Acsm5 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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63 records found for search term Acsm5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15164806	CV778234	single nucleotide variant	NM_017888.3(ACSM5):c.1001+10G>A	not provided [RCV000948435]	benign	16	20427877	20427877	Human		name
401938570	CV2807695	single nucleotide variant	NM_017888.3(ACSM5):c.165C>T (p.Phe55=)	not provided [RCV003417668]	likely benign	16	20411649	20411649	Human		name
401938571	CV2807696	single nucleotide variant	NM_017888.3(ACSM5):c.1059C>T (p.Asp353=)	not provided [RCV003417669]	likely benign	16	20429735	20429735	Human		name
405772840	CV3299919	single nucleotide variant	NM_017888.3(ACSM5):c.262A>G (p.Ile88Val)	not specified [RCV004435591]	likely benign	16	20418116	20418116	Human		name
407501187	CV3424750	single nucleotide variant	NM_017888.3(ACSM5):c.245A>G (p.Asn82Ser)	not specified [RCV004607322]	uncertain significance	16	20418099	20418099	Human		name
597785149	CV3647245	single nucleotide variant	NM_017888.3(ACSM5):c.239G>T (p.Trp80Leu)	not specified [RCV004900687]	uncertain significance	16	20418093	20418093	Human		name
156094568	CV2213407	single nucleotide variant	NM_017888.3(ACSM5):c.940A>G (p.Ile314Val)	not specified [RCV004087387]	uncertain significance	16	20427806	20427806	Human		name
156332875	CV2220751	single nucleotide variant	NM_017888.3(ACSM5):c.857G>T (p.Trp286Leu)	not specified [RCV004097919]	uncertain significance	16	20424005	20424005	Human		name
156022626	CV2223243	single nucleotide variant	NM_017888.3(ACSM5):c.769C>T (p.Arg257Trp)	not specified [RCV004105864]	uncertain significance	16	20423917	20423917	Human		name
156384941	CV2231229	single nucleotide variant	NM_017888.3(ACSM5):c.404G>T (p.Cys135Phe)	not specified [RCV004094428]	uncertain significance	16	20418258	20418258	Human		name
156084887	CV2249291	single nucleotide variant	NM_017888.3(ACSM5):c.760A>G (p.Ser254Gly)	not specified [RCV004118317]	uncertain significance	16	20421394	20421394	Human		name
156164566	CV2389707	single nucleotide variant	NM_017888.3(ACSM5):c.622C>T (p.Arg208Trp)	not specified [RCV004243756]	uncertain significance	16	20419434	20419434	Human		name
329353977	CV2436708	single nucleotide variant	NM_017888.3(ACSM5):c.589C>T (p.Arg197Trp)	not specified [RCV004258076]	uncertain significance	16	20419401	20419401	Human		name
329374582	CV2443960	single nucleotide variant	NM_017888.3(ACSM5):c.923C>T (p.Thr308Ile)	not specified [RCV004258288]	uncertain significance	16	20427789	20427789	Human		name
329352320	CV2452865	single nucleotide variant	NM_017888.3(ACSM5):c.310A>C (p.Asn104His)	not specified [RCV004277515]	uncertain significance	16	20418164	20418164	Human		name
401755125	CV2717654	single nucleotide variant	NM_017888.3(ACSM5):c.763G>A (p.Gly255Arg)	not specified [RCV004330337]	uncertain significance	16	20421397	20421397	Human		name
401881947	CV2784896	single nucleotide variant	NM_017888.3(ACSM5):c.911T>C (p.Val304Ala)	not specified [RCV004352674]	uncertain significance	16	20424059	20424059	Human		name
405772876	CV3299925	single nucleotide variant	NM_017888.3(ACSM5):c.404G>A (p.Cys135Tyr)	not specified [RCV004435597]	uncertain significance	16	20418258	20418258	Human		name
405772909	CV3299930	single nucleotide variant	NM_017888.3(ACSM5):c.583A>T (p.Ser195Cys)	not specified [RCV004435602]	uncertain significance	16	20419395	20419395	Human		name
405772961	CV3299940	single nucleotide variant	NM_017888.3(ACSM5):c.638A>C (p.Glu213Ala)	not specified [RCV004435612]	uncertain significance	16	20421272	20421272	Human		name
405772989	CV3299945	single nucleotide variant	NM_017888.3(ACSM5):c.742G>A (p.Gly248Arg)	not specified [RCV004435617]	uncertain significance	16	20421376	20421376	Human		name
405773039	CV3299953	single nucleotide variant	NM_017888.3(ACSM5):c.845T>C (p.Leu282Pro)	not specified [RCV004435625]	uncertain significance	16	20423993	20423993	Human		name
405773103	CV3299963	single nucleotide variant	NM_017888.3(ACSM5):c.994C>G (p.Leu332Val)	not specified [RCV004435635]	uncertain significance	16	20427860	20427860	Human		name
407475414	CV3424728	single nucleotide variant	NM_017888.3(ACSM5):c.469C>T (p.Arg157Trp)	not specified [RCV004600867]	uncertain significance	16	20419281	20419281	Human		name
407475560	CV3424755	single nucleotide variant	NM_017888.3(ACSM5):c.340C>T (p.Pro114Ser)	not specified [RCV004600891]	uncertain significance	16	20418194	20418194	Human		name
407475584	CV3424761	single nucleotide variant	NM_017888.3(ACSM5):c.796A>G (p.Ile266Val)	not specified [RCV004600895]	uncertain significance	16	20423944	20423944	Human		name
598173269	CV3938813	single nucleotide variant	NM_017888.3(ACSM5):c.482C>T (p.Ser161Phe)	not specified [RCV005309524]	uncertain significance	16	20419294	20419294	Human		name
598173410	CV3938838	single nucleotide variant	NM_017888.3(ACSM5):c.627G>C (p.Glu209Asp)	not specified [RCV005309548]	uncertain significance	16	20421261	20421261	Human		name
598173464	CV3938849	single nucleotide variant	NM_017888.3(ACSM5):c.913A>G (p.Ile305Val)	not specified [RCV005309556]	uncertain significance	16	20424061	20424061	Human		name
598173516	CV3938860	single nucleotide variant	NM_017888.3(ACSM5):c.928T>C (p.Ser310Pro)	not specified [RCV005309565]	uncertain significance	16	20427794	20427794	Human		name
598173570	CV3938870	single nucleotide variant	NM_017888.3(ACSM5):c.319G>A (p.Gly107Arg)	not specified [RCV005309573]	uncertain significance	16	20418173	20418173	Human		name
598173615	CV3938879	single nucleotide variant	NM_017888.3(ACSM5):c.391G>C (p.Val131Leu)	not specified [RCV005309580]	uncertain significance	16	20418245	20418245	Human		name
598173654	CV3938888	single nucleotide variant	NM_017888.3(ACSM5):c.787G>C (p.Glu263Gln)	not specified [RCV005309588]	uncertain significance	16	20423935	20423935	Human		name
598210757	CV3938897	single nucleotide variant	NM_017888.3(ACSM5):c.791C>A (p.Ser264Tyr)	not specified [RCV005315910]	uncertain significance	16	20423939	20423939	Human		name
155925591	CV2277327	single nucleotide variant	NM_017888.3(ACSM5):c.1558C>G (p.Leu520Val)	not specified [RCV004142936]	uncertain significance	16	20439821	20439821	Human		name
155906349	CV2283507	single nucleotide variant	NM_017888.3(ACSM5):c.1409G>A (p.Arg470Lys)	not specified [RCV004139722]	uncertain significance	16	20437152	20437152	Human		name
156064734	CV2316211	single nucleotide variant	NM_017888.3(ACSM5):c.1532G>T (p.Gly511Val)	not specified [RCV004174251]	uncertain significance	16	20437363	20437363	Human		name
155985600	CV2343862	single nucleotide variant	NM_017888.3(ACSM5):c.1386T>A (p.Asp462Glu)	not specified [RCV004193445]	uncertain significance	16	20437129	20437129	Human		name
156096710	CV2399113	single nucleotide variant	NM_017888.3(ACSM5):c.1373G>T (p.Arg458Leu)	not specified [RCV004246547]	uncertain significance	16	20437116	20437116	Human		name
329356974	CV2431210	single nucleotide variant	NM_017888.3(ACSM5):c.1598C>T (p.Thr533Met)	not specified [RCV004250554]	uncertain significance	16	20439861	20439861	Human		name
401721366	CV2709930	single nucleotide variant	NM_017888.3(ACSM5):c.1223G>A (p.Gly408Asp)	not specified [RCV004315004]	uncertain significance	16	20431236	20431236	Human		name
401896093	CV2777464	single nucleotide variant	NM_017888.3(ACSM5):c.1214A>G (p.Asp405Gly)	not specified [RCV004356237]	uncertain significance	16	20431227	20431227	Human		name
401894553	CV2788414	single nucleotide variant	NM_017888.3(ACSM5):c.1648C>T (p.Pro550Ser)	not specified [RCV004354946]	uncertain significance	16	20439911	20439911	Human		name
401938572	CV2807697	single nucleotide variant	NM_017888.3(ACSM5):c.1259C>T (p.Ala420Val)	not provided [RCV003417670]	likely benign	16	20431272	20431272	Human		name
405772492	CV3299859	single nucleotide variant	NM_017888.3(ACSM5):c.1033A>C (p.Thr345Pro)	not specified [RCV004435531]	uncertain significance	16	20429709	20429709	Human		name
405772514	CV3299863	single nucleotide variant	NM_017888.3(ACSM5):c.1074G>T (p.Trp358Cys)	not specified [RCV004435535]	uncertain significance	16	20429750	20429750	Human		name
405772521	CV3299864	single nucleotide variant	NM_017888.3(ACSM5):c.1123A>G (p.Thr375Ala)	not specified [RCV004435536]	uncertain significance	16	20429799	20429799	Human		name
405772574	CV3299873	single nucleotide variant	NM_017888.3(ACSM5):c.1274C>G (p.Pro425Arg)	not specified [RCV004435545]	uncertain significance	16	20431287	20431287	Human		name
405772579	CV3299874	single nucleotide variant	NM_017888.3(ACSM5):c.1336G>A (p.Glu446Lys)	not specified [RCV004435546]	uncertain significance	16	20437079	20437079	Human		name
405772673	CV3299890	single nucleotide variant	NM_017888.3(ACSM5):c.1409G>T (p.Arg470Ile)	not specified [RCV004435562]	uncertain significance	16	20437152	20437152	Human		name
405772696	CV3299894	single nucleotide variant	NM_017888.3(ACSM5):c.1421T>A (p.Val474Glu)	not specified [RCV004435566]	uncertain significance	16	20437164	20437164	Human		name
405772724	CV3299899	single nucleotide variant	NM_017888.3(ACSM5):c.1526T>C (p.Ile509Thr)	not specified [RCV004435571]	uncertain significance	16	20437357	20437357	Human		name
405772792	CV3299911	single nucleotide variant	NM_017888.3(ACSM5):c.1619T>A (p.Val540Glu)	not specified [RCV004435583]	uncertain significance	16	20439882	20439882	Human		name
405772818	CV3299915	single nucleotide variant	NM_017888.3(ACSM5):c.1639T>C (p.Tyr547His)	not specified [RCV004435587]	uncertain significance	16	20439902	20439902	Human		name
407475475	CV3424739	single nucleotide variant	NM_017888.3(ACSM5):c.1060G>A (p.Val354Met)	not specified [RCV004600877]	uncertain significance	16	20429736	20429736	Human		name
407475632	CV3424770	single nucleotide variant	NM_017888.3(ACSM5):c.1724A>G (p.Gln575Arg)	not specified [RCV004600904]	uncertain significance	16	20440411	20440411	Human		name
598173239	CV3938807	single nucleotide variant	NM_017888.3(ACSM5):c.1685C>T (p.Thr562Met)	not specified [RCV005309519]	uncertain significance	16	20440372	20440372	Human		name
598173251	CV3938809	single nucleotide variant	NM_017888.3(ACSM5):c.1219G>A (p.Glu407Lys)	not specified [RCV005309521]	uncertain significance	16	20431232	20431232	Human		name
598173320	CV3938822	single nucleotide variant	NM_017888.3(ACSM5):c.1540G>T (p.Val514Leu)	not specified [RCV005309533]	uncertain significance	16	20439803	20439803	Human		name
598173353	CV3938828	single nucleotide variant	NM_017888.3(ACSM5):c.1087G>A (p.Gly363Ser)	not specified [RCV005309538]	uncertain significance	16	20429763	20429763	Human		name
14746806	CV672097	single nucleotide variant	NM_017888.3(ACSM5):c.1157A>C (p.Lys386Thr)	not provided [RCV000845046]	not provided	16	20431024	20431024	Human		name
15164811	CV703546	single nucleotide variant	NM_017888.3(ACSM5):c.1079A>G (p.His360Arg)	not provided [RCV000948436]	benign	16	20429755	20429755	Human		name
8635694	CV90917	single nucleotide variant	NM_017888.2(ACSM5):c.1733G>A (p.Gly578Glu)	Malignant melanoma [RCV000071015]	not provided	16	20440420	20440420	Human		name

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