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18 variations found. Os07g0145400/LOC_Os07g05190 (leucine-rich repeat family protein; putative; expressed), ranging from 2,313,395 bp to 2,319,009 bp (including 0 kb upstream and 0 kb downstream of the gene).

Gene IDAnnotation
LOC_Os07g05190 leucine-rich repeat family protein, putative, expressed; RAP ID: Os07g0145400; MSU ID: LOC_Os07g05190

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
vg0702313507 (J) chr07 2313507 C A 99.90% 0.00% C -> A NA
LOC_Os07g05190.1 Alt: A| 3_prime_UTR_variant MODIFIER(snpEff)
LOC_Os07g05180.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 67.158; most accessible tissue: Zhenshan97 panicle, score: 94.026
vg0702313558 (J) chr07 2313558 T C 57.70% 0.28% C -> T
mr1004 (All); LR P-value: 1.44E-06;
mr1005 (All); LR P-value: 1.17E-11;
mr1146 (All); LR P-value: 2.53E-14;
mr1150 (All); LR P-value: 7.77E-22;
mr1874 (All); LR P-value: 3.57E-14;
mr1950 (All); LR P-value: 5.37E-15;
mr1158_2 (Ind_All); LR P-value: 5.49E-10;
mr1383_2 (Ind_All); LR P-value: 6.19E-11;
mr1520_2 (All); LR P-value: 2.10E-11;
mr1645_2 (All); LR P-value: 9.59E-08;
mr1654_2 (All); LR P-value: 2.67E-07;
mr1874_2 (All); LR P-value: 1.31E-18
N Alt: DEL/silent_mutation(CooVar)
LOC_Os07g05190.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g05180.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 66.210; most accessible tissue: Zhenshan97 panicle, score: 94.594
vg0702313588 (J) chr07 2313588 C T 93.70% 0.00% C -> T
mr1006 (All); LR P-value: 4.91E-06;
mr1028 (All); LR P-value: 2.87E-06;
mr1030 (All); LR P-value: 7.40E-06;
mr1058 (All); LR P-value: 1.65E-06;
mr1073 (All); LR P-value: 4.33E-08;
mr1095 (All); LR P-value: 1.93E-26;
mr1098 (All); LR P-value: 1.77E-38;
mr1099 (All); LR P-value: 1.40E-34;
mr1101 (All); LR P-value: 4.35E-32;
mr1113 (All); LR P-value: 5.94E-16;
mr1114 (All); LR P-value: 1.42E-18;
mr1117 (All); LR P-value: 4.22E-21;
mr1119 (All); LR P-value: 4.60E-17;
mr1120 (All); LR P-value: 8.00E-24;
mr1123 (All); LR P-value: 3.18E-28;
mr1126 (All); LR P-value: 2.32E-06;
mr1146 (All); LR P-value: 1.68E-15;
mr1153 (All); LR P-value: 3.43E-06;
mr1158 (All); LR P-value: 2.74E-15;
mr1168 (All); LR P-value: 1.51E-21;
mr1210 (All); LR P-value: 2.04E-22;
mr1230 (All); LR P-value: 1.08E-07;
mr1231 (All); LR P-value: 3.44E-13;
mr1240 (All); LR P-value: 7.90E-19;
mr1247 (All); LR P-value: 3.94E-24;
mr1262 (All); LR P-value: 2.17E-06;
mr1305 (All); LR P-value: 1.14E-25;
mr1331 (All); LR P-value: 3.97E-06;
mr1345 (All); LR P-value: 4.63E-07;
mr1348 (All); LR P-value: 3.24E-08;
mr1365 (All); LR P-value: 6.97E-09;
mr1367 (All); LR P-value: 6.50E-06;
mr1382 (All); LR P-value: 7.03E-07;
mr1393 (All); LR P-value: 2.96E-06;
mr1409 (All); LR P-value: 2.65E-12;
mr1417 (All); LR P-value: 9.55E-06;
mr1424 (All); LR P-value: 7.73E-06;
mr1427 (All); LR P-value: 2.17E-06;
mr1442 (All); LR P-value: 9.31E-09;
mr1453 (All); LR P-value: 5.73E-07;
mr1496 (All); LR P-value: 1.30E-14;
mr1499 (All); LR P-value: 4.48E-12;
mr1512 (All); LR P-value: 7.09E-06;
mr1515 (All); LR P-value: 4.17E-20;
mr1522 (All); LR P-value: 8.63E-12;
mr1523 (All); LR P-value: 3.12E-06;
mr1545 (All); LR P-value: 8.50E-06;
mr1549 (All); LR P-value: 4.88E-41;
mr1550 (All); LMM P-value: 3.41E-06; LR P-value: 1.09E-47;
mr1574 (All); LR P-value: 4.35E-06;
mr1586 (All); LR P-value: 1.12E-28;
mr1589 (All); LR P-value: 5.89E-28;
mr1612 (All); LR P-value: 9.93E-13;
mr1621 (All); LR P-value: 6.94E-07;
mr1634 (All); LR P-value: 1.08E-07;
mr1649 (All); LR P-value: 9.64E-14;
mr1665 (All); LR P-value: 1.95E-06;
mr1696 (All); LR P-value: 1.86E-11;
mr1727 (All); LR P-value: 8.73E-06;
mr1730 (All); LR P-value: 1.81E-09;
mr1757 (All); LR P-value: 2.82E-42;
mr1762 (All); LR P-value: 6.48E-07;
mr1765 (All); LR P-value: 3.12E-18;
mr1774 (All); LR P-value: 2.97E-06;
mr1858 (All); LR P-value: 2.35E-29;
mr1859 (All); LR P-value: 2.13E-29;
mr1866 (All); LR P-value: 1.01E-08;
mr1868 (All); LR P-value: 1.18E-29;
mr1911 (All); LR P-value: 2.95E-18;
mr1918 (All); LR P-value: 3.13E-13;
mr1931 (All); LR P-value: 9.18E-07;
mr1936 (All); LR P-value: 2.09E-18;
mr1939 (All); LR P-value: 5.71E-09;
mr1942 (All); LR P-value: 1.24E-07;
mr1961 (All); LR P-value: 4.25E-23;
mr1047_2 (All); LR P-value: 4.87E-12;
mr1095_2 (All); LR P-value: 1.51E-21;
mr1098_2 (All); LR P-value: 9.31E-35;
mr1099_2 (All); LR P-value: 5.51E-27;
mr1123_2 (All); LR P-value: 5.27E-21;
mr1305_2 (All); LR P-value: 1.43E-20;
mr1409_2 (All); LR P-value: 1.08E-12;
mr1510_2 (All); LR P-value: 3.23E-09;
mr1549_2 (All); LR P-value: 1.82E-33;
mr1550_2 (All); LR P-value: 2.71E-46;
mr1740_2 (All); LR P-value: 3.84E-06;
mr1741_2 (All); LR P-value: 5.95E-09;
mr1757_2 (All); LR P-value: 2.37E-26;
mr1792_2 (All); LR P-value: 3.31E-07;
mr1803_2 (All); LR P-value: 5.91E-15;
mr1808_2 (All); LR P-value: 5.11E-07;
mr1815_2 (All); LR P-value: 1.65E-06;
mr1911_2 (All); LR P-value: 1.54E-15
LOC_Os07g05190.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g05180.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 62.985; most accessible tissue: Zhenshan97 panicle, score: 94.195
vg0702314188 (J) chr07 2314188 G A 99.40% 0.00% G -> A NA
LOC_Os07g05190.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 74.817; most accessible tissue: Zhenshan97 panicle, score: 94.278
vg0702314200 (J) chr07 2314200 G A 50.70% 0.32% A -> G,T
mr1216 (All); LR P-value: 4.61E-06;
mr1158_2 (All); LR P-value: 1.07E-06;
mr1158_2 (Ind_All); LR P-value: 2.19E-12;
mr1383_2 (Ind_All); LR P-value: 2.66E-12;
mr1478_2 (All); LR P-value: 1.91E-09;
mr1608_2 (Ind_All); LR P-value: 2.87E-06;
mr1648_2 (All); LR P-value: 4.16E-06;
mr1971_2 (All); LR P-value: 3.24E-22
LOC_Os07g05190.1 Alt: DEL/frameshift_variant(CooVar)
LOC_Os07g05190.1 Alt: G| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
LOC_Os07g05190.1 Alt: T| synonymous_variant LOW(snpEff)
LOC_Os07g05180.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 75.507; most accessible tissue: Zhenshan97 panicle, score: 94.360
vg0702314591 (J) chr07 2314591 C T 57.80% 0.25% T -> C
mr1004 (All); LR P-value: 2.12E-06;
mr1005 (All); LR P-value: 2.47E-11;
mr1146 (All); LR P-value: 2.07E-14;
mr1150 (All); LR P-value: 6.68E-22;
mr1874 (All); LR P-value: 4.12E-14;
mr1158_2 (Ind_All); LR P-value: 1.22E-09;
mr1195_2 (All); LR P-value: 1.60E-18;
mr1383_2 (Ind_All); LR P-value: 7.80E-12;
mr1520_2 (All); LR P-value: 1.73E-11;
mr1645_2 (All); LR P-value: 4.29E-08;
mr1654_2 (All); LR P-value: 2.31E-07;
mr1874_2 (All); LR P-value: 7.09E-19
LOC_Os07g05190.1 Alt: DEL/frameshift_variant(CooVar)
LOC_Os07g05190.1 Alt: C| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 62.236; most accessible tissue: Zhenshan97 panicle, score: 83.904
vg0702314970 (J) chr07 2314970 C T 99.80% 0.00% C -> T NA
LOC_Os07g05190.1 Alt: T| missense_variant MODERATE(snpEff)
LOC_Os07g05180.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 63.711; most accessible tissue: Zhenshan97 panicle, score: 87.451
vg0702315611 (J) chr07 2315611 G A 99.90% 0.00% G -> A NA
LOC_Os07g05190.1 Alt: A| synonymous_variant LOW(snpEff)
LOC_Os07g05180.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 41.683; most accessible tissue: Zhenshan97 young leaf, score: 60.208
vg0702315769 (J) chr07 2315769 C T 57.60% 0.11% T -> C
mr1004 (All); LR P-value: 7.29E-07;
mr1005 (All); LR P-value: 7.63E-12;
mr1059 (All); LR P-value: 2.12E-14;
mr1146 (All); LR P-value: 8.42E-15;
mr1150 (All); LR P-value: 1.43E-22;
mr1441 (All); LR P-value: 5.12E-13;
mr1675 (All); LR P-value: 1.08E-14;
mr1874 (All); LR P-value: 9.84E-15;
mr1950 (All); LR P-value: 3.22E-15;
mr1158_2 (Ind_All); LR P-value: 2.38E-09;
mr1195_2 (All); LR P-value: 6.60E-19;
mr1383_2 (Ind_All); LR P-value: 1.57E-10;
mr1520_2 (All); LR P-value: 1.37E-11;
mr1654_2 (All); LR P-value: 8.20E-08;
mr1874_2 (All); LR P-value: 1.14E-19
LOC_Os07g05190.1 Alt: DEL/frameshift_variant(CooVar)
LOC_Os07g05190.1 Alt: C| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 45.744; most accessible tissue: Callus, score: 77.773
vg0702317034 (J) chr07 2317034 A C 99.40% 0.00% A -> C NA
LOC_Os07g05190.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 42.118; most accessible tissue: Callus, score: 87.473
vg0702318162 (J) chr07 2318162 A G 56.70% 0.25% G -> A
mr1005 (All); LR P-value: 2.00E-09;
mr1059 (All); LR P-value: 2.05E-14;
mr1950 (All); LR P-value: 3.18E-15;
mr1158_2 (Ind_All); LR P-value: 9.74E-10;
mr1383_2 (Ind_All); LR P-value: 2.33E-10;
mr1482_2 (All); LR P-value: 2.69E-07;
mr1645_2 (All); LR P-value: 7.75E-08
N Alt: DEL/silent_mutation(CooVar)
LOC_Os07g05190.1 Alt: A| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 60.493; most accessible tissue: Zhenshan97 panicle, score: 83.904
vg0702318558 (J) chr07 2318558 C T 57.40% 0.00% T -> C
mr1005 (All); LR P-value: 3.77E-10;
mr1150 (All); LR P-value: 2.01E-21;
mr1441 (All); LR P-value: 9.75E-13;
mr1874 (All); LR P-value: 9.70E-14;
mr1902 (All); LR P-value: 2.63E-11;
mr1950 (All); LR P-value: 5.20E-15;
mr1158_2 (Ind_All); LR P-value: 5.73E-10;
mr1383_2 (Ind_All); LR P-value: 2.29E-10;
mr1520_2 (All); LR P-value: 7.85E-12;
mr1645_2 (All); LR P-value: 5.24E-08;
mr1654_2 (All); LR P-value: 1.80E-07;
mr1874_2 (All); LR P-value: 2.65E-18
LOC_Os07g05190.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 60.953; most accessible tissue: Zhenshan97 panicle, score: 91.030
vg0702318694 (J) chr07 2318694 G C 57.50% 0.04% C -> G
mr1004 (All); LR P-value: 7.43E-06;
mr1005 (All); LR P-value: 2.70E-10;
mr1146 (All); LR P-value: 2.09E-14;
mr1150 (All); LR P-value: 8.38E-22;
mr1441 (All); LR P-value: 6.96E-13;
mr1874 (All); LR P-value: 3.62E-14;
mr1902 (All); LR P-value: 1.09E-11;
mr1950 (All); LR P-value: 8.81E-15;
mr1158_2 (Ind_All); LR P-value: 7.12E-10;
mr1195_2 (All); LR P-value: 1.28E-18;
mr1383_2 (Ind_All); LR P-value: 2.72E-10;
mr1520_2 (All); LR P-value: 1.49E-11;
mr1645_2 (All); LR P-value: 3.44E-08;
mr1654_2 (All); LR P-value: 1.64E-07;
mr1874_2 (All); LR P-value: 1.21E-18
N Alt: DEL/silent_mutation(CooVar)
LOC_Os07g05190.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 67.159; most accessible tissue: Zhenshan97 panicle, score: 91.536
vg0702318720 (J) chr07 2318720 C T 57.70% 0.00% T -> C
mr1004 (All); LR P-value: 5.87E-06;
mr1005 (All); LR P-value: 1.83E-10;
mr1150 (All); LR P-value: 4.80E-22;
mr1441 (All); LR P-value: 1.05E-12;
mr1874 (All); LR P-value: 8.55E-14;
mr1950 (All); LR P-value: 4.12E-15;
mr1158_2 (Ind_All); LR P-value: 5.20E-10;
mr1383_2 (Ind_All); LR P-value: 1.87E-10;
mr1520_2 (All); LR P-value: 1.25E-11;
mr1645_2 (All); LR P-value: 3.80E-08;
mr1654_2 (All); LR P-value: 3.29E-07;
mr1874_2 (All); LR P-value: 7.41E-19
LOC_Os07g05190.1 Alt: C| splice_region_variant&intron_variant LOW(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 69.998; most accessible tissue: Zhenshan97 panicle, score: 92.403
vg0702318727 (J) chr07 2318727 C A 99.40% 0.00% C -> A NA
LOC_Os07g05190.1 Alt: A| splice_region_variant LOW(snpEff)/silent_mutation(CooVar)
LOC_Os07g05190.1 Alt: A| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 70.799; most accessible tissue: Zhenshan97 panicle, score: 92.784
vg0702318929 (J) chr07 2318929 G GAGA 50.90% 0.00% GAGA -> G NA
LOC_Os07g05190.1 Alt: G| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 83.716; most accessible tissue: Callus, score: 97.610
vg0702318932 (J) chr07 2318932 A G 99.80% 0.00% A -> G NA
LOC_Os07g05190.1 Alt: G| 5_prime_UTR_variant MODIFIER(snpEff)
The average chromatin accessibility score: 83.642; most accessible tissue: Callus, score: 97.610
vg0702318944 (J) chr07 2318944 A T 99.40% 0.00% A -> T NA
LOC_Os07g05190.1 Alt: T| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 84.229; most accessible tissue: Callus, score: 97.610