Synrg Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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123 records found for search term Synrg

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401937689	CV2796811	single nucleotide variant	NM_007247.6(SYNRG):c.372-1G>A	SYNRG-related disorder [RCV003416781]	uncertain significance	17	37585431	37585431	Human		name , trait , alternate_id
401914392	CV2811272	single nucleotide variant	NM_007247.6(SYNRG):c.3777+3A>G	not provided [RCV003428244]	likely benign	17	37520535	37520535	Human		name
405286859	CV3213801	single nucleotide variant	NM_007247.6(SYNRG):c.3518-6C>T	SYNRG-related disorder [RCV003924199]	likely benign	17	37536133	37536133	Human		name , trait , alternate_id
28907238	CV860376	single nucleotide variant	NM_007247.6(SYNRG):c.3813+5G>A	not provided [RCV001093340]	uncertain significance	17	37520174	37520174	Human		name
405726713	CV3334806	single nucleotide variant	NM_007247.6(SYNRG):c.4G>T (p.Ala2Ser)	not specified [RCV004463846]	uncertain significance	17	37609352	37609352	Human		name
597780327	CV3618911	single nucleotide variant	NM_007247.6(SYNRG):c.17G>T (p.Gly6Val)	not specified [RCV004873780]	uncertain significance	17	37609339	37609339	Human		name
597780350	CV3618917	single nucleotide variant	NM_007247.6(SYNRG):c.13C>G (p.Pro5Ala)	not specified [RCV004873786]	uncertain significance	17	37609343	37609343	Human		name
156399873	CV2202277	single nucleotide variant	NM_007247.6(SYNRG):c.32G>A (p.Gly11Asp)	not specified [RCV004078210]	uncertain significance	17	37609324	37609324	Human		name
156165505	CV2319867	single nucleotide variant	NM_007247.6(SYNRG):c.68G>T (p.Gly23Val)	not specified [RCV004167750]	uncertain significance	17	37609288	37609288	Human		name
405265725	CV3215670	single nucleotide variant	NM_007247.6(SYNRG):c.612C>T (p.Phe204=)	SYNRG-related disorder [RCV003946845]	likely benign	17	37577591	37577591	Human		name , trait , alternate_id
405726721	CV3334807	single nucleotide variant	NM_007247.6(SYNRG):c.50C>T (p.Ala17Val)	not specified [RCV004463847]	uncertain significance	17	37609306	37609306	Human		name
407505787	CV3478336	single nucleotide variant	NM_007247.6(SYNRG):c.68G>C (p.Gly23Ala)	not specified [RCV004670933]	uncertain significance	17	37609288	37609288	Human		name
597780336	CV3618913	single nucleotide variant	NM_007247.6(SYNRG):c.76G>A (p.Gly26Ser)	not specified [RCV004873782]	likely benign	17	37609280	37609280	Human		name
597780365	CV3618922	single nucleotide variant	NM_007247.6(SYNRG):c.91G>A (p.Val31Ile)	not specified [RCV004873790]	uncertain significance	17	37600390	37600390	Human		name
156085340	CV2390565	single nucleotide variant	NM_007247.6(SYNRG):c.134T>C (p.Met45Thr)	not specified [RCV004239097]	uncertain significance	17	37596329	37596329	Human		name
401737490	CV2679894	single nucleotide variant	NM_007247.6(SYNRG):c.154A>T (p.Met52Leu)	not specified [RCV004284182]	uncertain significance	17	37596309	37596309	Human		name
401935987	CV2811273	single nucleotide variant	NM_007247.6(SYNRG):c.1917A>G (p.Thr639=)	not provided [RCV003413208]	likely benign	17	37553806	37553806	Human		name
405292771	CV3192622	single nucleotide variant	NM_007247.6(SYNRG):c.2886A>C (p.Pro962=)	SYNRG-related disorder [RCV003929870]	benign	17	37542288	37542288	Human		name , trait , alternate_id
405726605	CV3334794	single nucleotide variant	NM_007247.6(SYNRG):c.217T>C (p.Ser73Pro)	not specified [RCV004463834]	uncertain significance	17	37596246	37596246	Human		name
405726634	CV3334797	single nucleotide variant	NM_007247.6(SYNRG):c.242C>G (p.Ala81Gly)	not specified [RCV004463837]	uncertain significance	17	37586548	37586548	Human		name
407505779	CV3478332	single nucleotide variant	NM_007247.6(SYNRG):c.134T>G (p.Met45Arg)	not specified [RCV004670931]	uncertain significance	17	37596329	37596329	Human		name
407530332	CV3478333	single nucleotide variant	NM_007247.6(SYNRG):c.109C>A (p.Pro37Thr)	not specified [RCV004681856]	uncertain significance	17	37600372	37600372	Human		name
408383286	CV3503766	single nucleotide variant	NM_007247.6(SYNRG):c.145G>A (p.Gly49Arg)	SYNRG-related disorder [RCV004730552]	uncertain significance	17	37596318	37596318	Human		name , trait , alternate_id
151663647	CV1334113	single nucleotide variant	NM_007247.6(SYNRG):c.811A>G (p.Ile271Val)	not provided [RCV001839287]	uncertain significance	17	37577392	37577392	Human		name
151663649	CV1334115	single nucleotide variant	NM_007247.6(SYNRG):c.635C>T (p.Thr212Ile)	not provided [RCV001839289]	uncertain significance	17	37577568	37577568	Human		name
156401641	CV2207517	single nucleotide variant	NM_007247.6(SYNRG):c.805C>G (p.Leu269Val)	not specified [RCV004089984]	uncertain significance	17	37577398	37577398	Human		name
156117381	CV2278822	single nucleotide variant	NM_007247.6(SYNRG):c.896T>C (p.Val299Ala)	not specified [RCV004145534]	uncertain significance	17	37576346	37576346	Human		name
401779356	CV2680252	single nucleotide variant	NM_007247.6(SYNRG):c.781G>A (p.Ala261Thr)	not specified [RCV004286721]	uncertain significance	17	37577422	37577422	Human		name
401771555	CV2711756	single nucleotide variant	NM_007247.6(SYNRG):c.577C>T (p.Pro193Ser)	not specified [RCV004309410]	uncertain significance	17	37584660	37584660	Human		name
401761840	CV2726927	single nucleotide variant	NM_007247.6(SYNRG):c.377G>A (p.Arg126Gln)	not specified [RCV004323210]	uncertain significance	17	37585425	37585425	Human		name
401887374	CV2775705	single nucleotide variant	NM_007247.6(SYNRG):c.821G>A (p.Ser274Asn)	not specified [RCV004350836]	uncertain significance	17	37577382	37577382	Human		name
405276828	CV3192409	single nucleotide variant	NM_007247.6(SYNRG):c.544G>A (p.Asp182Asn)	SYNRG-related disorder [RCV003917293]	likely benign	17	37584693	37584693	Human		name , trait , alternate_id
405291743	CV3206038	single nucleotide variant	NM_007247.6(SYNRG):c.3579G>C (p.Val1193=)	SYNRG-related disorder [RCV003964126]	likely benign	17	37536066	37536066	Human		name , trait , alternate_id
405291850	CV3206153	single nucleotide variant	NM_007247.6(SYNRG):c.3312G>A (p.Lys1104=)	SYNRG-related disorder [RCV003964217]	likely benign	17	37540434	37540434	Human		name , trait , alternate_id
405258953	CV3215235	single nucleotide variant	NM_007247.6(SYNRG):c.3639C>T (p.Ile1213=)	SYNRG-related disorder [RCV003942273]	likely benign	17	37536006	37536006	Human		name , trait , alternate_id
405293349	CV3221430	single nucleotide variant	NM_007247.6(SYNRG):c.3063G>A (p.Ser1021=)	SYNRG-related disorder [RCV003966913]	likely benign	17	37542111	37542111	Human		name , trait , alternate_id
405726706	CV3334805	single nucleotide variant	NM_007247.6(SYNRG):c.458T>C (p.Leu153Ser)	not specified [RCV004463845]	uncertain significance	17	37585344	37585344	Human		name
405726730	CV3334808	single nucleotide variant	NM_007247.6(SYNRG):c.616G>C (p.Val206Leu)	not specified [RCV004463848]	uncertain significance	17	37577587	37577587	Human		name
405726735	CV3334809	single nucleotide variant	NM_007247.6(SYNRG):c.623G>C (p.Cys208Ser)	not specified [RCV004463849]	uncertain significance	17	37577580	37577580	Human		name
597780332	CV3618912	single nucleotide variant	NM_007247.6(SYNRG):c.460A>G (p.Ser154Gly)	not specified [RCV004873781]	uncertain significance	17	37585342	37585342	Human		name
597780340	CV3618914	single nucleotide variant	NM_007247.6(SYNRG):c.884A>G (p.Asn295Ser)	not specified [RCV004873783]	uncertain significance	17	37576358	37576358	Human		name
597780358	CV3618920	single nucleotide variant	NM_007247.6(SYNRG):c.629T>C (p.Ile210Thr)	not specified [RCV004873788]	uncertain significance	17	37577574	37577574	Human		name
597780381	CV3618926	single nucleotide variant	NM_007247.6(SYNRG):c.682A>G (p.Lys228Glu)	not specified [RCV004873794]	uncertain significance	17	37577521	37577521	Human		name
598264122	CV3923417	single nucleotide variant	NM_007247.6(SYNRG):c.895G>C (p.Val299Leu)	not specified [RCV005280708]	uncertain significance	17	37576347	37576347	Human		name
151663648	CV1334114	single nucleotide variant	NM_007247.6(SYNRG):c.2905G>A (p.Asp969Asn)	not provided [RCV001839288]	uncertain significance	17	37542269	37542269	Human		name
156182298	CV2222277	single nucleotide variant	NM_007247.6(SYNRG):c.2600C>T (p.Pro867Leu)	not specified [RCV004105296]	uncertain significance	17	37553123	37553123	Human		name
156036335	CV2243537	single nucleotide variant	NM_007247.6(SYNRG):c.2758C>T (p.Pro920Ser)	not specified [RCV004112490]	likely benign	17	37542416	37542416	Human		name
155984310	CV2247747	single nucleotide variant	NM_007247.6(SYNRG):c.2104A>G (p.Ile702Val)	not specified [RCV004121218]	likely benign	17	37553619	37553619	Human		name
156064902	CV2272458	single nucleotide variant	NM_007247.6(SYNRG):c.2909C>T (p.Thr970Met)	not specified [RCV004133376]	likely benign	17	37542265	37542265	Human		name
156040587	CV2279130	single nucleotide variant	NM_007247.6(SYNRG):c.1348G>A (p.Val450Ile)	not specified [RCV004139374]	uncertain significance	17	37568924	37568924	Human		name
156000640	CV2296333	single nucleotide variant	NM_007247.6(SYNRG):c.2128G>T (p.Asp710Tyr)	not specified [RCV004148092]	uncertain significance	17	37553595	37553595	Human		name
156277236	CV2300128	single nucleotide variant	NM_007247.6(SYNRG):c.1903G>C (p.Ala635Pro)	not specified [RCV004151319]	uncertain significance	17	37553820	37553820	Human		name
156260513	CV2305104	single nucleotide variant	NM_007247.6(SYNRG):c.1031G>A (p.Arg344Gln)	not specified [RCV004168978]	uncertain significance	17	37571858	37571858	Human		name
156043555	CV2307934	single nucleotide variant	NM_007247.6(SYNRG):c.1556G>T (p.Gly519Val)	not specified [RCV004170380]	uncertain significance	17	37561515	37561515	Human		name
156336859	CV2342968	single nucleotide variant	NM_007247.6(SYNRG):c.1984A>G (p.Lys662Glu)	not specified [RCV004192573]	uncertain significance	17	37553739	37553739	Human		name
155901396	CV2345799	single nucleotide variant	NM_007247.6(SYNRG):c.1777C>G (p.Pro593Ala)	not specified [RCV004205725]	likely benign	17	37553946	37553946	Human		name
156200493	CV2350849	single nucleotide variant	NM_007247.6(SYNRG):c.2383G>A (p.Glu795Lys)	not specified [RCV004211689]	uncertain significance	17	37553340	37553340	Human		name
156149125	CV2359460	single nucleotide variant	NM_007247.6(SYNRG):c.1798A>G (p.Ile600Val)	not specified [RCV004214779]	uncertain significance	17	37553925	37553925	Human		name
155988298	CV2363960	single nucleotide variant	NM_007247.6(SYNRG):c.2813A>C (p.Asn938Thr)	not specified [RCV004218928]	uncertain significance	17	37542361	37542361	Human		name
156212110	CV2366910	single nucleotide variant	NM_007247.6(SYNRG):c.1193C>T (p.Pro398Leu)	not specified [RCV004213322]	uncertain significance	17	37570791	37570791	Human		name
156388898	CV2376193	single nucleotide variant	NM_007247.6(SYNRG):c.1795A>G (p.Thr599Ala)	not specified [RCV004220418]	likely benign	17	37553928	37553928	Human		name
329392813	CV2439198	single nucleotide variant	NM_007247.6(SYNRG):c.2663T>C (p.Val888Ala)	not specified [RCV004266472]	uncertain significance	17	37542511	37542511	Human		name
329385807	CV2462374	single nucleotide variant	NM_007247.6(SYNRG):c.1102G>T (p.Gly368Cys)	not specified [RCV004268139]	uncertain significance	17	37570882	37570882	Human		name
401770748	CV2685873	single nucleotide variant	NM_007247.6(SYNRG):c.1658C>G (p.Pro553Arg)	not specified [RCV004294855]	uncertain significance	17	37561200	37561200	Human		name
401761409	CV2702325	single nucleotide variant	NM_007247.6(SYNRG):c.1552A>G (p.Lys518Glu)	not specified [RCV004316857]	uncertain significance	17	37561519	37561519	Human		name
401899764	CV2762200	single nucleotide variant	NM_007247.6(SYNRG):c.2182G>A (p.Val728Met)	not specified [RCV004335328]	likely benign	17	37553541	37553541	Human		name
401897735	CV2772881	single nucleotide variant	NM_007247.6(SYNRG):c.1442C>T (p.Pro481Leu)	not specified [RCV004357657]	uncertain significance	17	37568830	37568830	Human		name
401880423	CV2780083	single nucleotide variant	NM_007247.6(SYNRG):c.1215A>G (p.Ile405Met)	not specified [RCV004355745]	likely benign	17	37570769	37570769	Human		name
401864457	CV2784774	single nucleotide variant	NM_007247.6(SYNRG):c.1979C>T (p.Ala660Val)	not specified [RCV004352569]	uncertain significance	17	37553744	37553744	Human		name
401879464	CV2785109	single nucleotide variant	NM_007247.6(SYNRG):c.1214T>C (p.Ile405Thr)	not specified [RCV004355118]	uncertain significance	17	37570770	37570770	Human		name
401876238	CV2789341	single nucleotide variant	NM_007247.6(SYNRG):c.1222G>A (p.Gly408Ser)	not specified [RCV004365360]	uncertain significance	17	37570762	37570762	Human		name
401898250	CV2791004	single nucleotide variant	NM_007247.6(SYNRG):c.1676C>G (p.Ala559Gly)	not specified [RCV004354622]	uncertain significance	17	37554047	37554047	Human		name
405271644	CV3206208	single nucleotide variant	NM_007247.6(SYNRG):c.1216C>A (p.Pro406Thr)	SYNRG-related disorder [RCV003971861]	likely benign	17	37570768	37570768	Human		name , trait , alternate_id
405258935	CV3215226	single nucleotide variant	NM_007247.6(SYNRG):c.2989G>C (p.Glu997Gln)	SYNRG-related disorder [RCV003942264]	benign	17	37542185	37542185	Human		name , trait , alternate_id
405289278	CV3218192	single nucleotide variant	NM_007247.6(SYNRG):c.1716T>A (p.Asp572Glu)	SYNRG-related disorder [RCV003983594]	uncertain significance	17	37554007	37554007	Human		name , trait , alternate_id
405271031	CV3218850	single nucleotide variant	NM_007247.6(SYNRG):c.2960A>C (p.Asp987Ala)	SYNRG-related disorder [RCV003971603]	likely benign	17	37542214	37542214	Human		name , trait , alternate_id
405726575	CV3334791	single nucleotide variant	NM_007247.6(SYNRG):c.1699G>T (p.Asp567Tyr)	not specified [RCV004463831]	uncertain significance	17	37554024	37554024	Human		name
405726584	CV3334792	single nucleotide variant	NM_007247.6(SYNRG):c.1877G>A (p.Ser626Asn)	not specified [RCV004463832]	uncertain significance	17	37553846	37553846	Human		name
405726597	CV3334793	single nucleotide variant	NM_007247.6(SYNRG):c.1982C>T (p.Thr661Ile)	not specified [RCV004463833]	uncertain significance	17	37553741	37553741	Human		name
405726616	CV3334795	single nucleotide variant	NM_007247.6(SYNRG):c.2300C>G (p.Thr767Ser)	not specified [RCV004463835]	uncertain significance	17	37553423	37553423	Human		name
405726625	CV3334796	single nucleotide variant	NM_007247.6(SYNRG):c.2302C>T (p.Pro768Ser)	not specified [RCV004463836]	uncertain significance	17	37553421	37553421	Human		name
405726642	CV3334798	single nucleotide variant	NM_007247.6(SYNRG):c.2576C>A (p.Pro859Gln)	not specified [RCV004463838]	uncertain significance	17	37553147	37553147	Human		name
405726651	CV3334799	single nucleotide variant	NM_007247.6(SYNRG):c.2728C>A (p.Pro910Thr)	not specified [RCV004463839]	uncertain significance	17	37542446	37542446	Human		name
405726662	CV3334800	single nucleotide variant	NM_007247.6(SYNRG):c.2768C>T (p.Thr923Ile)	not specified [RCV004463840]	uncertain significance	17	37542406	37542406	Human		name
405726670	CV3334801	single nucleotide variant	NM_007247.6(SYNRG):c.2866C>T (p.Leu956Phe)	not specified [RCV004463841]	uncertain significance	17	37542308	37542308	Human		name
405726679	CV3334802	single nucleotide variant	NM_007247.6(SYNRG):c.2893G>C (p.Ala965Pro)	not specified [RCV004463842]	uncertain significance	17	37542281	37542281	Human		name
405726687	CV3334803	single nucleotide variant	NM_007247.6(SYNRG):c.2963T>C (p.Phe988Ser)	not specified [RCV004463843]	uncertain significance	17	37542211	37542211	Human		name
407505771	CV3478330	single nucleotide variant	NM_007247.6(SYNRG):c.2984C>T (p.Thr995Met)	not specified [RCV004670929]	uncertain significance	17	37542190	37542190	Human		name
407505774	CV3478331	single nucleotide variant	NM_007247.6(SYNRG):c.1105G>A (p.Val369Ile)	not specified [RCV004670930]	uncertain significance	17	37570879	37570879	Human		name
407530334	CV3478334	single nucleotide variant	NM_007247.6(SYNRG):c.1994G>T (p.Ser665Ile)	not specified [RCV004681857]	uncertain significance	17	37553729	37553729	Human		name
407505784	CV3478335	single nucleotide variant	NM_007247.6(SYNRG):c.1655A>G (p.Lys552Arg)	not specified [RCV004670932]	uncertain significance	17	37561203	37561203	Human		name
407505792	CV3478337	single nucleotide variant	NM_007247.6(SYNRG):c.1750C>G (p.Pro584Ala)	not specified [RCV004670934]	uncertain significance	17	37553973	37553973	Human		name
407505796	CV3478338	single nucleotide variant	NM_007247.6(SYNRG):c.2194G>A (p.Val732Met)	not specified [RCV004670935]	uncertain significance	17	37553529	37553529	Human		name
597780343	CV3618915	single nucleotide variant	NM_007247.6(SYNRG):c.2857G>A (p.Glu953Lys)	not specified [RCV004873784]	uncertain significance	17	37542317	37542317	Human		name
597780347	CV3618916	single nucleotide variant	NM_007247.6(SYNRG):c.1913G>A (p.Ser638Asn)	not specified [RCV004873785]	uncertain significance	17	37553810	37553810	Human		name
597794679	CV3618918	single nucleotide variant	NM_007247.6(SYNRG):c.1324A>G (p.Ile442Val)	not specified [RCV004877936]	uncertain significance	17	37570660	37570660	Human		name
597780354	CV3618919	single nucleotide variant	NM_007247.6(SYNRG):c.1798A>C (p.Ile600Leu)	not specified [RCV004873787]	uncertain significance	17	37553925	37553925	Human		name
597780362	CV3618921	single nucleotide variant	NM_007247.6(SYNRG):c.1565C>T (p.Ala522Val)	not specified [RCV004873789]	uncertain significance	17	37561506	37561506	Human		name
597780369	CV3618923	single nucleotide variant	NM_007247.6(SYNRG):c.2630C>T (p.Ala877Val)	not specified [RCV004873791]	uncertain significance	17	37542544	37542544	Human		name
597780377	CV3618925	single nucleotide variant	NM_007247.6(SYNRG):c.1034C>G (p.Thr345Ser)	not specified [RCV004873793]	uncertain significance	17	37571855	37571855	Human		name
598180817	CV3923418	single nucleotide variant	NM_007247.6(SYNRG):c.1072G>A (p.Val358Ile)	not specified [RCV005286609]	uncertain significance	17	37571817	37571817	Human		name
598180823	CV3923419	single nucleotide variant	NM_007247.6(SYNRG):c.2803A>C (p.Ser935Arg)	not specified [RCV005286610]	uncertain significance	17	37542371	37542371	Human		name
598180830	CV3923420	single nucleotide variant	NM_007247.6(SYNRG):c.1441C>G (p.Pro481Ala)	not specified [RCV005286611]	uncertain significance	17	37568831	37568831	Human		name
598264128	CV3923422	single nucleotide variant	NM_007247.6(SYNRG):c.2361A>G (p.Ile787Met)	not specified [RCV005280710]	likely benign	17	37553362	37553362	Human		name
28907264	CV860377	single nucleotide variant	NM_007247.6(SYNRG):c.2813A>G (p.Asn938Ser)	not provided [RCV001093341]	uncertain significance	17	37542361	37542361	Human		name
153301331	CV1685947	single nucleotide variant	NM_007247.6(SYNRG):c.3605T>C (p.Leu1202Pro)	not provided [RCV002260916]	uncertain significance	17	37536040	37536040	Human		name
155920088	CV2254989	single nucleotide variant	NM_007247.6(SYNRG):c.3671A>G (p.Asp1224Gly)	not specified [RCV004117214]	uncertain significance	17	37520644	37520644	Human		name
156145619	CV2292511	single nucleotide variant	NM_007247.6(SYNRG):c.3018C>A (p.Ser1006Arg)	not specified [RCV004150289]	uncertain significance	17	37542156	37542156	Human		name
156297861	CV2297721	single nucleotide variant	NM_007247.6(SYNRG):c.3182C>G (p.Thr1061Ser)	not specified [RCV004155400]	uncertain significance	17	37541992	37541992	Human		name
156210150	CV2309640	single nucleotide variant	NM_007247.6(SYNRG):c.3427A>G (p.Lys1143Glu)	not specified [RCV004159005]	uncertain significance	17	37538414	37538414	Human		name
155918831	CV2333076	single nucleotide variant	NM_007247.6(SYNRG):c.3622G>A (p.Val1208Ile)	not specified [RCV004194371]	uncertain significance	17	37536023	37536023	Human		name
156228650	CV2393038	single nucleotide variant	NM_007247.6(SYNRG):c.3718A>G (p.Lys1240Glu)	not specified [RCV004242888]	uncertain significance	17	37520597	37520597	Human		name
401743087	CV2715392	single nucleotide variant	NM_007247.6(SYNRG):c.3678C>G (p.Asn1226Lys)	not specified [RCV004324713]	uncertain significance	17	37520637	37520637	Human		name
401913695	CV2799602	single nucleotide variant	NM_007247.6(SYNRG):c.3280T>G (p.Phe1094Val)	SYNRG-related disorder [RCV003427938]	uncertain significance	17	37540466	37540466	Human		name , trait , alternate_id
405271824	CV3206292	single nucleotide variant	NM_007247.6(SYNRG):c.3238G>A (p.Glu1080Lys)	SYNRG-related disorder [RCV003971926]	uncertain significance	17	37540508	37540508	Human		name , trait , alternate_id
405726698	CV3334804	single nucleotide variant	NM_007247.6(SYNRG):c.3325G>A (p.Val1109Ile)	not specified [RCV004463844]	uncertain significance	17	37540421	37540421	Human		name
597780373	CV3618924	single nucleotide variant	NM_007247.6(SYNRG):c.3020C>T (p.Pro1007Leu)	not specified [RCV004873792]	uncertain significance	17	37542154	37542154	Human		name
597780384	CV3618927	single nucleotide variant	NM_007247.6(SYNRG):c.3262C>T (p.Pro1088Ser)	not specified [RCV004873795]	uncertain significance	17	37540484	37540484	Human		name
598180805	CV3923415	single nucleotide variant	NM_007247.6(SYNRG):c.3236A>G (p.Lys1079Arg)	not specified [RCV005286607]	uncertain significance	17	37540510	37540510	Human		name
598264125	CV3923421	single nucleotide variant	NM_007247.6(SYNRG):c.3332G>C (p.Arg1111Pro)	not specified [RCV005280709]	uncertain significance	17	37540414	37540414	Human		name
598180837	CV3923423	single nucleotide variant	NM_007247.6(SYNRG):c.3128C>G (p.Thr1043Ser)	not specified [RCV005286612]	uncertain significance	17	37542046	37542046	Human		name
598180846	CV3923424	single nucleotide variant	NM_007247.6(SYNRG):c.3125C>T (p.Ala1042Val)	not specified [RCV005286613]	uncertain significance	17	37542049	37542049	Human		name
8636109	CV91332	single nucleotide variant	NM_001163544.2(SYNRG):c.1172C>T (p.Ser391Phe)	Malignant melanoma [RCV000071430]	not provided	17	37568866	37568866	Human		name

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