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Search Results:

4 variations found. LOC_Os07g48730 (tyrosine protein kinase domain containing protein; putative; expressed), ranging from 29,179,660 bp to 29,181,610 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
vg0729180318 (J) chr07 29180318 G A 63.50% 0.00% A -> G
mr1342 (All); LR P-value: 9.10E-09;
mr1592 (All); LR P-value: 6.22E-15;
mr1795 (All); LR P-value: 1.35E-51;
mr1837 (All); LR P-value: 5.51E-06;
mr1915 (All); LR P-value: 5.00E-07;
mr1592_2 (All); LR P-value: 2.28E-16;
mr1700_2 (All); LR P-value: 2.15E-08;
mr1713_2 (All); LR P-value: 1.41E-12;
mr1727_2 (All); LR P-value: 5.03E-07;
mr1756_2 (All); LR P-value: 3.68E-10;
mr1785_2 (All); LR P-value: 5.21E-06;
mr1837_2 (All); LR P-value: 1.77E-08;
mr1915_2 (All); LR P-value: 8.67E-07;
mr1938_2 (All); LR P-value: 5.37E-14
LOC_Os07g48750.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g48720.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g48720.2 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g48720.3 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g48730.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 87.192; most accessible tissue: Zhenshan97 root, score: 95.193
vg0729181278 (J) chr07 29181278 G C 99.90% 0.00% G -> C NA
LOC_Os07g48730.1 Alt: C| 3_prime_UTR_variant MODIFIER(snpEff)
LOC_Os07g48750.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)
LOC_Os07g48720.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)
LOC_Os07g48720.2 Alt: C| downstream_gene_variant MODIFIER(snpEff)
LOC_Os07g48720.3 Alt: C| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 75.477; most accessible tissue: Callus, score: 97.666
vg0729181313 (J) chr07 29181313 T C 92.60% 0.00% C -> T NA
LOC_Os07g48730.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g48750.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g48720.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g48720.2 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g48720.3 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 74.378; most accessible tissue: Callus, score: 97.666
vg0729181328 (J) chr07 29181328 A G 99.70% 0.00% A -> G NA
LOC_Os07g48730.1 Alt: G| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g48750.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g48720.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g48720.2 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os07g48720.3 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 72.518; most accessible tissue: Callus, score: 94.374