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Gene ID/Symbol/Name (e.g., LOC_Os01g08570 or hwh1 or Os01g0180900 or gly%ltransferase, note: wildcard character '%' is also acceptable.):
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Search Results:

10 variations found. LOC_Os12g06080 (expressed protein), ranging from 2,836,020 bp to 2,836,995 bp (including 0 kb upstream and 0 kb downstream of the gene).

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
vg1202836111 (J) chr12 2836111 C T 99.80% 0.00% C -> T NA
LOC_Os12g06080.1 Alt: T| synonymous_variant LOW(snpEff)
LOC_Os12g06070.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 72.266; most accessible tissue: Minghui63 panicle, score: 85.556
vg1202836137 (J) chr12 2836137 C T 99.80% 0.00% C -> T NA
LOC_Os12g06080.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 72.426; most accessible tissue: Minghui63 panicle, score: 84.552
vg1202836219 (J) chr12 2836219 T G 91.30% 0.00% T -> G
mr1073 (All); LR P-value: 5.01E-06;
mr1545 (All); LR P-value: 5.54E-06;
mr1549 (All); LR P-value: 2.56E-37;
mr1621 (All); LR P-value: 3.72E-07;
mr1757 (All); LR P-value: 2.08E-36;
mr1757_2 (All); LR P-value: 3.83E-30;
mr1762_2 (All); LR P-value: 8.22E-07
LOC_Os12g06080.1 Alt: G| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 75.255; most accessible tissue: Minghui63 panicle, score: 84.005
vg1202836274 (J) chr12 2836274 A G 99.80% 0.00% A -> G NA
LOC_Os12g06070.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os12g06080.1 Alt: G| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 77.228; most accessible tissue: Zhenshan97 flower, score: 85.807
vg1202836288 (J) chr12 2836288 T C 94.80% 0.00% T -> C NA
LOC_Os12g06070.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os12g06080.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 77.118; most accessible tissue: Zhenshan97 flower, score: 86.268
vg1202836464 (J) chr12 2836464 C A 99.80% 0.00% C -> A NA
LOC_Os12g06080.1 Alt: A| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/probably damaging(PolyPhen-2)
The average chromatin accessibility score: 76.372; most accessible tissue: Zhenshan97 flower, score: 87.550
vg1202836573 (J) chr12 2836573 G A 98.80% 0.00% G -> A NA
LOC_Os12g06080.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 80.863; most accessible tissue: Zhenshan97 panicle, score: 90.061
vg1202836786 (J) chr12 2836786 A G 89.40% 0.00% A -> G
mr1403 (All); LR P-value: 2.01E-08;
mr1621 (All); LR P-value: 3.27E-06;
mr1762_2 (All); LR P-value: 1.67E-06
LOC_Os12g06080.1 Alt: G| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 83.803; most accessible tissue: Zhenshan97 panicle, score: 92.270
vg1202836800 (J) chr12 2836800 C T 92.90% 0.00% C -> T NA
LOC_Os12g06080.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 83.882; most accessible tissue: Zhenshan97 panicle, score: 92.270
STR1202836794 (J) chr12 2836794 CGCCGCC GCCGA CGCCGCT GCCGA 93.20% 0.00% CGCCGCCGCC GA -> CGCCGCTGCC GA NA