Golgb1 Variant Search Result - Rat Genome Database

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286 records found for search term Golgb1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405770285	CV3258473	single nucleotide variant	NM_001366282.2(GOLGB1):c.7A>G (p.Ser3Gly)	not specified [RCV004395805]	uncertain significance	3	121730965	121730965	Human		name
155924836	CV2248879	single nucleotide variant	NM_001366282.2(GOLGB1):c.68A>T (p.Asp23Val)	not specified [RCV004115887]	uncertain significance	3	121730904	121730904	Human		name
401775373	CV2724075	single nucleotide variant	NM_001366282.2(GOLGB1):c.94C>A (p.Pro32Thr)	not specified [RCV004326219]	uncertain significance	3	121730878	121730878	Human		name
401892365	CV2777507	single nucleotide variant	NM_001366282.2(GOLGB1):c.77T>C (p.Met26Thr)	not specified [RCV004356266]	uncertain significance	3	121730895	121730895	Human		name
597788997	CV3688133	single nucleotide variant	NM_001366282.2(GOLGB1):c.56A>G (p.Asp19Gly)	not specified [RCV004932862]	uncertain significance	3	121730916	121730916	Human		name
401912521	CV2824855	single nucleotide variant	NM_001366282.2(GOLGB1):c.2925A>T (p.Gly975=)	not provided [RCV003427304]	likely benign	3	121697598	121697598	Human		name
401912445	CV2824856	single nucleotide variant	NM_001366282.2(GOLGB1):c.2712G>A (p.Lys904=)	not provided [RCV003427305]	likely benign	3	121697811	121697811	Human		name
407520428	CV3439799	single nucleotide variant	NM_001366282.2(GOLGB1):c.262G>T (p.Ala88Ser)	not specified [RCV004630041]	uncertain significance	3	121729328	121729328	Human		name
597788974	CV3688124	single nucleotide variant	NM_001366282.2(GOLGB1):c.103C>T (p.His35Tyr)	not specified [RCV004932857]	uncertain significance	3	121730011	121730011	Human		name
15123787	CV733715	single nucleotide variant	NM_001366282.2(GOLGB1):c.1296C>G (p.Leu432=)	not provided [RCV000896471]	likely benign	3	121714969	121714969	Human		name
8625477	CV80600	single nucleotide variant	NM_004487.4(GOLGB1):c.6046G>A (p.Glu2016Lys)	Malignant melanoma [RCV000060677]	not provided	3	121694462	121694462	Human		name
156230830	CV2199608	single nucleotide variant	NM_001366282.2(GOLGB1):c.429G>C (p.Glu143Asp)	not specified [RCV004072355]	uncertain significance	3	121727015	121727015	Human		name
156176054	CV2205296	single nucleotide variant	NM_001366282.2(GOLGB1):c.589G>A (p.Glu197Lys)	not specified [RCV004079915]	uncertain significance	3	121722321	121722321	Human		name
156120337	CV2233658	single nucleotide variant	NM_001366282.2(GOLGB1):c.595A>T (p.Ile199Phe)	not specified [RCV004100112]	uncertain significance	3	121722315	121722315	Human		name
156228161	CV2234868	single nucleotide variant	NM_001366282.2(GOLGB1):c.797T>A (p.Leu266His)	not specified [RCV004113084]	uncertain significance	3	121718476	121718476	Human		name
156078896	CV2248519	single nucleotide variant	NM_001366282.2(GOLGB1):c.530A>G (p.Gln177Arg)	not specified [RCV004119648]	uncertain significance	3	121726914	121726914	Human		name
155949845	CV2267729	single nucleotide variant	NM_001366282.2(GOLGB1):c.780G>C (p.Arg260Ser)	not specified [RCV004134263]	uncertain significance	3	121718493	121718493	Human		name
156161489	CV2323454	single nucleotide variant	NM_001366282.2(GOLGB1):c.544A>T (p.Met182Leu)	not specified [RCV004165668]	uncertain significance	3	121722366	121722366	Human		name
155926844	CV2365824	single nucleotide variant	NM_001366282.2(GOLGB1):c.326A>G (p.Lys109Arg)	not specified [RCV004214359]	uncertain significance	3	121729264	121729264	Human		name
329396805	CV2455806	single nucleotide variant	NM_001366282.2(GOLGB1):c.563T>C (p.Met188Thr)	not specified [RCV004279095]	uncertain significance	3	121722347	121722347	Human		name
401860720	CV2758594	single nucleotide variant	NM_001366282.2(GOLGB1):c.532A>T (p.Ser178Cys)	not specified [RCV004337677]	uncertain significance	3	121722378	121722378	Human		name
401898583	CV2782512	single nucleotide variant	NM_001366282.2(GOLGB1):c.961G>A (p.Glu321Lys)	not specified [RCV004359555]	uncertain significance	3	121717064	121717064	Human		name
401872149	CV2792994	single nucleotide variant	NM_001366282.2(GOLGB1):c.533G>C (p.Ser178Thr)	not specified [RCV004360333]	uncertain significance	3	121722377	121722377	Human		name
401912441	CV2824853	single nucleotide variant	NM_001366282.2(GOLGB1):c.8379C>T (p.Thr2793=)	not provided [RCV003427302]	likely benign	3	121690985	121690985	Human		name
401912443	CV2824854	single nucleotide variant	NM_001366282.2(GOLGB1):c.4635G>A (p.Arg1545=)	not provided [RCV003427303]	likely benign	3	121695888	121695888	Human		name
405770175	CV3258455	single nucleotide variant	NM_001366282.2(GOLGB1):c.475C>A (p.Leu159Ile)	not specified [RCV004395787]	uncertain significance	3	121726969	121726969	Human		name
405770214	CV3258462	single nucleotide variant	NM_001366282.2(GOLGB1):c.706C>T (p.Arg236Cys)	not specified [RCV004395794]	uncertain significance	3	121719711	121719711	Human		name
405770255	CV3258468	single nucleotide variant	NM_001366282.2(GOLGB1):c.734T>C (p.Leu245Ser)	not specified [RCV004395800]	uncertain significance	3	121719683	121719683	Human		name
405770262	CV3258469	single nucleotide variant	NM_001366282.2(GOLGB1):c.745G>A (p.Ala249Thr)	not specified [RCV004395801]	uncertain significance	3	121719672	121719672	Human		name
405770279	CV3258472	single nucleotide variant	NM_001366282.2(GOLGB1):c.808G>A (p.Glu270Lys)	not specified [RCV004395804]	uncertain significance	3	121718465	121718465	Human		name
407520415	CV3439795	single nucleotide variant	NM_001366282.2(GOLGB1):c.904C>A (p.Gln302Lys)	not specified [RCV004630037]	uncertain significance	3	121717121	121717121	Human		name
407520425	CV3439798	single nucleotide variant	NM_001366282.2(GOLGB1):c.674G>A (p.Arg225Gln)	not specified [RCV004630040]	uncertain significance	3	121719743	121719743	Human		name
407504071	CV3439801	single nucleotide variant	NM_001366282.2(GOLGB1):c.436A>G (p.Ile146Val)	not specified [RCV004623945]	likely benign	3	121727008	121727008	Human		name
407520432	CV3439803	single nucleotide variant	NM_001366282.2(GOLGB1):c.467A>G (p.Lys156Arg)	not specified [RCV004630043]	uncertain significance	3	121726977	121726977	Human		name
407504094	CV3439816	single nucleotide variant	NM_001366282.2(GOLGB1):c.385G>A (p.Glu129Lys)	not specified [RCV004623950]	uncertain significance	3	121729205	121729205	Human		name
407504098	CV3439818	single nucleotide variant	NM_001366282.2(GOLGB1):c.647A>T (p.Gln216Leu)	not specified [RCV004623951]	uncertain significance	3	121722263	121722263	Human		name
597731984	CV3688120	single nucleotide variant	NM_001366282.2(GOLGB1):c.313A>G (p.Thr105Ala)	not specified [RCV004919974]	uncertain significance	3	121729277	121729277	Human		name
597732004	CV3688125	single nucleotide variant	NM_001366282.2(GOLGB1):c.488T>C (p.Leu163Ser)	not specified [RCV004919976]	uncertain significance	3	121726956	121726956	Human		name
597788987	CV3688129	single nucleotide variant	NM_001366282.2(GOLGB1):c.371C>T (p.Thr124Ile)	not specified [RCV004932860]	uncertain significance	3	121729219	121729219	Human		name
597789009	CV3688140	single nucleotide variant	NM_001366282.2(GOLGB1):c.746C>G (p.Ala249Gly)	not specified [RCV004932865]	uncertain significance	3	121719671	121719671	Human		name
598233000	CV3974553	single nucleotide variant	NM_001366282.2(GOLGB1):c.522A>T (p.Gln174His)	not specified [RCV005342690]	uncertain significance	3	121726922	121726922	Human		name
598264783	CV3974555	single nucleotide variant	NM_001366282.2(GOLGB1):c.665A>T (p.Gln222Leu)	not specified [RCV005348923]	uncertain significance	3	121719752	121719752	Human		name
598264861	CV3974572	single nucleotide variant	NM_001366282.2(GOLGB1):c.614A>C (p.Gln205Pro)	not specified [RCV005348939]	uncertain significance	3	121722296	121722296	Human		name
598233020	CV3974575	single nucleotide variant	NM_001366282.2(GOLGB1):c.502A>G (p.Thr168Ala)	not specified [RCV005342693]	uncertain significance	3	121726942	121726942	Human		name
15123779	CV733714	single nucleotide variant	NM_001366282.2(GOLGB1):c.8514C>A (p.Ser2838=)	not provided [RCV000896470]	likely benign	3	121690850	121690850	Human		name
156380805	CV2218319	single nucleotide variant	NM_001366282.2(GOLGB1):c.1936A>C (p.Ser646Arg)	not specified [RCV004088836]	uncertain significance	3	121698587	121698587	Human		name
156280488	CV2224164	single nucleotide variant	NM_001366282.2(GOLGB1):c.1472C>G (p.Ala491Gly)	not specified [RCV004096016]	uncertain significance	3	121702528	121702528	Human		name
156002237	CV2287980	single nucleotide variant	NM_001366282.2(GOLGB1):c.1489A>G (p.Ile497Val)	not specified [RCV004147751]	likely benign	3	121702511	121702511	Human		name
156152656	CV2307649	single nucleotide variant	NM_001366282.2(GOLGB1):c.2562G>C (p.Glu854Asp)	not specified [RCV004168066]	uncertain significance	3	121697961	121697961	Human		name
156176064	CV2331142	single nucleotide variant	NM_001366282.2(GOLGB1):c.2575G>T (p.Val859Leu)	not specified [RCV004181753]	uncertain significance	3	121697948	121697948	Human		name
156100781	CV2367572	single nucleotide variant	NM_001366282.2(GOLGB1):c.2857C>G (p.Gln953Glu)	not specified [RCV004211501]	uncertain significance	3	121697666	121697666	Human		name
156389004	CV2376292	single nucleotide variant	NM_001366282.2(GOLGB1):c.2390A>G (p.Asn797Ser)	not specified [RCV004222556]	uncertain significance	3	121698133	121698133	Human		name
329369169	CV2424747	single nucleotide variant	NM_001366282.2(GOLGB1):c.2792T>C (p.Val931Ala)	not specified [RCV004248641]	uncertain significance	3	121697731	121697731	Human		name
329389513	CV2445177	single nucleotide variant	NM_001366282.2(GOLGB1):c.1231C>T (p.Leu411Phe)	not specified [RCV004263814]	uncertain significance	3	121716794	121716794	Human		name
329377701	CV2449950	single nucleotide variant	NM_001366282.2(GOLGB1):c.2251A>G (p.Arg751Gly)	not specified [RCV004269018]	uncertain significance	3	121698272	121698272	Human		name
329367362	CV2456775	single nucleotide variant	NM_001366282.2(GOLGB1):c.1711A>G (p.Met571Val)	not specified [RCV004270751]	uncertain significance	3	121698812	121698812	Human		name
329398296	CV2464988	single nucleotide variant	NM_001366282.2(GOLGB1):c.1237G>A (p.Asp413Asn)	not specified [RCV004284903]	uncertain significance	3	121716788	121716788	Human		name
329382648	CV2465306	single nucleotide variant	NM_001366282.2(GOLGB1):c.1310A>G (p.Lys437Arg)	not specified [RCV004281098]	uncertain significance	3	121714955	121714955	Human		name
329392414	CV2468067	single nucleotide variant	NM_001366282.2(GOLGB1):c.1655T>C (p.Val552Ala)	not specified [RCV004275677]	uncertain significance	3	121698868	121698868	Human		name
401746674	CV2691958	single nucleotide variant	NM_001366282.2(GOLGB1):c.1598G>A (p.Ser533Asn)	not specified [RCV004301688]	uncertain significance	3	121698925	121698925	Human		name
401772043	CV2712050	single nucleotide variant	NM_001366282.2(GOLGB1):c.1900G>A (p.Glu634Lys)	not specified [RCV004311469]	uncertain significance	3	121698623	121698623	Human		name
401763632	CV2714623	single nucleotide variant	NM_001366282.2(GOLGB1):c.2566G>A (p.Ala856Thr)	not specified [RCV004318116]	uncertain significance	3	121697957	121697957	Human		name
401784196	CV2721138	single nucleotide variant	NM_001366282.2(GOLGB1):c.2566G>T (p.Ala856Ser)	not specified [RCV004330143]	uncertain significance	3	121697957	121697957	Human		name
401762478	CV2723458	single nucleotide variant	NM_001366282.2(GOLGB1):c.1462G>A (p.Glu488Lys)	not specified [RCV004323529]	uncertain significance	3	121702538	121702538	Human		name
401864262	CV2767583	single nucleotide variant	NM_001366282.2(GOLGB1):c.1778C>G (p.Ala593Gly)	not specified [RCV004343731]	likely benign	3	121698745	121698745	Human		name
401883638	CV2785721	single nucleotide variant	NM_001366282.2(GOLGB1):c.1690T>G (p.Leu564Val)	not specified [RCV004364978]	uncertain significance	3	121698833	121698833	Human		name
401888089	CV2791236	single nucleotide variant	NM_001366282.2(GOLGB1):c.2257C>G (p.Gln753Glu)	not specified [RCV004356873]	uncertain significance	3	121698266	121698266	Human		name
405770054	CV3258434	single nucleotide variant	NM_001366282.2(GOLGB1):c.1045C>A (p.His349Asn)	not specified [RCV004395766]	uncertain significance	3	121716980	121716980	Human		name
405770059	CV3258435	single nucleotide variant	NM_001366282.2(GOLGB1):c.1161G>T (p.Leu387Phe)	not specified [RCV004395767]	uncertain significance	3	121716864	121716864	Human		name
405770067	CV3258436	single nucleotide variant	NM_001366282.2(GOLGB1):c.1293G>C (p.Gln431His)	not specified [RCV004395768]	uncertain significance	3	121714972	121714972	Human		name
405770073	CV3258437	single nucleotide variant	NM_001366282.2(GOLGB1):c.1660G>C (p.Glu554Gln)	not specified [RCV004395769]	uncertain significance	3	121698863	121698863	Human		name
405770078	CV3258438	single nucleotide variant	NM_001366282.2(GOLGB1):c.1696G>A (p.Val566Ile)	not specified [RCV004395770]	uncertain significance	3	121698827	121698827	Human		name
405770090	CV3258440	single nucleotide variant	NM_001366282.2(GOLGB1):c.2023A>G (p.Lys675Glu)	not specified [RCV004395772]	uncertain significance	3	121698500	121698500	Human		name
405770097	CV3258441	single nucleotide variant	NM_001366282.2(GOLGB1):c.2129A>C (p.Glu710Ala)	not specified [RCV004395773]	uncertain significance	3	121698394	121698394	Human		name
405770103	CV3258442	single nucleotide variant	NM_001366282.2(GOLGB1):c.2217C>G (p.Asn739Lys)	not specified [RCV004395774]	uncertain significance	3	121698306	121698306	Human		name
405770109	CV3258443	single nucleotide variant	NM_001366282.2(GOLGB1):c.2306C>A (p.Ala769Asp)	not specified [RCV004395775]	uncertain significance	3	121698217	121698217	Human		name
405770114	CV3258444	single nucleotide variant	NM_001366282.2(GOLGB1):c.2635G>A (p.Glu879Lys)	not specified [RCV004395776]	uncertain significance	3	121697888	121697888	Human		name
405770120	CV3258445	single nucleotide variant	NM_001366282.2(GOLGB1):c.2740A>C (p.Ser914Arg)	not specified [RCV004395777]	uncertain significance	3	121697783	121697783	Human		name
405770126	CV3258446	single nucleotide variant	NM_001366282.2(GOLGB1):c.2819T>C (p.Leu940Pro)	not specified [RCV004395778]	uncertain significance	3	121697704	121697704	Human		name
405770131	CV3258447	single nucleotide variant	NM_001366282.2(GOLGB1):c.2821A>G (p.Asn941Asp)	not specified [RCV004395779]	uncertain significance	3	121697702	121697702	Human		name
407520392	CV3439787	single nucleotide variant	NM_001366282.2(GOLGB1):c.2807T>A (p.Leu936His)	not specified [RCV004630029]	uncertain significance	3	121697716	121697716	Human		name
407520395	CV3439788	single nucleotide variant	NM_001366282.2(GOLGB1):c.1526T>C (p.Leu509Pro)	not specified [RCV004630030]	uncertain significance	3	121699879	121699879	Human		name
407520435	CV3439804	single nucleotide variant	NM_001366282.2(GOLGB1):c.2005A>G (p.Thr669Ala)	not specified [RCV004630044]	uncertain significance	3	121698518	121698518	Human		name
407504082	CV3439806	single nucleotide variant	NM_001366282.2(GOLGB1):c.2222G>A (p.Ser741Asn)	not specified [RCV004623947]	likely benign	3	121698301	121698301	Human		name
407520448	CV3439810	single nucleotide variant	NM_001366282.2(GOLGB1):c.1352A>G (p.His451Arg)	not specified [RCV004630048]	uncertain significance	3	121714913	121714913	Human		name
597788952	CV3688110	single nucleotide variant	NM_001366282.2(GOLGB1):c.2483A>T (p.Gln828Leu)	not specified [RCV004932852]	uncertain significance	3	121698040	121698040	Human		name
597788960	CV3688113	single nucleotide variant	NM_001366282.2(GOLGB1):c.2342C>G (p.Ala781Gly)	not specified [RCV004932854]	uncertain significance	3	121698181	121698181	Human		name
597731994	CV3688121	single nucleotide variant	NM_001366282.2(GOLGB1):c.1178G>A (p.Gly393Glu)	not specified [RCV004919975]	likely benign	3	121716847	121716847	Human		name
597732015	CV3688127	single nucleotide variant	NM_001366282.2(GOLGB1):c.2906A>T (p.Asp969Val)	not specified [RCV004919977]	uncertain significance	3	121697617	121697617	Human		name
597789005	CV3688139	single nucleotide variant	NM_001366282.2(GOLGB1):c.2470C>A (p.Leu824Met)	not specified [RCV004932864]	uncertain significance	3	121698053	121698053	Human		name
597789017	CV3688143	single nucleotide variant	NM_001366282.2(GOLGB1):c.1020C>A (p.Phe340Leu)	not specified [RCV004932867]	uncertain significance	3	121717005	121717005	Human		name
597732128	CV3688148	single nucleotide variant	NM_001366282.2(GOLGB1):c.1657C>G (p.Leu553Val)	not specified [RCV004919988]	uncertain significance	3	121698866	121698866	Human		name
598264778	CV3974554	single nucleotide variant	NM_001366282.2(GOLGB1):c.2573G>A (p.Arg858His)	not specified [RCV005348922]	likely benign	3	121697950	121697950	Human		name
598264804	CV3974559	single nucleotide variant	NM_001366282.2(GOLGB1):c.1649A>C (p.Gln550Pro)	not specified [RCV005348927]	uncertain significance	3	121698874	121698874	Human		name
598264812	CV3974561	single nucleotide variant	NM_001366282.2(GOLGB1):c.1979A>T (p.Asn660Ile)	not specified [RCV005348929]	uncertain significance	3	121698544	121698544	Human		name
598264833	CV3974566	single nucleotide variant	NM_001366282.2(GOLGB1):c.1107T>G (p.Ser369Arg)	not specified [RCV005348933]	uncertain significance	3	121716918	121716918	Human		name
598264853	CV3974570	single nucleotide variant	NM_001366282.2(GOLGB1):c.1043A>G (p.His348Arg)	not specified [RCV005348937]	likely benign	3	121716982	121716982	Human		name
598233014	CV3974574	single nucleotide variant	NM_001366282.2(GOLGB1):c.2210C>G (p.Ala737Gly)	not specified [RCV005342692]	uncertain significance	3	121698313	121698313	Human		name
598264882	CV3974579	single nucleotide variant	NM_001366282.2(GOLGB1):c.1041G>A (p.Met347Ile)	not specified [RCV005348943]	uncertain significance	3	121716984	121716984	Human		name
598264916	CV3974588	single nucleotide variant	NM_001366282.2(GOLGB1):c.2830T>C (p.Ser944Pro)	not specified [RCV005348949]	uncertain significance	3	121697693	121697693	Human		name
598264921	CV3974589	single nucleotide variant	NM_001366282.2(GOLGB1):c.2498A>G (p.Glu833Gly)	not specified [RCV005348950]	uncertain significance	3	121698025	121698025	Human		name
15169043	CV708500	single nucleotide variant	NM_001366282.2(GOLGB1):c.2557C>T (p.Leu853Phe)	not provided [RCV000971735]	benign	3	121697966	121697966	Human		name
156141584	CV2199944	single nucleotide variant	NM_001366282.2(GOLGB1):c.9553C>T (p.Arg3185Trp)	not specified [RCV004074118]	uncertain significance	3	121667477	121667477	Human		name
156037104	CV2218516	single nucleotide variant	NM_001366282.2(GOLGB1):c.5741C>T (p.Thr1914Ile)	not specified [RCV004090795]	uncertain significance	3	121694782	121694782	Human		name
156116229	CV2221652	single nucleotide variant	NM_001366282.2(GOLGB1):c.3933G>C (p.Gln1311His)	not specified [RCV004096897]	uncertain significance	3	121696590	121696590	Human		name
155940527	CV2222178	single nucleotide variant	NM_001366282.2(GOLGB1):c.3643G>T (p.Asp1215Tyr)	not specified [RCV004104929]	uncertain significance	3	121696880	121696880	Human		name
156187167	CV2226667	single nucleotide variant	NM_001366282.2(GOLGB1):c.5205G>T (p.Arg1735Ser)	not specified [RCV004101900]	uncertain significance	3	121695318	121695318	Human		name
156335431	CV2228392	single nucleotide variant	NM_001366282.2(GOLGB1):c.3214T>C (p.Ser1072Pro)	not specified [RCV004098371]	uncertain significance	3	121697309	121697309	Human		name
156077385	CV2230285	single nucleotide variant	NM_001366282.2(GOLGB1):c.4682A>T (p.Asp1561Val)	not specified [RCV004099899]	uncertain significance	3	121695841	121695841	Human		name
156294632	CV2233657	single nucleotide variant	NM_001366282.2(GOLGB1):c.3827C>T (p.Thr1276Ile)	not specified [RCV004100111]	uncertain significance	3	121696696	121696696	Human		name
156243591	CV2242943	single nucleotide variant	NM_001366282.2(GOLGB1):c.8912T>C (p.Met2971Thr)	not specified [RCV004107828]	uncertain significance	3	121677412	121677412	Human		name
156035193	CV2253001	single nucleotide variant	NM_001366282.2(GOLGB1):c.5137G>C (p.Asp1713His)	not specified [RCV004120804]	uncertain significance	3	121695386	121695386	Human		name
156135104	CV2256825	single nucleotide variant	NM_001366282.2(GOLGB1):c.4327G>A (p.Ala1443Thr)	not specified [RCV004121045]	uncertain significance	3	121696196	121696196	Human		name
156359943	CV2258038	single nucleotide variant	NM_001366282.2(GOLGB1):c.3644A>G (p.Asp1215Gly)	not specified [RCV004129835]	uncertain significance	3	121696879	121696879	Human		name
155969439	CV2262113	single nucleotide variant	NM_001366282.2(GOLGB1):c.4565C>T (p.Thr1522Ile)	not specified [RCV004126575]	uncertain significance	3	121695958	121695958	Human		name
156235966	CV2268067	single nucleotide variant	NM_001366282.2(GOLGB1):c.9599G>C (p.Gly3200Ala)	not specified [RCV004136612]	uncertain significance	3	121664987	121664987	Human		name
155984806	CV2270623	single nucleotide variant	NM_001366282.2(GOLGB1):c.8688C>A (p.Asp2896Glu)	not specified [RCV004137839]	uncertain significance	3	121690676	121690676	Human		name
155980771	CV2272765	single nucleotide variant	NM_001366282.2(GOLGB1):c.8898A>G (p.Ile2966Met)	not specified [RCV004135686]	uncertain significance	3	121677426	121677426	Human		name
155905089	CV2285828	single nucleotide variant	NM_001366282.2(GOLGB1):c.4529A>T (p.Glu1510Val)	not specified [RCV004143775]	uncertain significance	3	121695994	121695994	Human		name
155940688	CV2294121	single nucleotide variant	NM_001366282.2(GOLGB1):c.9641C>G (p.Thr3214Arg)	not specified [RCV004149491]	uncertain significance	3	121664945	121664945	Human		name
156091245	CV2300031	single nucleotide variant	NM_001366282.2(GOLGB1):c.3457A>G (p.Ser1153Gly)	not specified [RCV004151240]	uncertain significance	3	121697066	121697066	Human		name
156349555	CV2305647	single nucleotide variant	NM_001366282.2(GOLGB1):c.4364A>G (p.His1455Arg)	not specified [RCV004167478]	uncertain significance	3	121696159	121696159	Human		name
156241114	CV2310114	single nucleotide variant	NM_001366282.2(GOLGB1):c.6775A>G (p.Ile2259Val)	not specified [RCV004163238]	uncertain significance	3	121693748	121693748	Human		name
156211030	CV2314436	single nucleotide variant	NM_001366282.2(GOLGB1):c.4272A>C (p.Glu1424Asp)	not specified [RCV004168546]	uncertain significance	3	121696251	121696251	Human		name
156170419	CV2317139	single nucleotide variant	NM_001366282.2(GOLGB1):c.5510A>G (p.His1837Arg)	not specified [RCV004174609]	uncertain significance	3	121695013	121695013	Human		name
156052442	CV2320306	single nucleotide variant	NM_001366282.2(GOLGB1):c.3279G>T (p.Glu1093Asp)	not specified [RCV004178470]	uncertain significance	3	121697244	121697244	Human		name
156355427	CV2324485	single nucleotide variant	NM_001366282.2(GOLGB1):c.7403T>G (p.Val2468Gly)	not specified [RCV004178967]	uncertain significance	3	121691961	121691961	Human		name
156290623	CV2324921	single nucleotide variant	NM_001366282.2(GOLGB1):c.9286G>T (p.Ala3096Ser)	not specified [RCV004175179]	uncertain significance	3	121669247	121669247	Human		name
156178965	CV2327569	single nucleotide variant	NM_001366282.2(GOLGB1):c.8955G>T (p.Gln2985His)	not specified [RCV004176866]	uncertain significance	3	121677369	121677369	Human		name
156176078	CV2331143	single nucleotide variant	NM_001366282.2(GOLGB1):c.9301C>G (p.Gln3101Glu)	not specified [RCV004181754]	uncertain significance	3	121669232	121669232	Human		name
156071888	CV2337784	single nucleotide variant	NM_001366282.2(GOLGB1):c.4079G>A (p.Ser1360Asn)	not specified [RCV004183801]	uncertain significance	3	121696444	121696444	Human		name
156200968	CV2338318	single nucleotide variant	NM_001366282.2(GOLGB1):c.9500A>T (p.Asp3167Val)	not specified [RCV004186372]	uncertain significance	3	121667530	121667530	Human		name
155920530	CV2343364	single nucleotide variant	NM_001366282.2(GOLGB1):c.9641C>T (p.Thr3214Ile)	not specified [RCV004194978]	uncertain significance	3	121664945	121664945	Human		name
156168102	CV2345380	single nucleotide variant	NM_001366282.2(GOLGB1):c.4259T>C (p.Leu1420Pro)	not specified [RCV004198157]	uncertain significance	3	121696264	121696264	Human		name
156116881	CV2349420	single nucleotide variant	NM_001366282.2(GOLGB1):c.3209C>T (p.Thr1070Ile)	not specified [RCV004199347]	uncertain significance	3	121697314	121697314	Human		name
156402250	CV2363631	single nucleotide variant	NM_001366282.2(GOLGB1):c.3728T>C (p.Ile1243Thr)	not specified [RCV004216584]	uncertain significance	3	121696795	121696795	Human		name
156343744	CV2364157	single nucleotide variant	NM_001366282.2(GOLGB1):c.5755A>G (p.Thr1919Ala)	not specified [RCV004223401]	uncertain significance	3	121694768	121694768	Human		name
156387597	CV2372795	single nucleotide variant	NM_001366282.2(GOLGB1):c.4282A>G (p.Thr1428Ala)	not specified [RCV004221980]	uncertain significance	3	121696241	121696241	Human		name
155936465	CV2379831	single nucleotide variant	NM_001366282.2(GOLGB1):c.5363C>T (p.Thr1788Met)	not specified [RCV004219943]	likely benign	3	121695160	121695160	Human		name
156209338	CV2382616	single nucleotide variant	NM_001366282.2(GOLGB1):c.3916G>A (p.Gly1306Arg)	not specified [RCV004232940]	uncertain significance	3	121696607	121696607	Human		name
156098498	CV2392790	single nucleotide variant	NM_001366282.2(GOLGB1):c.4863A>C (p.Glu1621Asp)	not specified [RCV004247154]	uncertain significance	3	121695660	121695660	Human		name
156248645	CV2393991	single nucleotide variant	NM_001366282.2(GOLGB1):c.5465C>T (p.Ser1822Leu)	not specified [RCV004236214]	uncertain significance	3	121695058	121695058	Human		name
155931945	CV2399930	single nucleotide variant	NM_001366282.2(GOLGB1):c.9719G>A (p.Arg3240Gln)	not specified [RCV004246866]	uncertain significance	3	121664556	121664556	Human		name
329367433	CV2427409	single nucleotide variant	NM_001366282.2(GOLGB1):c.3863A>G (p.Asn1288Ser)	not specified [RCV004248263]	uncertain significance	3	121696660	121696660	Human		name
329372897	CV2428700	single nucleotide variant	NM_001366282.2(GOLGB1):c.7859C>T (p.Thr2620Ile)	not specified [RCV004255492]	uncertain significance	3	121691505	121691505	Human		name
329374086	CV2434693	single nucleotide variant	NM_001366282.2(GOLGB1):c.6688G>C (p.Glu2230Gln)	not specified [RCV004248409]	uncertain significance	3	121693835	121693835	Human		name
329377596	CV2435971	single nucleotide variant	NM_001366282.2(GOLGB1):c.8023G>A (p.Ala2675Thr)	not specified [RCV004255193]	uncertain significance	3	121691341	121691341	Human		name
329362725	CV2439157	single nucleotide variant	NM_001366282.2(GOLGB1):c.4716C>G (p.Ser1572Arg)	not specified [RCV004266437]	uncertain significance	3	121695807	121695807	Human		name
329390076	CV2441286	single nucleotide variant	NM_001366282.2(GOLGB1):c.7433G>A (p.Arg2478Gln)	not specified [RCV004257105]	uncertain significance	3	121691931	121691931	Human		name
329395118	CV2457877	single nucleotide variant	NM_001366282.2(GOLGB1):c.8299G>T (p.Asp2767Tyr)	not specified [RCV004271471]	uncertain significance	3	121691065	121691065	Human		name
329351644	CV2459222	single nucleotide variant	NM_001366282.2(GOLGB1):c.6797A>G (p.Lys2266Arg)	not specified [RCV004274661]	uncertain significance	3	121692567	121692567	Human		name
329385662	CV2462156	single nucleotide variant	NM_001366282.2(GOLGB1):c.6224G>A (p.Arg2075His)	not specified [RCV004266177]	uncertain significance	3	121694299	121694299	Human		name
329387544	CV2470812	single nucleotide variant	NM_001366282.2(GOLGB1):c.7152G>A (p.Met2384Ile)	not specified [RCV004276026]	uncertain significance	3	121692212	121692212	Human		name
329353176	CV2471532	single nucleotide variant	NM_001366282.2(GOLGB1):c.6667G>A (p.Ala2223Thr)	not specified [RCV004280519]	uncertain significance	3	121693856	121693856	Human		name
401742132	CV2676902	single nucleotide variant	NM_001366282.2(GOLGB1):c.4409A>T (p.Lys1470Met)	not specified [RCV004291065]	uncertain significance	3	121696114	121696114	Human		name
401741495	CV2677372	single nucleotide variant	NM_001366282.2(GOLGB1):c.3830A>G (p.Glu1277Gly)	not specified [RCV004289454]	uncertain significance	3	121696693	121696693	Human		name
401742780	CV2677678	single nucleotide variant	NM_001366282.2(GOLGB1):c.5107C>T (p.Arg1703Trp)	not specified [RCV004291764]	uncertain significance	3	121695416	121695416	Human		name
401734516	CV2688547	single nucleotide variant	NM_001366282.2(GOLGB1):c.6866G>A (p.Gly2289Glu)	not specified [RCV004301509]	uncertain significance	3	121692498	121692498	Human		name
401769500	CV2689796	single nucleotide variant	NM_001366282.2(GOLGB1):c.7400T>G (p.Phe2467Cys)	not specified [RCV004297702]	uncertain significance	3	121691964	121691964	Human		name
401769818	CV2693034	single nucleotide variant	NM_001366282.2(GOLGB1):c.5731T>C (p.Ser1911Pro)	not specified [RCV004308582]	uncertain significance	3	121694792	121694792	Human		name
401728689	CV2693743	single nucleotide variant	NM_001366282.2(GOLGB1):c.9058G>C (p.Ala3020Pro)	not specified [RCV004298068]	uncertain significance	3	121677012	121677012	Human		name
401763004	CV2710404	single nucleotide variant	NM_001366282.2(GOLGB1):c.4514A>G (p.Lys1505Arg)	not specified [RCV004317563]	uncertain significance	3	121696009	121696009	Human		name
401734213	CV2713369	single nucleotide variant	NM_001366282.2(GOLGB1):c.5269C>G (p.Leu1757Val)	not specified [RCV004318668]	uncertain significance	3	121695254	121695254	Human		name
401752119	CV2714187	single nucleotide variant	NM_001366282.2(GOLGB1):c.9085G>T (p.Val3029Phe)	not specified [RCV004317425]	uncertain significance	3	121676985	121676985	Human		name
401739211	CV2722082	single nucleotide variant	NM_001366282.2(GOLGB1):c.6665A>G (p.Asp2222Gly)	not specified [RCV004328347]	uncertain significance	3	121693858	121693858	Human		name
401781639	CV2722199	single nucleotide variant	NM_001366282.2(GOLGB1):c.3017A>G (p.Asn1006Ser)	not specified [RCV004328765]	uncertain significance	3	121697506	121697506	Human		name
401723731	CV2725011	single nucleotide variant	NM_001366282.2(GOLGB1):c.9320C>T (p.Ala3107Val)	not specified [RCV004319769]	uncertain significance	3	121669213	121669213	Human		name
401863084	CV2755847	single nucleotide variant	NM_001366282.2(GOLGB1):c.3427G>A (p.Val1143Ile)	not specified [RCV004342215]	uncertain significance	3	121697096	121697096	Human		name
401873278	CV2761410	single nucleotide variant	NM_001366282.2(GOLGB1):c.3421G>A (p.Asp1141Asn)	not specified [RCV004334589]	uncertain significance	3	121697102	121697102	Human		name
401890568	CV2768310	single nucleotide variant	NM_001366282.2(GOLGB1):c.4286A>G (p.Lys1429Arg)	not specified [RCV004350293]	uncertain significance	3	121696237	121696237	Human		name
401891326	CV2769003	single nucleotide variant	NM_001366282.2(GOLGB1):c.7583A>G (p.Asn2528Ser)	not specified [RCV004348877]	uncertain significance	3	121691781	121691781	Human		name
401880315	CV2770047	single nucleotide variant	NM_001366282.2(GOLGB1):c.3767C>T (p.Thr1256Ile)	not specified [RCV004353866]	uncertain significance	3	121696756	121696756	Human		name
401885228	CV2770972	single nucleotide variant	NM_001366282.2(GOLGB1):c.6009G>C (p.Gln2003His)	not specified [RCV004343993]	uncertain significance	3	121694514	121694514	Human		name
401879275	CV2774553	single nucleotide variant	NM_001366282.2(GOLGB1):c.9338A>G (p.Asp3113Gly)	not specified [RCV004350035]	uncertain significance	3	121668142	121668142	Human		name
401874842	CV2781291	single nucleotide variant	NM_001366282.2(GOLGB1):c.5423T>G (p.Leu1808Arg)	not specified [RCV004352314]	uncertain significance	3	121695100	121695100	Human		name
401884522	CV2789708	single nucleotide variant	NM_001366282.2(GOLGB1):c.5777A>T (p.Asp1926Val)	not specified [RCV004361832]	uncertain significance	3	121694746	121694746	Human		name
401869904	CV2792216	single nucleotide variant	NM_001366282.2(GOLGB1):c.5140A>G (p.Thr1714Ala)	not specified [RCV004361418]	uncertain significance	3	121695383	121695383	Human		name
405770138	CV3258448	single nucleotide variant	NM_001366282.2(GOLGB1):c.3135T>A (p.Asp1045Glu)	not specified [RCV004395780]	uncertain significance	3	121697388	121697388	Human		name
405770142	CV3258449	single nucleotide variant	NM_001366282.2(GOLGB1):c.3899C>G (p.Ala1300Gly)	not specified [RCV004395781]	uncertain significance	3	121696624	121696624	Human		name
405770148	CV3258450	single nucleotide variant	NM_001366282.2(GOLGB1):c.3899C>T (p.Ala1300Val)	not specified [RCV004395782]	uncertain significance	3	121696624	121696624	Human		name
405770153	CV3258451	single nucleotide variant	NM_001366282.2(GOLGB1):c.3919A>C (p.Thr1307Pro)	not specified [RCV004395783]	uncertain significance	3	121696604	121696604	Human		name
405770157	CV3258452	single nucleotide variant	NM_001366282.2(GOLGB1):c.4166T>A (p.Leu1389Gln)	not specified [RCV004395784]	uncertain significance	3	121696357	121696357	Human		name
405770163	CV3258453	single nucleotide variant	NM_001366282.2(GOLGB1):c.4316A>G (p.Asp1439Gly)	not specified [RCV004395785]	uncertain significance	3	121696207	121696207	Human		name
405770168	CV3258454	single nucleotide variant	NM_001366282.2(GOLGB1):c.4399T>C (p.Cys1467Arg)	not specified [RCV004395786]	uncertain significance	3	121696124	121696124	Human		name
405770189	CV3258458	single nucleotide variant	NM_001366282.2(GOLGB1):c.6485A>T (p.Glu2162Val)	not specified [RCV004395790]	uncertain significance	3	121694038	121694038	Human		name
405770196	CV3258459	single nucleotide variant	NM_001366282.2(GOLGB1):c.6621C>G (p.Asp2207Glu)	not specified [RCV004395791]	uncertain significance	3	121693902	121693902	Human		name
405770203	CV3258460	single nucleotide variant	NM_001366282.2(GOLGB1):c.6668C>G (p.Ala2223Gly)	not specified [RCV004395792]	uncertain significance	3	121693855	121693855	Human		name
405770207	CV3258461	single nucleotide variant	NM_001366282.2(GOLGB1):c.6870A>C (p.Glu2290Asp)	not specified [RCV004395793]	uncertain significance	3	121692494	121692494	Human		name
405770221	CV3258463	single nucleotide variant	NM_001366282.2(GOLGB1):c.6988A>G (p.Ser2330Gly)	not specified [RCV004395795]	uncertain significance	3	121692376	121692376	Human		name
405770228	CV3258464	single nucleotide variant	NM_001366282.2(GOLGB1):c.7072A>G (p.Lys2358Glu)	not specified [RCV004395796]	uncertain significance	3	121692292	121692292	Human		name
405770235	CV3258465	single nucleotide variant	NM_001366282.2(GOLGB1):c.7097C>T (p.Thr2366Ile)	not specified [RCV004395797]	uncertain significance	3	121692267	121692267	Human		name
405770242	CV3258466	single nucleotide variant	NM_001366282.2(GOLGB1):c.7108G>A (p.Ala2370Thr)	not specified [RCV004395798]	uncertain significance	3	121692256	121692256	Human		name
405770250	CV3258467	single nucleotide variant	NM_001366282.2(GOLGB1):c.7184G>T (p.Gly2395Val)	not specified [RCV004395799]	uncertain significance	3	121692180	121692180	Human		name
405770267	CV3258470	single nucleotide variant	NM_001366282.2(GOLGB1):c.7775G>A (p.Arg2592Gln)	not specified [RCV004395802]	likely benign	3	121691589	121691589	Human		name
405770273	CV3258471	single nucleotide variant	NM_001366282.2(GOLGB1):c.7907A>G (p.His2636Arg)	not specified [RCV004395803]	uncertain significance	3	121691457	121691457	Human		name
405770291	CV3258474	single nucleotide variant	NM_001366282.2(GOLGB1):c.8032G>C (p.Val2678Leu)	not specified [RCV004395806]	uncertain significance	3	121691332	121691332	Human		name
405770298	CV3258475	single nucleotide variant	NM_001366282.2(GOLGB1):c.8212A>G (p.Ile2738Val)	not specified [RCV004395807]	uncertain significance	3	121691152	121691152	Human		name
405770305	CV3258476	single nucleotide variant	NM_001366282.2(GOLGB1):c.8309T>C (p.Leu2770Pro)	not specified [RCV004395808]	uncertain significance	3	121691055	121691055	Human		name
405770312	CV3258477	single nucleotide variant	NM_001366282.2(GOLGB1):c.8350A>G (p.Arg2784Gly)	not specified [RCV004395809]	uncertain significance	3	121691014	121691014	Human		name
405770319	CV3258478	single nucleotide variant	NM_001366282.2(GOLGB1):c.9239G>A (p.Ser3080Asn)	not specified [RCV004395810]	uncertain significance	3	121669294	121669294	Human		name
405770327	CV3258479	single nucleotide variant	NM_001366282.2(GOLGB1):c.9463G>A (p.Val3155Met)	not specified [RCV004395811]	likely benign	3	121667567	121667567	Human		name
405770332	CV3258480	single nucleotide variant	NM_001366282.2(GOLGB1):c.9548T>A (p.Ile3183Asn)	not specified [RCV004395812]	uncertain significance	3	121667482	121667482	Human		name
405770338	CV3258481	single nucleotide variant	NM_001366282.2(GOLGB1):c.9626T>G (p.Leu3209Arg)	not specified [RCV004395813]	uncertain significance	3	121664960	121664960	Human		name
405770344	CV3258482	single nucleotide variant	NM_001366282.2(GOLGB1):c.9712C>T (p.Arg3238Trp)	not specified [RCV004395814]	uncertain significance	3	121664563	121664563	Human		name
405770351	CV3258483	single nucleotide variant	NM_001366282.2(GOLGB1):c.9739A>G (p.Ile3247Val)	not specified [RCV004395815]	uncertain significance	3	121664536	121664536	Human		name
407520402	CV3439791	single nucleotide variant	NM_001366282.2(GOLGB1):c.6788A>T (p.Glu2263Val)	not specified [RCV004630033]	uncertain significance	3	121692576	121692576	Human		name
407520405	CV3439792	single nucleotide variant	NM_001366282.2(GOLGB1):c.6173A>G (p.Gln2058Arg)	not specified [RCV004630034]	uncertain significance	3	121694350	121694350	Human		name
407520408	CV3439793	single nucleotide variant	NM_001366282.2(GOLGB1):c.5312A>G (p.Asn1771Ser)	not specified [RCV004630035]	uncertain significance	3	121695211	121695211	Human		name
407520412	CV3439794	single nucleotide variant	NM_001366282.2(GOLGB1):c.6587C>G (p.Thr2196Ser)	not specified [RCV004630036]	uncertain significance	3	121693936	121693936	Human		name
407520419	CV3439796	single nucleotide variant	NM_001366282.2(GOLGB1):c.3494C>T (p.Pro1165Leu)	not specified [RCV004630038]	uncertain significance	3	121697029	121697029	Human		name
407520421	CV3439797	single nucleotide variant	NM_001366282.2(GOLGB1):c.3809A>C (p.Glu1270Ala)	not specified [RCV004630039]	uncertain significance	3	121696714	121696714	Human		name
407504078	CV3439802	single nucleotide variant	NM_001366282.2(GOLGB1):c.9058G>A (p.Ala3020Thr)	not specified [RCV004623946]	uncertain significance	3	121677012	121677012	Human		name
407520438	CV3439805	single nucleotide variant	NM_001366282.2(GOLGB1):c.3303G>C (p.Gln1101His)	not specified [RCV004630045]	uncertain significance	3	121697220	121697220	Human		name
407520441	CV3439807	single nucleotide variant	NM_001366282.2(GOLGB1):c.4271A>C (p.Glu1424Ala)	not specified [RCV004630046]	uncertain significance	3	121696252	121696252	Human		name
407504086	CV3439808	single nucleotide variant	NM_001366282.2(GOLGB1):c.6167A>C (p.Glu2056Ala)	not specified [RCV004623948]	uncertain significance	3	121694356	121694356	Human		name
407520445	CV3439809	single nucleotide variant	NM_001366282.2(GOLGB1):c.3875A>G (p.Asp1292Gly)	not specified [RCV004630047]	uncertain significance	3	121696648	121696648	Human		name
407504089	CV3439811	single nucleotide variant	NM_001366282.2(GOLGB1):c.7961C>G (p.Ser2654Cys)	not specified [RCV004623949]	uncertain significance	3	121691403	121691403	Human		name
407520451	CV3439812	single nucleotide variant	NM_001366282.2(GOLGB1):c.5534A>C (p.Gln1845Pro)	not specified [RCV004630049]	uncertain significance	3	121694989	121694989	Human		name
407520454	CV3439813	single nucleotide variant	NM_001366282.2(GOLGB1):c.5126A>C (p.His1709Pro)	not specified [RCV004630050]	uncertain significance	3	121695397	121695397	Human		name
407520457	CV3439814	single nucleotide variant	NM_001366282.2(GOLGB1):c.7234G>T (p.Asp2412Tyr)	not specified [RCV004630051]	uncertain significance	3	121692130	121692130	Human		name
407520460	CV3439815	single nucleotide variant	NM_001366282.2(GOLGB1):c.8081A>G (p.His2694Arg)	not specified [RCV004630052]	uncertain significance	3	121691283	121691283	Human		name
407520463	CV3439817	single nucleotide variant	NM_001366282.2(GOLGB1):c.4418C>T (p.Pro1473Leu)	not specified [RCV004630053]	uncertain significance	3	121696105	121696105	Human		name
407520466	CV3439819	single nucleotide variant	NM_001366282.2(GOLGB1):c.3574C>G (p.Arg1192Gly)	not specified [RCV004630054]	uncertain significance	3	121696949	121696949	Human		name
407520469	CV3439820	single nucleotide variant	NM_001366282.2(GOLGB1):c.6301G>T (p.Ala2101Ser)	not specified [RCV004630055]	uncertain significance	3	121694222	121694222	Human		name
407520472	CV3439822	single nucleotide variant	NM_001366282.2(GOLGB1):c.6118A>G (p.Ile2040Val)	not specified [RCV004630057]	uncertain significance	3	121694405	121694405	Human		name
597731892	CV3688104	single nucleotide variant	NM_001366282.2(GOLGB1):c.7454A>G (p.Tyr2485Cys)	not specified [RCV004919964]	uncertain significance	3	121691910	121691910	Human		name
597788944	CV3688105	single nucleotide variant	NM_001366282.2(GOLGB1):c.7414T>G (p.Ser2472Ala)	not specified [RCV004932850]	uncertain significance	3	121691950	121691950	Human		name
597731901	CV3688106	single nucleotide variant	NM_001366282.2(GOLGB1):c.4589G>A (p.Ser1530Asn)	not specified [RCV004919965]	likely benign	3	121695934	121695934	Human		name
597788948	CV3688107	single nucleotide variant	NM_001366282.2(GOLGB1):c.7941C>G (p.His2647Gln)	not specified [RCV004932851]	likely benign	3	121691423	121691423	Human		name
597731912	CV3688108	single nucleotide variant	NM_001366282.2(GOLGB1):c.5456C>T (p.Ser1819Leu)	not specified [RCV004919966]	uncertain significance	3	121695067	121695067	Human		name
597731922	CV3688109	single nucleotide variant	NM_001366282.2(GOLGB1):c.5344G>A (p.Glu1782Lys)	not specified [RCV004919967]	uncertain significance	3	121695179	121695179	Human		name
597788956	CV3688111	single nucleotide variant	NM_001366282.2(GOLGB1):c.7571T>C (p.Met2524Thr)	not specified [RCV004932853]	uncertain significance	3	121691793	121691793	Human		name
597731930	CV3688112	single nucleotide variant	NM_001366282.2(GOLGB1):c.9067G>T (p.Asp3023Tyr)	not specified [RCV004919968]	uncertain significance	3	121677003	121677003	Human		name
597731938	CV3688114	single nucleotide variant	NM_001366282.2(GOLGB1):c.9559G>C (p.Glu3187Gln)	not specified [RCV004919969]	uncertain significance	3	121665027	121665027	Human		name
597788965	CV3688115	single nucleotide variant	NM_001366282.2(GOLGB1):c.5125C>A (p.His1709Asn)	not specified [RCV004932855]	uncertain significance	3	121695398	121695398	Human		name
597731947	CV3688116	single nucleotide variant	NM_001366282.2(GOLGB1):c.6559A>G (p.Ser2187Gly)	not specified [RCV004919970]	uncertain significance	3	121693964	121693964	Human		name
597731956	CV3688117	single nucleotide variant	NM_001366282.2(GOLGB1):c.6904C>T (p.Arg2302Cys)	not specified [RCV004919971]	uncertain significance	3	121692460	121692460	Human		name
597731966	CV3688118	single nucleotide variant	NM_001366282.2(GOLGB1):c.8662A>G (p.Met2888Val)	not specified [RCV004919972]	uncertain significance	3	121690702	121690702	Human		name
597731974	CV3688119	single nucleotide variant	NM_001366282.2(GOLGB1):c.8800A>G (p.Lys2934Glu)	not specified [RCV004919973]	uncertain significance	3	121681760	121681760	Human		name
597788970	CV3688122	single nucleotide variant	NM_001366282.2(GOLGB1):c.3860C>T (p.Ser1287Phe)	not specified [RCV004932856]	uncertain significance	3	121696663	121696663	Human		name
597788978	CV3688126	single nucleotide variant	NM_001366282.2(GOLGB1):c.3737G>T (p.Arg1246Met)	not specified [RCV004932858]	uncertain significance	3	121696786	121696786	Human		name
597788982	CV3688128	single nucleotide variant	NM_001366282.2(GOLGB1):c.3502G>C (p.Glu1168Gln)	not specified [RCV004932859]	uncertain significance	3	121697021	121697021	Human		name
597788992	CV3688130	single nucleotide variant	NM_001366282.2(GOLGB1):c.6140T>G (p.Val2047Gly)	not specified [RCV004932861]	uncertain significance	3	121694383	121694383	Human		name
597732027	CV3688131	single nucleotide variant	NM_001366282.2(GOLGB1):c.3821A>G (p.Lys1274Arg)	not specified [RCV004919978]	uncertain significance	3	121696702	121696702	Human		name
597732035	CV3688132	single nucleotide variant	NM_001366282.2(GOLGB1):c.7397C>G (p.Ser2466Cys)	not specified [RCV004919979]	uncertain significance	3	121691967	121691967	Human		name
597732043	CV3688134	single nucleotide variant	NM_001366282.2(GOLGB1):c.3955A>G (p.Ile1319Val)	not specified [RCV004919980]	uncertain significance	3	121696568	121696568	Human		name
597789001	CV3688135	single nucleotide variant	NM_001366282.2(GOLGB1):c.4175T>C (p.Leu1392Pro)	not specified [RCV004932863]	uncertain significance	3	121696348	121696348	Human		name
597732054	CV3688136	single nucleotide variant	NM_001366282.2(GOLGB1):c.3319C>A (p.Gln1107Lys)	not specified [RCV004919981]	uncertain significance	3	121697204	121697204	Human		name
597732064	CV3688137	single nucleotide variant	NM_001366282.2(GOLGB1):c.4642C>T (p.Leu1548Phe)	not specified [RCV004919982]	uncertain significance	3	121695881	121695881	Human		name
597732075	CV3688138	single nucleotide variant	NM_001366282.2(GOLGB1):c.5218T>C (p.Tyr1740His)	not specified [RCV004919983]	uncertain significance	3	121695305	121695305	Human		name
597732087	CV3688141	single nucleotide variant	NM_001366282.2(GOLGB1):c.3233T>C (p.Leu1078Pro)	not specified [RCV004919984]	uncertain significance	3	121697290	121697290	Human		name
597789013	CV3688142	single nucleotide variant	NM_001366282.2(GOLGB1):c.3503A>C (p.Glu1168Ala)	not specified [RCV004932866]	uncertain significance	3	121697020	121697020	Human		name
597789021	CV3688144	single nucleotide variant	NM_001366282.2(GOLGB1):c.8900A>G (p.His2967Arg)	not specified [RCV004932868]	uncertain significance	3	121677424	121677424	Human		name
597732097	CV3688145	single nucleotide variant	NM_001366282.2(GOLGB1):c.7304A>G (p.Glu2435Gly)	not specified [RCV004919985]	uncertain significance	3	121692060	121692060	Human		name
597732109	CV3688146	single nucleotide variant	NM_001366282.2(GOLGB1):c.9679T>G (p.Trp3227Gly)	not specified [RCV004919986]	uncertain significance	3	121664596	121664596	Human		name
597732120	CV3688147	single nucleotide variant	NM_001366282.2(GOLGB1):c.5476G>A (p.Ala1826Thr)	not specified [RCV004919987]	uncertain significance	3	121695047	121695047	Human		name
597732138	CV3688149	single nucleotide variant	NM_001366282.2(GOLGB1):c.7136A>G (p.His2379Arg)	not specified [RCV004919989]	uncertain significance	3	121692228	121692228	Human		name
598128796	CV3886594	single nucleotide variant	NM_001366282.2(GOLGB1):c.6668C>T (p.Ala2223Val)	not provided [RCV005244254]	benign	3	121693855	121693855	Human		name
598264789	CV3974556	single nucleotide variant	NM_001366282.2(GOLGB1):c.5951A>G (p.Lys1984Arg)	not specified [RCV005348924]	uncertain significance	3	121694572	121694572	Human		name
598264794	CV3974557	single nucleotide variant	NM_001366282.2(GOLGB1):c.5822G>A (p.Ser1941Asn)	not specified [RCV005348925]	uncertain significance	3	121694701	121694701	Human		name
598264799	CV3974558	single nucleotide variant	NM_001366282.2(GOLGB1):c.6590A>C (p.Lys2197Thr)	not specified [RCV005348926]	uncertain significance	3	121693933	121693933	Human		name
598264809	CV3974560	single nucleotide variant	NM_001366282.2(GOLGB1):c.9226G>A (p.Asp3076Asn)	not specified [RCV005348928]	uncertain significance	3	121669307	121669307	Human		name
598264817	CV3974562	single nucleotide variant	NM_001366282.2(GOLGB1):c.7483A>G (p.Ile2495Val)	not specified [RCV005348930]	likely benign	3	121691881	121691881	Human		name
598264823	CV3974563	single nucleotide variant	NM_001366282.2(GOLGB1):c.5180C>T (p.Ala1727Val)	not specified [RCV005348931]	uncertain significance	3	121695343	121695343	Human		name
598233008	CV3974564	single nucleotide variant	NM_001366282.2(GOLGB1):c.8425G>A (p.Glu2809Lys)	not specified [RCV005342691]	uncertain significance	3	121690939	121690939	Human		name
598264827	CV3974565	single nucleotide variant	NM_001366282.2(GOLGB1):c.6340A>G (p.Lys2114Glu)	not specified [RCV005348932]	uncertain significance	3	121694183	121694183	Human		name
598264838	CV3974567	single nucleotide variant	NM_001366282.2(GOLGB1):c.4144A>G (p.Ser1382Gly)	not specified [RCV005348934]	uncertain significance	3	121696379	121696379	Human		name
598264843	CV3974568	single nucleotide variant	NM_001366282.2(GOLGB1):c.9139C>A (p.His3047Asn)	not specified [RCV005348935]	uncertain significance	3	121676931	121676931	Human		name
598264847	CV3974569	single nucleotide variant	NM_001366282.2(GOLGB1):c.8491G>A (p.Asp2831Asn)	not specified [RCV005348936]	uncertain significance	3	121690873	121690873	Human		name
598264857	CV3974571	single nucleotide variant	NM_001366282.2(GOLGB1):c.4079G>T (p.Ser1360Ile)	not specified [RCV005348938]	uncertain significance	3	121696444	121696444	Human		name
598264867	CV3974573	single nucleotide variant	NM_001366282.2(GOLGB1):c.5659G>A (p.Gly1887Ser)	not specified [RCV005348940]	uncertain significance	3	121694864	121694864	Human		name
598233026	CV3974576	single nucleotide variant	NM_001366282.2(GOLGB1):c.6519G>T (p.Lys2173Asn)	not specified [RCV005342694]	uncertain significance	3	121694004	121694004	Human		name
598264873	CV3974577	single nucleotide variant	NM_001366282.2(GOLGB1):c.7651A>G (p.Ile2551Val)	not specified [RCV005348941]	uncertain significance	3	121691713	121691713	Human		name
598264877	CV3974578	single nucleotide variant	NM_001366282.2(GOLGB1):c.7660A>G (p.Ser2554Gly)	not specified [RCV005348942]	uncertain significance	3	121691704	121691704	Human		name
598264887	CV3974580	single nucleotide variant	NM_001366282.2(GOLGB1):c.6616C>T (p.Arg2206Cys)	not specified [RCV005348944]	uncertain significance	3	121693907	121693907	Human		name
598264891	CV3974581	single nucleotide variant	NM_001366282.2(GOLGB1):c.6214G>T (p.Val2072Phe)	not specified [RCV005348945]	uncertain significance	3	121694309	121694309	Human		name
598264896	CV3974582	single nucleotide variant	NM_001366282.2(GOLGB1):c.6008A>G (p.Gln2003Arg)	not specified [RCV005348946]	uncertain significance	3	121694515	121694515	Human		name
598264903	CV3974583	single nucleotide variant	NM_001366282.2(GOLGB1):c.7367A>C (p.Glu2456Ala)	not specified [RCV005348947]	uncertain significance	3	121691997	121691997	Human		name
598233031	CV3974584	single nucleotide variant	NM_001366282.2(GOLGB1):c.3179G>A (p.Cys1060Tyr)	not specified [RCV005342695]	uncertain significance	3	121697344	121697344	Human		name
598233037	CV3974585	single nucleotide variant	NM_001366282.2(GOLGB1):c.3374C>T (p.Ala1125Val)	not specified [RCV005342696]	likely benign	3	121697149	121697149	Human		name
598233045	CV3974586	single nucleotide variant	NM_001366282.2(GOLGB1):c.5426G>T (p.Ser1809Ile)	not specified [RCV005342697]	uncertain significance	3	121695097	121695097	Human		name
598264909	CV3974587	single nucleotide variant	NM_001366282.2(GOLGB1):c.4162G>T (p.Gly1388Cys)	not specified [RCV005348948]	uncertain significance	3	121696361	121696361	Human		name
598264926	CV3974590	single nucleotide variant	NM_001366282.2(GOLGB1):c.9766C>G (p.Leu3256Val)	not specified [RCV005348951]	uncertain significance	3	121664509	121664509	Human		name
15169038	CV708499	single nucleotide variant	NM_001366282.2(GOLGB1):c.3656G>C (p.Arg1219Pro)	not provided [RCV000971734]	likely benign	3	121696867	121696867	Human	6	name
15169038	CV708499	single nucleotide variant	NM_001366282.2(GOLGB1):c.3656G>C (p.Arg1219Pro)	not provided [RCV000971734]	likely benign	3	121696867	121696868	Human	6	name
8625476	CV80599	deletion	NM_004487.4(GOLGB1):c.8271delG (p.Arg2759Glyfs)	Malignant melanoma [RCV000060676]	not provided	3	121691078	121691078	Human		name

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