not specified [RCV004118726]	uncertain significance	5	141199938	141199938	Human		name
156070521	CV2267169	single nucleotide variant	NM_018932.4(PCDHB12):c.109G>A (p.Glu37Lys)	not specified [RCV004133857]	uncertain significance	5	141209016	141209016	Human		name
155972919	CV2271589	single nucleotide variant	NM_018934.4(PCDHB14):c.151G>C (p.Asp51His)	not specified [RCV004128670]	uncertain significance	5	141223656	141223656	Human		name
156182340	CV2298605	single nucleotide variant	NM_018930.4(PCDHB10):c.213C>A (p.Asn71Lys)	not specified [RCV004162252]	uncertain significance	5	141192765	141192765	Human		name
156290171	CV2299465	single nucleotide variant	NM_020957.4(PCDHB16):c.184C>G (p.Arg62Gly)	not specified [RCV004154542]	uncertain significance	5	141182743	141182743	Human		name
156348937	CV2309154	single nucleotide variant	NM_020957.4(PCDHB16):c.169A>T (p.Thr57Ser)	not specified [RCV004171506]	uncertain significance	5	141182728	141182728	Human		name
156096520	CV2310191	single nucleotide variant	NM_018932.4(PCDHB12):c.142T>G (p.Leu48Val)	not specified [RCV004163296]	uncertain significance	5	141209049	141209049	Human		name
156175538	CV2317240	single nucleotide variant	NM_018935.4(PCDHB15):c.214G>A (p.Glu72Lys)	not specified [RCV004178737]	uncertain significance	5	141245792	141245792	Human		name
156274753	CV2320083	single nucleotide variant	NM_018933.4(PCDHB13):c.140C>G (p.Thr47Ser)	not specified [RCV004167934]	uncertain significance	5	141214263	141214263	Human		name
156273729	CV2320206	single nucleotide variant	NM_018930.4(PCDHB10):c.178G>A (p.Ala60Thr)	not specified [RCV004169827]	uncertain significance	5	141192730	141192730	Human		name
156272703	CV2323411	single nucleotide variant	NM_018934.4(PCDHB14):c.163G>A (p.Gly55Arg)	not specified [RCV004171805]	uncertain significance	5	141223668	141223668	Human		name
155914321	CV2341971	single nucleotide variant	NM_018933.4(PCDHB13):c.216C>G (p.Asn72Lys)	not specified [RCV004184913]	uncertain significance	5	141214339	141214339	Human		name
156338551	CV2351439	single nucleotide variant	NM_018931.3(PCDHB11):c.167T>A (p.Val56Glu)	not specified [RCV004193126]	uncertain significance	5	141199941	141199941	Human		name
156183035	CV2353202	single nucleotide variant	NM_020957.4(PCDHB16):c.284T>C (p.Leu95Pro)	not specified [RCV004203671]	uncertain significance	5	141182843	141182843	Human		name
155910488	CV2366455	single nucleotide variant	NM_018932.4(PCDHB12):c.247G>T (p.Asp83Tyr)	not specified [RCV004208435]	uncertain significance	5	141209154	141209154	Human		name
156172514	CV2380828	single nucleotide variant	NM_018931.3(PCDHB11):c.178T>C (p.Ser60Pro)	not specified [RCV004218384]	uncertain significance	5	141199952	141199952	Human		name
155961268	CV2390850	single nucleotide variant	NM_018931.3(PCDHB11):c.104T>C (p.Val35Ala)	not specified [RCV004241123]	uncertain significance	5	141199878	141199878	Human		name
329368073	CV2427681	single nucleotide variant	NM_018931.3(PCDHB11):c.227A>G (p.Gln76Arg)	not specified [RCV004250303]	uncertain significance	5	141200001	141200001	Human		name
329365167	CV2440091	single nucleotide variant	NM_018931.3(PCDHB11):c.203C>T (p.Ser68Phe)	not specified [RCV004260557]	uncertain significance	5	141199977	141199977	Human		name
401754644	CV2682259	single nucleotide variant	NM_018931.3(PCDHB11):c.241A>G (p.Thr81Ala)	not specified [RCV004297215]	uncertain significance	5	141200015	141200015	Human		name
401771466	CV2711702	single nucleotide variant	NM_018930.4(PCDHB10):c.120G>C (p.Glu40Asp)	not specified [RCV004309372]	uncertain significance	5	141192672	141192672	Human		name
401879904	CV2769807	single nucleotide variant	NM_018935.4(PCDHB15):c.200T>C (p.Val67Ala)	not specified [RCV004353672]	uncertain significance	5	141245778	141245778	Human		name
401874788	CV2781244	single nucleotide variant	NM_018935.4(PCDHB15):c.268C>G (p.Leu90Val)	not specified [RCV004352278]	uncertain significance	5	141245846	141245846	Human		name
401915324	CV2825314	single nucleotide variant	NM_020957.4(PCDHB16):c.1251T>C (p.Tyr417=)	not provided [RCV003428636]	likely benign	5	141183810	141183810	Human		name
401917924	CV2825315	single nucleotide variant	NM_020957.4(PCDHB16):c.1542C>T (p.Phe514=)	not provided [RCV003429832]	likely benign	5	141184101	141184101	Human		name
401917926	CV2825316	single nucleotide variant	NM_020957.4(PCDHB16):c.1647G>A (p.Val549=)	not provided [RCV003429833]	likely benign	5	141184206	141184206	Human		name
401915147	CV2825322	single nucleotide variant	NM_018930.4(PCDHB10):c.1905A>G (p.Ala635=)	not provided [RCV003428639]	likely benign	5	141194457	141194457	Human		name
401915149	CV2825323	single nucleotide variant	NM_018931.3(PCDHB11):c.1416T>C (p.Ser472=)	not provided [RCV003428640]	likely benign	5	141201190	141201190	Human		name
401917932	CV2825324	single nucleotide variant	NM_018931.3(PCDHB11):c.1596C>A (p.Gly532=)	not provided [RCV003429837]	likely benign	5	141201370	141201370	Human		name
401915153	CV2825325	single nucleotide variant	NM_018932.4(PCDHB12):c.1086G>A (p.Glu362=)	not provided [RCV003428641]	likely benign	5	141209993	141209993	Human		name
401915160	CV2825328	single nucleotide variant	NM_018934.4(PCDHB14):c.1398C>T (p.Pro466=)	not provided [RCV003428644]	likely benign	5	141224903	141224903	Human		name
401917933	CV2825329	single nucleotide variant	NM_018934.4(PCDHB14):c.1440A>G (p.Ser480=)	not provided [RCV003429838]	likely benign	5	141224945	141224945	Human		name
401917934	CV2825330	single nucleotide variant	NM_018934.4(PCDHB14):c.1992C>T (p.Asp664=)	not provided [RCV003429839]	likely benign	5	141225497	141225497	Human		name
405742680	CV3367911	single nucleotide variant	NM_018933.4(PCDHB13):c.143A>G (p.Asn48Ser)	not specified [RCV004497978]	uncertain significance	5	141214266	141214266	Human		name
405742704	CV3367914	single nucleotide variant	NM_018933.4(PCDHB13):c.164T>C (p.Leu55Pro)	not specified [RCV004497981]	uncertain significance	5	141214287	141214287	Human		name
405742744	CV3367920	single nucleotide variant	NM_018933.4(PCDHB13):c.283G>C (p.Asp95His)	not specified [RCV004497987]	uncertain significance	5	141214406	141214406	Human		name
405744518	CV3367963	single nucleotide variant	NM_018935.4(PCDHB15):c.236T>C (p.Leu79Pro)	not specified [RCV004498030]	uncertain significance	5	141245814	141245814	Human		name
405742244	CV3371870	single nucleotide variant	NM_018931.3(PCDHB11):c.190G>T (p.Ala64Ser)	not specified [RCV004497943]	uncertain significance	5	141199964	141199964	Human		name
405742302	CV3371878	single nucleotide variant	NM_018931.3(PCDHB11):c.290G>C (p.Gly97Ala)	not specified [RCV004497951]	uncertain significance	5	141200064	141200064	Human		name
405742566	CV3371889	single nucleotide variant	NM_018932.4(PCDHB12):c.157G>A (p.Gly53Arg)	not specified [RCV004497962]	uncertain significance	5	141209064	141209064	Human		name
407480350	CV3463093	single nucleotide variant	NM_018931.3(PCDHB11):c.106G>A (p.Ala36Thr)	not specified [RCV004664389]	uncertain significance	5	141199880	141199880	Human		name
407523267	CV3463121	single nucleotide variant	NM_018934.4(PCDHB14):c.163G>C (p.Gly55Arg)	not specified [RCV004653179]	uncertain significance	5	141223668	141223668	Human		name
407523287	CV3463131	single nucleotide variant	NM_018935.4(PCDHB15):c.172G>A (p.Glu58Lys)	not specified [RCV004653186]	uncertain significance	5	141245750	141245750	Human		name
407480485	CV3463138	single nucleotide variant	NM_018935.4(PCDHB15):c.269T>G (p.Leu90Arg)	not specified [RCV004664410]	uncertain significance	5	141245847	141245847	Human		name
407480496	CV3463143	single nucleotide variant	NM_020957.4(PCDHB16):c.131T>C (p.Phe44Ser)	not specified [RCV004664412]	uncertain significance	5	141182690	141182690	Human		name
407480504	CV3463144	single nucleotide variant	NM_020957.4(PCDHB16):c.195G>T (p.Arg65Ser)	not specified [RCV004664413]	uncertain significance	5	141182754	141182754	Human		name
597737016	CV3575045	single nucleotide variant	NM_018932.4(PCDHB12):c.233A>G (p.Asp78Gly)	not specified [RCV004843826]	uncertain significance	5	141209140	141209140	Human		name
597756089	CV3575052	single nucleotide variant	NM_018933.4(PCDHB13):c.158T>C (p.Leu53Pro)	not specified [RCV004848073]	uncertain significance	5	141214281	141214281	Human		name
597737058	CV3575056	single nucleotide variant	NM_018933.4(PCDHB13):c.203T>C (p.Val68Ala)	not specified [RCV004843835]	uncertain significance	5	141214326	141214326	Human		name
597737089	CV3575096	single nucleotide variant	NM_018935.4(PCDHB15):c.271G>T (p.Asp91Tyr)	not specified [RCV004843865]	uncertain significance	5	141245849	141245849	Human		name
597756249	CV3575104	single nucleotide variant	NM_020957.4(PCDHB16):c.254T>C (p.Leu85Pro)	not specified [RCV004848086]	uncertain significance	5	141182813	141182813	Human		name
597737143	CV3575112	single nucleotide variant	NM_020957.4(PCDHB16):c.118G>A (p.Glu40Lys)	not specified [RCV004843876]	uncertain significance	5	141182677	141182677	Human		name
597736793	CV3578886	single nucleotide variant	NM_018930.4(PCDHB10):c.241A>G (p.Thr81Ala)	not specified [RCV004843780]	uncertain significance	5	141192793	141192793	Human		name
597736812	CV3578891	single nucleotide variant	NM_018930.4(PCDHB10):c.170G>A (p.Gly57Glu)	not specified [RCV004843784]	uncertain significance	5	141192722	141192722	Human		name
597736831	CV3578896	single nucleotide variant	NM_018931.3(PCDHB11):c.151G>A (p.Asp51Asn)	not specified [RCV004843788]	uncertain significance	5	141199925	141199925	Human		name
597736865	CV3578904	single nucleotide variant	NM_018931.3(PCDHB11):c.293C>G (p.Ser98Cys)	not specified [RCV004843795]	uncertain significance	5	141200067	141200067	Human		name
597736929	CV3578921	single nucleotide variant	NM_018931.3(PCDHB11):c.199G>A (p.Val67Ile)	not specified [RCV004843808]	uncertain significance	5	141199973	141199973	Human		name
598195458	CV3996056	single nucleotide variant	NM_018931.3(PCDHB11):c.259A>T (p.Ser87Cys)	not specified [RCV005397538]	uncertain significance	5	141200033	141200033	Human		name
598269529	CV3996057	single nucleotide variant	NM_018931.3(PCDHB11):c.190G>A (p.Ala64Thr)	not specified [RCV005388803]	uncertain significance	5	141199964	141199964	Human		name
598269581	CV3996072	single nucleotide variant	NM_018932.4(PCDHB12):c.160C>T (p.Leu54Phe)	not specified [RCV005388816]	uncertain significance	5	141209067	141209067	Human		name
598269667	CV3996092	single nucleotide variant	NM_018933.4(PCDHB13):c.236A>G (p.Asn79Ser)	not specified [RCV005388834]	uncertain significance	5	141214359	141214359	Human		name
598269794	CV3996120	single nucleotide variant	NM_018935.4(PCDHB15):c.275G>A (p.Arg92Gln)	not specified [RCV005388860]	uncertain significance	5	141245853	141245853	Human		name
598195512	CV3996126	single nucleotide variant	NM_018935.4(PCDHB15):c.274C>G (p.Arg92Gly)	not specified [RCV005397546]	uncertain significance	5	141245852	141245852	Human		name
598269854	CV3996136	single nucleotide variant	NM_020957.4(PCDHB16):c.146G>A (p.Gly49Glu)	not specified [RCV005388872]	likely benign	5	141182705	141182705	Human		name
617153870	CV4022136	deletion	NM_020957.4(PCDHB16):c.894del (p.Glu300fs)	not provided [RCV005429190]	not provided	5	141183453	141183453	Human		name
8625942	CV81081	single nucleotide variant	NM_018933.3(PCDHB13):c.1587C>T (p.Phe529=)	Malignant melanoma [RCV000061159]	not provided	5	141215710	141215710	Human		name
8631447	CV86634	single nucleotide variant	NM_018932.3(PCDHB12):c.1167C>T (p.Ile389=)	Malignant melanoma [RCV000066725]	not provided	5	141210074	141210074	Human		name
156320652	CV2197363	single nucleotide variant	NM_018934.4(PCDHB14):c.392C>T (p.Pro131Leu)	not specified [RCV004081105]	uncertain significance	5	141223897	141223897	Human		name
156063438	CV2199917	single nucleotide variant	NM_018934.4(PCDHB14):c.866G>C (p.Arg289Pro)	not specified [RCV004074097]	uncertain significance	5	141224371	141224371	Human		name
155915643	CV2200443	single nucleotide variant	NM_018930.4(PCDHB10):c.401A>G (p.Gln134Arg)	not specified [RCV004076757]	uncertain significance	5	141192953	141192953	Human		name
155961068	CV2204434	single nucleotide variant	NM_018930.4(PCDHB10):c.520C>T (p.Pro174Ser)	not specified [RCV004079241]	uncertain significance	5	141193072	141193072	Human		name
156083718	CV2205538	single nucleotide variant	NM_018930.4(PCDHB10):c.863T>C (p.Ile288Thr)	not specified [RCV004082469]	uncertain significance	5	141193415	141193415	Human		name
156034043	CV2211686	single nucleotide variant	NM_020957.4(PCDHB16):c.512A>C (p.Lys171Thr)	not specified [RCV004084572]	uncertain significance	5	141183071	141183071	Human		name
156032393	CV2218294	single nucleotide variant	NM_018931.3(PCDHB11):c.341C>A (p.Thr114Lys)	not specified [RCV004088481]	uncertain significance	5	141200115	141200115	Human		name
156282377	CV2220781	single nucleotide variant	NM_018932.4(PCDHB12):c.682G>A (p.Val228Ile)	not specified [RCV004092231]	uncertain significance	5	141209589	141209589	Human		name
156185655	CV2222634	single nucleotide variant	NM_018931.3(PCDHB11):c.389C>T (p.Ser130Phe)	not specified [RCV004099458]	uncertain significance	5	141200163	141200163	Human		name
156023282	CV2223450	single nucleotide variant	NM_018933.4(PCDHB13):c.746G>C (p.Arg249Thr)	not specified [RCV004106027]	uncertain significance	5	141214869	141214869	Human		name
156121204	CV2227009	single nucleotide variant	NM_018931.3(PCDHB11):c.566G>A (p.Arg189Lys)	not specified [RCV004097395]	uncertain significance	5	141200340	141200340	Human		name
156241444	CV2231357	single nucleotide variant	NM_018934.4(PCDHB14):c.896G>A (p.Gly299Glu)	not specified [RCV004096451]	uncertain significance	5	141224401	141224401	Human		name
155983817	CV2241049	single nucleotide variant	NM_018933.4(PCDHB13):c.308G>A (p.Cys103Tyr)	not specified [RCV004104096]	uncertain significance	5	141214431	141214431	Human		name
155912824	CV2245653	single nucleotide variant	NM_018931.3(PCDHB11):c.887A>G (p.Gln296Arg)	not specified [RCV004111537]	uncertain significance	5	141200661	141200661	Human		name
156298051	CV2246991	single nucleotide variant	NM_018932.4(PCDHB12):c.465A>C (p.Glu155Asp)	not specified [RCV004112774]	uncertain significance	5	141209372	141209372	Human		name
156284492	CV2249846	single nucleotide variant	NM_018930.4(PCDHB10):c.683T>C (p.Val228Ala)	not specified [RCV004122592]	uncertain significance	5	141193235	141193235	Human		name
156182932	CV2255290	single nucleotide variant	NM_018934.4(PCDHB14):c.790A>G (p.Ile264Val)	not specified [RCV004117671]	likely benign	5	141224295	141224295	Human		name
156356773	CV2257540	single nucleotide variant	NM_018931.3(PCDHB11):c.866G>T (p.Arg289Leu)	not specified [RCV004125593]	uncertain significance	5	141200640	141200640	Human		name
155988168	CV2259542	single nucleotide variant	NM_020957.4(PCDHB16):c.428C>A (p.Pro143Gln)	not specified [RCV004122730]	uncertain significance	5	141182987	141182987	Human		name
156058439	CV2262891	single nucleotide variant	NM_018934.4(PCDHB14):c.875T>A (p.Phe292Tyr)	not specified [RCV004125035]	uncertain significance	5	141224380	141224380	Human		name
155967569	CV2265784	single nucleotide variant	NM_018930.4(PCDHB10):c.715G>A (p.Ala239Thr)	not specified [RCV004126403]	uncertain significance	5	141193267	141193267	Human		name
156169324	CV2266741	single nucleotide variant	NM_020957.4(PCDHB16):c.779T>A (p.Leu260Gln)	not specified [RCV004137570]	uncertain significance	5	141183338	141183338	Human		name
156071731	CV2267338	single nucleotide variant	NM_020957.4(PCDHB16):c.754C>G (p.Pro252Ala)	not specified [RCV004133999]	uncertain significance	5	141183313	141183313	Human		name
156151359	CV2268948	single nucleotide variant	NM_020957.4(PCDHB16):c.821A>G (p.Asn274Ser)	not specified [RCV004128352]	uncertain significance	5	141183380	141183380	Human		name
156336653	CV2270868	single nucleotide variant	NM_020957.4(PCDHB16):c.338C>T (p.Pro113Leu)	not specified [RCV004131911]	uncertain significance	5	141182897	141182897	Human		name
155957873	CV2282125	single nucleotide variant	NM_018931.3(PCDHB11):c.547A>G (p.Arg183Gly)	not specified [RCV004138861]	uncertain significance	5	141200321	141200321	Human		name
156245167	CV2283406	single nucleotide variant	NM_018933.4(PCDHB13):c.673G>C (p.Gly225Arg)	not specified [RCV004139635]	uncertain significance	5	141214796	141214796	Human		name
156063992	CV2287034	single nucleotide variant	NM_018933.4(PCDHB13):c.520A>G (p.Ser174Gly)	not specified [RCV004144915]	uncertain significance	5	141214643	141214643	Human		name
156294015	CV2293142	single nucleotide variant	NM_018930.4(PCDHB10):c.581T>C (p.Leu194Pro)	not specified [RCV004150664]	uncertain significance	5	141193133	141193133	Human		name
156018382	CV2302834	single nucleotide variant	NM_018930.4(PCDHB10):c.514A>C (p.Ile172Leu)	not specified [RCV004162737]	uncertain significance	5	141193066	141193066	Human		name
156305351	CV2305085	single nucleotide variant	NM_020957.4(PCDHB16):c.719C>T (p.Pro240Leu)	not specified [RCV004168962]	uncertain significance	5	141183278	141183278	Human		name
155951676	CV2309737	single nucleotide variant	NM_018935.4(PCDHB15):c.341T>C (p.Leu114Ser)	not specified [RCV004160865]	uncertain significance	5	141245919	141245919	Human		name
156305564	CV2314658	single nucleotide variant	NM_018932.4(PCDHB12):c.616C>A (p.Pro206Thr)	not specified [RCV004170811]	uncertain significance	5	141209523	141209523	Human		name
156196130	CV2319058	single nucleotide variant	NM_018935.4(PCDHB15):c.664C>G (p.Arg222Gly)	not specified [RCV004178139]	uncertain significance	5	141246242	141246242	Human		name
156296744	CV2319155	single nucleotide variant	NM_018931.3(PCDHB11):c.470C>T (p.Ala157Val)	not specified [RCV004178221]	uncertain significance	5	141200244	141200244	Human		name
156058112	CV2322901	single nucleotide variant	NM_020957.4(PCDHB16):c.322G>T (p.Val108Leu)	not specified [RCV004185352]	uncertain significance	5	141182881	141182881	Human		name
156396273	CV2326188	single nucleotide variant	NM_018933.4(PCDHB13):c.749T>C (p.Val250Ala)	not specified [RCV004180456]	uncertain significance	5	141214872	141214872	Human		name
156182553	CV2327904	single nucleotide variant	NM_018932.4(PCDHB12):c.598C>A (p.Leu200Met)	not specified [RCV004179227]	uncertain significance	5	141209505	141209505	Human		name
156176634	CV2331181	single nucleotide variant	NM_018932.4(PCDHB12):c.904A>C (p.Thr302Pro)	not specified [RCV004181785]	uncertain significance	5	141209811	141209811	Human		name
156072449	CV2331508	single nucleotide variant	NM_018933.4(PCDHB13):c.310G>A (p.Val104Met)	not specified [RCV004182114]	uncertain significance	5	141214433	141214433	Human		name
156077437	CV2331880	single nucleotide variant	NM_018931.3(PCDHB11):c.919C>G (p.Leu307Val)	not specified [RCV004186535]	uncertain significance	5	141200693	141200693	Human		name
156334578	CV2333406	single nucleotide variant	NM_018930.4(PCDHB10):c.845T>C (p.Phe282Ser)	not specified [RCV004190113]	uncertain significance	5	141193397	141193397	Human		name
156049390	CV2336518	single nucleotide variant	NM_018932.4(PCDHB12):c.916C>T (p.Pro306Ser)	not specified [RCV004194726]	likely benign	5	141209823	141209823	Human		name
155983592	CV2344323	single nucleotide variant	NM_018932.4(PCDHB12):c.815G>T (p.Gly272Val)	not specified [RCV004195081]	uncertain significance	5	141209722	141209722	Human		name
155902064	CV2345923	single nucleotide variant	NM_018930.4(PCDHB10):c.430G>C (p.Glu144Gln)	not specified [RCV004198961]	uncertain significance	5	141192982	141192982	Human		name
156240679	CV2350359	single nucleotide variant	NM_018932.4(PCDHB12):c.537C>A (p.His179Gln)	not specified [RCV004202304]	uncertain significance	5	141209444	141209444	Human		name
156119777	CV2354107	single nucleotide variant	NM_018932.4(PCDHB12):c.823A>G (p.Ser275Gly)	not specified [RCV004206545]	likely benign	5	141209730	141209730	Human		name
156119797	CV2354108	single nucleotide variant	NM_018932.4(PCDHB12):c.829C>A (p.Leu277Ile)	not specified [RCV004206546]	likely benign	5	141209736	141209736	Human		name
155930114	CV2354109	single nucleotide variant	NM_018932.4(PCDHB12):c.833C>G (p.Ser278Cys)	not specified [RCV004206547]	uncertain significance	5	141209740	141209740	Human		name
155927920	CV2366005	single nucleotide variant	NM_020957.4(PCDHB16):c.901G>C (p.Val301Leu)	not provided [RCV004695694]\|not specified [RCV004207606]	uncertain significance	5	141183460	141183460	Human		name
156287240	CV2370475	single nucleotide variant	NM_018930.4(PCDHB10):c.617G>A (p.Gly206Glu)	not specified [RCV004215823]	uncertain significance	5	141193169	141193169	Human		name
155998299	CV2373274	single nucleotide variant	NM_018935.4(PCDHB15):c.518C>A (p.Ser173Tyr)	not specified [RCV004217942]	uncertain significance	5	141246096	141246096	Human		name
156388884	CV2376182	single nucleotide variant	NM_018930.4(PCDHB10):c.556G>A (p.Asp186Asn)	not specified [RCV004220408]	uncertain significance	5	141193108	141193108	Human		name
156048868	CV2378130	single nucleotide variant	NM_018930.4(PCDHB10):c.686G>T (p.Arg229Leu)	not specified [RCV004233047]	uncertain significance	5	141193238	141193238	Human		name
156156724	CV2397900	single nucleotide variant	NM_018933.4(PCDHB13):c.694G>C (p.Glu232Gln)	not specified [RCV004239725]	uncertain significance	5	141214817	141214817	Human		name
329381915	CV2424264	single nucleotide variant	NM_018930.4(PCDHB10):c.631A>C (p.Thr211Pro)	not specified [RCV004252175]	uncertain significance	5	141193183	141193183	Human		name
329369919	CV2424981	single nucleotide variant	NM_018930.4(PCDHB10):c.704T>C (p.Val235Ala)	not specified [RCV004250644]	uncertain significance	5	141193256	141193256	Human		name
329390874	CV2437371	single nucleotide variant	NM_020957.4(PCDHB16):c.938C>G (p.Thr313Arg)	not specified [RCV004256241]	uncertain significance	5	141183497	141183497	Human		name
329354326	CV2437866	single nucleotide variant	NM_018930.4(PCDHB10):c.682G>A (p.Val228Ile)	not specified [RCV004261155]	likely benign	5	141193234	141193234	Human		name
329388961	CV2448539	single nucleotide variant	NM_018930.4(PCDHB10):c.331G>T (p.Asp111Tyr)	not specified [RCV004259221]	uncertain significance	5	141192883	141192883	Human		name
329382653	CV2449287	single nucleotide variant	NM_018935.4(PCDHB15):c.554G>T (p.Arg185Leu)	not specified [RCV004257418]	uncertain significance	5	141246132	141246132	Human		name
329358221	CV2450225	single nucleotide variant	NM_018930.4(PCDHB10):c.607G>C (p.Glu203Gln)	not specified [RCV004271331]	uncertain significance	5	141193159	141193159	Human		name
329402746	CV2451313	single nucleotide variant	NM_018935.4(PCDHB15):c.644T>C (p.Val215Ala)	not specified [RCV004272007]	uncertain significance	5	141246222	141246222	Human		name
329379853	CV2456512	single nucleotide variant	NM_018930.4(PCDHB10):c.821A>G (p.Asn274Ser)	not specified [RCV004275653]	uncertain significance	5	141193373	141193373	Human		name
329370544	CV2461756	single nucleotide variant	NM_018934.4(PCDHB14):c.652G>A (p.Gly218Arg)	not specified [RCV004269903]	uncertain significance	5	141224157	141224157	Human		name
401751847	CV2672597	single nucleotide variant	NM_018931.3(PCDHB11):c.911G>C (p.Arg304Thr)	not specified [RCV004287628]	likely benign	5	141200685	141200685	Human		name
401728863	CV2673072	single nucleotide variant	NM_018931.3(PCDHB11):c.900A>C (p.Glu300Asp)	not specified [RCV004284059]	likely benign	5	141200674	141200674	Human		name
401731285	CV2674322	single nucleotide variant	NM_018935.4(PCDHB15):c.688A>C (p.Ile230Leu)	not specified [RCV004289198]	uncertain significance	5	141246266	141246266	Human		name
401742866	CV2677701	single nucleotide variant	NM_018933.4(PCDHB13):c.721C>T (p.Pro241Ser)	not specified [RCV004291783]	uncertain significance	5	141214844	141214844	Human		name
401747452	CV2688919	single nucleotide variant	NM_018933.4(PCDHB13):c.947A>T (p.Tyr316Phe)	not specified [RCV004303924]	uncertain significance	5	141215070	141215070	Human		name
401758460	CV2694114	single nucleotide variant	NM_020957.4(PCDHB16):c.597G>C (p.Glu199Asp)	not specified [RCV004302546]	uncertain significance	5	141183156	141183156	Human		name
401746531	CV2694876	single nucleotide variant	NM_018930.4(PCDHB10):c.664A>G (p.Arg222Gly)	not specified [RCV004300946]	uncertain significance	5	141193216	141193216	Human		name
401760320	CV2695001	single nucleotide variant	NM_018935.4(PCDHB15):c.905G>A (p.Arg302Gln)	not specified [RCV004301375]	uncertain significance	5	141246483	141246483	Human		name
401725651	CV2697500	single nucleotide variant	NM_018932.4(PCDHB12):c.322G>T (p.Val108Leu)	not specified [RCV004297889]	uncertain significance	5	141209229	141209229	Human		name
401737278	CV2699716	single nucleotide variant	NM_018930.4(PCDHB10):c.332A>G (p.Asp111Gly)	not specified [RCV004308060]	uncertain significance	5	141192884	141192884	Human		name
401720801	CV2702122	single nucleotide variant	NM_018930.4(PCDHB10):c.458G>A (p.Arg153Lys)	not specified [RCV004314482]	uncertain significance	5	141193010	141193010	Human		name
401724861	CV2714999	single nucleotide variant	NM_018930.4(PCDHB10):c.724T>C (p.Phe242Leu)	not specified [RCV004322315]	uncertain significance	5	141193276	141193276	Human		name
401766002	CV2717970	single nucleotide variant	NM_018932.4(PCDHB12):c.974G>A (p.Gly325Glu)	not specified [RCV004321919]	uncertain significance	5	141209881	141209881	Human		name
401763533	CV2720357	single nucleotide variant	NM_018932.4(PCDHB12):c.613C>T (p.Arg205Cys)	not specified [RCV004325670]	uncertain significance	5	141209520	141209520	Human		name
401779952	CV2725790	single nucleotide variant	NM_018930.4(PCDHB10):c.476A>T (p.Asp159Val)	not provided [RCV004696463]\|not specified [RCV004316266]	uncertain significance	5	141193028	141193028	Human		name
401879390	CV2758297	single nucleotide variant	NM_018932.4(PCDHB12):c.844T>C (p.Ser282Pro)	not specified [RCV004341651]	uncertain significance	5	141209751	141209751	Human		name
401889857	CV2763465	single nucleotide variant	NM_018935.4(PCDHB15):c.649G>A (p.Gly217Ser)	not specified [RCV004349349]	uncertain significance	5	141246227	141246227	Human		name
401854337	CV2766656	single nucleotide variant	NM_018931.3(PCDHB11):c.659C>T (p.Pro220Leu)	not specified [RCV004347265]	uncertain significance	5	141200433	141200433	Human		name
401862472	CV2775319	single nucleotide variant	NM_018933.4(PCDHB13):c.596A>C (p.Lys199Thr)	not specified [RCV004348431]	uncertain significance	5	141214719	141214719	Human		name
401897609	CV2776448	single nucleotide variant	NM_018933.4(PCDHB13):c.389A>G (p.His130Arg)	not specified [RCV004355564]	uncertain significance	5	141214512	141214512	Human		name
401899976	CV2780138	single nucleotide variant	NM_018931.3(PCDHB11):c.703A>G (p.Ile235Val)	not specified [RCV004355794]	likely benign	5	141200477	141200477	Human		name
401883128	CV2785545	single nucleotide variant	NM_018934.4(PCDHB14):c.784G>C (p.Ala262Pro)	not specified [RCV004363065]	uncertain significance	5	141224289	141224289	Human		name
401917923	CV2825313	single nucleotide variant	NM_020957.4(PCDHB16):c.641C>T (p.Ala214Val)	not provided [RCV003429831]	likely benign	5	141183200	141183200	Human		name
405742644	CV3367906	single nucleotide variant	NM_018932.4(PCDHB12):c.329T>A (p.Met110Lys)	not specified [RCV004497973]	uncertain significance	5	141209236	141209236	Human		name
405742650	CV3367907	single nucleotide variant	NM_018932.4(PCDHB12):c.548G>A (p.Arg183Lys)	not specified [RCV004497974]	uncertain significance	5	141209455	141209455	Human		name
405742657	CV3367908	single nucleotide variant	NM_018932.4(PCDHB12):c.583G>A (p.Val195Ile)	not specified [RCV004497975]	uncertain significance	5	141209490	141209490	Human		name
405742751	CV3367921	single nucleotide variant	NM_018933.4(PCDHB13):c.407A>G (p.Asp136Gly)	not specified [RCV004497988]	uncertain significance	5	141214530	141214530	Human		name
405742762	CV3367923	single nucleotide variant	NM_018933.4(PCDHB13):c.703G>A (p.Asp235Asn)	not specified [RCV004497990]	uncertain significance	5	141214826	141214826	Human		name
405742768	CV3367924	single nucleotide variant	NM_018933.4(PCDHB13):c.743A>G (p.Tyr248Cys)	not specified [RCV004497991]	uncertain significance	5	141214866	141214866	Human		name
405742775	CV3367925	single nucleotide variant	NM_018933.4(PCDHB13):c.807T>G (p.Asp269Glu)	not specified [RCV004497992]	uncertain significance	5	141214930	141214930	Human		name
405742939	CV3367950	single nucleotide variant	NM_018934.4(PCDHB14):c.508T>A (p.Tyr170Asn)	not specified [RCV004498017]	uncertain significance	5	141224013	141224013	Human		name
405744615	CV3367951	single nucleotide variant	NM_018934.4(PCDHB14):c.550G>C (p.Asp184His)	not specified [RCV004498018]	uncertain significance	5	141224055	141224055	Human		name
405744600	CV3367953	single nucleotide variant	NM_018934.4(PCDHB14):c.677C>T (p.Thr226Ile)	not specified [RCV004498020]	uncertain significance	5	141224182	141224182	Human		name
405744595	CV3367954	single nucleotide variant	NM_018934.4(PCDHB14):c.781A>T (p.Ile261Phe)	not specified [RCV004498021]	uncertain significance	5	141224286	141224286	Human		name
405744507	CV3367964	single nucleotide variant	NM_018935.4(PCDHB15):c.445G>A (p.Gly149Arg)	not specified [RCV004498031]	uncertain significance	5	141246023	141246023	Human		name
405744497	CV3367965	single nucleotide variant	NM_018935.4(PCDHB15):c.469G>A (p.Ala157Thr)	not specified [RCV004498032]	uncertain significance	5	141246047	141246047	Human		name
405744227	CV3367966	single nucleotide variant	NM_018935.4(PCDHB15):c.536A>G (p.His179Arg)	not specified [RCV004498033]	uncertain significance	5	141246114	141246114	Human		name
405744176	CV3367968	single nucleotide variant	NM_018935.4(PCDHB15):c.693G>C (p.Leu231Phe)	not specified [RCV004498035]	uncertain significance	5	141246271	141246271	Human		name
405743997	CV3367969	single nucleotide variant	NM_018935.4(PCDHB15):c.704C>G (p.Ala235Gly)	not specified [RCV004498036]	uncertain significance	5	141246282	141246282	Human		name
405743778	CV3367970	single nucleotide variant	NM_018935.4(PCDHB15):c.708T>A (p.Asn236Lys)	not specified [RCV004498037]	uncertain significance	5	141246286	141246286	Human		name
405743049	CV3367990	single nucleotide variant	NM_020957.4(PCDHB16):c.353A>T (p.Gln118Leu)	not specified [RCV004498057]	uncertain significance	5	141182912	141182912	Human		name
405743054	CV3367991	single nucleotide variant	NM_020957.4(PCDHB16):c.443T>C (p.Leu148Pro)	not specified [RCV004498058]	uncertain significance	5	141183002	141183002	Human		name
405744622	CV3367992	single nucleotide variant	NM_020957.4(PCDHB16):c.612G>C (p.Glu204Asp)	not specified [RCV004498059]	uncertain significance	5	141183171	141183171	Human		name
405743070	CV3367993	single nucleotide variant	NM_020957.4(PCDHB16):c.662C>A (p.Pro221Gln)	not specified [RCV004498060]	uncertain significance	5	141183221	141183221	Human		name
405743075	CV3367994	single nucleotide variant	NM_020957.4(PCDHB16):c.715G>A (p.Ala239Thr)	not specified [RCV004498061]	uncertain significance	5	141183274	141183274	Human		name
405743082	CV3367995	single nucleotide variant	NM_020957.4(PCDHB16):c.752T>C (p.Ile251Thr)	not specified [RCV004498062]	uncertain significance	5	141183311	141183311	Human		name
405742514	CV3371849	single nucleotide variant	NM_018930.4(PCDHB10):c.372G>T (p.Arg124Ser)	not specified [RCV004497922]	uncertain significance	5	141192924	141192924	Human		name
405742107	CV3371850	single nucleotide variant	NM_018930.4(PCDHB10):c.524A>G (p.Asn175Ser)	not specified [RCV004497923]	uncertain significance	5	141193076	141193076	Human		name
405742114	CV3371851	single nucleotide variant	NM_018930.4(PCDHB10):c.563G>C (p.Gly188Ala)	not specified [RCV004497924]	uncertain significance	5	141193115	141193115	Human		name
405742121	CV3371852	single nucleotide variant	NM_018930.4(PCDHB10):c.578A>T (p.Glu193Val)	not specified [RCV004497925]	uncertain significance	5	141193130	141193130	Human		name
405742127	CV3371853	single nucleotide variant	NM_018930.4(PCDHB10):c.701A>C (p.Asp234Ala)	not specified [RCV004497926]	uncertain significance	5	141193253	141193253	Human		name
405742135	CV3371854	single nucleotide variant	NM_018930.4(PCDHB10):c.805G>A (p.Val269Ile)	not specified [RCV004497927]	likely benign	5	141193357	141193357	Human		name
405742143	CV3371855	single nucleotide variant	NM_018930.4(PCDHB10):c.869C>G (p.Thr290Arg)	not specified [RCV004497928]	uncertain significance	5	141193421	141193421	Human		name
405742149	CV3371856	single nucleotide variant	NM_018930.4(PCDHB10):c.940T>A (p.Ser314Thr)	not specified [RCV004497929]	uncertain significance	5	141193492	141193492	Human		name
405742157	CV3371857	single nucleotide variant	NM_018930.4(PCDHB10):c.980T>C (p.Leu327Pro)	not specified [RCV004497930]	uncertain significance	5	141193532	141193532	Human		name
405742308	CV3371879	single nucleotide variant	NM_018931.3(PCDHB11):c.360G>C (p.Glu120Asp)	not specified [RCV004497952]	uncertain significance	5	141200134	141200134	Human		name
405742315	CV3371880	single nucleotide variant	NM_018931.3(PCDHB11):c.391C>T (p.Pro131Ser)	not specified [RCV004497953]	uncertain significance	5	141200165	141200165	Human		name
405742524	CV3371883	single nucleotide variant	NM_018931.3(PCDHB11):c.668C>T (p.Ser223Phe)	not specified [RCV004497956]	uncertain significance	5	141200442	141200442	Human		name
405742533	CV3371884	single nucleotide variant	NM_018931.3(PCDHB11):c.745G>A (p.Val249Met)	not specified [RCV004497957]	uncertain significance	5	141200519	141200519	Human		name
407523422	CV3463077	single nucleotide variant	NM_018930.4(PCDHB10):c.733G>A (p.Ala245Thr)	not specified [RCV004653158]	uncertain significance	5	141193285	141193285	Human		name
407523414	CV3463083	single nucleotide variant	NM_018930.4(PCDHB10):c.322A>T (p.Ile108Phe)	not specified [RCV004653161]	uncertain significance	5	141192874	141192874	Human		name
407523411	CV3463084	single nucleotide variant	NM_018930.4(PCDHB10):c.523A>G (p.Asn175Asp)	not specified [RCV004653162]	uncertain significance	5	141193075	141193075	Human		name
407523405	CV3463086	single nucleotide variant	NM_018930.4(PCDHB10):c.353G>C (p.Arg118Pro)	not specified [RCV004653164]	uncertain significance	5	141192905	141192905	Human		name
407480327	CV3463087	single nucleotide variant	NM_018930.4(PCDHB10):c.581T>G (p.Leu194Arg)	not specified [RCV004664385]	uncertain significance	5	141193133	141193133	Human		name
407480338	CV3463091	single nucleotide variant	NM_018931.3(PCDHB11):c.648T>G (p.Asp216Glu)	not specified [RCV004664387]	uncertain significance	5	141200422	141200422	Human		name
407480343	CV3463092	single nucleotide variant	NM_018931.3(PCDHB11):c.755G>T (p.Arg252Leu)	not specified [RCV004664388]	uncertain significance	5	141200529	141200529	Human		name
407523302	CV3463095	single nucleotide variant	NM_018931.3(PCDHB11):c.955A>G (p.Ile319Val)	not specified [RCV004653167]	uncertain significance	5	141200729	141200729	Human		name
407480361	CV3463097	single nucleotide variant	NM_018931.3(PCDHB11):c.340A>T (p.Thr114Ser)	not specified [RCV004664391]	uncertain significance	5	141200114	141200114	Human		name
407523269	CV3463123	single nucleotide variant	NM_018934.4(PCDHB14):c.889A>G (p.Ile297Val)	not specified [RCV004653180]	uncertain significance	5	141224394	141224394	Human		name
407523279	CV3463128	single nucleotide variant	NM_018934.4(PCDHB14):c.992G>A (p.Cys331Tyr)	not specified [RCV004653183]	uncertain significance	5	141224497	141224497	Human		name
407523284	CV3463130	single nucleotide variant	NM_018935.4(PCDHB15):c.443T>C (p.Leu148Pro)	not specified [RCV004653185]	likely benign	5	141246021	141246021	Human		name
407523290	CV3463132	single nucleotide variant	NM_018935.4(PCDHB15):c.322G>C (p.Val108Leu)	not specified [RCV004653187]	uncertain significance	5	141245900	141245900	Human		name
407523305	CV3463140	single nucleotide variant	NM_020957.4(PCDHB16):c.842T>A (p.Leu281His)	not specified [RCV004653192]	uncertain significance	5	141183401	141183401	Human		name
407480511	CV3463146	single nucleotide variant	NM_020957.4(PCDHB16):c.520C>G (p.Pro174Ala)	not specified [RCV004664414]	uncertain significance	5	141183079	141183079	Human		name
597736968	CV3575033	single nucleotide variant	NM_018932.4(PCDHB12):c.674C>T (p.Thr225Ile)	not specified [RCV004843816]	uncertain significance	5	141209581	141209581	Human		name
597736978	CV3575035	single nucleotide variant	NM_018932.4(PCDHB12):c.763A>G (p.Ser255Gly)	not specified [RCV004843818]	uncertain significance	5	141209670	141209670	Human		name
597736988	CV3575038	single nucleotide variant	NM_018932.4(PCDHB12):c.524A>G (p.Asn175Ser)	not specified [RCV004843820]	uncertain significance	5	141209431	141209431	Human		name
597736996	CV3575040	single nucleotide variant	NM_018932.4(PCDHB12):c.301C>A (p.Pro101Thr)	not specified [RCV004843822]	uncertain significance	5	141209208	141209208	Human		name
597737021	CV3575046	single nucleotide variant	NM_018932.4(PCDHB12):c.751A>G (p.Ile251Val)	not specified [RCV004843827]	uncertain significance	5	141209658	141209658	Human		name
597737035	CV3575049	single nucleotide variant	NM_018932.4(PCDHB12):c.509A>G (p.Tyr170Cys)	not specified [RCV004843830]	uncertain significance	5	141209416	141209416	Human		name
597737055	CV3575055	single nucleotide variant	NM_018933.4(PCDHB13):c.484G>C (p.Asp162His)	not specified [RCV004843834]	uncertain significance	5	141214607	141214607	Human		name
597756097	CV3575063	single nucleotide variant	NM_018933.4(PCDHB13):c.442C>T (p.Pro148Ser)	not specified [RCV004848075]	uncertain significance	5	141214565	141214565	Human		name
597737310	CV3575073	single nucleotide variant	NM_018934.4(PCDHB14):c.985G>A (p.Gly329Arg)	not specified [RCV004843848]	uncertain significance	5	141224490	141224490	Human		name
597737291	CV3575077	single nucleotide variant	NM_018934.4(PCDHB14):c.944A>G (p.Tyr315Cys)	not specified [RCV004843852]	uncertain significance	5	141224449	141224449	Human		name
597737278	CV3575081	single nucleotide variant	NM_018934.4(PCDHB14):c.754C>T (p.Pro252Ser)	not specified [RCV004843855]	uncertain significance	5	141224259	141224259	Human		name
597756118	CV3575082	single nucleotide variant	NM_018934.4(PCDHB14):c.695T>C (p.Val232Ala)	not specified [RCV004848080]	uncertain significance	5	141224200	141224200	Human		name
597737241	CV3575092	single nucleotide variant	NM_018935.4(PCDHB15):c.773G>C (p.Gly258Ala)	not specified [RCV004843862]	uncertain significance	5	141246351	141246351	Human		name
597737079	CV3575093	single nucleotide variant	NM_018935.4(PCDHB15):c.682A>T (p.Ile228Phe)	not specified [RCV004843863]	uncertain significance	5	141246260	141246260	Human		name
597756131	CV3575094	single nucleotide variant	NM_018935.4(PCDHB15):c.517T>C (p.Ser173Pro)	not specified [RCV004848083]	uncertain significance	5	141246095	141246095	Human		name
597737138	CV3575111	single nucleotide variant	NM_020957.4(PCDHB16):c.785C>T (p.Ala262Val)	not specified [RCV004843875]	likely benign	5	141183344	141183344	Human		name
597737153	CV3575114	single nucleotide variant	NM_020957.4(PCDHB16):c.905G>A (p.Arg302Gln)	not specified [RCV004843878]	uncertain significance	5	141183464	141183464	Human		name
597736808	CV3578890	single nucleotide variant	NM_018930.4(PCDHB10):c.553G>C (p.Gly185Arg)	not specified [RCV004843783]	uncertain significance	5	141193105	141193105	Human		name
597736826	CV3578895	single nucleotide variant	NM_018931.3(PCDHB11):c.559G>A (p.Asp187Asn)	not specified [RCV004843787]	uncertain significance	5	141200333	141200333	Human		name
597736836	CV3578897	single nucleotide variant	NM_018931.3(PCDHB11):c.428C>T (p.Pro143Leu)	not specified [RCV004843789]	uncertain significance	5	141200202	141200202	Human		name
597736875	CV3578907	single nucleotide variant	NM_018931.3(PCDHB11):c.626G>A (p.Ser209Asn)	not specified [RCV004843797]	uncertain significance	5	141200400	141200400	Human		name
597736885	CV3578910	single nucleotide variant	NM_018931.3(PCDHB11):c.610G>C (p.Glu204Gln)	not specified [RCV004843799]	uncertain significance	5	141200384	141200384	Human		name
597736895	CV3578912	single nucleotide variant	NM_018931.3(PCDHB11):c.893C>A (p.Ser298Tyr)	not specified [RCV004843801]	uncertain significance	5	141200667	141200667	Human		name
597736910	CV3578916	single nucleotide variant	NM_018931.3(PCDHB11):c.691G>A (p.Val231Met)	not specified [RCV004843804]	uncertain significance	5	141200465	141200465	Human		name
598269488	CV3996044	single nucleotide variant	NM_018930.4(PCDHB10):c.803A>G (p.Asp268Gly)	not specified [RCV005388794]	uncertain significance	5	141193355	141193355	Human		name
598269492	CV3996045	single nucleotide variant	NM_018930.4(PCDHB10):c.478C>A (p.Pro160Thr)	not specified [RCV005388795]	uncertain significance	5	141193030	141193030	Human		name
598269533	CV3996058	single nucleotide variant	NM_018931.3(PCDHB11):c.836A>G (p.Tyr279Cys)	not specified [RCV005388804]	uncertain significance	5	141200610	141200610	Human		name
598269544	CV3996062	single nucleotide variant	NM_018931.3(PCDHB11):c.545T>C (p.Met182Thr)	not specified [RCV005388807]	uncertain significance	5	141200319	141200319	Human		name
598269548	CV3996063	single nucleotide variant	NM_018931.3(PCDHB11):c.687G>T (p.Arg229Ser)	not specified [RCV005388808]	uncertain significance	5	141200461	141200461	Human		name
598195473	CV3996065	single nucleotide variant	NM_018931.3(PCDHB11):c.923A>G (p.Asp308Gly)	not specified [RCV005397540]	uncertain significance	5	141200697	141200697	Human		name
598269558	CV3996066	single nucleotide variant	NM_018931.3(PCDHB11):c.695T>C (p.Val232Ala)	not specified [RCV005388810]	uncertain significance	5	141200469	141200469	Human		name
598269563	CV3996067	single nucleotide variant	NM_018931.3(PCDHB11):c.366G>T (p.Gln122His)	not specified [RCV005388811]	uncertain significance	5	141200140	141200140	Human		name
598269585	CV3996073	single nucleotide variant	NM_018932.4(PCDHB12):c.888A>C (p.Gln296His)	not specified [RCV005388817]	uncertain significance	5	141209795	141209795	Human		name
598269615	CV3996080	single nucleotide variant	NM_018932.4(PCDHB12):c.574C>G (p.Pro192Ala)	not specified [RCV005388823]	uncertain significance	5	141209481	141209481	Human		name
598269639	CV3996085	single nucleotide variant	NM_018932.4(PCDHB12):c.822C>G (p.Asn274Lys)	not specified [RCV005388828]	uncertain significance	5	141209729	141209729	Human		name
598269642	CV3996086	single nucleotide variant	NM_018932.4(PCDHB12):c.939G>C (p.Glu313Asp)	not specified [RCV005388829]	uncertain significance	5	141209846	141209846	Human		name
598269647	CV3996087	single nucleotide variant	NM_018932.4(PCDHB12):c.715T>A (p.Ser239Thr)	not specified [RCV005388830]	uncertain significance	5	141209622	141209622	Human		name
598269672	CV3996093	single nucleotide variant	NM_018933.4(PCDHB13):c.446C>T (p.Pro149Leu)	not specified [RCV005388835]	uncertain significance	5	141214569	141214569	Human		name
598269677	CV3996094	single nucleotide variant	NM_018933.4(PCDHB13):c.626T>C (p.Leu209Pro)	not specified [RCV005388836]	uncertain significance	5	141214749	141214749	Human		name
598269682	CV3996095	single nucleotide variant	NM_018933.4(PCDHB13):c.691A>G (p.Ile231Val)	not specified [RCV005388837]	likely benign	5	141214814	141214814	Human		name
598269692	CV3996097	single nucleotide variant	NM_018933.4(PCDHB13):c.776G>C (p.Gly259Ala)	not specified [RCV005388839]	uncertain significance	5	141214899	141214899	Human		name
598269708	CV3996102	single nucleotide variant	NM_018933.4(PCDHB13):c.944C>G (p.Ser315Cys)	not specified [RCV005388843]	uncertain significance	5	141215067	141215067	Human		name
598269713	CV3996103	single nucleotide variant	NM_018933.4(PCDHB13):c.671C>G (p.Ser224Cys)	not specified [RCV005388844]	uncertain significance	5	141214794	141214794	Human		name
598269734	CV3996107	single nucleotide variant	NM_018934.4(PCDHB14):c.703A>G (p.Ile235Val)	not specified [RCV005388848]	uncertain significance	5	141224208	141224208	Human		name
598195506	CV3996121	single nucleotide variant	NM_018935.4(PCDHB15):c.715G>A (p.Ala239Thr)	not specified [RCV005397545]	uncertain significance	5	141246293	141246293	Human		name
598269803	CV3996123	single nucleotide variant	NM_018935.4(PCDHB15):c.365T>G (p.Leu122Arg)	not specified [RCV005388862]	uncertain significance	5	141245943	141245943	Human		name
598269849	CV3996135	single nucleotide variant	NM_020957.4(PCDHB16):c.950T>G (p.Val317Gly)	not specified [RCV005388871]	uncertain significance	5	141183509	141183509	Human		name
598269859	CV3996137	single nucleotide variant	NM_020957.4(PCDHB16):c.488G>T (p.Gly163Val)	not specified [RCV005388873]	uncertain significance	5	141183047	141183047	Human		name
598269863	CV3996138	single nucleotide variant	NM_020957.4(PCDHB16):c.814G>A (p.Gly272Arg)	not specified [RCV005388874]	uncertain significance	5	141183373	141183373	Human		name
598269873	CV3996140	single nucleotide variant	NM_020957.4(PCDHB16):c.315T>G (p.His105Gln)	not specified [RCV005388876]	uncertain significance	5	141182874	141182874	Human		name
598269878	CV3996141	single nucleotide variant	NM_020957.4(PCDHB16):c.529C>T (p.His177Tyr)	not specified [RCV005388877]	uncertain significance	5	141183088	141183088	Human		name
8625939	CV81078	single nucleotide variant	NM_018932.4(PCDHB12):c.971G>A (p.Gly324Glu)	not specified [RCV004277215]	uncertain significance\|not provided	5	141209878	141209878	Human		name
8625941	CV81080	single nucleotide variant	NM_018933.3(PCDHB13):c.385G>A (p.Asp129Asn)	Malignant melanoma [RCV000061158]	not provided	5	141214508	141214508	Human		name
8631446	CV86633	single nucleotide variant	NM_018932.3(PCDHB12):c.742G>A (p.Glu248Lys)	Malignant melanoma [RCV000066724]	not provided	5	141209649	141209649	Human		name
8631451	CV86638	single nucleotide variant	NM_018935.3(PCDHB15):c.603T>G (p.Asp201Glu)	Malignant melanoma [RCV000066729]	not provided	5	141246181	141246181	Human		name
156027659	CV2195537	single nucleotide variant	NM_018930.4(PCDHB10):c.1886T>C (p.Leu629Pro)	not specified [RCV004082752]	uncertain significance	5	141194438	141194438	Human		name
156144265	CV2200147	single nucleotide variant	NM_020957.4(PCDHB16):c.1214C>A (p.Thr405Lys)	not specified [RCV004069718]	uncertain significance	5	141183773	141183773	Human		name
156397439	CV2200501	single nucleotide variant	NM_018930.4(PCDHB10):c.1411G>A (p.Gly471Ser)	not specified [RCV004078856]	uncertain significance	5	141193963	141193963	Human		name
156373515	CV2201230	single nucleotide variant	NM_018934.4(PCDHB14):c.1420A>G (p.Ser474Gly)	not specified [RCV004077371]	uncertain significance	5	141224925	141224925	Human		name
156259777	CV2204760	single nucleotide variant	NM_018935.4(PCDHB15):c.1977A>C (p.Gln659His)	not specified [RCV004075020]	likely benign	5	141247555	141247555	Human		name
156399284	CV2205029	single nucleotide variant	NM_018931.3(PCDHB11):c.1431C>G (p.Asp477Glu)	not specified [RCV004077644]	uncertain significance	5	141201205	141201205	Human		name
156399448	CV2205124	single nucleotide variant	NM_018933.4(PCDHB13):c.2323C>A (p.Pro775Thr)	not specified [RCV004077722]	uncertain significance	5	141216446	141216446	Human		name
156376232	CV2210497	single nucleotide variant	NM_018931.3(PCDHB11):c.2015C>T (p.Pro672Leu)	not specified [RCV004089627]	uncertain significance	5	141201789	141201789	Human		name
155923864	CV2212455	single nucleotide variant	NM_018932.4(PCDHB12):c.1202A>G (p.Tyr401Cys)	not specified [RCV004091353]	uncertain significance	5	141210109	141210109	Human		name
155924006	CV2212529	single nucleotide variant	NM_018934.4(PCDHB14):c.1591G>C (p.Val531Leu)	not specified [RCV004091412]	uncertain significance	5	141225096	141225096	Human		name
156240339	CV2213605	single nucleotide variant	NM_018930.4(PCDHB10):c.1199T>C (p.Phe400Ser)	not specified [RCV004089691]	uncertain significance	5	141193751	141193751	Human		name
155977572	CV2214881	single nucleotide variant	NM_018933.4(PCDHB13):c.2135G>T (p.Arg712Leu)	not specified [RCV004084676]	uncertain significance	5	141216258	141216258	Human		name
155978108	CV2214968	single nucleotide variant	NM_018934.4(PCDHB14):c.1136G>A (p.Gly379Glu)	not specified [RCV004084746]	uncertain significance	5	141224641	141224641	Human		name
155979133	CV2215153	single nucleotide variant	NM_020957.4(PCDHB16):c.1993G>A (p.Gly665Ser)	not specified [RCV004086873]	uncertain significance	5	141184552	141184552	Human		name
156326997	CV2217186	single nucleotide variant	NM_018931.3(PCDHB11):c.1670A>G (p.Asn557Ser)	not specified [RCV004087642]	uncertain significance	5	141201444	141201444	Human		name
156331848	CV2218223	single nucleotide variant	NM_018933.4(PCDHB13):c.1977C>A (p.His659Gln)	not specified [RCV004088425]	uncertain significance	5	141216100	141216100	Human		name
156067398	CV2221821	single nucleotide variant	NM_018930.4(PCDHB10):c.1538T>G (p.Leu513Arg)	not specified [RCV004102850]	uncertain significance	5	141194090	141194090	Human		name
156386818	CV2225212	single nucleotide variant	NM_018931.3(PCDHB11):c.1825G>C (p.Ala609Pro)	not specified [RCV004095008]	uncertain significance	5	141201599	141201599	Human		name
156225403	CV2226184	single nucleotide variant	NM_018931.3(PCDHB11):c.1355C>T (p.Thr452Ile)	not specified [RCV004105584]	uncertain significance	5	141201129	141201129	Human		name
156226264	CV2226404	single nucleotide variant	NM_018930.4(PCDHB10):c.1522G>C (p.Ala508Pro)	not specified [RCV004099622]	uncertain significance	5	141194074	141194074	Human		name
156292062	CV2226405	single nucleotide variant	NM_018932.4(PCDHB12):c.1534C>T (p.His512Tyr)	not specified [RCV004099623]	uncertain significance	5	141210441	141210441	Human		name
156226282	CV2226406	single nucleotide variant	NM_018935.4(PCDHB15):c.1355C>T (p.Thr452Ile)	not specified [RCV004099624]	uncertain significance	5	141246933	141246933	Human		name
155941734	CV2229281	single nucleotide variant	NM_020957.4(PCDHB16):c.1955G>T (p.Arg652Leu)	not specified [RCV004101081]	likely benign	5	141184514	141184514	Human		name
156334572	CV2230940	single nucleotide variant	NM_018930.4(PCDHB10):c.1342G>A (p.Ala448Thr)	not specified [RCV004092404]	uncertain significance	5	141193894	141193894	Human		name
156243058	CV2231481	single nucleotide variant	NM_018931.3(PCDHB11):c.1583A>G (p.Asp528Gly)	not specified [RCV004096553]	uncertain significance	5	141201357	141201357	Human		name
156244479	CV2231606	single nucleotide variant	NM_018931.3(PCDHB11):c.1566G>T (p.Glu522Asp)	not specified [RCV004096648]	uncertain significance	5	141201340	141201340	Human		name
155983433	CV2233302	single nucleotide variant	NM_020957.4(PCDHB16):c.1171T>G (p.Phe391Val)	not specified [RCV004105683]	uncertain significance	5	141183730	141183730	Human		name
156292555	CV2233463	single nucleotide variant	NM_018934.4(PCDHB14):c.1439C>T (p.Ser480Leu)	not specified [RCV004106087]	uncertain significance	5	141224944	141224944	Human		name
156295351	CV2233725	single nucleotide variant	NM_018935.4(PCDHB15):c.1687T>G (p.Tyr563Asp)	not specified [RCV004100170]	uncertain significance	5	141247265	141247265	Human		name
155946508	CV2238130	single nucleotide variant	NM_018934.4(PCDHB14):c.1009G>A (p.Val337Ile)	not specified [RCV004111143]	uncertain significance	5	141224514	141224514	Human		name
156028929	CV2238271	single nucleotide variant	NM_018932.4(PCDHB12):c.1331T>C (p.Val444Ala)	not specified [RCV004113352]	uncertain significance	5	141210238	141210238	Human		name
156296017	CV2239870	single nucleotide variant	NM_018931.3(PCDHB11):c.2162C>G (p.Ser721Trp)	not specified [RCV004108380]	uncertain significance	5	141201936	141201936	Human		name
156064159	CV2240206	single nucleotide variant	NM_018931.3(PCDHB11):c.1588C>T (p.Arg530Cys)	not specified [RCV004112783]	uncertain significance	5	141201362	141201362	Human		name
156244866	CV2243235	single nucleotide variant	NM_018931.3(PCDHB11):c.2147G>A (p.Arg716Lys)	not specified [RCV004110123]	uncertain significance	5	141201921	141201921	Human		name
156082076	CV2244368	single nucleotide variant	NM_018931.3(PCDHB11):c.2204A>G (p.His735Arg)	not specified [RCV004100347]	uncertain significance	5	141201978	141201978	Human		name
156235100	CV2245404	single nucleotide variant	NM_018932.4(PCDHB12):c.1801T>C (p.Trp601Arg)	not specified [RCV004109193]	uncertain significance	5	141210708	141210708	Human		name
155976920	CV2246126	single nucleotide variant	NM_018930.4(PCDHB10):c.1921G>C (p.Val641Leu)	not specified [RCV004114027]	likely benign	5	141194473	141194473	Human		name
156241565	CV2246127	single nucleotide variant	NM_018932.4(PCDHB12):c.1431C>A (p.Asp477Glu)	not specified [RCV004114028]	uncertain significance	5	141210338	141210338	Human		name
156163217	CV2246614	single nucleotide variant	NM_018934.4(PCDHB14):c.1787C>T (p.Ser596Leu)	not specified [RCV004110357]	uncertain significance	5	141225292	141225292	Human		name
156283639	CV2249778	single nucleotide variant	NM_018933.4(PCDHB13):c.1474C>A (p.Pro492Thr)	not specified [RCV004122544]	uncertain significance	5	141215597	141215597	Human		name
155993278	CV2252220	single nucleotide variant	NM_018935.4(PCDHB15):c.2293A>C (p.Lys765Gln)	not specified [RCV004122226]	uncertain significance	5	141247871	141247871	Human		name
155993582	CV2253600	single nucleotide variant	NM_020957.4(PCDHB16):c.1610G>C (p.Gly537Ala)	not specified [RCV004125287]	uncertain significance	5	141184169	141184169	Human		name
155993595	CV2253601	single nucleotide variant	NM_020957.4(PCDHB16):c.1615C>T (p.Pro539Ser)	not specified [RCV004125288]	uncertain significance	5	141184174	141184174	Human		name
155989090	CV2259654	single nucleotide variant	NM_018935.4(PCDHB15):c.1304A>T (p.Gln435Leu)	not specified [RCV004116690]	uncertain significance	5	141246882	141246882	Human		name
156242999	CV2262208	single nucleotide variant	NM_018935.4(PCDHB15):c.1651G>T (p.Val551Leu)	not specified [RCV004126636]	uncertain significance	5	141247229	141247229	Human		name
156334396	CV2263265	single nucleotide variant	NM_018934.4(PCDHB14):c.1708G>A (p.Ala570Thr)	not specified [RCV004133554]	uncertain significance	5	141225213	141225213	Human		name
156044326	CV2268516	single nucleotide variant	NM_018934.4(PCDHB14):c.1529A>G (p.Asn510Ser)	not specified [RCV004130201]	uncertain significance	5	141225034	141225034	Human		name
156065186	CV2272483	single nucleotide variant	NM_018932.4(PCDHB12):c.2138T>A (p.Leu713Gln)	not specified [RCV004133397]	uncertain significance	5	141211045	141211045	Human		name
155984938	CV2274776	single nucleotide variant	NM_018931.3(PCDHB11):c.1222C>T (p.Pro408Ser)	not specified [RCV004139127]	uncertain significance	5	141200996	141200996	Human		name
155900834	CV2275271	single nucleotide variant	NM_020957.4(PCDHB16):c.1516A>G (p.Ile506Val)	not specified [RCV004137050]	uncertain significance	5	141184075	141184075	Human		name
156121004	CV2275973	single nucleotide variant	NM_018935.4(PCDHB15):c.1573C>A (p.Gln525Lys)	not specified [RCV004139614]	uncertain significance	5	141247151	141247151	Human		name
156121763	CV2276041	single nucleotide variant	NM_018931.3(PCDHB11):c.1478C>T (p.Pro493Leu)	not specified [RCV004141717]	uncertain significance	5	141201252	141201252	Human		name
155967048	CV2280233	single nucleotide variant	NM_020957.4(PCDHB16):c.1384G>C (p.Glu462Gln)	not specified [RCV004140451]	uncertain significance	5	141183943	141183943	Human		name
156001746	CV2284515	single nucleotide variant	NM_018930.4(PCDHB10):c.1964C>G (p.Thr655Ser)	not specified [RCV004140693]	likely benign	5	141194516	141194516	Human		name
156066291	CV2284517	single nucleotide variant	NM_018931.3(PCDHB11):c.1702G>C (p.Gly568Arg)	not specified [RCV004140695]	uncertain significance	5	141201476	141201476	Human		name
156279785	CV2285114	single nucleotide variant	NM_018931.3(PCDHB11):c.2215G>A (p.Val739Met)	not specified [RCV004145340]	likely benign	5	141201989	141201989	Human		name
155993975	CV2286355	single nucleotide variant	NM_018935.4(PCDHB15):c.1217A>T (p.Glu406Val)	not specified [RCV004139886]	uncertain significance	5	141246795	141246795	Human		name
155965324	CV2286915	single nucleotide variant	NM_018930.4(PCDHB10):c.1189G>C (p.Val397Leu)	not specified [RCV004144524]	uncertain significance	5	141193741	141193741	Human		name
156007684	CV2288332	single nucleotide variant	NM_018930.4(PCDHB10):c.1168C>T (p.Pro390Ser)	not specified [RCV004150102]	uncertain significance	5	141193720	141193720	Human		name
156150328	CV2289650	single nucleotide variant	NM_018934.4(PCDHB14):c.1730C>T (p.Pro577Leu)	not specified [RCV004148563]	uncertain significance	5	141225235	141225235	Human		name
156004823	CV2290238	single nucleotide variant	NM_018932.4(PCDHB12):c.2006C>A (p.Pro669His)	not specified [RCV004152888]	uncertain significance	5	141210913	141210913	Human		name
156285055	CV2291954	single nucleotide variant	NM_018935.4(PCDHB15):c.1634C>T (p.Ala545Val)	not specified [RCV004158465]	uncertain significance	5	141247212	141247212	Human		name
156280077	CV2293939	single nucleotide variant	NM_018930.4(PCDHB10):c.1955G>T (p.Arg652Leu)	not specified [RCV004155482]	likely benign	5	141194507	141194507	Human		name
156185869	CV2294982	single nucleotide variant	NM_018932.4(PCDHB12):c.1222C>A (p.Pro408Thr)	not specified [RCV004156125]	likely benign	5	141210129	141210129	Human		name
156185890	CV2294983	single nucleotide variant	NM_018935.4(PCDHB15):c.1396C>T (p.Pro466Ser)	not specified [RCV004156126]	uncertain significance	5	141246974	141246974	Human		name
156177706	CV2298236	single nucleotide variant	NM_018934.4(PCDHB14):c.2162C>T (p.Ser721Leu)	not specified [RCV004160159]	uncertain significance	5	141225667	141225667	Human		name
155943396	CV2298550	single nucleotide variant	NM_018930.4(PCDHB10):c.2224A>G (p.Arg742Gly)	not specified [RCV004162204]	uncertain significance	5	141194776	141194776	Human		name
156080358	CV2300996	single nucleotide variant	NM_018933.4(PCDHB13):c.1630G>A (p.Glu544Lys)	not specified [RCV004158162]	uncertain significance	5	141215753	141215753	Human		name
155907872	CV2302307	single nucleotide variant	NM_020957.4(PCDHB16):c.2174G>A (p.Cys725Tyr)	not specified [RCV004161068]	uncertain significance	5	141184733	141184733	Human		name
156100011	CV2306584	single nucleotide variant	NM_018934.4(PCDHB14):c.1528A>T (p.Asn510Tyr)	not specified [RCV004157188]	uncertain significance	5	141225033	141225033	Human		name
156300173	CV2306925	single nucleotide variant	NM_018933.4(PCDHB13):c.1717A>C (p.Thr573Pro)	not specified [RCV004157446]	uncertain significance	5	141215840	141215840	Human		name
155965660	CV2308533	single nucleotide variant	NM_018932.4(PCDHB12):c.1591G>A (p.Val531Met)	not specified [RCV004166810]	uncertain significance	5	141210498	141210498	Human		name
156054336	CV2308660	single nucleotide variant	NM_018930.4(PCDHB10):c.1045G>T (p.Val349Leu)	not specified [RCV004167210]	uncertain significance	5	141193597	141193597	Human		name
156298043	CV2310580	single nucleotide variant	NM_020957.4(PCDHB16):c.1088T>C (p.Ile363Thr)	not specified [RCV004163597]	likely benign	5	141183647	141183647	Human		name
156348307	CV2312714	single nucleotide variant	NM_018933.4(PCDHB13):c.1556T>C (p.Leu519Pro)	not specified [RCV004169439]	uncertain significance	5	141215679	141215679	Human		name
155974594	CV2317996	single nucleotide variant	NM_018934.4(PCDHB14):c.2174G>T (p.Cys725Phe)	not specified [RCV004177112]	uncertain significance	5	141225679	141225679	Human		name
156165839	CV2319897	single nucleotide variant	NM_018935.4(PCDHB15):c.2159C>A (p.Ala720Asp)	not specified [RCV004167777]	uncertain significance	5	141247737	141247737	Human		name
156396463	CV2326286	single nucleotide variant	NM_018932.4(PCDHB12):c.1307A>G (p.Asn436Ser)	not specified [RCV004180532]	uncertain significance	5	141210214	141210214	Human		name
156289002	CV2327461	single nucleotide variant	NM_018931.3(PCDHB11):c.2134C>T (p.Arg712Trp)	not specified [RCV004174875]	uncertain significance	5	141201908	141201908	Human		name
156289406	CV2327500	single nucleotide variant	NM_018932.4(PCDHB12):c.1622T>C (p.Leu541Ser)	not specified [RCV004176812]	uncertain significance	5	141210529	141210529	Human		name
156180494	CV2327742	single nucleotide variant	NM_018933.4(PCDHB13):c.1723C>A (p.Leu575Met)	not specified [RCV004179094]	uncertain significance	5	141215846	141215846	Human		name
156155406	CV2328766	single nucleotide variant	NM_020957.4(PCDHB16):c.1528A>T (p.Asn510Tyr)	not specified [RCV004177992]	uncertain significance	5	141184087	141184087	Human		name
156396680	CV2330209	single nucleotide variant	NM_018931.3(PCDHB11):c.2212G>T (p.Asp738Tyr)	not specified [RCV004187670]	uncertain significance	5	141201986	141201986	Human		name
155918782	CV2333069	single nucleotide variant	NM_018932.4(PCDHB12):c.2144G>A (p.Arg715Lys)	not specified [RCV004194364]	uncertain significance	5	141211051	141211051	Human		name
155918868	CV2333085	single nucleotide variant	NM_018933.4(PCDHB13):c.1028A>G (p.Asp343Gly)	not specified [RCV004194380]	uncertain significance	5	141215151	141215151	Human		name
156173790	CV2333744	single nucleotide variant	NM_018930.4(PCDHB10):c.1928T>C (p.Leu643Pro)	not specified [RCV004181255]	uncertain significance	5	141194480	141194480	Human		name
156272002	CV2333888	single nucleotide variant	NM_018930.4(PCDHB10):c.1022A>G (p.Asn341Ser)	not specified [RCV004181383]	uncertain significance	5	141193574	141193574	Human		name
156272657	CV2333946	single nucleotide variant	NM_018934.4(PCDHB14):c.1780G>A (p.Gly594Ser)	not specified [RCV004183478]	uncertain significance	5	141225285	141225285	Human		name
156201989	CV2334615	single nucleotide variant	NM_018930.4(PCDHB10):c.1576G>T (p.Ala526Ser)	not specified [RCV004188602]	uncertain significance	5	141194128	141194128	Human		name
156325655	CV2335340	single nucleotide variant	NM_018930.4(PCDHB10):c.2149A>G (p.Arg717Gly)	not specified [RCV004186900]	uncertain significance	5	141194701	141194701	Human		name
155916221	CV2336107	single nucleotide variant	NM_018933.4(PCDHB13):c.1914C>G (p.His638Gln)	not specified [RCV004189702]	uncertain significance	5	141216037	141216037	Human		name
156292929	CV2336345	single nucleotide variant	NM_018932.4(PCDHB12):c.1148G>T (p.Cys383Phe)	not specified [RCV004194568]	uncertain significance	5	141210055	141210055	Human		name
156088097	CV2337108	single nucleotide variant	NM_018935.4(PCDHB15):c.1348G>T (p.Ala450Ser)	not specified [RCV004192870]	uncertain significance	5	141246926	141246926	Human		name
155914847	CV2339008	single nucleotide variant	NM_018931.3(PCDHB11):c.1208T>C (p.Leu403Ser)	not specified [RCV004187063]	uncertain significance	5	141200982	141200982	Human		name
155968743	CV2339345	single nucleotide variant	NM_018935.4(PCDHB15):c.2327G>A (p.Ser776Asn)	not specified [RCV004191575]	uncertain significance	5	141247905	141247905	Human		name
155902076	CV2345924	single nucleotide variant	NM_018933.4(PCDHB13):c.1081G>A (p.Ala361Thr)	not specified [RCV004198962]	uncertain significance	5	141215204	141215204	Human		name
156235989	CV2346405	single nucleotide variant	NM_018930.4(PCDHB10):c.1329C>G (p.Asp443Glu)	not specified [RCV004203883]	uncertain significance	5	141193881	141193881	Human		name
155923337	CV2347486	single nucleotide variant	NM_018932.4(PCDHB12):c.1522G>A (p.Ala508Thr)	not specified [RCV004200435]	uncertain significance	5	141210429	141210429	Human		name
155905270	CV2349724	single nucleotide variant	NM_020957.4(PCDHB16):c.1607G>C (p.Arg536Pro)	not specified [RCV004204138]	uncertain significance	5	141184166	141184166	Human		name
156275000	CV2351781	single nucleotide variant	NM_018932.4(PCDHB12):c.2035G>A (p.Ala679Thr)	not specified [RCV004197938]	uncertain significance	5	141210942	141210942	Human		name
156224950	CV2352621	single nucleotide variant	NM_018931.3(PCDHB11):c.1936G>A (p.Asp646Asn)	not specified [RCV004198654]	uncertain significance	5	141201710	141201710	Human		name
156122405	CV2354327	single nucleotide variant	NM_018934.4(PCDHB14):c.2189G>T (p.Gly730Val)	not specified [RCV004206744]	uncertain significance	5	141225694	141225694	Human		name
156109796	CV2355524	single nucleotide variant	NM_018931.3(PCDHB11):c.1705T>C (p.Ser569Pro)	not specified [RCV004205373]	uncertain significance	5	141201479	141201479	Human		name
156177899	CV2355887	single nucleotide variant	NM_018935.4(PCDHB15):c.2189G>A (p.Gly730Asp)	not specified [RCV004201275]	uncertain significance	5	141247767	141247767	Human		name
155930716	CV2361233	single nucleotide variant	NM_018934.4(PCDHB14):c.1745C>T (p.Pro582Leu)	not specified [RCV004216409]	uncertain significance	5	141225250	141225250	Human		name
156009223	CV2361975	single nucleotide variant	NM_020957.4(PCDHB16):c.2194T>C (p.Phe732Leu)	not specified [RCV004207741]	uncertain significance	5	141184753	141184753	Human		name
155925764	CV2365641	single nucleotide variant	NM_018935.4(PCDHB15):c.1819C>T (p.Leu607Phe)	not specified [RCV004214201]	uncertain significance	5	141247397	141247397	Human		name
155927402	CV2365920	single nucleotide variant	NM_018934.4(PCDHB14):c.1526A>G (p.Asp509Gly)	not specified [RCV004207535]	uncertain significance	5	141225031	141225031	Human		name
156101914	CV2367716	single nucleotide variant	NM_018933.4(PCDHB13):c.1868A>T (p.Glu623Val)	not specified [RCV004213678]	uncertain significance	5	141215991	141215991	Human		name
156287719	CV2370553	single nucleotide variant	NM_020957.4(PCDHB16):c.1146T>G (p.Ile382Met)	not specified [RCV004215886]	uncertain significance	5	141183705	141183705	Human		name
155931769	CV2371011	single nucleotide variant	NM_018933.4(PCDHB13):c.1954C>T (p.Arg652Cys)	not specified [RCV004220778]	uncertain significance	5	141216077	141216077	Human		name
156385087	CV2371693	single nucleotide variant	NM_018935.4(PCDHB15):c.1648C>G (p.Leu550Val)	not specified [RCV004218977]	uncertain significance	5	141247226	141247226	Human		name
156076491	CV2375040	single nucleotide variant	NM_018934.4(PCDHB14):c.1979T>C (p.Val660Ala)	not specified [RCV004230091]	uncertain significance	5	141225484	141225484	Human		name
156185988	CV2377907	single nucleotide variant	NM_018933.4(PCDHB13):c.1947G>T (p.Glu649Asp)	not specified [RCV004230475]	uncertain significance	5	141216070	141216070	Human		name
156095240	CV2377908	single nucleotide variant	NM_018933.4(PCDHB13):c.2033C>T (p.Pro678Leu)	not specified [RCV004230476]	uncertain significance	5	141216156	141216156	Human		name
156346378	CV2378007	single nucleotide variant	NM_018930.4(PCDHB10):c.1645G>A (p.Val549Met)	not specified [RCV004232574]	uncertain significance	5	141194197	141194197	Human		name
156392299	CV2378495	single nucleotide variant	NM_018932.4(PCDHB12):c.1410C>G (p.Ile470Met)	not specified [RCV004228549]	uncertain significance	5	141210317	141210317	Human		name
155954038	CV2379126	single nucleotide variant	NM_018935.4(PCDHB15):c.1342G>T (p.Ala448Ser)	not specified [RCV004235923]	uncertain significance	5	141246920	141246920	Human		name
156070740	CV2381339	single nucleotide variant	NM_020957.4(PCDHB16):c.1584G>C (p.Glu528Asp)	not specified [RCV004227397]	uncertain significance	5	141184143	141184143	Human		name
155903113	CV2386433	single nucleotide variant	NM_018933.4(PCDHB13):c.1594G>A (p.Gly532Ser)	not specified [RCV004228758]	uncertain significance	5	141215717	141215717	Human		name
156091247	CV2389430	single nucleotide variant	NM_018931.3(PCDHB11):c.1264A>G (p.Thr422Ala)	not specified [RCV004238156]	uncertain significance	5	141201038	141201038	Human		name
156100305	CV2392934	single nucleotide variant	NM_020957.4(PCDHB16):c.1399G>A (p.Ala467Thr)	not specified [RCV004247280]	uncertain significance	5	141183958	141183958	Human		name
156149514	CV2394584	single nucleotide variant	NM_018933.4(PCDHB13):c.1460C>T (p.Thr487Ile)	not specified [RCV004240933]	uncertain significance	5	141215583	141215583	Human		name
155958688	CV2395235	single nucleotide variant	NM_018930.4(PCDHB10):c.1651G>A (p.Val551Met)	not specified [RCV004236897]	uncertain significance	5	141194203	141194203	Human		name
156259052	CV2395441	single nucleotide variant	NM_020957.4(PCDHB16):c.2050A>C (p.Asn684His)	not specified [RCV004241312]	uncertain significance	5	141184609	141184609	Human		name
156260322	CV2395541	single nucleotide variant	NM_018935.4(PCDHB15):c.2009A>T (p.Tyr670Phe)	not specified [RCV004241399]	uncertain significance	5	141247587	141247587	Human		name
156254239	CV2397530	single nucleotide variant	NM_018934.4(PCDHB14):c.2278G>A (p.Gly760Arg)	not specified [RCV004236996]	uncertain significance	5	141225783	141225783	Human		name
156255421	CV2397648	single nucleotide variant	NM_018930.4(PCDHB10):c.2260G>A (p.Glu754Lys)	not specified [RCV004237096]	uncertain significance	5	141194812	141194812	Human		name
156224025	CV2399311	single nucleotide variant	NM_018934.4(PCDHB14):c.1477C>T (p.Pro493Ser)	not specified [RCV004242602]	likely benign	5	141224982	141224982	Human		name
156222048	CV2399657	single nucleotide variant	NM_018930.4(PCDHB10):c.1601C>T (p.Thr534Ile)	not specified [RCV004245477]	uncertain significance	5	141194153	141194153	Human		name
156222668	CV2399802	single nucleotide variant	NM_018930.4(PCDHB10):c.1660G>A (p.Ala554Thr)	not specified [RCV004245607]	uncertain significance	5	141194212	141194212	Human		name
329356393	CV2430728	single nucleotide variant	NM_018932.4(PCDHB12):c.1985T>C (p.Leu662Pro)	not specified [RCV004253911]	uncertain significance	5	141210892	141210892	Human		name
329385068	CV2435250	single nucleotide variant	NM_018935.4(PCDHB15):c.1531G>C (p.Gly511Arg)	not specified [RCV004252885]	uncertain significance	5	141247109	141247109	Human		name
329376845	CV2435717	single nucleotide variant	NM_018933.4(PCDHB13):c.1531G>A (p.Gly511Ser)	not specified [RCV004253349]	uncertain significance	5	141215654	141215654	Human		name
329399281	CV2436548	single nucleotide variant	NM_018931.3(PCDHB11):c.1139G>T (p.Arg380Ile)	not specified [RCV004253706]	uncertain significance	5	141200913	141200913	Human		name
329353931	CV2436663	single nucleotide variant	NM_018931.3(PCDHB11):c.1378G>A (p.Val460Ile)	not specified [RCV004258035]	uncertain significance	5	141201152	141201152	Human		name
329353932	CV2436664	single nucleotide variant	NM_018935.4(PCDHB15):c.1118G>C (p.Arg373Pro)	not specified [RCV004258036]	uncertain significance	5	141246696	141246696	Human		name
329400747	CV2438735	single nucleotide variant	NM_020957.4(PCDHB16):c.1894G>A (p.Glu632Lys)	not specified [RCV004261884]	uncertain significance	5	141184453	141184453	Human		name
329360713	CV2439631	single nucleotide variant	NM_018932.4(PCDHB12):c.1775T>C (p.Val592Ala)	not specified [RCV004255648]	uncertain significance	5	141210682	141210682	Human		name
329353706	CV2443583	single nucleotide variant	NM_018931.3(PCDHB11):c.2327C>A (p.Ala776Glu)	not specified [RCV004262407]	uncertain significance	5	141202101	141202101	Human		name
329374686	CV2444021	single nucleotide variant	NM_018935.4(PCDHB15):c.1584G>C (p.Glu528Asp)	not specified [RCV004258342]	uncertain significance	5	141247162	141247162	Human		name
329400011	CV2444312	single nucleotide variant	NM_018930.4(PCDHB10):c.2237C>A (p.Thr746Asn)	not specified [RCV004263072]	uncertain significance	5	141194789	141194789	Human		name
329391718	CV2444968	single nucleotide variant	NM_020957.4(PCDHB16):c.1483G>A (p.Asp495Asn)	not specified [RCV004261590]	uncertain significance	5	141184042	141184042	Human		name
329357768	CV2453779	single nucleotide variant	NM_018930.4(PCDHB10):c.1475C>T (p.Pro492Leu)	not specified [RCV004269400]	uncertain significance	5	141194027	141194027	Human		name
329384849	CV2454445	single nucleotide variant	NM_018934.4(PCDHB14):c.2033C>A (p.Pro678Gln)	not specified [RCV004267948]	uncertain significance	5	141225538	141225538	Human		name
329390935	CV2455619	single nucleotide variant	NM_018933.4(PCDHB13):c.1423G>T (p.Ala475Ser)	not specified [RCV004276866]	uncertain significance	5	141215546	141215546	Human		name
329379856	CV2456513	single nucleotide variant	NM_018934.4(PCDHB14):c.1052C>T (p.Ser351Leu)	not specified [RCV004275654]	uncertain significance	5	141224557	141224557	Human		name
329394812	CV2457650	single nucleotide variant	NM_018931.3(PCDHB11):c.2276C>T (p.Ser759Phe)	not specified [RCV004269503]	uncertain significance	5	141202050	141202050	Human		name
329395212	CV2458212	single nucleotide variant	NM_018930.4(PCDHB10):c.1298C>G (p.Thr433Ser)	not specified [RCV004265875]	uncertain significance	5	141193850	141193850	Human		name
329356548	CV2460401	single nucleotide variant	NM_018933.4(PCDHB13):c.2243G>T (p.Ser748Ile)	not specified [RCV004268713]	uncertain significance	5	141216366	141216366	Human		name
329394476	CV2461370	single nucleotide variant	NM_018930.4(PCDHB10):c.1885C>A (p.Leu629Met)	not specified [RCV004267530]	uncertain significance	5	141194437	141194437	Human		name
329360689	CV2462873	single nucleotide variant	NM_018933.4(PCDHB13):c.1280G>A (p.Gly427Glu)	not specified [RCV004272721]	uncertain significance	5	141215403	141215403	Human		name
329374239	CV2463459	single nucleotide variant	NM_018931.3(PCDHB11):c.1329C>A (p.Asp443Glu)	not specified [RCV004277290]	uncertain significance	5	141201103	141201103	Human		name
329382539	CV2465251	single nucleotide variant	NM_018931.3(PCDHB11):c.1318T>G (p.Leu440Val)	not specified [RCV004281053]	uncertain significance	5	141201092	141201092	Human		name
329376281	CV2465455	single nucleotide variant	NM_018934.4(PCDHB14):c.1897C>A (p.Arg633Ser)	not specified [RCV004281225]	uncertain significance	5	141225402	141225402	Human		name
329392030	CV2470310	single nucleotide variant	NM_018932.4(PCDHB12):c.2285A>G (p.Asn762Ser)	not specified [RCV004279704]	likely benign	5	141211192	141211192	Human		name
329398532	CV2471592	single nucleotide variant	NM_018930.4(PCDHB10):c.1916G>A (p.Arg639Lys)	not specified [RCV004286890]	uncertain significance	5	141194468	141194468	Human		name
401755897	CV2675576	single nucleotide variant	NM_020957.4(PCDHB16):c.1062C>A (p.Ser354Arg)	not specified [RCV004295189]	uncertain significance	5	141183621	141183621	Human		name
401738450	CV2676289	single nucleotide variant	NM_018934.4(PCDHB14):c.1591G>A (p.Val531Met)	not specified [RCV004286327]	uncertain significance	5	141225096	141225096	Human		name
401779546	CV2676607	single nucleotide variant	NM_018935.4(PCDHB15):c.1846G>C (p.Gly616Arg)	not specified [RCV004288790]	uncertain significance	5	141247424	141247424	Human		name
401747031	CV2678990	single nucleotide variant	NM_018931.3(PCDHB11):c.1346C>G (p.Pro449Arg)	not specified [RCV004295002]	uncertain significance	5	141201120	141201120	Human		name
401722275	CV2680880	single nucleotide variant	NM_018934.4(PCDHB14):c.2348T>C (p.Met783Thr)	not specified [RCV004293524]	uncertain significance	5	141225853	141225853	Human		name
401781213	CV2681930	single nucleotide variant	NM_018931.3(PCDHB11):c.1680C>G (p.Phe560Leu)	not specified [RCV004296918]	uncertain significance	5	141201454	141201454	Human		name
401723794	CV2684869	single nucleotide variant	NM_018933.4(PCDHB13):c.1327G>T (p.Asp443Tyr)	not specified [RCV004296375]	uncertain significance	5	141215450	141215450	Human		name
401770548	CV2685763	single nucleotide variant	NM_018932.4(PCDHB12):c.1913A>G (p.His638Arg)	not specified [RCV004294754]	uncertain significance	5	141210820	141210820	Human		name
401728250	CV2685969	single nucleotide variant	NM_018933.4(PCDHB13):c.1012G>C (p.Val338Leu)	not specified [RCV004296987]	uncertain significance	5	141215135	141215135	Human		name
401749322	CV2693077	single nucleotide variant	NM_018930.4(PCDHB10):c.1711C>T (p.Pro571Ser)	not specified [RCV004308619]	uncertain significance	5	141194263	141194263	Human		name
401745547	CV2693278	single nucleotide variant	NM_018935.4(PCDHB15):c.1411G>C (p.Gly471Arg)	not specified [RCV004295246]	uncertain significance	5	141246989	141246989	Human		name
401737510	CV2695820	single nucleotide variant	NM_018931.3(PCDHB11):c.1069C>T (p.Pro357Ser)	not specified [RCV004308104]	uncertain significance	5	141200843	141200843	Human		name
401750305	CV2696011	single nucleotide variant	NM_018930.4(PCDHB10):c.1690C>T (p.Pro564Ser)	not specified [RCV004308269]	uncertain significance	5	141194242	141194242	Human		name
401759244	CV2701454	single nucleotide variant	NM_018931.3(PCDHB11):c.1829C>T (p.Thr610Met)	not specified [RCV004312126]	uncertain significance	5	141201603	141201603	Human		name
401776617	CV2703294	single nucleotide variant	NM_018935.4(PCDHB15):c.1537C>A (p.Leu513Met)	not specified [RCV004315651]	uncertain significance	5	141247115	141247115	Human		name
401749280	CV2704575	single nucleotide variant	NM_018933.4(PCDHB13):c.1753C>G (p.Leu585Val)	not specified [RCV004313618]	uncertain significance	5	141215876	141215876	Human		name
401750037	CV2704912	single nucleotide variant	NM_018933.4(PCDHB13):c.1884G>T (p.Arg628Ser)	not specified [RCV004307484]	uncertain significance	5	141216007	141216007	Human		name
401734412	CV2709492	single nucleotide variant	NM_018933.4(PCDHB13):c.1147A>T (p.Ser383Cys)	not specified [RCV004318734]	uncertain significance	5	141215270	141215270	Human		name
401759595	CV2712583	single nucleotide variant	NM_020957.4(PCDHB16):c.1431C>G (p.Asp477Glu)	not specified [RCV004307914]	uncertain significance	5	141183990	141183990	Human		name
401774613	CV2713571	single nucleotide variant	NM_018930.4(PCDHB10):c.1520A>G (p.Asn507Ser)	not specified [RCV004320950]	uncertain significance	5	141194072	141194072	Human		name
401750150	CV2715523	single nucleotide variant	NM_020957.4(PCDHB16):c.1849G>T (p.Val617Leu)	not specified [RCV004326924]	uncertain significance	5	141184408	141184408	Human		name
401751122	CV2715872	single nucleotide variant	NM_018934.4(PCDHB14):c.1426A>G (p.Thr476Ala)	not specified [RCV004328986]	uncertain significance	5	141224931	141224931	Human		name
401751129	CV2715874	single nucleotide variant	NM_020957.4(PCDHB16):c.1277T>C (p.Met426Thr)	not specified [RCV004328988]	uncertain significance	5	141183836	141183836	Human		name
401777217	CV2721651	single nucleotide variant	NM_018935.4(PCDHB15):c.1411G>A (p.Gly471Ser)	not specified [RCV004316144]	uncertain significance	5	141246989	141246989	Human		name
401764035	CV2725409	single nucleotide variant	NM_018934.4(PCDHB14):c.2032C>T (p.Pro678Ser)	not specified [RCV004320048]	uncertain significance	5	141225537	141225537	Human		name
401770947	CV2726311	single nucleotide variant	NM_018930.4(PCDHB10):c.2257T>C (p.Tyr753His)	not specified [RCV004326753]	uncertain significance	5	141194809	141194809	Human		name
401771195	CV2726395	single nucleotide variant	NM_018931.3(PCDHB11):c.1893C>A (p.Ser631Arg)	not specified [RCV004328610]	uncertain significance	5	141201667	141201667	Human		name
401761580	CV2726822	single nucleotide variant	NM_020957.4(PCDHB16):c.1086G>T (p.Glu362Asp)	not specified [RCV004323129]	uncertain significance	5	141183645	141183645	Human		name
401780573	CV2727452	single nucleotide variant	NM_018931.3(PCDHB11):c.1664A>G (p.Asn555Ser)	not specified [RCV004329658]	uncertain significance	5	141201438	141201438	Human		name
401778763	CV2735491	single nucleotide variant	NM_018931.3(PCDHB11):c.2098C>T (p.Leu700Phe)	not specified [RCV004331050]	uncertain significance	5	141201872	141201872	Human		name
401873699	CV2757723	single nucleotide variant	NM_018933.4(PCDHB13):c.1378G>C (p.Val460Leu)	not specified [RCV004336876]	uncertain significance	5	141215501	141215501	Human		name
401889432	CV2758103	single nucleotide variant	NM_018930.4(PCDHB10):c.1031C>A (p.Pro344His)	not specified [RCV004341484]	uncertain significance	5	141193583	141193583	Human		name
401880834	CV2763156	single nucleotide variant	NM_018930.4(PCDHB10):c.1329C>A (p.Asp443Glu)	not specified [RCV004336199]	uncertain significance	5	141193881	141193881	Human		name
401888766	CV2764671	single nucleotide variant	NM_018932.4(PCDHB12):c.1238G>C (p.Ser413Thr)	not specified [RCV004341472]	uncertain significance	5	141210145	141210145	Human		name
401856437	CV2764784	single nucleotide variant	NM_020957.4(PCDHB16):c.1831G>A (p.Glu611Lys)	not specified [RCV004334891]	uncertain significance	5	141184390	141184390	Human		name
401863230	CV2765605	single nucleotide variant	NM_018934.4(PCDHB14):c.1346C>T (p.Pro449Leu)	not specified [RCV004335618]	uncertain significance	5	141224851	141224851	Human		name
401863394	CV2765664	single nucleotide variant	NM_018932.4(PCDHB12):c.2158G>A (p.Ala720Thr)	not specified [RCV004335674]	uncertain significance	5	141211065	141211065	Human		name
401864002	CV2767460	single nucleotide variant	NM_018934.4(PCDHB14):c.1150T>C (p.Ser384Pro)	not specified [RCV004343626]	uncertain significance	5	141224655	141224655	Human		name
401887802	CV2772265	single nucleotide variant	NM_018931.3(PCDHB11):c.1001T>C (p.Ile334Thr)	not specified [RCV004346898]	uncertain significance	5	141200775	141200775	Human		name
401870260	CV2772665	single nucleotide variant	NM_020957.4(PCDHB16):c.1907C>T (p.Ala636Val)	not specified [RCV004355406]	uncertain significance	5	141184466	141184466	Human		name
401878905	CV2773774	single nucleotide variant	NM_018934.4(PCDHB14):c.2362A>C (p.Asn788His)	not specified [RCV004356440]	uncertain significance	5	141225867	141225867	Human		name
401865967	CV2775360	single nucleotide variant	NM_018934.4(PCDHB14):c.2305C>T (p.Pro769Ser)	not specified [RCV004348765]	uncertain significance	5	141225810	141225810	Human		name
401887114	CV2775618	single nucleotide variant	NM_018935.4(PCDHB15):c.1616C>T (p.Pro539Leu)	not specified [RCV004350769]	uncertain significance	5	141247194	141247194	Human		name
401872005	CV2775813	single nucleotide variant	NM_018931.3(PCDHB11):c.1151C>A (p.Ser384Tyr)	not specified [RCV004344853]	uncertain significance	5	141200925	141200925	Human		name
401864762	CV2778025	single nucleotide variant	NM_020957.4(PCDHB16):c.2179A>G (p.Met727Val)	not specified [RCV004347980]	likely benign	5	141184738	141184738	Human		name
401885614	CV2778173	single nucleotide variant	NM_018933.4(PCDHB13):c.1748G>T (p.Gly583Val)	not specified [RCV004349898]	uncertain significance	5	141215871	141215871	Human		name
401896552	CV2782185	single nucleotide variant	NM_018932.4(PCDHB12):c.1117A>G (p.Arg373Gly)	not specified [RCV004359161]	uncertain significance	5	141210024	141210024	Human		name
401898762	CV2782669	single nucleotide variant	NM_018932.4(PCDHB12):c.1001G>T (p.Arg334Ile)	not specified [RCV004359686]	uncertain significance	5	141209908	141209908	Human		name
401880272	CV2783153	single nucleotide variant	NM_018930.4(PCDHB10):c.1031C>G (p.Pro344Arg)	not specified [RCV004363501]	uncertain significance	5	141193583	141193583	Human		name
401880275	CV2783154	single nucleotide variant	NM_018931.3(PCDHB11):c.2165T>C (p.Val722Ala)	not specified [RCV004363502]	uncertain significance	5	141201939	141201939	Human		name
401880277	CV2783155	single nucleotide variant	NM_018933.4(PCDHB13):c.1447A>G (p.Asn483Asp)	not specified [RCV004363503]	uncertain significance	5	141215570	141215570	Human		name
401899173	CV2783725	single nucleotide variant	NM_018931.3(PCDHB11):c.2214C>G (p.Asp738Glu)	not specified [RCV004360645]	uncertain significance	5	141201988	141201988	Human		name
401863907	CV2784764	single nucleotide variant	NM_018933.4(PCDHB13):c.2212G>T (p.Asp738Tyr)	not specified [RCV004352560]	uncertain significance	5	141216335	141216335	Human		name
401896729	CV2788721	single nucleotide variant	NM_018932.4(PCDHB12):c.1291C>G (p.Leu431Val)	not specified [RCV004361197]	uncertain significance	5	141210198	141210198	Human		name
401895245	CV2789796	single nucleotide variant	NM_020957.4(PCDHB16):c.1585T>A (p.Phe529Ile)	not specified [RCV004361901]	uncertain significance	5	141184144	141184144	Human		name
405742624	CV3367903	single nucleotide variant	NM_018932.4(PCDHB12):c.2221G>A (p.Gly741Ser)	not specified [RCV004497970]	uncertain significance	5	141211128	141211128	Human		name
405742630	CV3367904	single nucleotide variant	NM_018932.4(PCDHB12):c.2278A>G (p.Arg760Gly)	not specified [RCV004497971]	likely benign	5	141211185	141211185	Human		name
405742664	CV3367909	single nucleotide variant	NM_018933.4(PCDHB13):c.1204A>G (p.Thr402Ala)	not specified [RCV004497976]	uncertain significance	5	141215327	141215327	Human		name
405742673	CV3367910	single nucleotide variant	NM_018933.4(PCDHB13):c.1416C>G (p.Ser472Arg)	not specified [RCV004497977]	uncertain significance	5	141215539	141215539	Human		name
405742688	CV3367912	single nucleotide variant	NM_018933.4(PCDHB13):c.1576G>A (p.Gly526Arg)	not specified [RCV004497979]	uncertain significance	5	141215699	141215699	Human		name
405742697	CV3367913	single nucleotide variant	NM_018933.4(PCDHB13):c.1608C>G (p.His536Gln)	not specified [RCV004497980]	uncertain significance	5	141215731	141215731	Human		name
405742718	CV3367916	single nucleotide variant	NM_018933.4(PCDHB13):c.1988T>C (p.Val663Ala)	not specified [RCV004497983]	uncertain significance	5	141216111	141216111	Human		name
405742730	CV3367918	single nucleotide variant	NM_018933.4(PCDHB13):c.2233C>G (p.Leu745Val)	not specified [RCV004497985]	uncertain significance	5	141216356	141216356	Human		name
405742738	CV3367919	single nucleotide variant	NM_018933.4(PCDHB13):c.2257G>A (p.Val753Met)	not specified [RCV004497986]	uncertain significance	5	141216380	141216380	Human		name
405742778	CV3367926	single nucleotide variant	NM_018934.4(PCDHB14):c.1046T>G (p.Ile349Arg)	not specified [RCV004497993]	uncertain significance	5	141224551	141224551	Human		name
405742787	CV3367927	single nucleotide variant	NM_018934.4(PCDHB14):c.1102T>C (p.Phe368Leu)	not specified [RCV004497994]	uncertain significance	5	141224607	141224607	Human		name
405742795	CV3367928	single nucleotide variant	NM_018934.4(PCDHB14):c.1130A>G (p.Asp377Gly)	not specified [RCV004497995]	uncertain significance	5	141224635	141224635	Human		name
405742801	CV3367929	single nucleotide variant	NM_018934.4(PCDHB14):c.1148G>C (p.Cys383Ser)	not specified [RCV004497996]	uncertain significance	5	141224653	141224653	Human		name
405742810	CV3367930	single nucleotide variant	NM_018934.4(PCDHB14):c.1159G>A (p.Asp387Asn)	not specified [RCV004497997]	uncertain significance	5	141224664	141224664	Human		name
405742815	CV3367931	single nucleotide variant	NM_018934.4(PCDHB14):c.1160A>G (p.Asp387Gly)	not specified [RCV004497998]	uncertain significance	5	141224665	141224665	Human		name
405742821	CV3367932	single nucleotide variant	NM_018934.4(PCDHB14):c.1168C>T (p.Pro390Ser)	not specified [RCV004497999]	uncertain significance	5	141224673	141224673	Human		name
405742825	CV3367933	single nucleotide variant	NM_018934.4(PCDHB14):c.1313C>T (p.Thr438Ile)	not specified [RCV004498000]	uncertain significance	5	141224818	141224818	Human		name
405742833	CV3367934	single nucleotide variant	NM_018934.4(PCDHB14):c.1411G>C (p.Gly471Arg)	not specified [RCV004498001]	uncertain significance	5	141224916	141224916	Human		name
405742840	CV3367935	single nucleotide variant	NM_018934.4(PCDHB14):c.1553C>T (p.Ser518Leu)	not specified [RCV004498002]	uncertain significance	5	141225058	141225058	Human		name
405742847	CV3367936	single nucleotide variant	NM_018934.4(PCDHB14):c.1581C>A (p.Phe527Leu)	not specified [RCV004498003]	uncertain significance	5	141225086	141225086	Human		name
405742866	CV3367939	single nucleotide variant	NM_018934.4(PCDHB14):c.1786T>G (p.Ser596Ala)	not specified [RCV004498006]	uncertain significance	5	141225291	141225291	Human		name
405742881	CV3367941	single nucleotide variant	NM_018934.4(PCDHB14):c.1873C>A (p.Arg625Ser)	not specified [RCV004498008]	uncertain significance	5	141225378	141225378	Human		name
405742888	CV3367942	single nucleotide variant	NM_018934.4(PCDHB14):c.1906G>C (p.Ala636Pro)	not specified [RCV004498009]	likely benign	5	141225411	141225411	Human		name
405742895	CV3367943	single nucleotide variant	NM_018934.4(PCDHB14):c.1930G>A (p.Val644Ile)	not specified [RCV004498010]	uncertain significance	5	141225435	141225435	Human		name
405742907	CV3367945	single nucleotide variant	NM_018934.4(PCDHB14):c.2005C>G (p.Pro669Ala)	not specified [RCV004498012]	uncertain significance	5	141225510	141225510	Human		name
405742912	CV3367946	single nucleotide variant	NM_018934.4(PCDHB14):c.2035G>A (p.Ala679Thr)	not specified [RCV004498013]	uncertain significance	5	141225540	141225540	Human		name
405742919	CV3367947	single nucleotide variant	NM_018934.4(PCDHB14):c.2134C>T (p.Arg712Trp)	not specified [RCV004498014]	uncertain significance	5	141225639	141225639	Human		name
405742926	CV3367948	single nucleotide variant	NM_018934.4(PCDHB14):c.2154G>C (p.Arg718Ser)	not specified [RCV004498015]	uncertain significance	5	141225659	141225659	Human		name
405742932	CV3367949	single nucleotide variant	NM_018934.4(PCDHB14):c.2188G>T (p.Gly730Cys)	not specified [RCV004498016]	uncertain significance	5	141225693	141225693	Human		name
405744588	CV3367955	single nucleotide variant	NM_018935.4(PCDHB15):c.1305G>C (p.Gln435His)	not specified [RCV004498022]	likely benign	5	141246883	141246883	Human		name
405744579	CV3367956	single nucleotide variant	NM_018935.4(PCDHB15):c.1307G>A (p.Ser436Asn)	not specified [RCV004498023]	likely benign	5	141246885	141246885	Human		name
405744571	CV3367957	single nucleotide variant	NM_018935.4(PCDHB15):c.1460C>A (p.Thr487Asn)	not specified [RCV004498024]	uncertain significance	5	141247038	141247038	Human		name
405744564	CV3367958	single nucleotide variant	NM_018935.4(PCDHB15):c.1726G>A (p.Val576Met)	not specified [RCV004498025]	uncertain significance	5	141247304	141247304	Human		name
405744558	CV3367959	single nucleotide variant	NM_018935.4(PCDHB15):c.1759A>T (p.Thr587Ser)	not specified [RCV004498026]	uncertain significance	5	141247337	141247337	Human		name
405744549	CV3367960	single nucleotide variant	NM_018935.4(PCDHB15):c.1935G>C (p.Lys645Asn)	not specified [RCV004498027]	uncertain significance	5	141247513	141247513	Human		name
405744524	CV3367962	single nucleotide variant	NM_018935.4(PCDHB15):c.2205T>G (p.His735Gln)	not specified [RCV004498029]	uncertain significance	5	141247783	141247783	Human		name
405743207	CV3367973	single nucleotide variant	NM_020957.4(PCDHB16):c.1178T>C (p.Leu393Pro)	not specified [RCV004498040]	uncertain significance	5	141183737	141183737	Human		name
405743063	CV3367974	single nucleotide variant	NM_020957.4(PCDHB16):c.1320G>C (p.Gln440His)	not specified [RCV004498041]	uncertain significance	5	141183879	141183879	Human		name
405742945	CV3367975	single nucleotide variant	NM_020957.4(PCDHB16):c.1321A>G (p.Ile441Val)	not specified [RCV004498042]	likely benign	5	141183880	141183880	Human		name
405742951	CV3367976	single nucleotide variant	NM_020957.4(PCDHB16):c.1460C>A (p.Thr487Asn)	not specified [RCV004498043]	uncertain significance	5	141184019	141184019	Human		name
405742959	CV3367977	single nucleotide variant	NM_020957.4(PCDHB16):c.1466C>T (p.Ser489Leu)	not specified [RCV004498044]	uncertain significance	5	141184025	141184025	Human		name
405742965	CV3367978	single nucleotide variant	NM_020957.4(PCDHB16):c.1610G>A (p.Gly537Asp)	not specified [RCV004498045]	uncertain significance	5	141184169	141184169	Human		name
405742977	CV3367980	single nucleotide variant	NM_020957.4(PCDHB16):c.1681G>C (p.Val561Leu)	not specified [RCV004498047]	uncertain significance	5	141184240	141184240	Human		name
405742984	CV3367981	single nucleotide variant	NM_020957.4(PCDHB16):c.1760C>G (p.Thr587Ser)	not specified [RCV004498048]	uncertain significance	5	141184319	141184319	Human		name
405742989	CV3367982	single nucleotide variant	NM_020957.4(PCDHB16):c.1952C>G (p.Pro651Arg)	not specified [RCV004498049]	uncertain significance	5	141184511	141184511	Human		name
405742994	CV3367983	single nucleotide variant	NM_020957.4(PCDHB16):c.2006C>T (p.Pro669Leu)	not specified [RCV004498050]	uncertain significance	5	141184565	141184565	Human		name
405743003	CV3367984	single nucleotide variant	NM_020957.4(PCDHB16):c.2009T>A (p.Phe670Tyr)	not specified [RCV004498051]	likely benign	5	141184568	141184568	Human		name
405743010	CV3367985	single nucleotide variant	NM_020957.4(PCDHB16):c.2135G>T (p.Arg712Leu)	not specified [RCV004498052]	uncertain significance	5	141184694	141184694	Human		name
405743016	CV3367986	single nucleotide variant	NM_020957.4(PCDHB16):c.2227G>T (p.Gly743Trp)	not specified [RCV004498053]	uncertain significance	5	141184786	141184786	Human		name
405743023	CV3367987	single nucleotide variant	NM_020957.4(PCDHB16):c.2228G>T (p.Gly743Val)	not specified [RCV004498054]	uncertain significance	5	141184787	141184787	Human		name
405743032	CV3367988	single nucleotide variant	NM_020957.4(PCDHB16):c.2257G>C (p.Val753Leu)	not specified [RCV004498055]	uncertain significance	5	141184816	141184816	Human		name
405743038	CV3367989	single nucleotide variant	NM_020957.4(PCDHB16):c.2273G>A (p.Gly758Asp)	not specified [RCV004498056]	uncertain significance	5	141184832	141184832	Human		name
405741981	CV3371832	single nucleotide variant	NM_018930.4(PCDHB10):c.1034C>T (p.Pro345Leu)	not specified [RCV004497905]	uncertain significance	5	141193586	141193586	Human		name
405741989	CV3371833	single nucleotide variant	NM_018930.4(PCDHB10):c.1153A>G (p.Ile385Val)	not specified [RCV004497906]	uncertain significance	5	141193705	141193705	Human		name
405741997	CV3371834	single nucleotide variant	NM_018930.4(PCDHB10):c.1223C>T (p.Ala408Val)	not specified [RCV004497907]	uncertain significance	5	141193775	141193775	Human		name
405742004	CV3371835	single nucleotide variant	NM_018930.4(PCDHB10):c.1361C>T (p.Thr454Ile)	not specified [RCV004497908]	uncertain significance	5	141193913	141193913	Human		name
405742012	CV3371836	single nucleotide variant	NM_018930.4(PCDHB10):c.1403T>A (p.Leu468Gln)	not specified [RCV004497909]	uncertain significance	5	141193955	141193955	Human		name
405742019	CV3371837	single nucleotide variant	NM_018930.4(PCDHB10):c.1468C>A (p.Leu490Met)	not specified [RCV004497910]	uncertain significance	5	141194020	141194020	Human		name
405742026	CV3371838	single nucleotide variant	NM_018930.4(PCDHB10):c.1478C>A (p.Pro493His)	not specified [RCV004497911]	uncertain significance	5	141194030	141194030	Human		name
405742036	CV3371840	single nucleotide variant	NM_018930.4(PCDHB10):c.1760C>T (p.Thr587Ile)	not specified [RCV004497913]	uncertain significance	5	141194312	141194312	Human		name
405742043	CV3371841	single nucleotide variant	NM_018930.4(PCDHB10):c.1823A>T (p.Lys608Met)	not specified [RCV004497914]	uncertain significance	5	141194375	141194375	Human		name
405742059	CV3371843	single nucleotide variant	NM_018930.4(PCDHB10):c.2119G>T (p.Val707Leu)	not specified [RCV004497916]	uncertain significance	5	141194671	141194671	Human		name
405742065	CV3371844	single nucleotide variant	NM_018930.4(PCDHB10):c.2134G>T (p.Ala712Ser)	not specified [RCV004497917]	uncertain significance	5	141194686	141194686	Human		name
405742080	CV3371846	single nucleotide variant	NM_018930.4(PCDHB10):c.2317A>G (p.Ile773Val)	not specified [RCV004497919]	uncertain significance	5	141194869	141194869	Human		name
405742087	CV3371847	single nucleotide variant	NM_018930.4(PCDHB10):c.2368A>T (p.Thr790Ser)	not specified [RCV004497920]	uncertain significance	5	141194920	141194920	Human		name
405742093	CV3371848	single nucleotide variant	NM_018930.4(PCDHB10):c.2369C>G (p.Thr790Ser)	not specified [RCV004497921]	uncertain significance	5	141194921	141194921	Human		name
405742173	CV3371859	single nucleotide variant	NM_018931.3(PCDHB11):c.1192G>C (p.Glu398Gln)	not specified [RCV004497932]	uncertain significance	5	141200966	141200966	Human		name
405742185	CV3371861	single nucleotide variant	NM_018931.3(PCDHB11):c.1411G>C (p.Gly471Arg)	not specified [RCV004497934]	uncertain significance	5	141201185	141201185	Human		name
405742189	CV3371862	single nucleotide variant	NM_018931.3(PCDHB11):c.1558G>A (p.Asp520Asn)	not specified [RCV004497935]	uncertain significance	5	141201332	141201332	Human		name
405742196	CV3371863	single nucleotide variant	NM_018931.3(PCDHB11):c.1600A>G (p.Thr534Ala)	not specified [RCV004497936]	uncertain significance	5	141201374	141201374	Human		name
405742202	CV3371864	single nucleotide variant	NM_018931.3(PCDHB11):c.1600A>T (p.Thr534Ser)	not specified [RCV004497937]	uncertain significance	5	141201374	141201374	Human		name
405742211	CV3371865	single nucleotide variant	NM_018931.3(PCDHB11):c.1607G>A (p.Arg536His)	not specified [RCV004497938]	uncertain significance	5	141201381	141201381	Human		name
405742216	CV3371866	single nucleotide variant	NM_018931.3(PCDHB11):c.1660G>A (p.Ala554Thr)	not specified [RCV004497939]	uncertain significance	5	141201434	141201434	Human		name
405742223	CV3371867	single nucleotide variant	NM_018931.3(PCDHB11):c.1733G>A (p.Arg578Gln)	not specified [RCV004497940]	uncertain significance	5	141201507	141201507	Human		name
405742236	CV3371869	single nucleotide variant	NM_018931.3(PCDHB11):c.1801T>C (p.Trp601Arg)	not specified [RCV004497942]	uncertain significance	5	141201575	141201575	Human		name
405742254	CV3371871	single nucleotide variant	NM_018931.3(PCDHB11):c.1922T>C (p.Val641Ala)	not specified [RCV004497944]	uncertain significance	5	141201696	141201696	Human		name
405742260	CV3371872	single nucleotide variant	NM_018931.3(PCDHB11):c.2054C>G (p.Ser685Trp)	not specified [RCV004497945]	uncertain significance	5	141201828	141201828	Human		name
405742268	CV3371873	single nucleotide variant	NM_018931.3(PCDHB11):c.2180T>G (p.Val727Gly)	not specified [RCV004497946]	uncertain significance	5	141201954	141201954	Human		name
405742275	CV3371874	single nucleotide variant	NM_018931.3(PCDHB11):c.2185A>G (p.Lys729Glu)	not specified [RCV004497947]	likely benign	5	141201959	141201959	Human		name
405742290	CV3371876	single nucleotide variant	NM_018931.3(PCDHB11):c.2354A>G (p.Glu785Gly)	not specified [RCV004497949]	uncertain significance	5	141202128	141202128	Human		name
405742295	CV3371877	single nucleotide variant	NM_018931.3(PCDHB11):c.2362A>G (p.Thr788Ala)	not specified [RCV004497950]	uncertain significance	5	141202136	141202136	Human		name
405742538	CV3371885	single nucleotide variant	NM_018932.4(PCDHB12):c.1088C>T (p.Thr363Ile)	not specified [RCV004497958]	uncertain significance	5	141209995	141209995	Human		name
405742544	CV3371886	single nucleotide variant	NM_018932.4(PCDHB12):c.1310T>C (p.Ile437Thr)	not specified [RCV004497959]	uncertain significance	5	141210217	141210217	Human		name
405742558	CV3371888	single nucleotide variant	NM_018932.4(PCDHB12):c.1348G>A (p.Ala450Thr)	not specified [RCV004497961]	uncertain significance	5	141210255	141210255	Human		name
405742574	CV3371890	single nucleotide variant	NM_018932.4(PCDHB12):c.1588C>T (p.Arg530Cys)	not specified [RCV004497963]	uncertain significance	5	141210495	141210495	Human		name
405742581	CV3371891	single nucleotide variant	NM_018932.4(PCDHB12):c.1607A>T (p.His536Leu)	not specified [RCV004497964]	uncertain significance	5	141210514	141210514	Human		name
405742589	CV3371892	single nucleotide variant	NM_018932.4(PCDHB12):c.1856C>T (p.Ala619Val)	not specified [RCV004497965]	uncertain significance	5	141210763	141210763	Human		name
405742595	CV3371893	single nucleotide variant	NM_018932.4(PCDHB12):c.1930G>A (p.Val644Ile)	not specified [RCV004497966]	uncertain significance	5	141210837	141210837	Human		name
405742602	CV3371894	single nucleotide variant	NM_018932.4(PCDHB12):c.1943G>A (p.Gly648Asp)	not specified [RCV004497967]	uncertain significance	5	141210850	141210850	Human		name
405742610	CV3371895	single nucleotide variant	NM_018932.4(PCDHB12):c.1961C>A (p.Ala654Asp)	not specified [RCV004497968]	uncertain significance	5	141210868	141210868	Human		name
405742617	CV3371896	single nucleotide variant	NM_018932.4(PCDHB12):c.2131G>C (p.Val711Leu)	not specified [RCV004497969]	uncertain significance	5	141211038	141211038	Human		name
407480309	CV3463078	single nucleotide variant	NM_018930.4(PCDHB10):c.2035G>T (p.Ala679Ser)	not specified [RCV004664382]	uncertain significance	5	141194587	141194587	Human		name
407480316	CV3463079	single nucleotide variant	NM_018930.4(PCDHB10):c.1495C>T (p.Pro499Ser)	not specified [RCV004664383]	uncertain significance	5	141194047	141194047	Human		name
407523419	CV3463080	single nucleotide variant	NM_018930.4(PCDHB10):c.2220C>G (p.Asp740Glu)	not specified [RCV004653159]	uncertain significance	5	141194772	141194772	Human		name
407523416	CV3463081	single nucleotide variant	NM_018930.4(PCDHB10):c.1648C>G (p.Leu550Val)	not specified [RCV004653160]	uncertain significance	5	141194200	141194200	Human		name
407480322	CV3463082	single nucleotide variant	NM_018930.4(PCDHB10):c.1384G>C (p.Glu462Gln)	not specified [RCV004664384]	uncertain significance	5	141193936	141193936	Human		name
407523408	CV3463085	single nucleotide variant	NM_018930.4(PCDHB10):c.1270A>G (p.Thr424Ala)	not specified [RCV004653163]	uncertain significance	5	141193822	141193822	Human		name
407523402	CV3463088	single nucleotide variant	NM_018930.4(PCDHB10):c.1093C>G (p.Leu365Val)	not specified [RCV004653165]	uncertain significance	5	141193645	141193645	Human		name
407480331	CV3463089	single nucleotide variant	NM_018930.4(PCDHB10):c.1642C>A (p.Arg548Ser)	not specified [RCV004664386]	uncertain significance	5	141194194	141194194	Human		name
407523399	CV3463090	single nucleotide variant	NM_018930.4(PCDHB10):c.1262T>C (p.Ile421Thr)	not specified [RCV004653166]	uncertain significance	5	141193814	141193814	Human		name
407480353	CV3463094	single nucleotide variant	NM_018931.3(PCDHB11):c.2389T>A (p.Phe797Ile)	not specified [RCV004664390]	uncertain significance	5	141202163	141202163	Human		name
407523233	CV3463096	single nucleotide variant	NM_018931.3(PCDHB11):c.1315G>A (p.Val439Met)	not specified [RCV004653168]	uncertain significance	5	141201089	141201089	Human		name
407480366	CV3463098	single nucleotide variant	NM_018931.3(PCDHB11):c.2228G>A (p.Gly743Glu)	not specified [RCV004664392]	uncertain significance	5	141202002	141202002	Human		name
407480374	CV3463099	single nucleotide variant	NM_018931.3(PCDHB11):c.1048T>C (p.Ser350Pro)	not specified [RCV004664393]	uncertain significance	5	141200822	141200822	Human		name
407523236	CV3463100	single nucleotide variant	NM_018931.3(PCDHB11):c.1492C>A (p.Leu498Met)	not specified [RCV004653169]	uncertain significance	5	141201266	141201266	Human		name
407480387	CV3463102	single nucleotide variant	NM_018932.4(PCDHB12):c.1156C>A (p.Pro386Thr)	not specified [RCV004664395]	uncertain significance	5	141210063	141210063	Human		name
407523239	CV3463103	single nucleotide variant	NM_018932.4(PCDHB12):c.2107T>C (p.Phe703Leu)	not specified [RCV004653170]	likely benign	5	141211014	141211014	Human		name
407480393	CV3463104	single nucleotide variant	NM_018932.4(PCDHB12):c.1075A>G (p.Asn359Asp)	not specified [RCV004664396]	uncertain significance	5	141209982	141209982	Human		name
407480401	CV3463106	single nucleotide variant	NM_018932.4(PCDHB12):c.2183C>A (p.Pro728His)	not specified [RCV004664397]	uncertain significance	5	141211090	141211090	Human		name
407480407	CV3463107	single nucleotide variant	NM_018932.4(PCDHB12):c.1098G>T (p.Met366Ile)	not specified [RCV004664398]	uncertain significance	5	141210005	141210005	Human		name
407523245	CV3463108	single nucleotide variant	NM_018932.4(PCDHB12):c.1576G>A (p.Gly526Arg)	not specified [RCV004653172]	uncertain significance	5	141210483	141210483	Human		name
407480414	CV3463109	single nucleotide variant	NM_018933.4(PCDHB13):c.2317A>T (p.Asn773Tyr)	not specified [RCV004664399]	uncertain significance	5	141216440	141216440	Human		name
407523249	CV3463110	single nucleotide variant	NM_018933.4(PCDHB13):c.1873C>A (p.Arg625Ser)	not specified [RCV004653173]	uncertain significance	5	141215996	141215996	Human		name
407480420	CV3463111	single nucleotide variant	NM_018933.4(PCDHB13):c.1377C>G (p.Phe459Leu)	not specified [RCV004664400]	uncertain significance	5	141215500	141215500	Human		name
407523252	CV3463112	single nucleotide variant	NM_018933.4(PCDHB13):c.2053T>A (p.Leu685Met)	not specified [RCV004653174]	uncertain significance	5	141216176	141216176	Human		name
407523255	CV3463113	single nucleotide variant	NM_018933.4(PCDHB13):c.1523C>T (p.Ala508Val)	not specified [RCV004653175]	uncertain significance	5	141215646	141215646	Human		name
407480426	CV3463114	single nucleotide variant	NM_018933.4(PCDHB13):c.2189G>T (p.Gly730Val)	not specified [RCV004664401]	uncertain significance	5	141216312	141216312	Human		name
407523258	CV3463115	single nucleotide variant	NM_018933.4(PCDHB13):c.1013T>C (p.Val338Ala)	not specified [RCV004653176]	uncertain significance	5	141215136	141215136	Human		name
407523261	CV3463116	single nucleotide variant	NM_018934.4(PCDHB14):c.1871T>G (p.Val624Gly)	not specified [RCV004653177]	uncertain significance	5	141225376	141225376	Human		name
407523264	CV3463117	single nucleotide variant	NM_018934.4(PCDHB14):c.2201G>A (p.Gly734Glu)	not specified [RCV004653178]	uncertain significance	5	141225706	141225706	Human		name
407480441	CV3463119	single nucleotide variant	NM_018934.4(PCDHB14):c.2116C>T (p.Leu706Phe)	not specified [RCV004664403]	uncertain significance	5	141225621	141225621	Human		name
407480445	CV3463120	single nucleotide variant	NM_018934.4(PCDHB14):c.1521C>A (p.Asn507Lys)	not specified [RCV004664404]	uncertain significance	5	141225026	141225026	Human		name
407480453	CV3463122	single nucleotide variant	NM_018934.4(PCDHB14):c.1060A>G (p.Lys354Glu)	not specified [RCV004664405]	uncertain significance	5	141224565	141224565	Human		name
407480460	CV3463124	single nucleotide variant	NM_018934.4(PCDHB14):c.2345A>G (p.Asn782Ser)	not specified [RCV004664406]	uncertain significance	5	141225850	141225850	Human		name
407523273	CV3463125	single nucleotide variant	NM_018934.4(PCDHB14):c.1709C>T (p.Ala570Val)	not specified [RCV004653181]	uncertain significance	5	141225214	141225214	Human		name
407480465	CV3463126	single nucleotide variant	NM_018934.4(PCDHB14):c.1993G>C (p.Gly665Arg)	not specified [RCV004664407]	uncertain significance	5	141225498	141225498	Human		name
407523276	CV3463127	single nucleotide variant	NM_018934.4(PCDHB14):c.1340A>G (p.Asn447Ser)	not specified [RCV004653182]	uncertain significance	5	141224845	141224845	Human		name
407523293	CV3463133	single nucleotide variant	NM_018935.4(PCDHB15):c.2116T>C (p.Phe706Leu)	not specified [RCV004653188]	likely benign	5	141247694	141247694	Human		name
407523296	CV3463134	single nucleotide variant	NM_018935.4(PCDHB15):c.1708G>T (p.Ala570Ser)	not specified [RCV004653189]	uncertain significance	5	141247286	141247286	Human		name
407480472	CV3463135	single nucleotide variant	NM_018935.4(PCDHB15):c.1732C>T (p.Arg578Trp)	not specified [RCV004664408]	uncertain significance	5	141247310	141247310	Human		name
407480477	CV3463136	single nucleotide variant	NM_018935.4(PCDHB15):c.1928T>C (p.Leu643Pro)	not specified [RCV004664409]	uncertain significance	5	141247506	141247506	Human		name
407523299	CV3463137	single nucleotide variant	NM_018935.4(PCDHB15):c.2134C>T (p.Arg712Trp)	not specified [RCV004653190]	uncertain significance	5	141247712	141247712	Human		name
407523467	CV3463139	single nucleotide variant	NM_018935.4(PCDHB15):c.1487C>G (p.Pro496Arg)	not specified [RCV004653191]	uncertain significance	5	141247065	141247065	Human		name
407523308	CV3463141	single nucleotide variant	NM_020957.4(PCDHB16):c.1657G>A (p.Asp553Asn)	not specified [RCV004653193]	uncertain significance	5	141184216	141184216	Human		name
407480490	CV3463142	single nucleotide variant	NM_020957.4(PCDHB16):c.1045A>G (p.Met349Val)	not specified [RCV004664411]	uncertain significance	5	141183604	141183604	Human		name
407523311	CV3463145	single nucleotide variant	NM_020957.4(PCDHB16):c.2014C>A (p.Pro672Thr)	not specified [RCV004653194]	uncertain significance	5	141184573	141184573	Human		name
407523313	CV3463147	single nucleotide variant	NM_020957.4(PCDHB16):c.1028A>G (p.Asn343Ser)	not specified [RCV004653195]	uncertain significance	5	141183587	141183587	Human		name
407523316	CV3463148	single nucleotide variant	NM_020957.4(PCDHB16):c.1856C>T (p.Ala619Val)	not specified [RCV004653196]	uncertain significance	5	141184415	141184415	Human		name
407523319	CV3463149	single nucleotide variant	NM_020957.4(PCDHB16):c.1495C>T (p.Pro499Ser)	not specified [RCV004653197]	uncertain significance	5	141184054	141184054	Human		name
597736945	CV3575028	single nucleotide variant	NM_018932.4(PCDHB12):c.1600A>T (p.Thr534Ser)	not specified [RCV004843811]	uncertain significance	5	141210507	141210507	Human		name
597736949	CV3575029	single nucleotide variant	NM_018932.4(PCDHB12):c.2093C>G (p.Ser698Trp)	not specified [RCV004843812]	uncertain significance	5	141211000	141211000	Human		name
597736954	CV3575030	single nucleotide variant	NM_018932.4(PCDHB12):c.1849G>C (p.Val617Leu)	not specified [RCV004843813]	uncertain significance	5	141210756	141210756	Human		name
597736958	CV3575031	single nucleotide variant	NM_018932.4(PCDHB12):c.2264T>G (p.Val755Gly)	not specified [RCV004843814]	uncertain significance	5	141211171	141211171	Human		name
597736964	CV3575032	single nucleotide variant	NM_018932.4(PCDHB12):c.1136G>C (p.Gly379Ala)	not specified [RCV004843815]	uncertain significance	5	141210043	141210043	Human		name
597736973	CV3575034	single nucleotide variant	NM_018932.4(PCDHB12):c.2161C>T (p.Pro721Ser)	not specified [RCV004843817]	likely benign	5	141211068	141211068	Human		name
597736983	CV3575036	single nucleotide variant	NM_018932.4(PCDHB12):c.2009A>T (p.Tyr670Phe)	not specified [RCV004843819]	uncertain significance	5	141210916	141210916	Human		name
597756081	CV3575037	single nucleotide variant	NM_018932.4(PCDHB12):c.1169C>T (p.Pro390Leu)	not specified [RCV004848071]	uncertain significance	5	141210076	141210076	Human		name
597736993	CV3575039	single nucleotide variant	NM_018932.4(PCDHB12):c.1979T>A (p.Val660Glu)	not specified [RCV004843821]	uncertain significance	5	141210886	141210886	Human		name
597737001	CV3575041	single nucleotide variant	NM_018932.4(PCDHB12):c.1897C>T (p.Arg633Cys)	not specified [RCV004843823]	uncertain significance	5	141210804	141210804	Human		name
597756085	CV3575042	single nucleotide variant	NM_018932.4(PCDHB12):c.1604A>G (p.Asp535Gly)	not specified [RCV004848072]	uncertain significance	5	141210511	141210511	Human		name
597737006	CV3575043	single nucleotide variant	NM_018932.4(PCDHB12):c.1975C>T (p.His659Tyr)	not specified [RCV004843824]	uncertain significance	5	141210882	141210882	Human		name
597737011	CV3575044	single nucleotide variant	NM_018932.4(PCDHB12):c.1267G>A (p.Val423Ile)	not specified [RCV004843825]	uncertain significance	5	141210174	141210174	Human		name
597737026	CV3575047	single nucleotide variant	NM_018932.4(PCDHB12):c.2167G>A (p.Gly723Ser)	not specified [RCV004843828]	uncertain significance	5	141211074	141211074	Human		name
597737031	CV3575048	single nucleotide variant	NM_018932.4(PCDHB12):c.1225C>G (p.Leu409Val)	not specified [RCV004843829]	uncertain significance	5	141210132	141210132	Human		name
597737040	CV3575050	single nucleotide variant	NM_018932.4(PCDHB12):c.1993G>C (p.Gly665Arg)	not specified [RCV004843831]	uncertain significance	5	141210900	141210900	Human		name
597737046	CV3575051	single nucleotide variant	NM_018933.4(PCDHB13):c.1278G>C (p.Leu426Phe)	not specified [RCV004843832]	uncertain significance	5	141215401	141215401	Human		name
597756093	CV3575054	single nucleotide variant	NM_018933.4(PCDHB13):c.1342G>T (p.Ala448Ser)	not specified [RCV004848074]	uncertain significance	5	141215465	141215465	Human		name
597737065	CV3575057	single nucleotide variant	NM_018933.4(PCDHB13):c.1871T>G (p.Val624Gly)	not specified [RCV004843836]	uncertain significance	5	141215994	141215994	Human		name
597737069	CV3575058	single nucleotide variant	NM_018933.4(PCDHB13):c.1049T>C (p.Met350Thr)	not specified [RCV004843837]	uncertain significance	5	141215172	141215172	Human		name
597737075	CV3575059	single nucleotide variant	NM_018933.4(PCDHB13):c.1258A>G (p.Thr420Ala)	not specified [RCV004843838]	uncertain significance	5	141215381	141215381	Human		name
597737354	CV3575060	single nucleotide variant	NM_018933.4(PCDHB13):c.2141G>C (p.Cys714Ser)	not specified [RCV004843839]	uncertain significance	5	141216264	141216264	Human		name
597737349	CV3575061	single nucleotide variant	NM_018933.4(PCDHB13):c.2228G>A (p.Arg743Lys)	not specified [RCV004843840]	uncertain significance	5	141216351	141216351	Human		name
597737345	CV3575062	single nucleotide variant	NM_018933.4(PCDHB13):c.2240A>G (p.Gln747Arg)	not specified [RCV004843841]	uncertain significance	5	141216363	141216363	Human		name
597756101	CV3575064	single nucleotide variant	NM_018933.4(PCDHB13):c.2287G>A (p.Glu763Lys)	not specified [RCV004848076]	uncertain significance	5	141216410	141216410	Human		name
597756105	CV3575065	single nucleotide variant	NM_018933.4(PCDHB13):c.2260T>A (p.Cys754Ser)	not specified [RCV004848077]	uncertain significance	5	141216383	141216383	Human		name
597737337	CV3575067	single nucleotide variant	NM_018933.4(PCDHB13):c.2225C>T (p.Thr742Ile)	not specified [RCV004843843]	uncertain significance	5	141216348	141216348	Human		name
597737332	CV3575068	single nucleotide variant	NM_018933.4(PCDHB13):c.2289G>T (p.Glu763Asp)	not specified [RCV004843844]	uncertain significance	5	141216412	141216412	Human		name
597737326	CV3575069	single nucleotide variant	NM_018933.4(PCDHB13):c.1382G>C (p.Arg461Pro)	not specified [RCV004843845]	uncertain significance	5	141215505	141215505	Human		name
597737321	CV3575070	single nucleotide variant	NM_018933.4(PCDHB13):c.1551G>T (p.Arg517Ser)	not specified [RCV004843846]	uncertain significance	5	141215674	141215674	Human		name
597756108	CV3575071	single nucleotide variant	NM_018933.4(PCDHB13):c.2113G>A (p.Val705Met)	not specified [RCV004848078]	uncertain significance	5	141216236	141216236	Human		name
597737315	CV3575072	single nucleotide variant	NM_018933.4(PCDHB13):c.1483G>A (p.Asp495Asn)	not specified [RCV004843847]	uncertain significance	5	141215606	141215606	Human		name
597737305	CV3575074	single nucleotide variant	NM_018934.4(PCDHB14):c.1634C>A (p.Ala545Glu)	not specified [RCV004843849]	uncertain significance	5	141225139	141225139	Human		name
597737302	CV3575075	single nucleotide variant	NM_018934.4(PCDHB14):c.1954C>T (p.Arg652Cys)	not specified [RCV004843850]	uncertain significance	5	141225459	141225459	Human		name
597737296	CV3575076	single nucleotide variant	NM_018934.4(PCDHB14):c.2293A>C (p.Lys765Gln)	not specified [RCV004843851]	uncertain significance	5	141225798	141225798	Human		name
597737287	CV3575078	single nucleotide variant	NM_018934.4(PCDHB14):c.1423G>T (p.Ala475Ser)	not specified [RCV004843853]	uncertain significance	5	141224928	141224928	Human		name
597756112	CV3575079	single nucleotide variant	NM_018934.4(PCDHB14):c.1348A>G (p.Thr450Ala)	not specified [RCV004848079]	likely benign	5	141224853	141224853	Human		name
597737281	CV3575080	single nucleotide variant	NM_018934.4(PCDHB14):c.1690C>A (p.Pro564Thr)	not specified [RCV004843854]	uncertain significance	5	141225195	141225195	Human		name
597756123	CV3575083	single nucleotide variant	NM_018934.4(PCDHB14):c.1797C>G (p.Asn599Lys)	not specified [RCV004848081]	uncertain significance	5	141225302	141225302	Human		name
597737271	CV3575084	single nucleotide variant	NM_018935.4(PCDHB15):c.2103C>A (p.Phe701Leu)	not specified [RCV004843856]	uncertain significance	5	141247681	141247681	Human		name
597737266	CV3575085	single nucleotide variant	NM_018935.4(PCDHB15):c.1243G>A (p.Ala415Thr)	not specified [RCV004843857]	uncertain significance	5	141246821	141246821	Human		name
597737262	CV3575086	single nucleotide variant	NM_018935.4(PCDHB15):c.1034C>T (p.Pro345Leu)	not specified [RCV004843858]	uncertain significance	5	141246612	141246612	Human		name
597737256	CV3575087	single nucleotide variant	NM_018935.4(PCDHB15):c.1922T>C (p.Val641Ala)	not specified [RCV004843859]	uncertain significance	5	141247500	141247500	Human		name
597756127	CV3575089	single nucleotide variant	NM_018935.4(PCDHB15):c.2144G>A (p.Arg715Lys)	not specified [RCV004848082]	uncertain significance	5	141247722	141247722	Human		name
597737251	CV3575090	single nucleotide variant	NM_018935.4(PCDHB15):c.1300G>A (p.Glu434Lys)	not specified [RCV004843860]	uncertain significance	5	141246878	141246878	Human		name
597737245	CV3575091	single nucleotide variant	NM_018935.4(PCDHB15):c.1744C>A (p.Pro582Thr)	not specified [RCV004843861]	uncertain significance	5	141247322	141247322	Human		name
597737084	CV3575095	single nucleotide variant	NM_018935.4(PCDHB15):c.2000C>T (p.Ser667Phe)	not specified [RCV004843864]	uncertain significance	5	141247578	141247578	Human		name
597737094	CV3575097	single nucleotide variant	NM_018935.4(PCDHB15):c.2032C>A (p.Pro678Thr)	not specified [RCV004843866]	uncertain significance	5	141247610	141247610	Human		name
597737099	CV3575098	single nucleotide variant	NM_020957.4(PCDHB16):c.1745C>G (p.Pro582Arg)	not specified [RCV004843867]	uncertain significance	5	141184304	141184304	Human		name
597737103	CV3575100	single nucleotide variant	NM_020957.4(PCDHB16):c.1241G>A (p.Arg414Lys)	not specified [RCV004843868]	uncertain significance	5	141183800	141183800	Human		name
597737108	CV3575101	single nucleotide variant	NM_020957.4(PCDHB16):c.1573C>T (p.Gln525Ter)	not specified [RCV004843869]	uncertain significance	5	141184132	141184132	Human		name
597756240	CV3575102	single nucleotide variant	NM_020957.4(PCDHB16):c.1741G>A (p.Glu581Lys)	not specified [RCV004848084]	uncertain significance	5	141184300	141184300	Human		name
597756245	CV3575103	single nucleotide variant	NM_020957.4(PCDHB16):c.1531G>T (p.Gly511Cys)	not specified [RCV004848085]	uncertain significance	5	141184090	141184090	Human		name
597737113	CV3575105	single nucleotide variant	NM_020957.4(PCDHB16):c.1279G>A (p.Gly427Arg)	not specified [RCV004843870]	uncertain significance	5	141183838	141183838	Human		name
597737118	CV3575106	single nucleotide variant	NM_020957.4(PCDHB16):c.1879G>A (p.Ala627Thr)	not specified [RCV004843871]	uncertain significance	5	141184438	141184438	Human		name
597737123	CV3575107	single nucleotide variant	NM_020957.4(PCDHB16):c.1846G>T (p.Gly616Cys)	not specified [RCV004843872]	uncertain significance	5	141184405	141184405	Human		name
597737127	CV3575108	single nucleotide variant	NM_020957.4(PCDHB16):c.1912C>G (p.Gln638Glu)	not specified [RCV004843873]	uncertain significance	5	141184471	141184471	Human		name
597737132	CV3575110	single nucleotide variant	NM_020957.4(PCDHB16):c.1234G>A (p.Glu412Lys)	not specified [RCV004843874]	uncertain significance	5	141183793	141183793	Human		name
597737148	CV3575113	single nucleotide variant	NM_020957.4(PCDHB16):c.2191C>T (p.Pro731Ser)	not specified [RCV004843877]	uncertain significance	5	141184750	141184750	Human		name
597756254	CV3575115	single nucleotide variant	NM_020957.4(PCDHB16):c.1108G>C (p.Val370Leu)	not specified [RCV004848087]	uncertain significance	5	141183667	141183667	Human		name
597756047	CV3578881	single nucleotide variant	NM_018930.4(PCDHB10):c.1914C>G (p.His638Gln)	not specified [RCV004848062]	uncertain significance	5	141194466	141194466	Human		name
597736774	CV3578882	single nucleotide variant	NM_018930.4(PCDHB10):c.1238T>G (p.Ile413Ser)	not specified [RCV004843776]	likely benign	5	141193790	141193790	Human		name
597736779	CV3578883	single nucleotide variant	NM_018930.4(PCDHB10):c.1241G>A (p.Arg414Lys)	not specified [RCV004843777]	uncertain significance	5	141193793	141193793	Human		name
597736783	CV3578884	single nucleotide variant	NM_018930.4(PCDHB10):c.1665C>G (p.Asn555Lys)	not specified [RCV004843778]	uncertain significance	5	141194217	141194217	Human		name
597736798	CV3578887	single nucleotide variant	NM_018930.4(PCDHB10):c.1106A>T (p.Lys369Met)	not specified [RCV004843781]	uncertain significance	5	141193658	141193658	Human		name
597756051	CV3578888	single nucleotide variant	NM_018930.4(PCDHB10):c.1241G>C (p.Arg414Thr)	not specified [RCV004848063]	uncertain significance	5	141193793	141193793	Human		name
597736803	CV3578889	single nucleotide variant	NM_018930.4(PCDHB10):c.1714T>C (p.Cys572Arg)	not specified [RCV004843782]	uncertain significance	5	141194266	141194266	Human		name
597756055	CV3578892	single nucleotide variant	NM_018930.4(PCDHB10):c.1127G>C (p.Gly376Ala)	not specified [RCV004848064]	uncertain significance	5	141193679	141193679	Human		name
597736817	CV3578893	single nucleotide variant	NM_018930.4(PCDHB10):c.2221G>T (p.Val741Leu)	not specified [RCV004843785]	uncertain significance	5	141194773	141194773	Human		name
597736821	CV3578894	single nucleotide variant	NM_018931.3(PCDHB11):c.2220C>A (p.Ser740Arg)	not specified [RCV004843786]	uncertain significance	5	141201994	141201994	Human		name
597736841	CV3578898	single nucleotide variant	NM_018931.3(PCDHB11):c.1517T>A (p.Ile506Asn)	not specified [RCV004843790]	uncertain significance	5	141201291	141201291	Human		name
597756058	CV3578899	single nucleotide variant	NM_018931.3(PCDHB11):c.1783G>A (p.Asp595Asn)	not specified [RCV004848065]	uncertain significance	5	141201557	141201557	Human		name
597736846	CV3578900	single nucleotide variant	NM_018931.3(PCDHB11):c.1642C>T (p.Arg548Cys)	not specified [RCV004843791]	uncertain significance	5	141201416	141201416	Human		name
597736861	CV3578903	single nucleotide variant	NM_018931.3(PCDHB11):c.1780G>C (p.Gly594Arg)	not specified [RCV004843794]	uncertain significance	5	141201554	141201554	Human		name
597756062	CV3578905	single nucleotide variant	NM_018931.3(PCDHB11):c.1531G>C (p.Gly511Arg)	not specified [RCV004848066]	uncertain significance	5	141201305	141201305	Human		name
597736870	CV3578906	single nucleotide variant	NM_018931.3(PCDHB11):c.1433G>C (p.Arg478Thr)	not specified [RCV004843796]	uncertain significance	5	141201207	141201207	Human		name
597736880	CV3578908	single nucleotide variant	NM_018931.3(PCDHB11):c.1001T>G (p.Ile334Arg)	not specified [RCV004843798]	likely benign	5	141200775	141200775	Human		name
597756066	CV3578909	single nucleotide variant	NM_018931.3(PCDHB11):c.1477C>T (p.Pro493Ser)	not specified [RCV004848067]	uncertain significance	5	141201251	141201251	Human		name
597736890	CV3578911	single nucleotide variant	NM_018931.3(PCDHB11):c.1897C>G (p.Arg633Gly)	not specified [RCV004843800]	uncertain significance	5	141201671	141201671	Human		name
597736900	CV3578913	single nucleotide variant	NM_018931.3(PCDHB11):c.1379T>C (p.Val460Ala)	not specified [RCV004843802]	uncertain significance	5	141201153	141201153	Human		name
597756070	CV3578914	single nucleotide variant	NM_018931.3(PCDHB11):c.1164C>G (p.Asp388Glu)	not specified [RCV004848068]	uncertain significance	5	141200938	141200938	Human		name
597736905	CV3578915	single nucleotide variant	NM_018931.3(PCDHB11):c.1334A>G (p.Asn445Ser)	not specified [RCV004843803]	uncertain significance	5	141201108	141201108	Human		name
597756074	CV3578917	single nucleotide variant	NM_018931.3(PCDHB11):c.2376C>A (p.Ser792Arg)	not specified [RCV004848069]	uncertain significance	5	141202150	141202150	Human		name
597736916	CV3578918	single nucleotide variant	NM_018931.3(PCDHB11):c.1173C>A (p.Phe391Leu)	not specified [RCV004843805]	uncertain significance	5	141200947	141200947	Human		name
597736920	CV3578919	single nucleotide variant	NM_018931.3(PCDHB11):c.1243G>A (p.Ala415Thr)	not specified [RCV004843806]	uncertain significance	5	141201017	141201017	Human		name
597736925	CV3578920	single nucleotide variant	NM_018931.3(PCDHB11):c.1655T>C (p.Leu552Pro)	not specified [RCV004843807]	uncertain significance	5	141201429	141201429	Human		name
597756077	CV3578922	single nucleotide variant	NM_018931.3(PCDHB11):c.2205T>G (p.His735Gln)	not specified [RCV004848070]	uncertain significance	5	141201979	141201979	Human		name
597736935	CV3578924	single nucleotide variant	NM_018931.3(PCDHB11):c.2206C>A (p.Leu736Met)	not specified [RCV004843809]	uncertain significance	5	141201980	141201980	Human		name
597736940	CV3578925	single nucleotide variant	NM_018931.3(PCDHB11):c.1291C>A (p.Leu431Met)	not specified [RCV004843810]	uncertain significance	5	141201065	141201065	Human		name
598269498	CV3996046	single nucleotide variant	NM_018930.4(PCDHB10):c.1789G>A (p.Gly597Ser)	not specified [RCV005388796]	uncertain significance	5	141194341	141194341	Human		name
598269504	CV3996047	single nucleotide variant	NM_018930.4(PCDHB10):c.1104T>A (p.Phe368Leu)	not specified [RCV005388797]	uncertain significance	5	141193656	141193656	Human		name
598195440	CV3996048	single nucleotide variant	NM_018930.4(PCDHB10):c.2024A>G (p.Glu675Gly)	not specified [RCV005397535]	uncertain significance	5	141194576	141194576	Human		name
598269513	CV3996051	single nucleotide variant	NM_018930.4(PCDHB10):c.1008A>T (p.Glu336Asp)	not specified [RCV005388800]	uncertain significance	5	141193560	141193560	Human		name
598195446	CV3996052	single nucleotide variant	NM_018930.4(PCDHB10):c.1448A>G (p.Asn483Ser)	not specified [RCV005397536]	uncertain significance	5	141194000	141194000	Human		name
598269518	CV3996053	single nucleotide variant	NM_018930.4(PCDHB10):c.1681G>T (p.Val561Leu)	not specified [RCV005388801]	uncertain significance	5	141194233	141194233	Human		name
598269524	CV3996054	single nucleotide variant	NM_018931.3(PCDHB11):c.1460A>C (p.Asn487Thr)	not specified [RCV005388802]	likely benign	5	141201234	141201234	Human		name
598195452	CV3996055	single nucleotide variant	NM_018931.3(PCDHB11):c.2158G>A (p.Ala720Thr)	not specified [RCV005397537]	uncertain significance	5	141201932	141201932	Human		name
598195466	CV3996059	single nucleotide variant	NM_018931.3(PCDHB11):c.2107T>C (p.Phe703Leu)	not specified [RCV005397539]	likely benign	5	141201881	141201881	Human		name
598269540	CV3996061	single nucleotide variant	NM_018931.3(PCDHB11):c.1252A>G (p.Asn418Asp)	not specified [RCV005388806]	uncertain significance	5	141201026	141201026	Human		name
598269553	CV3996064	single nucleotide variant	NM_018931.3(PCDHB11):c.2144G>A (p.Arg715Lys)	not specified [RCV005388809]	uncertain significance	5	141201918	141201918	Human		name
598269569	CV3996069	single nucleotide variant	NM_018932.4(PCDHB12):c.2074G>A (p.Val692Met)	not specified [RCV005388813]	uncertain significance	5	141210981	141210981	Human		name
598269574	CV3996070	single nucleotide variant	NM_018932.4(PCDHB12):c.1591G>C (p.Val531Leu)	not specified [RCV005388814]	uncertain significance	5	141210498	141210498	Human		name
598269579	CV3996071	single nucleotide variant	NM_018932.4(PCDHB12):c.2204A>G (p.His735Arg)	not specified [RCV005388815]	uncertain significance	5	141211111	141211111	Human		name
598269591	CV3996074	single nucleotide variant	NM_018932.4(PCDHB12):c.1030G>T (p.Ala344Ser)	not specified [RCV005388818]	uncertain significance	5	141209937	141209937	Human		name
598269596	CV3996075	single nucleotide variant	NM_018932.4(PCDHB12):c.1835C>T (p.Pro612Leu)	not specified [RCV005388819]	uncertain significance	5	141210742	141210742	Human		name
598195481	CV3996076	single nucleotide variant	NM_018932.4(PCDHB12):c.1879G>T (p.Ala627Ser)	not specified [RCV005397541]	uncertain significance	5	141210786	141210786	Human		name
598269601	CV3996077	single nucleotide variant	NM_018932.4(PCDHB12):c.1016A>G (p.Asp339Gly)	not specified [RCV005388820]	uncertain significance	5	141209923	141209923	Human		name
598269610	CV3996079	single nucleotide variant	NM_018932.4(PCDHB12):c.1741G>A (p.Glu581Lys)	not specified [RCV005388822]	uncertain significance	5	141210648	141210648	Human		name
598269620	CV3996081	single nucleotide variant	NM_018932.4(PCDHB12):c.1483G>A (p.Asp495Asn)	not specified [RCV005388824]	uncertain significance	5	141210390	141210390	Human		name
598269623	CV3996082	single nucleotide variant	NM_018932.4(PCDHB12):c.1546C>G (p.Leu516Val)	not specified [RCV005388825]	uncertain significance	5	141210453	141210453	Human		name
598269630	CV3996083	single nucleotide variant	NM_018932.4(PCDHB12):c.2222G>A (p.Gly741Asp)	not specified [RCV005388826]	uncertain significance	5	141211129	141211129	Human		name
598269632	CV3996084	single nucleotide variant	NM_018932.4(PCDHB12):c.1634C>T (p.Ala545Val)	not specified [RCV005388827]	uncertain significance	5	141210541	141210541	Human		name
598269655	CV3996088	single nucleotide variant	NM_018933.4(PCDHB13):c.1417G>A (p.Val473Ile)	not specified [RCV005388831]	uncertain significance	5	141215540	141215540	Human		name
598269662	CV3996090	single nucleotide variant	NM_018933.4(PCDHB13):c.2305C>G (p.Pro769Ala)	not specified [RCV005388833]	uncertain significance	5	141216428	141216428	Human		name
598195487	CV3996091	single nucleotide variant	NM_018933.4(PCDHB13):c.1874G>C (p.Arg625Pro)	not specified [RCV005397542]	uncertain significance	5	141215997	141215997	Human		name
598269687	CV3996096	single nucleotide variant	NM_018933.4(PCDHB13):c.1327G>A (p.Asp443Asn)	not specified [RCV005388838]	uncertain significance	5	141215450	141215450	Human		name
598269697	CV3996098	single nucleotide variant	NM_018933.4(PCDHB13):c.2116C>T (p.Leu706Phe)	not specified [RCV005388840]	uncertain significance	5	141216239	141216239	Human		name
598195493	CV3996099	single nucleotide variant	NM_018933.4(PCDHB13):c.2389A>G (p.Ile797Val)	not specified [RCV005397543]	uncertain significance	5	141216512	141216512	Human		name
598269703	CV3996101	single nucleotide variant	NM_018933.4(PCDHB13):c.1532G>A (p.Gly511Asp)	not specified [RCV005388842]	uncertain significance	5	141215655	141215655	Human		name
598269718	CV3996104	single nucleotide variant	NM_018934.4(PCDHB14):c.2246A>G (p.Tyr749Cys)	not specified [RCV005388845]	uncertain significance	5	141225751	141225751	Human		name
598269723	CV3996105	single nucleotide variant	NM_018934.4(PCDHB14):c.1248G>C (p.Glu416Asp)	not specified [RCV005388846]	uncertain significance	5	141224753	141224753	Human		name
598269728	CV3996106	single nucleotide variant	NM_018934.4(PCDHB14):c.1660G>A (p.Ala554Thr)	not specified [RCV005388847]	uncertain significance	5	141225165	141225165	Human		name
598269738	CV3996108	single nucleotide variant	NM_018934.4(PCDHB14):c.2332G>C (p.Asp778His)	not specified [RCV005388849]	uncertain significance	5	141225837	141225837	Human		name
598195499	CV3996109	single nucleotide variant	NM_018934.4(PCDHB14):c.1516A>G (p.Ile506Val)	not specified [RCV005397544]	uncertain significance	5	141225021	141225021	Human		name
598269743	CV3996110	single nucleotide variant	NM_018934.4(PCDHB14):c.1308C>G (p.Asn436Lys)	not specified [RCV005388850]	uncertain significance	5	141224813	141224813	Human		name
598269753	CV3996112	single nucleotide variant	NM_018934.4(PCDHB14):c.1530T>G (p.Asn510Lys)	not specified [RCV005388852]	uncertain significance	5	141225035	141225035	Human		name
598269759	CV3996113	single nucleotide variant	NM_018934.4(PCDHB14):c.1480C>G (p.Gln494Glu)	not specified [RCV005388853]	uncertain significance	5	141224985	141224985	Human		name
598269763	CV3996114	single nucleotide variant	NM_018934.4(PCDHB14):c.1702G>A (p.Gly568Ser)	not specified [RCV005388854]	uncertain significance	5	141225207	141225207	Human		name
598269768	CV3996115	single nucleotide variant	NM_018934.4(PCDHB14):c.1390A>C (p.Asn464His)	not specified [RCV005388855]	uncertain significance	5	141224895	141224895	Human		name
598269774	CV3996116	single nucleotide variant	NM_018935.4(PCDHB15):c.1315G>T (p.Val439Leu)	not specified [RCV005388856]	uncertain significance	5	141246893	141246893	Human		name
598269779	CV3996117	single nucleotide variant	NM_018935.4(PCDHB15):c.2060C>A (p.Thr687Asn)	not specified [RCV005388857]	uncertain significance	5	141247638	141247638	Human		name
598269783	CV3996118	single nucleotide variant	NM_018935.4(PCDHB15):c.1720G>A (p.Glu574Lys)	not specified [RCV005388858]	uncertain significance	5	141247298	141247298	Human		name
598269788	CV3996119	single nucleotide variant	NM_018935.4(PCDHB15):c.2062G>C (p.Val688Leu)	not specified [RCV005388859]	uncertain significance	5	141247640	141247640	Human		name
598269798	CV3996122	single nucleotide variant	NM_018935.4(PCDHB15):c.2060C>G (p.Thr687Ser)	not specified [RCV005388861]	uncertain significance	5	141247638	141247638	Human		name
598269808	CV3996124	single nucleotide variant	NM_018935.4(PCDHB15):c.1787C>T (p.Ser596Leu)	not specified [RCV005388863]	uncertain significance	5	141247365	141247365	Human		name
598269813	CV3996125	single nucleotide variant	NM_018935.4(PCDHB15):c.1370C>T (p.Thr457Ile)	not specified [RCV005388864]	uncertain significance	5	141246948	141246948	Human		name
598269818	CV3996127	single nucleotide variant	NM_018935.4(PCDHB15):c.2125G>A (p.Val709Met)	not specified [RCV005388865]	uncertain significance	5	141247703	141247703	Human		name
598269823	CV3996128	single nucleotide variant	NM_018935.4(PCDHB15):c.1228G>A (p.Asp410Asn)	not specified [RCV005388866]	uncertain significance	5	141246806	141246806	Human		name
598195518	CV3996129	single nucleotide variant	NM_018935.4(PCDHB15):c.1378G>C (p.Val460Leu)	not specified [RCV005397547]	uncertain significance	5	141246956	141246956	Human		name
598269833	CV3996131	single nucleotide variant	NM_020957.4(PCDHB16):c.2215G>A (p.Val739Ile)	not specified [RCV005388868]	uncertain significance	5	141184774	141184774	Human		name
598269839	CV3996132	single nucleotide variant	NM_020957.4(PCDHB16):c.1334A>G (p.Asn445Ser)	not specified [RCV005388869]	uncertain significance	5	141183893	141183893	Human		name
598195524	CV3996133	single nucleotide variant	NM_020957.4(PCDHB16):c.1192A>G (p.Lys398Glu)	not specified [RCV005397548]	uncertain significance	5	141183751	141183751	Human		name
598269844	CV3996134	single nucleotide variant	NM_020957.4(PCDHB16):c.2230A>G (p.Thr744Ala)	not specified [RCV005388870]	uncertain significance	5	141184789	141184789	Human		name
598269884	CV3996142	single nucleotide variant	NM_020957.4(PCDHB16):c.1237G>A (p.Ala413Thr)	not specified [RCV005388878]	uncertain significance	5	141183796	141183796	Human		name
598269889	CV3996143	single nucleotide variant	NM_020957.4(PCDHB16):c.1648C>G (p.Leu550Val)	not specified [RCV005388879]	uncertain significance	5	141184207	141184207	Human		name
598269894	CV3996144	single nucleotide variant	NM_020957.4(PCDHB16):c.1589G>C (p.Arg530Pro)	not specified [RCV005388880]	uncertain significance	5	141184148	141184148	Human		name
598269897	CV3996145	single nucleotide variant	NM_020957.4(PCDHB16):c.2083G>A (p.Ala695Thr)	not specified [RCV005388881]	uncertain significance	5	141184642	141184642	Human		name
598269903	CV3996146	single nucleotide variant	NM_020957.4(PCDHB16):c.1765G>A (p.Val589Met)	not specified [RCV005388882]	uncertain significance	5	141184324	141184324	Human		name
598195434	CV3999532	single nucleotide variant	NM_018930.4(PCDHB10):c.2083G>A (p.Ala695Thr)	not specified [RCV005397534]	uncertain significance	5	141194635	141194635	Human		name
598269466	CV3999533	single nucleotide variant	NM_018930.4(PCDHB10):c.1378G>C (p.Val460Leu)	not specified [RCV005388789]	uncertain significance	5	141193930	141193930	Human		name
598269471	CV3999534	single nucleotide variant	NM_018930.4(PCDHB10):c.2140C>G (p.Arg714Gly)	not specified [RCV005388790]	uncertain significance	5	141194692	141194692	Human		name
598269478	CV3999536	single nucleotide variant	NM_018930.4(PCDHB10):c.1313C>T (p.Thr438Met)	not specified [RCV005388792]	uncertain significance	5	141193865	141193865	Human		name
598269484	CV3999537	single nucleotide variant	NM_018930.4(PCDHB10):c.2275G>A (p.Gly759Arg)	not specified [RCV005388793]	uncertain significance	5	141194827	141194827	Human		name
15157429	CV698873	single nucleotide variant	NM_018931.3(PCDHB11):c.1584C>G (p.Asp528Glu)	not provided [RCV000946882]	benign	5	141201358	141201358	Human		name
8625938	CV81077	single nucleotide variant	NM_018931.2(PCDHB11):c.2231C>T (p.Thr744Ile)	Malignant melanoma [RCV000061155]	not provided	5	141202005	141202005	Human		name
8625940	CV81079	single nucleotide variant	NM_018932.3(PCDHB12):c.2327C>T (p.Pro776Leu)	Malignant melanoma [RCV000061157]	not provided	5	141211234	141211234	Human		name
8625943	CV81082	single nucleotide variant	NM_018935.3(PCDHB15):c.2153G>A (p.Arg718Lys)	Malignant melanoma [RCV000061160]	not provided	5	141247731	141247731	Human		name
8631440	CV86627	single nucleotide variant	NM_020957.3(PCDHB16):c.2014C>T (p.Pro672Ser)	Malignant melanoma [RCV000066718]	not provided	5	141184573	141184573	Human		name
8631441	CV86628	single nucleotide variant	NM_020957.3(PCDHB16):c.2015C>T (p.Pro672Leu)	Malignant melanoma [RCV000066719]	not provided	5	141184574	141184574	Human		name
8631444	CV86631	single nucleotide variant	NM_018930.3(PCDHB10):c.2321C>T (p.Ser774Leu)	Malignant melanoma [RCV000066722]	not provided	5	141194873	141194873	Human		name
8631445	CV86632	single nucleotide variant	NM_018931.2(PCDHB11):c.2314C>T (p.Pro772Ser)	Malignant melanoma [RCV000066723]	not provided	5	141202088	141202088	Human		name
8631448	CV86635	single nucleotide variant	NM_018933.3(PCDHB13):c.2344G>A (p.Glu782Lys)	Malignant melanoma [RCV000066726]	not provided	5	141216467	141216467	Human		name

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