Trim31 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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50 records found for search term Trim31

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8581847	CV116292	single nucleotide variant	NM_007028.3(TRIM31):c.767+310T>C	Lung cancer [RCV000096815]	uncertain significance	6	30108716	30108716	Human		name
15123916	CV710388	single nucleotide variant	NM_007028.5(TRIM31):c.18T>G (p.Phe6Leu)	not provided [RCV000963327]	benign	6	30112788	30112788	Human		name
15129502	CV710389	single nucleotide variant	NM_007028.5(TRIM31):c.15G>T (p.Gln5His)	not provided [RCV000964268]\|not specified [RCV004029912]	likely benign\|uncertain significance	6	30112791	30112791	Human		name
401915511	CV2822807	single nucleotide variant	NM_007028.5(TRIM31):c.318C>T (p.Cys106=)	not provided [RCV003428777]	likely benign	6	30112488	30112488	Human		name
598274106	CV3935413	single nucleotide variant	NM_007028.5(TRIM31):c.82A>C (p.Thr28Pro)	not specified [RCV005303762]	uncertain significance	6	30112724	30112724	Human		name
15197114	CV699505	single nucleotide variant	NM_007028.5(TRIM31):c.50C>G (p.Pro17Arg)	not provided [RCV000956376]	benign	6	30112756	30112756	Human		name
156334929	CV2333455	single nucleotide variant	NM_007028.5(TRIM31):c.276G>C (p.Glu92Asp)	not specified [RCV004190156]	uncertain significance	6	30112530	30112530	Human		name
155927542	CV2365945	single nucleotide variant	NM_007028.5(TRIM31):c.260A>G (p.Gln87Arg)	not specified [RCV004207555]	uncertain significance	6	30112546	30112546	Human		name
401920416	CV2822806	single nucleotide variant	NM_007028.5(TRIM31):c.1029C>A (p.Gly343=)	not provided [RCV003431708]	likely benign	6	30103785	30103785	Human		name
405790176	CV3336904	single nucleotide variant	NM_007028.5(TRIM31):c.272A>G (p.Lys91Arg)	not specified [RCV004473783]	uncertain significance	6	30112534	30112534	Human		name
597801720	CV3617686	single nucleotide variant	NM_007028.5(TRIM31):c.215G>A (p.Arg72Gln)	not specified [RCV004880866]	uncertain significance	6	30112591	30112591	Human		name
598274102	CV3935411	single nucleotide variant	NM_007028.5(TRIM31):c.242T>C (p.Leu81Pro)	not specified [RCV005303760]	uncertain significance	6	30112564	30112564	Human		name
598274112	CV3935416	single nucleotide variant	NM_007028.5(TRIM31):c.128T>C (p.Ile43Thr)	not specified [RCV005303765]	uncertain significance	6	30112678	30112678	Human		name
15197110	CV699504	single nucleotide variant	NM_007028.5(TRIM31):c.214C>T (p.Arg72Trp)	not provided [RCV000956375]	benign	6	30112592	30112592	Human		name
15165573	CV710385	single nucleotide variant	NM_007028.5(TRIM31):c.1044G>A (p.Gly348=)	not provided [RCV000970979]	benign	6	30103770	30103770	Human		name
155927817	CV2227396	single nucleotide variant	NM_007028.5(TRIM31):c.298G>A (p.Glu100Lys)	not specified [RCV004092062]	uncertain significance	6	30112508	30112508	Human		name
156046406	CV2304268	single nucleotide variant	NM_007028.5(TRIM31):c.805C>T (p.Pro269Ser)	not specified [RCV004164392]	uncertain significance	6	30108131	30108131	Human		name
156058311	CV2322916	single nucleotide variant	NM_007028.5(TRIM31):c.631A>G (p.Thr211Ala)	not specified [RCV004185364]	likely benign	6	30110561	30110561	Human		name
156104759	CV2361040	single nucleotide variant	NM_007028.5(TRIM31):c.769A>G (p.Ser257Gly)	not specified [RCV004216236]	uncertain significance	6	30108167	30108167	Human		name
155918271	CV2362549	single nucleotide variant	NM_007028.5(TRIM31):c.328G>A (p.Gly110Arg)	not specified [RCV004215211]	uncertain significance	6	30112478	30112478	Human		name
156083326	CV2369011	single nucleotide variant	NM_007028.5(TRIM31):c.950T>C (p.Met317Thr)	not specified [RCV004207950]	uncertain significance	6	30105176	30105176	Human		name
155953478	CV2379020	single nucleotide variant	NM_007028.5(TRIM31):c.923T>A (p.Phe308Tyr)	not specified [RCV004233781]	uncertain significance	6	30105203	30105203	Human		name
156053438	CV2385551	single nucleotide variant	NM_007028.5(TRIM31):c.446T>C (p.Leu149Ser)	not specified [RCV004233191]	uncertain significance	6	30111715	30111715	Human		name
329357361	CV2456737	single nucleotide variant	NM_007028.5(TRIM31):c.443T>C (p.Val148Ala)	not specified [RCV004270718]	uncertain significance	6	30111718	30111718	Human		name
401737274	CV2679271	single nucleotide variant	NM_007028.5(TRIM31):c.757G>A (p.Val253Ile)	not specified [RCV004285819]	uncertain significance	6	30109036	30109036	Human		name
405790178	CV3336905	single nucleotide variant	NM_007028.5(TRIM31):c.381T>A (p.Asn127Lys)	not specified [RCV004473784]	uncertain significance	6	30112425	30112425	Human		name
405790181	CV3336906	single nucleotide variant	NM_007028.5(TRIM31):c.595C>A (p.Leu199Met)	not specified [RCV004473785]	uncertain significance	6	30110597	30110597	Human		name
405790184	CV3336907	single nucleotide variant	NM_007028.5(TRIM31):c.611A>C (p.Tyr204Ser)	not specified [RCV004473786]	uncertain significance	6	30110581	30110581	Human		name
405790186	CV3336908	single nucleotide variant	NM_007028.5(TRIM31):c.638C>T (p.Ala213Val)	not specified [RCV004473787]	uncertain significance	6	30110554	30110554	Human		name
405790190	CV3336909	single nucleotide variant	NM_007028.5(TRIM31):c.734A>C (p.Gln245Pro)	not specified [RCV004473788]	uncertain significance	6	30110458	30110458	Human		name
407453721	CV3490482	single nucleotide variant	NM_007028.5(TRIM31):c.519G>C (p.Gln173His)	not specified [RCV004684642]	uncertain significance	6	30110673	30110673	Human		name
407453725	CV3490483	single nucleotide variant	NM_007028.5(TRIM31):c.632C>T (p.Thr211Met)	not specified [RCV004684643]	uncertain significance	6	30110560	30110560	Human		name
597801721	CV3617687	single nucleotide variant	NM_007028.5(TRIM31):c.998C>T (p.Thr333Ile)	not specified [RCV004880867]	uncertain significance	6	30104128	30104128	Human		name
597801725	CV3617689	single nucleotide variant	NM_007028.5(TRIM31):c.301A>G (p.Met101Val)	not specified [RCV004880869]	uncertain significance	6	30112505	30112505	Human		name
597801727	CV3617691	single nucleotide variant	NM_007028.5(TRIM31):c.653T>G (p.Val218Gly)	not specified [RCV004880870]	uncertain significance	6	30110539	30110539	Human		name
598274100	CV3935410	single nucleotide variant	NM_007028.5(TRIM31):c.850G>A (p.Asp284Asn)	not specified [RCV005303759]	uncertain significance	6	30108086	30108086	Human		name
598274104	CV3935412	single nucleotide variant	NM_007028.5(TRIM31):c.381T>G (p.Asn127Lys)	not specified [RCV005303761]	uncertain significance	6	30112425	30112425	Human		name
598274110	CV3935415	single nucleotide variant	NM_007028.5(TRIM31):c.518A>C (p.Gln173Pro)	not specified [RCV005303764]	uncertain significance	6	30110674	30110674	Human		name
15157659	CV699500	single nucleotide variant	NM_007028.5(TRIM31):c.734A>G (p.Gln245Arg)	not provided [RCV000946925]	benign	6	30110458	30110458	Human		name
15197099	CV699501	single nucleotide variant	NM_007028.5(TRIM31):c.704T>C (p.Leu235Pro)	not provided [RCV000956372]	benign	6	30110488	30110488	Human		name
15197103	CV699502	single nucleotide variant	NM_007028.5(TRIM31):c.379A>G (p.Asn127Asp)	not provided [RCV000956373]	benign	6	30112427	30112427	Human		name
15197107	CV699503	single nucleotide variant	NM_007028.5(TRIM31):c.303G>A (p.Met101Ile)	not provided [RCV000956374]	benign	6	30112503	30112503	Human		name
15129490	CV710386	single nucleotide variant	NM_007028.5(TRIM31):c.559C>T (p.Leu187Phe)	not provided [RCV000964266]\|not specified [RCV004029910]	likely benign\|uncertain significance	6	30110633	30110633	Human		name
15129497	CV710387	single nucleotide variant	NM_007028.5(TRIM31):c.525A>C (p.Glu175Asp)	not provided [RCV000964267]\|not specified [RCV004029911]	likely benign\|uncertain significance	6	30110667	30110667	Human		name
15176508	CV721926	single nucleotide variant	NM_007028.5(TRIM31):c.707A>G (p.Lys236Arg)	not provided [RCV000884600]	likely benign	6	30110485	30110485	Human		name
401868689	CV2767311	single nucleotide variant	NM_007028.5(TRIM31):c.1048C>G (p.Pro350Ala)	not specified [RCV004349478]	uncertain significance	6	30103766	30103766	Human		name
401895307	CV2786348	single nucleotide variant	NM_007028.5(TRIM31):c.1196C>T (p.Ala399Val)	not specified [RCV004361952]	uncertain significance	6	30103618	30103618	Human		name
405790173	CV3336903	single nucleotide variant	NM_007028.5(TRIM31):c.1022C>T (p.Ala341Val)	not specified [RCV004473782]	uncertain significance	6	30104104	30104104	Human		name
597801723	CV3617688	single nucleotide variant	NM_007028.5(TRIM31):c.1245C>G (p.Ile415Met)	not specified [RCV004880868]	uncertain significance	6	30103569	30103569	Human		name
15163571	CV721925	single nucleotide variant	NM_007028.5(TRIM31):c.1228G>T (p.Glu410Ter)	not provided [RCV000881999]	likely benign	6	30103586	30103586	Human		name

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