Ppp1r13b Variant Search Result - Rat Genome Database

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127 records found for search term Ppp1r13b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329354298	CV2437858	single nucleotide variant	NM_015316.3(PPP1R13B):c.86G>A (p.Arg29Gln)	not specified [RCV004261147]	uncertain significance	14	103797442	103797442	Human		name
597758807	CV3587617	single nucleotide variant	NM_015316.3(PPP1R13B):c.77C>T (p.Thr26Ile)	not specified [RCV004848613]	uncertain significance	14	103797451	103797451	Human		name
10448556	CV204622	single nucleotide variant	NM_015316.3(PPP1R13B):c.215G>A (p.Arg72Gln)	Childhood-onset schizophrenia [RCV000202339]	benign	14	103784857	103784857	Human	1	name
155929198	CV2277998	single nucleotide variant	NM_015316.3(PPP1R13B):c.283C>T (p.Arg95Cys)	not specified [RCV004141234]	uncertain significance	14	103778816	103778816	Human		name
156049293	CV2319295	single nucleotide variant	NM_015316.3(PPP1R13B):c.181A>G (p.Met61Val)	not specified [RCV004180121]	uncertain significance	14	103784891	103784891	Human		name
156071943	CV2325264	single nucleotide variant	NM_015316.3(PPP1R13B):c.194A>G (p.His65Arg)	not specified [RCV004177662]	uncertain significance	14	103784878	103784878	Human		name
156154495	CV2388715	single nucleotide variant	NM_015316.3(PPP1R13B):c.259A>G (p.Thr87Ala)	not specified [RCV004239585]	likely benign	14	103784813	103784813	Human		name
401915570	CV2807309	single nucleotide variant	NM_015316.3(PPP1R13B):c.2271T>C (p.Asp757=)	not provided [RCV003400648]	likely benign	14	103740145	103740145	Human		name
405795094	CV3366579	single nucleotide variant	NM_015316.3(PPP1R13B):c.218G>C (p.Arg73Thr)	not specified [RCV004507281]	uncertain significance	14	103784854	103784854	Human		name
597758872	CV3587630	single nucleotide variant	NM_015316.3(PPP1R13B):c.190G>A (p.Glu64Lys)	not specified [RCV004848626]	uncertain significance	14	103784882	103784882	Human		name
15139355	CV714011	single nucleotide variant	NM_015316.3(PPP1R13B):c.2790C>T (p.Cys930=)	not provided [RCV000965951]	benign	14	103738753	103738753	Human		name
15147430	CV714013	single nucleotide variant	NM_015316.3(PPP1R13B):c.2154C>T (p.Gly718=)	not provided [RCV000967338]	benign	14	103740262	103740262	Human		name
15147438	CV714014	single nucleotide variant	NM_015316.3(PPP1R13B):c.1884C>T (p.His628=)	not provided [RCV000967339]	benign	14	103740532	103740532	Human		name
15159104	CV714015	single nucleotide variant	NM_015316.3(PPP1R13B):c.1659T>C (p.Ile553=)	not provided [RCV000969647]	benign	14	103741953	103741953	Human		name
15167240	CV725573	single nucleotide variant	NM_015316.3(PPP1R13B):c.2880C>T (p.Cys960=)	not provided [RCV000882806]	benign	14	103737845	103737845	Human		name
156182867	CV2222334	single nucleotide variant	NM_015316.3(PPP1R13B):c.881A>T (p.Glu294Val)	not specified [RCV004105343]	uncertain significance	14	103749882	103749882	Human		name
156288543	CV2229779	single nucleotide variant	NM_015316.3(PPP1R13B):c.494G>A (p.Arg165His)	not specified [RCV004105356]	uncertain significance	14	103754207	103754207	Human		name
156229547	CV2234981	single nucleotide variant	NM_015316.3(PPP1R13B):c.791C>T (p.Ala264Val)	not specified [RCV004113177]	uncertain significance	14	103753037	103753037	Human		name
156142376	CV2288695	single nucleotide variant	NM_015316.3(PPP1R13B):c.526C>A (p.Leu176Ile)	not specified [RCV004153986]	uncertain significance	14	103754175	103754175	Human		name
156120290	CV2354155	single nucleotide variant	NM_015316.3(PPP1R13B):c.374A>G (p.Glu125Gly)	not specified [RCV004206590]	uncertain significance	14	103757732	103757732	Human		name
156148622	CV2394504	single nucleotide variant	NM_015316.3(PPP1R13B):c.882A>T (p.Glu294Asp)	not specified [RCV004240863]	uncertain significance	14	103749881	103749881	Human		name
329395074	CV2457844	single nucleotide variant	NM_015316.3(PPP1R13B):c.314A>G (p.Asn105Ser)	not specified [RCV004269654]	uncertain significance	14	103778785	103778785	Human		name
401719324	CV2679496	single nucleotide variant	NM_015316.3(PPP1R13B):c.367C>T (p.Arg123Cys)	not specified [RCV004287800]	uncertain significance	14	103757739	103757739	Human		name
401738461	CV2721883	single nucleotide variant	NM_015316.3(PPP1R13B):c.946C>T (p.Arg316Cys)	not specified [RCV004326391]	uncertain significance	14	103749817	103749817	Human		name
401768346	CV2735272	single nucleotide variant	NM_015316.3(PPP1R13B):c.491G>A (p.Arg164His)	not specified [RCV004333944]	uncertain significance	14	103754210	103754210	Human		name
401915567	CV2807308	single nucleotide variant	NM_015316.3(PPP1R13B):c.3123C>T (p.His1041=)	not provided [RCV003400647]	likely benign	14	103736111	103736111	Human		name
405795133	CV3366592	single nucleotide variant	NM_015316.3(PPP1R13B):c.302G>A (p.Arg101Gln)	not specified [RCV004507294]	uncertain significance	14	103778797	103778797	Human		name
405795250	CV3366596	single nucleotide variant	NM_015316.3(PPP1R13B):c.340C>T (p.Arg114Cys)	not specified [RCV004507298]	uncertain significance	14	103778759	103778759	Human		name
405795148	CV3366597	single nucleotide variant	NM_015316.3(PPP1R13B):c.859T>C (p.Ser287Pro)	not specified [RCV004507299]	uncertain significance	14	103749904	103749904	Human		name
407529767	CV3471564	single nucleotide variant	NM_015316.3(PPP1R13B):c.605A>G (p.Tyr202Cys)	not specified [RCV004656207]	uncertain significance	14	103754096	103754096	Human		name
407529769	CV3471565	single nucleotide variant	NM_015316.3(PPP1R13B):c.947G>A (p.Arg316His)	not specified [RCV004656208]	uncertain significance	14	103749816	103749816	Human		name
597758821	CV3587620	single nucleotide variant	NM_015316.3(PPP1R13B):c.794C>A (p.Ala265Glu)	not specified [RCV004848616]	uncertain significance	14	103753034	103753034	Human		name
597758826	CV3587621	single nucleotide variant	NM_015316.3(PPP1R13B):c.782C>T (p.Thr261Met)	not specified [RCV004848617]	uncertain significance	14	103753046	103753046	Human		name
597758830	CV3587622	single nucleotide variant	NM_015316.3(PPP1R13B):c.833G>A (p.Arg278His)	not specified [RCV004848618]	uncertain significance	14	103749930	103749930	Human		name
597758867	CV3587629	single nucleotide variant	NM_015316.3(PPP1R13B):c.890A>G (p.Asn297Ser)	not specified [RCV004848625]	uncertain significance	14	103749873	103749873	Human		name
597758882	CV3587632	single nucleotide variant	NM_015316.3(PPP1R13B):c.580C>T (p.Arg194Cys)	not specified [RCV004848628]	uncertain significance	14	103754121	103754121	Human		name
598169334	CV3897562	single nucleotide variant	NM_015316.3(PPP1R13B):c.931A>G (p.Ser311Gly)	not specified [RCV005262773]	uncertain significance	14	103749832	103749832	Human		name
598169343	CV3897564	single nucleotide variant	NM_015316.3(PPP1R13B):c.853C>G (p.Gln285Glu)	not specified [RCV005262775]	uncertain significance	14	103749910	103749910	Human		name
598169393	CV3897574	single nucleotide variant	NM_015316.3(PPP1R13B):c.729A>C (p.Glu243Asp)	not specified [RCV005262784]	uncertain significance	14	103753099	103753099	Human		name
15106893	CV714016	single nucleotide variant	NM_015316.3(PPP1R13B):c.508A>G (p.Ile170Val)	not provided [RCV000960174]	benign\|likely benign	14	103754193	103754193	Human		name
156234472	CV2193311	single nucleotide variant	NM_015316.3(PPP1R13B):c.1792C>T (p.His598Tyr)	not specified [RCV004071613]	uncertain significance	14	103741820	103741820	Human		name
156324494	CV2198724	single nucleotide variant	NM_015316.3(PPP1R13B):c.2641G>A (p.Gly881Arg)	not specified [RCV004075731]	uncertain significance	14	103738975	103738975	Human		name
156400334	CV2199115	single nucleotide variant	NM_015316.3(PPP1R13B):c.1310C>T (p.Thr437Met)	not specified [RCV004080511]	uncertain significance	14	103742664	103742664	Human		name
156098250	CV2207035	single nucleotide variant	NM_015316.3(PPP1R13B):c.2447C>T (p.Pro816Leu)	not specified [RCV004085648]	uncertain significance	14	103739969	103739969	Human		name
155940552	CV2222186	single nucleotide variant	NM_015316.3(PPP1R13B):c.2785G>A (p.Val929Ile)	not specified [RCV004104936]	uncertain significance	14	103738758	103738758	Human		name
155980094	CV2222973	single nucleotide variant	NM_015316.3(PPP1R13B):c.2599C>T (p.Arg867Trp)	not specified [RCV004103565]	uncertain significance	14	103739017	103739017	Human		name
156179910	CV2225797	single nucleotide variant	NM_015316.3(PPP1R13B):c.1483C>A (p.Pro495Thr)	not specified [RCV004103204]	uncertain significance	14	103742129	103742129	Human		name
155974564	CV2235726	single nucleotide variant	NM_015316.3(PPP1R13B):c.1969C>T (p.Pro657Ser)	not specified [RCV004111863]	uncertain significance	14	103740447	103740447	Human		name
155981176	CV2244046	single nucleotide variant	NM_015316.3(PPP1R13B):c.1549C>A (p.Gln517Lys)	not specified [RCV004108529]	uncertain significance	14	103742063	103742063	Human		name
155960892	CV2249533	single nucleotide variant	NM_015316.3(PPP1R13B):c.1349C>A (p.Pro450His)	not specified [RCV004120562]	uncertain significance	14	103742263	103742263	Human		name
155901730	CV2294628	single nucleotide variant	NM_015316.3(PPP1R13B):c.1570G>C (p.Val524Leu)	not specified [RCV004161883]	uncertain significance	14	103742042	103742042	Human		name
156193007	CV2301930	single nucleotide variant	NM_015316.3(PPP1R13B):c.2945C>T (p.Ala982Val)	not specified [RCV004156710]	uncertain significance	14	103737780	103737780	Human		name
156117422	CV2349468	single nucleotide variant	NM_015316.3(PPP1R13B):c.2840T>C (p.Val947Ala)	not specified [RCV004201441]	uncertain significance	14	103738703	103738703	Human		name
155981581	CV2351365	single nucleotide variant	NM_015316.3(PPP1R13B):c.1682G>A (p.Gly561Glu)	not specified [RCV004193063]	uncertain significance	14	103741930	103741930	Human		name
156248824	CV2362276	single nucleotide variant	NM_015316.3(PPP1R13B):c.1847C>T (p.Ser616Leu)	not specified [RCV004210065]	uncertain significance	14	103740569	103740569	Human		name
156033672	CV2376610	single nucleotide variant	NM_015316.3(PPP1R13B):c.1684T>G (p.Ser562Ala)	not specified [RCV004222815]	uncertain significance	14	103741928	103741928	Human		name
155959446	CV2390533	single nucleotide variant	NM_015316.3(PPP1R13B):c.1784C>T (p.Pro595Leu)	not specified [RCV004239068]	uncertain significance	14	103741828	103741828	Human		name
329383339	CV2434504	single nucleotide variant	NM_015316.3(PPP1R13B):c.2398G>A (p.Glu800Lys)	not specified [RCV004254211]	uncertain significance	14	103740018	103740018	Human		name
329399892	CV2444338	single nucleotide variant	NM_015316.3(PPP1R13B):c.2186G>A (p.Arg729His)	not specified [RCV004263092]	uncertain significance	14	103740230	103740230	Human		name
329354547	CV2448390	single nucleotide variant	NM_015316.3(PPP1R13B):c.1355C>T (p.Pro452Leu)	not provided [RCV004696371]\|not specified [RCV004256675]	uncertain significance	14	103742257	103742257	Human		name
401719237	CV2679464	single nucleotide variant	NM_015316.3(PPP1R13B):c.1502C>T (p.Thr501Ile)	not specified [RCV004287773]	uncertain significance	14	103742110	103742110	Human		name
401726076	CV2699069	single nucleotide variant	NM_015316.3(PPP1R13B):c.2489C>T (p.Thr830Met)	not specified [RCV004303583]	uncertain significance	14	103739927	103739927	Human		name
401762312	CV2723395	single nucleotide variant	NM_015316.3(PPP1R13B):c.1956T>A (p.Asp652Glu)	not specified [RCV004329601]	likely benign	14	103740460	103740460	Human		name
401783685	CV2723841	single nucleotide variant	NM_015316.3(PPP1R13B):c.2522C>T (p.Pro841Leu)	not specified [RCV004325983]	uncertain significance	14	103739894	103739894	Human		name
401857203	CV2755657	single nucleotide variant	NM_015316.3(PPP1R13B):c.1111A>C (p.Ser371Arg)	not specified [RCV004342042]	uncertain significance	14	103746412	103746412	Human		name
401860167	CV2765486	single nucleotide variant	NM_015316.3(PPP1R13B):c.1510C>T (p.Pro504Ser)	not specified [RCV004341798]	uncertain significance	14	103742102	103742102	Human		name
401887928	CV2781766	single nucleotide variant	NM_015316.3(PPP1R13B):c.2209A>G (p.Met737Val)	not specified [RCV004356730]	uncertain significance	14	103740207	103740207	Human		name
405795246	CV3366570	single nucleotide variant	NM_015316.3(PPP1R13B):c.1019C>T (p.Ser340Leu)	not specified [RCV004507272]	uncertain significance	14	103746504	103746504	Human		name
405795144	CV3366571	single nucleotide variant	NM_015316.3(PPP1R13B):c.1043C>G (p.Pro348Arg)	not specified [RCV004507273]	uncertain significance	14	103746480	103746480	Human		name
405795073	CV3366572	single nucleotide variant	NM_015316.3(PPP1R13B):c.1139G>T (p.Arg380Ile)	not specified [RCV004507274]	uncertain significance	14	103746384	103746384	Human		name
405795075	CV3366573	single nucleotide variant	NM_015316.3(PPP1R13B):c.1241G>T (p.Ser414Ile)	not specified [RCV004507275]	uncertain significance	14	103742733	103742733	Human		name
405795078	CV3366574	single nucleotide variant	NM_015316.3(PPP1R13B):c.1533G>T (p.Gln511His)	not specified [RCV004507276]	uncertain significance	14	103742079	103742079	Human		name
405795081	CV3366575	single nucleotide variant	NM_015316.3(PPP1R13B):c.1898C>T (p.Thr633Met)	not specified [RCV004507277]	uncertain significance	14	103740518	103740518	Human		name
405795084	CV3366576	single nucleotide variant	NM_015316.3(PPP1R13B):c.1954G>A (p.Asp652Asn)	not specified [RCV004507278]	uncertain significance	14	103740462	103740462	Human		name
405795088	CV3366577	single nucleotide variant	NM_015316.3(PPP1R13B):c.2131A>G (p.Ile711Val)	not specified [RCV004507279]	uncertain significance	14	103740285	103740285	Human		name
405795091	CV3366578	single nucleotide variant	NM_015316.3(PPP1R13B):c.2152G>A (p.Gly718Ser)	not specified [RCV004507280]	uncertain significance	14	103740264	103740264	Human		name
405795097	CV3366580	single nucleotide variant	NM_015316.3(PPP1R13B):c.2308G>A (p.Glu770Lys)	not specified [RCV004507282]	uncertain significance	14	103740108	103740108	Human		name
405795100	CV3366581	single nucleotide variant	NM_015316.3(PPP1R13B):c.2323G>A (p.Ala775Thr)	not specified [RCV004507283]	uncertain significance	14	103740093	103740093	Human		name
405795103	CV3366582	single nucleotide variant	NM_015316.3(PPP1R13B):c.2375A>G (p.Asn792Ser)	not specified [RCV004507284]	uncertain significance	14	103740041	103740041	Human		name
405795106	CV3366583	single nucleotide variant	NM_015316.3(PPP1R13B):c.2395C>T (p.Pro799Ser)	not specified [RCV004507285]	uncertain significance	14	103740021	103740021	Human		name
405795109	CV3366584	single nucleotide variant	NM_015316.3(PPP1R13B):c.2428A>G (p.Thr810Ala)	not specified [RCV004507286]	uncertain significance	14	103739988	103739988	Human		name
405795112	CV3366585	single nucleotide variant	NM_015316.3(PPP1R13B):c.2496G>C (p.Gln832His)	not specified [RCV004507287]	uncertain significance	14	103739920	103739920	Human		name
405795116	CV3366586	single nucleotide variant	NM_015316.3(PPP1R13B):c.2497A>T (p.Ile833Phe)	not specified [RCV004507288]	uncertain significance	14	103739919	103739919	Human		name
405795119	CV3366587	single nucleotide variant	NM_015316.3(PPP1R13B):c.2521C>T (p.Pro841Ser)	not specified [RCV004507289]	uncertain significance	14	103739895	103739895	Human		name
405795121	CV3366588	single nucleotide variant	NM_015316.3(PPP1R13B):c.2596A>G (p.Lys866Glu)	not specified [RCV004507290]	uncertain significance	14	103739020	103739020	Human		name
405795124	CV3366589	single nucleotide variant	NM_015316.3(PPP1R13B):c.2666T>C (p.Leu889Pro)	not specified [RCV004507291]	uncertain significance	14	103738950	103738950	Human		name
405795127	CV3366590	single nucleotide variant	NM_015316.3(PPP1R13B):c.2791G>A (p.Ala931Thr)	not specified [RCV004507292]	uncertain significance	14	103738752	103738752	Human		name
405795130	CV3366591	single nucleotide variant	NM_015316.3(PPP1R13B):c.2806A>G (p.Ile936Val)	not specified [RCV004507293]	uncertain significance	14	103738737	103738737	Human		name
407529753	CV3471557	single nucleotide variant	NM_015316.3(PPP1R13B):c.1474G>A (p.Ala492Thr)	not specified [RCV004656200]	uncertain significance	14	103742138	103742138	Human		name
407529755	CV3471558	single nucleotide variant	NM_015316.3(PPP1R13B):c.2291A>G (p.Asn764Ser)	not specified [RCV004656201]	uncertain significance	14	103740125	103740125	Human		name
407529757	CV3471559	single nucleotide variant	NM_015316.3(PPP1R13B):c.2002C>T (p.Arg668Trp)	not specified [RCV004656202]	uncertain significance	14	103740414	103740414	Human		name
407529759	CV3471560	single nucleotide variant	NM_015316.3(PPP1R13B):c.1987G>A (p.Val663Met)	not specified [RCV004656203]	uncertain significance	14	103740429	103740429	Human		name
407529761	CV3471561	single nucleotide variant	NM_015316.3(PPP1R13B):c.2256G>C (p.Met752Ile)	not specified [RCV004656204]	uncertain significance	14	103740160	103740160	Human		name
407529763	CV3471562	single nucleotide variant	NM_015316.3(PPP1R13B):c.2563C>T (p.Pro855Ser)	not specified [RCV004656205]	uncertain significance	14	103739853	103739853	Human		name
407529771	CV3471566	single nucleotide variant	NM_015316.3(PPP1R13B):c.1513G>A (p.Ala505Thr)	not specified [RCV004656209]	uncertain significance	14	103742099	103742099	Human		name
597758803	CV3587616	single nucleotide variant	NM_015316.3(PPP1R13B):c.2455G>A (p.Asp819Asn)	not specified [RCV004848612]	uncertain significance	14	103739961	103739961	Human		name
597758811	CV3587618	single nucleotide variant	NM_015316.3(PPP1R13B):c.1901G>A (p.Gly634Asp)	not specified [RCV004848614]	uncertain significance	14	103740515	103740515	Human		name
597758835	CV3587623	single nucleotide variant	NM_015316.3(PPP1R13B):c.2905C>T (p.Leu969Phe)	not specified [RCV004848619]	uncertain significance	14	103737820	103737820	Human		name
597758839	CV3587624	single nucleotide variant	NM_015316.3(PPP1R13B):c.2629C>T (p.Arg877Trp)	not specified [RCV004848620]	uncertain significance	14	103738987	103738987	Human		name
597758849	CV3587626	single nucleotide variant	NM_015316.3(PPP1R13B):c.2203G>A (p.Gly735Ser)	not specified [RCV004848622]	uncertain significance	14	103740213	103740213	Human		name
597758854	CV3587627	single nucleotide variant	NM_015316.3(PPP1R13B):c.1889C>T (p.Ser630Leu)	not specified [RCV004848623]	uncertain significance	14	103740527	103740527	Human		name
597758877	CV3587631	single nucleotide variant	NM_015316.3(PPP1R13B):c.2758G>A (p.Glu920Lys)	not specified [RCV004848627]	uncertain significance	14	103738785	103738785	Human		name
597758887	CV3587633	single nucleotide variant	NM_015316.3(PPP1R13B):c.1663C>T (p.Pro555Ser)	not specified [RCV004848629]	uncertain significance	14	103741949	103741949	Human		name
598169340	CV3897563	single nucleotide variant	NM_015316.3(PPP1R13B):c.1471A>C (p.Ser491Arg)	not specified [RCV005262774]	uncertain significance	14	103742141	103742141	Human		name
598169349	CV3897565	single nucleotide variant	NM_015316.3(PPP1R13B):c.1424C>T (p.Ser475Leu)	not specified [RCV005262776]	uncertain significance	14	103742188	103742188	Human		name
598169356	CV3897566	single nucleotide variant	NM_015316.3(PPP1R13B):c.1798G>A (p.Ala600Thr)	not specified [RCV005262777]	likely benign	14	103741814	103741814	Human		name
598202872	CV3897567	single nucleotide variant	NM_015316.3(PPP1R13B):c.2395C>G (p.Pro799Ala)	not specified [RCV005269286]	uncertain significance	14	103740021	103740021	Human		name
598169361	CV3897568	single nucleotide variant	NM_015316.3(PPP1R13B):c.1742C>A (p.Ser581Tyr)	not specified [RCV005262778]	uncertain significance	14	103741870	103741870	Human		name
598169367	CV3897569	single nucleotide variant	NM_015316.3(PPP1R13B):c.2045C>T (p.Pro682Leu)	not specified [RCV005262779]	uncertain significance	14	103740371	103740371	Human		name
598169372	CV3897570	single nucleotide variant	NM_015316.3(PPP1R13B):c.1045T>C (p.Tyr349His)	not specified [RCV005262780]	uncertain significance	14	103746478	103746478	Human		name
598169378	CV3897571	single nucleotide variant	NM_015316.3(PPP1R13B):c.1219G>A (p.Gly407Ser)	not specified [RCV005262781]	likely benign	14	103742755	103742755	Human		name
598169388	CV3897573	single nucleotide variant	NM_015316.3(PPP1R13B):c.1488T>A (p.Ser496Arg)	not specified [RCV005262783]	uncertain significance	14	103742124	103742124	Human		name
598169399	CV3897575	single nucleotide variant	NM_015316.3(PPP1R13B):c.1070G>A (p.Ser357Asn)	not specified [RCV005262785]	uncertain significance	14	103746453	103746453	Human		name
598169404	CV3897576	single nucleotide variant	NM_015316.3(PPP1R13B):c.2536G>A (p.Glu846Lys)	not specified [RCV005262786]	uncertain significance	14	103739880	103739880	Human		name
15155401	CV714012	single nucleotide variant	NM_015316.3(PPP1R13B):c.2531G>A (p.Gly844Glu)	not provided [RCV000968918]	benign	14	103739885	103739885	Human		name
15164722	CV739135	single nucleotide variant	NM_015316.3(PPP1R13B):c.1663C>A (p.Pro555Thr)	not provided [RCV000904066]	benign	14	103741949	103741949	Human		name
155935131	CV2225503	single nucleotide variant	NM_015316.3(PPP1R13B):c.3198C>A (p.Asp1066Glu)	not specified [RCV004100895]	uncertain significance	14	103736036	103736036	Human		name
329369648	CV2461174	single nucleotide variant	NM_015316.3(PPP1R13B):c.3142A>G (p.Ile1048Val)	not specified [RCV004267375]	uncertain significance	14	103736092	103736092	Human		name
405795136	CV3366593	single nucleotide variant	NM_015316.3(PPP1R13B):c.3152G>A (p.Arg1051His)	not specified [RCV004507295]	uncertain significance	14	103736082	103736082	Human		name
405795138	CV3366594	single nucleotide variant	NM_015316.3(PPP1R13B):c.3200G>A (p.Arg1067Gln)	not specified [RCV004507296]	uncertain significance	14	103736034	103736034	Human		name
405795141	CV3366595	single nucleotide variant	NM_015316.3(PPP1R13B):c.3254G>A (p.Arg1085Gln)	not specified [RCV004507297]	uncertain significance	14	103735173	103735173	Human		name
407529765	CV3471563	single nucleotide variant	NM_015316.3(PPP1R13B):c.3187C>T (p.Arg1063Cys)	not specified [RCV004656206]	uncertain significance	14	103736047	103736047	Human		name
597758816	CV3587619	single nucleotide variant	NM_015316.3(PPP1R13B):c.3089A>G (p.Tyr1030Cys)	not specified [RCV004848615]	uncertain significance	14	103736145	103736145	Human		name
597758844	CV3587625	single nucleotide variant	NM_015316.3(PPP1R13B):c.3151C>T (p.Arg1051Cys)	not specified [RCV004848621]	uncertain significance	14	103736083	103736083	Human		name
598169382	CV3897572	single nucleotide variant	NM_015316.3(PPP1R13B):c.3133G>A (p.Ala1045Thr)	not specified [RCV005262782]	uncertain significance	14	103736101	103736101	Human		name
8635113	CV90335	single nucleotide variant	NM_015316.2(PPP1R13B):c.3194G>A (p.Gly1065Glu)	Malignant melanoma [RCV000070433]	not provided	14	103736040	103736040	Human		name
596924806	CV3496648	single nucleotide variant	NM_175634.3(RUNX1T1):c.1642C>T (p.His548Tyr)	PPP1R13B related disorder [RCV005055237]\|not provided [RCV004794696]	uncertain significance\|no classifications from unflagged records	8	91960415	91960415	Human		trait

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