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15 variations found. Os01g0750400/LOC_Os01g54630 (leucine rich repeat family protein; putative; expressed), ranging from 31,431,622 bp to 31,433,202 bp (including 0 kb upstream and 0 kb downstream of the gene).

Gene IDAnnotation
LOC_Os01g54630 leucine rich repeat family protein, putative, expressed; RAP ID: Os01g0750400; MSU ID: LOC_Os01g54630

Gene Expression Atlas:

The expression data is from the CREP database. And the expression value is log2-transformed. Move the mouse over the cells of the heat map to get detailed tissue information and expression values.

Variation Map (with Chromatin Accessibility Map/ Non-coding Varation Scores Map) in Searched Region:

The 'big effect' variations are marked out:

ColorExplainDetails
red High impact variants defined by snpEff 'STOP_LOST', 'START_LOST', 'STOP_GAINED', 'FRAME_SHIFT' et. al., the details can be found at http://snpef f.sourceforge.net/SnpEff_manual.html#eff.
purple 'Damaging' or 'probably damaging' non-synonymous SNPs defined by PolyPhen-2 This is a qualitative result of nonsynonymous SNP annotation, where 'damaging' or 'probably damaging' means that the variant is more likely to affect protein function. Details can be found here.

Detailed Variation Information:

Var ID Chrom Position Primary Allele Secondary Allele Primary Allele Frequency DEL Frequency Var GWAS Results Effect
vg0131431638 (J) chr01 31431638 A T 67.40% 0.00% T -> A
mr1003 (All); LR P-value: 1.35E-22;
mr1008 (All); LR P-value: 1.02E-105;
mr1009 (All); LR P-value: 5.47E-105;
mr1010 (All); LR P-value: 2.88E-13;
mr1163 (All); LR P-value: 1.54E-21;
mr1239 (All); LR P-value: 6.60E-14;
mr1242 (All); LR P-value: 3.96E-20;
mr1781 (All); LR P-value: 3.39E-07;
mr1010_2 (All); LR P-value: 3.52E-21;
mr1051_2 (All); LR P-value: 5.64E-27;
mr1114_2 (All); LR P-value: 2.53E-16;
mr1118_2 (All); LR P-value: 1.01E-14;
mr1242_2 (All); LR P-value: 6.04E-24;
mr1496_2 (All); LR P-value: 3.52E-15;
mr1645_2 (All); LR P-value: 5.78E-08;
mr1700_2 (All); LR P-value: 2.13E-08;
mr1781_2 (All); LR P-value: 5.38E-11;
mr1840_2 (All); LR P-value: 6.39E-06
LOC_Os01g54630.1 Alt: A| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g54620.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g54640.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 73.145; most accessible tissue: Zhenshan97 panicle, score: 93.752
vg0131431837 (J) chr01 31431837 A G 87.50% 0.00% A -> G NA
LOC_Os01g54630.1 Alt: G| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g54620.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g54640.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 77.761; most accessible tissue: Zhenshan97 panicle, score: 93.752
vg0131431842 (J) chr01 31431842 C T 99.00% 0.00% C -> T NA
LOC_Os01g54630.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g54620.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g54640.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 77.753; most accessible tissue: Zhenshan97 panicle, score: 93.936
vg0131431925 (J) chr01 31431925 G A 99.00% 0.00% G -> A NA
LOC_Os01g54630.1 Alt: A| 3_prime_UTR_variant MODIFIER(snpEff)
LOC_Os01g54620.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os01g54640.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 80.155; most accessible tissue: Zhenshan97 panicle, score: 92.784
vg0131432101 (J) chr01 31432101 G GCGCCGT 66.90% 0.00% GCGCCGT -> G NA
LOC_Os01g54630.1 Alt: G| inframe_deletion MODERATE(snpEff)/inframe_variant(CooVar)
The average chromatin accessibility score: 82.230; most accessible tissue: Zhenshan97 panicle, score: 94.360
vg0131432613 (J) chr01 31432613 A C 64.00% 0.00% C -> A NA
LOC_Os01g54630.1 Alt: A| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 87.777; most accessible tissue: Zhenshan97 panicle, score: 95.323
vg0131432651 (J) chr01 31432651 G A 90.60% 0.00% G -> A
mr1240 (All); LR P-value: 8.55E-17;
mr1530 (All); LR P-value: 3.84E-07;
mr1858 (All); LR P-value: 3.20E-28;
mr1859 (All); LR P-value: 2.95E-28;
mr1897 (All); LR P-value: 6.01E-12;
mr1098_2 (All); LR P-value: 6.53E-32;
mr1099_2 (All); LR P-value: 3.92E-23;
mr1123_2 (All); LR P-value: 5.63E-23;
mr1240_2 (All); LR P-value: 9.55E-20;
mr1918_2 (All); LR P-value: 2.72E-14;
mr1936_2 (All); LR P-value: 8.42E-16
LOC_Os01g54630.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 87.414; most accessible tissue: Zhenshan97 panicle, score: 94.949
vg0131432655 (J) chr01 31432655 G A 99.00% 0.00% G -> A NA
LOC_Os01g54630.1 Alt: A| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/possibly damaging(PolyPhen-2)
The average chromatin accessibility score: 87.517; most accessible tissue: Zhenshan97 panicle, score: 95.016
vg0131432734 (J) chr01 31432734 C A 68.20% 0.00% C -> A
Plant_height (All); LR P-value: 3.21E-19;
Plant_height (Ind_All); LR P-value: 1.35E-16;
mr1003 (All); LR P-value: 4.24E-25;
mr1003 (Ind_All); LR P-value: 3.64E-07;
mr1011 (All); LR P-value: 3.25E-06;
mr1013 (All); LR P-value: 8.92E-15;
mr1013 (Ind_All); LR P-value: 3.24E-06;
mr1031 (All); LR P-value: 9.23E-15;
mr1031 (Ind_All); LR P-value: 8.97E-07;
mr1034 (All); LR P-value: 1.62E-12;
mr1034 (Ind_All); LR P-value: 4.21E-06;
mr1042 (Ind_All); LR P-value: 2.66E-06;
mr1043 (Ind_All); LR P-value: 1.01E-06;
mr1051 (All); LR P-value: 1.05E-25;
mr1051 (Ind_All); LR P-value: 2.91E-07;
mr1056 (All); LR P-value: 1.24E-13;
mr1201 (Ind_All); LR P-value: 3.19E-06;
mr1219 (Ind_All); LR P-value: 3.71E-06;
mr1677 (Ind_All); LR P-value: 1.71E-06;
mr1912 (Ind_All); LR P-value: 6.48E-06;
mr1060_2 (Ind_All); LR P-value: 3.70E-06;
mr1084_2 (All); LR P-value: 4.00E-08;
mr1115_2 (Ind_All); LR P-value: 2.23E-07;
mr1174_2 (All); LR P-value: 3.57E-11;
mr1180_2 (All); LR P-value: 1.92E-15;
mr1183_2 (All); LR P-value: 3.79E-22;
mr1207_2 (Ind_All); LR P-value: 9.72E-06;
mr1215_2 (All); LR P-value: 1.00E-09;
mr1260_2 (All); LR P-value: 9.55E-19;
mr1268_2 (Ind_All); LR P-value: 2.00E-06;
mr1274_2 (Ind_All); LR P-value: 2.34E-07;
mr1302_2 (All); LR P-value: 2.29E-08;
mr1306_2 (Ind_All); LR P-value: 3.67E-06;
mr1319_2 (All); LR P-value: 3.49E-10;
mr1327_2 (All); LR P-value: 2.48E-09;
mr1327_2 (Ind_All); LR P-value: 8.73E-10;
mr1330_2 (All); LR P-value: 1.33E-14;
mr1330_2 (Ind_All); LR P-value: 1.32E-06;
mr1352_2 (All); LR P-value: 3.64E-23;
mr1352_2 (Ind_All); LR P-value: 1.25E-10;
mr1376_2 (All); LR P-value: 3.26E-09;
mr1422_2 (All); LR P-value: 1.69E-24;
mr1428_2 (All); LR P-value: 8.46E-07;
mr1431_2 (All); LR P-value: 9.19E-10;
mr1565_2 (All); LR P-value: 7.27E-12;
mr1565_2 (Ind_All); LR P-value: 1.01E-09;
mr1611_2 (Ind_All); LR P-value: 1.95E-06;
mr1624_2 (Ind_All); LR P-value: 3.91E-08;
mr1653_2 (Ind_All); LR P-value: 2.84E-07;
mr1681_2 (All); LR P-value: 1.75E-08;
mr1681_2 (Ind_All); LR P-value: 8.67E-06;
mr1696_2 (Ind_All); LR P-value: 8.54E-06;
mr1735_2 (Ind_All); LR P-value: 9.23E-06;
mr1739_2 (Ind_All); LR P-value: 2.51E-09;
mr1751_2 (All); LR P-value: 1.42E-08;
mr1758_2 (Ind_All); LR P-value: 6.84E-10;
mr1771_2 (Ind_All); LR P-value: 1.31E-06;
mr1784_2 (Ind_All); LR P-value: 7.03E-06;
mr1824_2 (All); LR P-value: 2.80E-07;
mr1885_2 (All); LR P-value: 3.61E-07;
mr1959_2 (Ind_All); LR P-value: 3.92E-06
LOC_Os01g54630.1 Alt: A| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 90.196; most accessible tissue: Zhenshan97 panicle, score: 95.951
vg0131432852 (J) chr01 31432852 C T 99.00% 0.00% C -> T NA
LOC_Os01g54630.1 Alt: T| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 87.704; most accessible tissue: Zhenshan97 panicle, score: 95.855
vg0131433010 (J) chr01 31433010 C T 89.10% 4.02% C -> T NA
LOC_Os01g54630.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
LOC_Os01g54630.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 91.639; most accessible tissue: Zhenshan97 panicle, score: 97.556
vg0131433018 (J) chr01 31433018 C T 89.20% 3.89% C -> T NA
LOC_Os01g54630.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
LOC_Os01g54630.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 91.591; most accessible tissue: Zhenshan97 panicle, score: 97.641
vg0131433146 (J) chr01 31433146 T C 99.70% 0.00% T -> C NA
LOC_Os01g54630.1 Alt: C| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 95.118; most accessible tissue: Zhenshan97 panicle, score: 99.328
vg0131433190 (J) chr01 31433190 T C 87.50% 0.00% T -> C NA
LOC_Os01g54630.1 Alt: C| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 97.242; most accessible tissue: Zhenshan97 panicle, score: 99.519
STR0131432102 (J) chr01 31432102 C CGCCGTC 60.70% 0.00% CGCCGTC -> C NA