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Search Results:

28 variations found. Os03g0379700/LOC_Os03g26250 (expressed protein), ranging from 15,011,161 bp to 15,011,736 bp (including 0 kb upstream and 0 kb downstream of the gene).

Gene IDAnnotation
LOC_Os03g26250 conserved hypothetical protein; RAP ID: Os03g0379700; MSU ID: LOC_Os03g26250

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
vg0315011173 (J) chr03 15011173 G A 99.60% 0.00% G -> A NA
LOC_Os03g26250.1 Alt: A| synonymous_variant LOW(snpEff)
LOC_Os03g26240.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26260.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26229.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 66.620; most accessible tissue: Minghui63 root, score: 82.511
vg0315011284 (J) chr03 15011284 G A 77.20% 0.00% G -> A
mr1082 (Jap_All); LR P-value: 2.47E-06;
mr1083 (Jap_All); LR P-value: 1.13E-06;
mr1088 (Ind_All); LR P-value: 9.25E-06;
mr1217 (Jap_All); LR P-value: 1.03E-07;
mr1237 (Ind_All); LR P-value: 4.05E-08;
mr1526 (Ind_All); LR P-value: 8.37E-07;
mr1560 (Jap_All); LR P-value: 9.11E-06;
mr1634 (Ind_All); LR P-value: 8.00E-06;
mr1852 (Jap_All); LR P-value: 4.42E-08
LOC_Os03g26250.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 70.461; most accessible tissue: Callus, score: 84.841
vg0315011318 (J) chr03 15011318 C T 85.50% 0.00% C -> T
mr1045 (All); LR P-value: 2.26E-08;
mr1045 (Jap_All); LR P-value: 2.90E-07;
mr1072 (Jap_All); LR P-value: 8.00E-06;
mr1077 (All); LR P-value: 1.45E-18;
mr1077 (Jap_All); LR P-value: 1.75E-07;
mr1202 (Jap_All); LR P-value: 8.02E-07;
mr1330 (Jap_All); LR P-value: 7.13E-10;
mr1521 (Jap_All); LR P-value: 5.71E-07;
mr1530 (Jap_All); LR P-value: 6.72E-07;
mr1576 (All); LR P-value: 2.76E-07;
mr1576 (Jap_All); LR P-value: 7.71E-06;
mr1627 (Jap_All); LR P-value: 2.17E-06;
mr1629 (Jap_All); LR P-value: 1.13E-06;
mr1668 (Jap_All); LR P-value: 1.56E-06;
mr1703 (All); LMM P-value: 3.63E-07; LR P-value: 3.62E-07;
mr1703 (Jap_All); LMM P-value: 2.15E-06; LR P-value: 2.15E-06;
mr1729 (Jap_All); LR P-value: 1.88E-06;
mr1804 (All); LR P-value: 8.24E-08;
mr1844 (All); LR P-value: 6.56E-13;
mr1844 (Jap_All); LR P-value: 3.57E-06;
mr1865 (Jap_All); LR P-value: 4.62E-07;
mr1880 (All); LR P-value: 2.20E-06;
mr1977 (All); LR P-value: 1.01E-07;
mr1977 (Jap_All); LR P-value: 4.48E-06;
mr1982 (All); LR P-value: 1.91E-13;
mr1182_2 (All); LR P-value: 1.41E-14;
mr1182_2 (Jap_All); LR P-value: 2.53E-07;
mr1282_2 (All); LR P-value: 3.42E-10;
mr1530_2 (Jap_All); LR P-value: 2.78E-10
LOC_Os03g26250.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/probably damaging(PolyPhen-2)
The average chromatin accessibility score: 70.414; most accessible tissue: Callus, score: 84.841
vg0315011365 (J) chr03 15011365 C T 79.20% 0.00% C -> T,G
mr1448 (Jap_All); LR P-value: 4.89E-06;
mr1549 (Jap_All); LR P-value: 1.01E-09;
mr1627 (Jap_All); LR P-value: 1.80E-06;
mr1757 (Jap_All); LR P-value: 3.26E-08
LOC_Os03g26250.1 Alt: T| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
LOC_Os03g26250.1 Alt: G| synonymous_variant LOW(snpEff)
LOC_Os03g26240.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26260.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26229.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 67.981; most accessible tissue: Minghui63 root, score: 82.967
vg0315011380 (J) chr03 15011380 C T 98.20% 0.00% C -> T NA
LOC_Os03g26250.1 Alt: T| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 67.408; most accessible tissue: Minghui63 root, score: 82.818
vg0315011440 (J) chr03 15011440 G A 99.10% 0.74% G -> A NA
LOC_Os03g26240.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 62.408; most accessible tissue: Minghui63 root, score: 79.068
vg0315011446 (J) chr03 15011446 A AT 99.10% 0.00% A -> AT NA
LOC_Os03g26240.1 Alt: AT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: AT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: AT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: AT| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 62.065; most accessible tissue: Callus, score: 78.971
vg0315011458 (J) chr03 15011458 C T 92.70% 0.00% T -> C NA
LOC_Os03g26240.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 61.981; most accessible tissue: Callus, score: 78.971
vg0315011459 (J) chr03 15011459 G A 96.90% 0.00% A -> G NA
LOC_Os03g26240.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 61.981; most accessible tissue: Callus, score: 78.971
vg0315011468 (J) chr03 15011468 C T 96.90% 0.00% T -> C NA
LOC_Os03g26240.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 61.154; most accessible tissue: Callus, score: 78.971
vg0315011508 (J) chr03 15011508 C T 99.70% 0.00% C -> T NA
LOC_Os03g26240.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26260.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26229.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26250.1 Alt: T| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 58.812; most accessible tissue: Callus, score: 78.971
vg0315011511 (J) chr03 15011511 C T 76.90% 0.00% C -> T
mr1082 (Jap_All); LR P-value: 2.47E-06;
mr1083 (Jap_All); LR P-value: 1.13E-06;
mr1217 (Jap_All); LR P-value: 1.03E-07;
mr1237 (Ind_All); LR P-value: 5.09E-08;
mr1526 (Ind_All); LR P-value: 1.22E-06;
mr1560 (Jap_All); LR P-value: 9.11E-06;
mr1634 (Ind_All); LR P-value: 3.05E-06;
mr1852 (Jap_All); LR P-value: 4.42E-08
LOC_Os03g26240.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 59.174; most accessible tissue: Callus, score: 78.971
vg0315011517 (J) chr03 15011517 C T 79.10% 0.00% C -> T
mr1448 (Jap_All); LR P-value: 4.89E-06;
mr1549 (Jap_All); LR P-value: 1.01E-09;
mr1575 (All); LR P-value: 5.79E-09;
mr1627 (Jap_All); LR P-value: 1.80E-06;
mr1757 (Jap_All); LR P-value: 3.26E-08;
mr1952_2 (All); LR P-value: 6.48E-07
LOC_Os03g26240.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 58.735; most accessible tissue: Callus, score: 78.971
vg0315011523 (J) chr03 15011523 ATTT TTTT 79.10% 0.00% ATTT -> TTTT,A
mr1077 (All); LR P-value: 1.67E-18;
mr1330 (Jap_All); LR P-value: 3.46E-06;
mr1448 (Jap_All); LR P-value: 6.00E-06;
mr1549 (Jap_All); LR P-value: 8.20E-09;
mr1575 (All); LR P-value: 9.30E-09;
mr1757 (Jap_All); LR P-value: 7.92E-08;
mr1090_2 (Jap_All); LR P-value: 2.63E-07;
mr1096_2 (Jap_All); LR P-value: 1.39E-06
LOC_Os03g26240.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26240.1 Alt: TTTT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: TTTT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: TTTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: TTTT| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 58.935; most accessible tissue: Callus, score: 78.971
vg0315011536 (J) chr03 15011536 A G 97.80% 0.00% A -> G NA
LOC_Os03g26240.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 59.121; most accessible tissue: Callus, score: 78.971
vg0315011608 (J) chr03 15011608 G A 99.80% 0.00% G -> A NA
LOC_Os03g26240.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26260.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26229.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26250.1 Alt: A| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 48.961; most accessible tissue: Minghui63 panicle, score: 64.459
vg0315011619 (J) chr03 15011619 G A 50.40% 0.00% G -> A
Grain_length (Jap_All); LR P-value: 1.26E-14;
mr1088 (Jap_All); LR P-value: 7.94E-07;
mr1104 (Jap_All); LR P-value: 2.84E-06;
mr1179 (Jap_All); LR P-value: 1.50E-06;
mr1213 (Jap_All); LR P-value: 8.12E-06;
mr1236 (Jap_All); LR P-value: 5.59E-06;
mr1502 (Jap_All); LR P-value: 3.36E-06;
mr1620 (Jap_All); LR P-value: 3.06E-07;
mr1769 (Jap_All); LR P-value: 8.42E-13;
mr1422_2 (Jap_All); LR P-value: 2.38E-07;
mr1533_2 (Jap_All); LR P-value: 7.00E-12;
mr1583_2 (Jap_All); LR P-value: 2.50E-06
LOC_Os03g26240.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 48.956; most accessible tissue: Zhenshan97 panicle, score: 65.386
vg0315011627 (J) chr03 15011627 C T 99.90% 0.00% C -> T NA
LOC_Os03g26240.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26260.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26229.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26250.1 Alt: T| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 47.736; most accessible tissue: Zhenshan97 panicle, score: 65.386
vg0315011628 (J) chr03 15011628 G A 96.80% 0.00% A -> G NA
LOC_Os03g26240.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 47.736; most accessible tissue: Zhenshan97 panicle, score: 65.386
vg0315011642 (J) chr03 15011642 G A 97.60% 0.00% G -> A
mr1073 (Jap_All); LR P-value: 1.85E-06;
mr1217 (Jap_All); LR P-value: 1.52E-07;
mr1852 (Jap_All); LR P-value: 1.72E-08;
mr1786_2 (Jap_All); LR P-value: 9.05E-06
LOC_Os03g26240.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 40.430; most accessible tissue: Zhenshan97 panicle, score: 59.590
vg0315011650 (J) chr03 15011650 A T 99.20% 0.00% A -> T NA
LOC_Os03g26240.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26260.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26229.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26250.1 Alt: T| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 39.847; most accessible tissue: Minghui63 panicle, score: 62.157
vg0315011651 (J) chr03 15011651 A G 99.20% 0.00% A -> G NA
LOC_Os03g26240.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26260.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26229.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os03g26250.1 Alt: G| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 39.337; most accessible tissue: Minghui63 panicle, score: 62.157
vg0315011654 (J) chr03 15011654 CAACGGC GTCATCT ATTAAAA TAACGGC GTCATCT ATTAAAA 92.00% 0.00% CAACGGCGTC ATCTATTAAA A -> TAACGGCGTC ATCTATTAAA A,C NA
LOC_Os03g26240.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26240.1 Alt: TAACGGCGTCATCTATTAAAA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: TAACGGCGTCATCTATTAAAA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: TAACGGCGTCATCTATTAAAA| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: TAACGGCGTCATCTATTAAAA| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 38.710; most accessible tissue: Minghui63 panicle, score: 62.157
vg0315011663 (J) chr03 15011663 C T 51.40% 0.00% C -> T
Grain_length (Jap_All); LR P-value: 1.26E-14;
mr1088 (Jap_All); LR P-value: 7.94E-07;
mr1104 (Jap_All); LR P-value: 2.84E-06;
mr1179 (Jap_All); LR P-value: 1.50E-06;
mr1213 (Jap_All); LR P-value: 8.12E-06;
mr1236 (Jap_All); LR P-value: 5.59E-06;
mr1502 (Jap_All); LR P-value: 3.36E-06;
mr1620 (Jap_All); LR P-value: 3.06E-07;
mr1769 (Jap_All); LR P-value: 8.42E-13;
mr1422_2 (Jap_All); LR P-value: 2.38E-07;
mr1533_2 (Jap_All); LR P-value: 7.00E-12;
mr1583_2 (Jap_All); LR P-value: 2.50E-06
LOC_Os03g26240.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 39.111; most accessible tissue: Minghui63 panicle, score: 62.157
vg0315011675 (J) chr03 15011675 A T 78.40% 0.34% A -> T,ATTTAAT
mr1448 (Jap_All); LR P-value: 4.89E-06;
mr1549 (Jap_All); LR P-value: 1.01E-09;
mr1575 (All); LR P-value: 5.79E-09;
mr1627 (Jap_All); LR P-value: 1.80E-06;
mr1757 (Jap_All); LR P-value: 3.26E-08;
mr1952_2 (All); LR P-value: 6.48E-07
LOC_Os03g26240.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26240.1 Alt: ATTTAAT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: ATTTAAT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: ATTTAAT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: ATTTAAT| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 41.124; most accessible tissue: Callus, score: 67.433
vg0315011678 (J) chr03 15011678 CGGAGGT AGT TGGAGGT AGT 97.20% 0.00% CGGAGGTAGT -> TGGAGGTAGT ,C NA
LOC_Os03g26240.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26240.1 Alt: TGGAGGTAGT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: TGGAGGTAGT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: TGGAGGTAGT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: TGGAGGTAGT| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 41.230; most accessible tissue: Callus, score: 67.433
vg0315011702 (J) chr03 15011702 T C 98.20% 0.00% T -> C NA
LOC_Os03g26240.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26260.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26229.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os03g26250.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 41.658; most accessible tissue: Callus, score: 67.433
STR0315011534 (J) chr03 15011534 ATA ATG 92.90% 0.00% ATA -> ATG NA