Sh2d3c Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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75 records found for search term Sh2d3c

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155931450	CV2293520	single nucleotide variant	NM_170600.3(SH2D3C):c.50T>C (p.Phe17Ser)	not specified [RCV004153053]	uncertain significance	9	127774455	127774455	Human		name
401893414	CV2766830	single nucleotide variant	NM_170600.3(SH2D3C):c.82C>T (p.Arg28Trp)	not specified [RCV004349215]	uncertain significance	9	127774423	127774423	Human		name
401918459	CV2826407	single nucleotide variant	NM_170600.3(SH2D3C):c.444C>A (p.Pro148=)	not provided [RCV003430255]	likely benign	9	127774061	127774061	Human		name
405707739	CV3317868	single nucleotide variant	NM_170600.3(SH2D3C):c.74A>G (p.Asn25Ser)	not specified [RCV004448032]	uncertain significance	9	127774431	127774431	Human		name
405707750	CV3317869	single nucleotide variant	NM_170600.3(SH2D3C):c.86C>T (p.Ser29Phe)	not specified [RCV004448033]	uncertain significance	9	127774419	127774419	Human		name
405707756	CV3317870	single nucleotide variant	NM_170600.3(SH2D3C):c.98G>A (p.Arg33Lys)	not specified [RCV004448034]	uncertain significance	9	127774407	127774407	Human		name
597695291	CV3605983	single nucleotide variant	NM_170600.3(SH2D3C):c.91A>G (p.Thr31Ala)	not specified [RCV004859284]	uncertain significance	9	127774414	127774414	Human		name
598239835	CV3917720	single nucleotide variant	NM_170600.3(SH2D3C):c.516G>A (p.Arg172=)	not specified [RCV005276095]	likely benign	9	127761650	127761650	Human		name
329361063	CV2463249	single nucleotide variant	NM_170600.3(SH2D3C):c.137A>C (p.Glu46Ala)	not specified [RCV004275015]	uncertain significance	9	127774368	127774368	Human		name
405707659	CV3317856	single nucleotide variant	NM_170600.3(SH2D3C):c.137A>T (p.Glu46Val)	not specified [RCV004448020]	uncertain significance	9	127774368	127774368	Human		name
405707707	CV3317863	single nucleotide variant	NM_170600.3(SH2D3C):c.205C>T (p.Arg69Cys)	not specified [RCV004448027]	uncertain significance	9	127774300	127774300	Human		name
597695249	CV3605979	single nucleotide variant	NM_170600.3(SH2D3C):c.284G>A (p.Arg95Gln)	not specified [RCV004859280]	likely benign	9	127774221	127774221	Human		name
597695272	CV3605981	single nucleotide variant	NM_170600.3(SH2D3C):c.211A>G (p.Ser71Gly)	not specified [RCV004859282]	uncertain significance	9	127774294	127774294	Human		name
15193567	CV700801	single nucleotide variant	NM_170600.3(SH2D3C):c.1737G>A (p.Lys579=)	not provided [RCV000955408]	benign	9	127744627	127744627	Human		name
156399532	CV2205175	single nucleotide variant	NM_170600.3(SH2D3C):c.325G>A (p.Gly109Arg)	not specified [RCV004077770]	likely benign	9	127774180	127774180	Human		name
156377076	CV2206957	single nucleotide variant	NM_170600.3(SH2D3C):c.565G>A (p.Glu189Lys)	not specified [RCV004085579]	uncertain significance	9	127751291	127751291	Human		name
156175154	CV2299524	single nucleotide variant	NM_170600.3(SH2D3C):c.893G>A (p.Arg298His)	not specified [RCV004154867]	uncertain significance	9	127749457	127749457	Human		name
156110630	CV2387674	single nucleotide variant	NM_170600.3(SH2D3C):c.476T>C (p.Val159Ala)	not specified [RCV004234217]	uncertain significance	9	127774029	127774029	Human		name
329351524	CV2462077	single nucleotide variant	NM_170600.3(SH2D3C):c.828G>T (p.Glu276Asp)	not specified [RCV004266111]	uncertain significance	9	127749522	127749522	Human		name
401735698	CV2692175	single nucleotide variant	NM_170600.3(SH2D3C):c.910C>A (p.Arg304Ser)	not specified [RCV004301873]	uncertain significance	9	127749440	127749440	Human		name
401893462	CV2765319	single nucleotide variant	NM_170600.3(SH2D3C):c.652C>T (p.His218Tyr)	not specified [RCV004339832]	uncertain significance	9	127751204	127751204	Human		name
405707718	CV3317865	single nucleotide variant	NM_170600.3(SH2D3C):c.459G>T (p.Glu153Asp)	not specified [RCV004448029]	uncertain significance	9	127774046	127774046	Human		name
405707725	CV3317866	single nucleotide variant	NM_170600.3(SH2D3C):c.506A>G (p.His169Arg)	not specified [RCV004448030]	uncertain significance	9	127773999	127773999	Human		name
405707733	CV3317867	single nucleotide variant	NM_170600.3(SH2D3C):c.558C>G (p.Phe186Leu)	not specified [RCV004448031]	uncertain significance	9	127751298	127751298	Human		name
597695261	CV3605980	single nucleotide variant	NM_170600.3(SH2D3C):c.707G>A (p.Arg236His)	not specified [RCV004859281]	uncertain significance	9	127749643	127749643	Human		name
597695326	CV3605986	single nucleotide variant	NM_170600.3(SH2D3C):c.950G>T (p.Cys317Phe)	not specified [RCV004859287]	uncertain significance	9	127749400	127749400	Human		name
598239818	CV3917717	single nucleotide variant	NM_170600.3(SH2D3C):c.535G>A (p.Ala179Thr)	not specified [RCV005276092]	uncertain significance	9	127761631	127761631	Human		name
156032596	CV2214480	single nucleotide variant	NM_170600.3(SH2D3C):c.1622C>T (p.Thr541Ile)	not specified [RCV004088535]	uncertain significance	9	127744742	127744742	Human		name
156043367	CV2215846	single nucleotide variant	NM_170600.3(SH2D3C):c.1861A>G (p.Met621Val)	not specified [RCV004096946]	uncertain significance	9	127742904	127742904	Human		name
156384414	CV2231079	single nucleotide variant	NM_170600.3(SH2D3C):c.1954C>G (p.Leu652Val)	not specified [RCV004094304]	uncertain significance	9	127741922	127741922	Human		name
156032040	CV2239299	single nucleotide variant	NM_170600.3(SH2D3C):c.1270C>T (p.Arg424Cys)	not specified [RCV004112261]	uncertain significance	9	127745094	127745094	Human		name
156205677	CV2249893	single nucleotide variant	NM_170600.3(SH2D3C):c.1504G>A (p.Val502Met)	not specified [RCV004122869]	uncertain significance	9	127744860	127744860	Human		name
156165327	CV2270337	single nucleotide variant	NM_170600.3(SH2D3C):c.1033G>A (p.Val345Ile)	not specified [RCV004135541]	uncertain significance	9	127749317	127749317	Human		name
156074841	CV2281473	single nucleotide variant	NM_170600.3(SH2D3C):c.1073G>A (p.Arg358His)	not specified [RCV004153797]	uncertain significance	9	127749277	127749277	Human		name
155959917	CV2285336	single nucleotide variant	NM_170600.3(SH2D3C):c.1938G>T (p.Met646Ile)	not specified [RCV004139212]	uncertain significance	9	127741938	127741938	Human		name
156327711	CV2332140	single nucleotide variant	NM_170600.3(SH2D3C):c.2000A>G (p.Lys667Arg)	not specified [RCV004189177]	uncertain significance	9	127741876	127741876	Human		name
155922260	CV2340592	single nucleotide variant	NM_170600.3(SH2D3C):c.1702C>T (p.Arg568Trp)	not specified [RCV004197300]	uncertain significance	9	127744662	127744662	Human		name
155975633	CV2342688	single nucleotide variant	NM_170600.3(SH2D3C):c.1327G>T (p.Ala443Ser)	not specified [RCV004196769]	uncertain significance	9	127745037	127745037	Human		name
156254744	CV2358851	single nucleotide variant	NM_170600.3(SH2D3C):c.1639G>A (p.Val547Met)	not specified [RCV004212198]	uncertain significance	9	127744725	127744725	Human		name
156305664	CV2359659	single nucleotide variant	NM_170600.3(SH2D3C):c.1762C>T (p.Arg588Trp)	not specified [RCV004210486]	uncertain significance	9	127744602	127744602	Human		name
156135326	CV2362237	single nucleotide variant	NM_170600.3(SH2D3C):c.1154G>A (p.Arg385His)	not specified [RCV004210033]	likely benign	9	127747257	127747257	Human		name
156268542	CV2372057	single nucleotide variant	NM_170600.3(SH2D3C):c.2497C>A (p.Gln833Lys)	not specified [RCV004221726]	uncertain significance	9	127738832	127738832	Human		name
155954393	CV2379205	single nucleotide variant	NM_170600.3(SH2D3C):c.1172G>A (p.Arg391His)	not specified [RCV004235990]	uncertain significance	9	127747239	127747239	Human		name
329376340	CV2425078	single nucleotide variant	NM_170600.3(SH2D3C):c.2507G>A (p.Arg836His)	not specified [RCV004248974]	uncertain significance	9	127738822	127738822	Human		name
329364603	CV2443730	single nucleotide variant	NM_170600.3(SH2D3C):c.1948G>A (p.Asp650Asn)	not specified [RCV004256029]	uncertain significance	9	127741928	127741928	Human		name
329358097	CV2453891	single nucleotide variant	NM_170600.3(SH2D3C):c.1197G>C (p.Gln399His)	not specified [RCV004271280]	uncertain significance	9	127747214	127747214	Human		name
401747133	CV2679016	single nucleotide variant	NM_170600.3(SH2D3C):c.1511G>T (p.Gly504Val)	not specified [RCV004295025]	uncertain significance	9	127744853	127744853	Human		name
401759164	CV2712455	single nucleotide variant	NM_170600.3(SH2D3C):c.1517G>A (p.Arg506Gln)	not specified [RCV004313917]	uncertain significance	9	127744847	127744847	Human		name
401768578	CV2735352	single nucleotide variant	NM_170600.3(SH2D3C):c.1822A>G (p.Thr608Ala)	not specified [RCV004334009]	uncertain significance	9	127742943	127742943	Human		name
401889978	CV2762067	single nucleotide variant	NM_170600.3(SH2D3C):c.1069C>T (p.Arg357Trp)	not specified [RCV004341884]	uncertain significance	9	127749281	127749281	Human		name
401891544	CV2779241	single nucleotide variant	NM_170600.3(SH2D3C):c.1402C>T (p.His468Tyr)	not specified [RCV004350925]	likely benign	9	127744962	127744962	Human		name
401918458	CV2826406	single nucleotide variant	NM_170600.3(SH2D3C):c.1159C>G (p.Arg387Gly)	not provided [RCV003430254]	likely benign	9	127747252	127747252	Human		name
405708272	CV3317850	single nucleotide variant	NM_170600.3(SH2D3C):c.1070G>A (p.Arg357Gln)	not specified [RCV004448014]	uncertain significance	9	127749280	127749280	Human		name
405708078	CV3317851	single nucleotide variant	NM_170600.3(SH2D3C):c.1151C>A (p.Pro384His)	not specified [RCV004448015]	uncertain significance	9	127747260	127747260	Human		name
405707907	CV3317852	single nucleotide variant	NM_170600.3(SH2D3C):c.1171C>T (p.Arg391Cys)	not specified [RCV004448016]	uncertain significance	9	127747240	127747240	Human		name
405707762	CV3317853	single nucleotide variant	NM_170600.3(SH2D3C):c.1229T>C (p.Ile410Thr)	not specified [RCV004448017]	uncertain significance	9	127747182	127747182	Human		name
405707644	CV3317854	single nucleotide variant	NM_170600.3(SH2D3C):c.1312C>G (p.Pro438Ala)	not specified [RCV004448018]	uncertain significance	9	127745052	127745052	Human		name
405707665	CV3317857	single nucleotide variant	NM_170600.3(SH2D3C):c.1453A>G (p.Ser485Gly)	not specified [RCV004448021]	uncertain significance	9	127744911	127744911	Human		name
405707674	CV3317858	single nucleotide variant	NM_170600.3(SH2D3C):c.1496A>T (p.Gln499Leu)	not specified [RCV004448022]	uncertain significance	9	127744868	127744868	Human		name
405707681	CV3317859	single nucleotide variant	NM_170600.3(SH2D3C):c.1726C>T (p.Arg576Cys)	not specified [RCV004448023]	uncertain significance	9	127744638	127744638	Human		name
405707687	CV3317860	single nucleotide variant	NM_170600.3(SH2D3C):c.1812A>G (p.Ile604Met)	not specified [RCV004448024]	uncertain significance	9	127742953	127742953	Human		name
405707694	CV3317861	single nucleotide variant	NM_170600.3(SH2D3C):c.1835A>G (p.Gln612Arg)	not specified [RCV004448025]	uncertain significance	9	127742930	127742930	Human		name
405707700	CV3317862	single nucleotide variant	NM_170600.3(SH2D3C):c.1987G>A (p.Ala663Thr)	not specified [RCV004448026]	uncertain significance	9	127741889	127741889	Human		name
405707712	CV3317864	single nucleotide variant	NM_170600.3(SH2D3C):c.2506C>T (p.Arg836Cys)	not specified [RCV004448028]	uncertain significance	9	127738823	127738823	Human		name
407490362	CV3484171	single nucleotide variant	NM_170600.3(SH2D3C):c.1507C>T (p.Arg503Cys)	not specified [RCV004666288]	uncertain significance	9	127744857	127744857	Human		name
407490366	CV3484172	single nucleotide variant	NM_170600.3(SH2D3C):c.1234G>A (p.Glu412Lys)	not specified [RCV004666289]	uncertain significance	9	127747177	127747177	Human		name
407490369	CV3484173	single nucleotide variant	NM_170600.3(SH2D3C):c.2317G>A (p.Val773Met)	not specified [RCV004666290]	uncertain significance	9	127739772	127739772	Human		name
597695240	CV3605978	single nucleotide variant	NM_170600.3(SH2D3C):c.1282G>A (p.Ala428Thr)	not specified [RCV004859279]	likely benign	9	127745082	127745082	Human		name
597695280	CV3605982	single nucleotide variant	NM_170600.3(SH2D3C):c.2217C>G (p.Ser739Arg)	not specified [RCV004859283]	uncertain significance	9	127739872	127739872	Human		name
597695303	CV3605984	single nucleotide variant	NM_170600.3(SH2D3C):c.2233C>T (p.His745Tyr)	not specified [RCV004859285]	uncertain significance	9	127739856	127739856	Human		name
597695314	CV3605985	single nucleotide variant	NM_170600.3(SH2D3C):c.1370C>T (p.Pro457Leu)	not specified [RCV004859286]	uncertain significance	9	127744994	127744994	Human		name
597695335	CV3605987	single nucleotide variant	NM_170600.3(SH2D3C):c.2050A>G (p.Ser684Gly)	not specified [RCV004859288]	uncertain significance	9	127741826	127741826	Human		name
597695346	CV3605988	single nucleotide variant	NM_170600.3(SH2D3C):c.1078G>A (p.Val360Ile)	not specified [RCV004859289]	uncertain significance	9	127749272	127749272	Human		name
598239823	CV3917718	single nucleotide variant	NM_170600.3(SH2D3C):c.2312A>G (p.His771Arg)	not specified [RCV005276093]	uncertain significance	9	127739777	127739777	Human		name
598239828	CV3917719	single nucleotide variant	NM_170600.3(SH2D3C):c.1548G>C (p.Gln516His)	not specified [RCV005276094]	uncertain significance	9	127744816	127744816	Human		name

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