Search for Variation by Gene:

Gene ID/Symbol/Name (e.g., LOC_Os01g08570 or hwh1 or Os01g0180900 or gly%ltransferase, note: wildcard character '%' is also acceptable.):
Upstream (kb, optional, must <= 10 kb) : Downstream (kb, optional, must <= 10 kb) :
Variations Type:

Optional: (The selected data will be displayed in the result page.)

 Show Gene Expression Atlas  Show Chromatin Accessibility Map
 Show Non-coding variation Scores

Search Results:

7 variations found. LOC_Os08g18850 (hypothetical protein), ranging from 11,251,537 bp to 11,251,841 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
vg0811251553 (J) chr08 11251553 T C 91.00% 0.00% T -> C NA
LOC_Os08g18850.1 Alt: C| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 15.984; most accessible tissue: Zhenshan97 panicle, score: 24.575
vg0811251629 (J) chr08 11251629 A T 18.20% 47.33% A -> T NA
LOC_Os08g18850.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
LOC_Os08g18850.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
LOC_Os08g18850.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 14.934; most accessible tissue: Zhenshan97 panicle, score: 32.308
vg0811251630 (J) chr08 11251630 T C 17.40% 53.53% T -> C
Heading_date (All); LR P-value: 7.83E-10;
Spikelet_length (All); LR P-value: 2.00E-16;
Spikelet_length (Jap_All); LR P-value: 1.25E-12;
mr1137 (All); LR P-value: 1.62E-32;
mr1137 (Jap_All); LR P-value: 9.48E-09;
mr1576 (All); LR P-value: 6.93E-06;
mr1708 (All); LR P-value: 1.04E-06;
mr1864 (Jap_All); LR P-value: 5.81E-10;
mr1043_2 (Jap_All); LR P-value: 5.95E-06;
mr1115_2 (All); LR P-value: 1.57E-27;
mr1115_2 (Jap_All); LR P-value: 3.55E-15;
mr1129_2 (Jap_All); LR P-value: 4.79E-06;
mr1137_2 (All); LR P-value: 4.44E-35;
mr1229_2 (All); LR P-value: 1.43E-06;
mr1229_2 (Jap_All); LR P-value: 7.95E-07;
mr1251_2 (Jap_All); LR P-value: 1.40E-09;
mr1252_2 (All); LR P-value: 3.23E-07;
mr1252_2 (Jap_All); LR P-value: 8.78E-06;
mr1404_2 (Jap_All); LR P-value: 4.71E-06;
mr1435_2 (Jap_All); LR P-value: 1.45E-09;
mr1502_2 (Jap_All); LR P-value: 2.13E-07;
mr1521_2 (Jap_All); LR P-value: 3.73E-09;
mr1555_2 (All); LR P-value: 2.58E-06;
mr1570_2 (Jap_All); LR P-value: 4.68E-07;
mr1580_2 (Jap_All); LR P-value: 6.84E-10;
mr1596_2 (Jap_All); LR P-value: 7.79E-06;
mr1611_2 (All); LR P-value: 4.10E-24;
mr1611_2 (Jap_All); LR P-value: 1.63E-12;
mr1671_2 (Jap_All); LR P-value: 5.71E-07;
mr1693_2 (All); LR P-value: 1.92E-07;
mr1693_2 (Jap_All); LR P-value: 1.53E-06;
mr1746_2 (All); LR P-value: 1.16E-16;
mr1746_2 (Jap_All); LR P-value: 5.05E-09;
mr1789_2 (All); LR P-value: 7.22E-29;
mr1800_2 (All); LR P-value: 4.80E-14;
mr1825_2 (Jap_All); LR P-value: 2.43E-09;
mr1844_2 (All); LR P-value: 3.80E-11;
mr1880_2 (All); LR P-value: 2.35E-07;
mr1880_2 (Jap_All); LR P-value: 1.21E-07
LOC_Os08g18850.1 Alt: C| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
LOC_Os08g18850.1 Alt: C| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
LOC_Os08g18850.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 14.934; most accessible tissue: Zhenshan97 panicle, score: 32.308
vg0811251643 (J) chr08 11251643 A G 53.90% 0.21% A -> G NA
LOC_Os08g18860.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g18850.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 14.671; most accessible tissue: Zhenshan97 panicle, score: 32.308
vg0811251683 (J) chr08 11251683 G A 98.90% 0.00% G -> A
mr1028 (Jap_All); LR P-value: 6.10E-07;
mr1369 (Jap_All); LMM P-value: 4.76E-06; LR P-value: 4.76E-06;
mr1453 (Jap_All); LR P-value: 3.17E-06;
mr1648 (Jap_All); LR P-value: 6.12E-07;
mr1652 (Jap_All); LR P-value: 3.31E-06;
mr1697 (Jap_All); LR P-value: 5.49E-08
LOC_Os08g18850.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 14.368; most accessible tissue: Zhenshan97 panicle, score: 32.308
vg0811251725 (J) chr08 11251725 G T 50.50% 0.02% T -> G NA
LOC_Os08g18850.1 Alt: G| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
LOC_Os08g18850.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 13.917; most accessible tissue: Zhenshan97 panicle, score: 36.038
vg0811251746 (J) chr08 11251746 G T 98.00% 0.00% G -> T,A NA
LOC_Os08g18850.1 Alt: T| stop_gained HIGH(snpEff)/stop_gained(CooVar)
LOC_Os08g18850.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 13.727; most accessible tissue: Zhenshan97 panicle, score: 36.038