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:

9 variations found. LOC_Os11g04690 (zinc finger; C3HC4 type domain containing protein; expressed), ranging from 1,998,789 bp to 1,999,485 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
vg1101998790 (J) chr11 1998790 A T 79.50% 0.00% A -> T
mr1593 (Ind_All); LR P-value: 8.00E-07;
mr1607 (All); LR P-value: 2.06E-09;
mr1662 (All); LR P-value: 6.13E-07;
mr1686 (Ind_All); LR P-value: 1.00E-06;
mr1835 (All); LR P-value: 1.10E-08;
mr1835 (Ind_All); LR P-value: 7.22E-08;
mr1904 (All); LMM P-value: 5.54E-06; LR P-value: 7.62E-17;
mr1904 (Ind_All); LMM P-value: 9.12E-09; LR P-value: 4.05E-15;
mr1942 (All); LR P-value: 9.40E-08;
mr1024_2 (Ind_All); LR P-value: 5.37E-10;
mr1072_2 (Ind_All); LR P-value: 2.82E-08;
mr1075_2 (Ind_All); LR P-value: 1.55E-08;
mr1077_2 (Ind_All); LR P-value: 5.90E-09;
mr1078_2 (Ind_All); LR P-value: 3.13E-09;
mr1199_2 (Ind_All); LR P-value: 6.26E-06;
mr1200_2 (Ind_All); LR P-value: 1.51E-07;
mr1265_2 (All); LR P-value: 6.45E-09;
mr1265_2 (Ind_All); LR P-value: 3.98E-09;
mr1482_2 (All); LR P-value: 2.20E-07;
mr1486_2 (Ind_All); LR P-value: 3.66E-07;
mr1528_2 (All); LR P-value: 2.46E-11;
mr1528_2 (Ind_All); LR P-value: 7.32E-09;
mr1558_2 (Ind_All); LR P-value: 1.15E-07;
mr1565_2 (Ind_All); LR P-value: 7.29E-12;
mr1593_2 (Ind_All); LR P-value: 2.36E-08;
mr1598_2 (Ind_All); LR P-value: 9.38E-11;
mr1641_2 (Ind_All); LR P-value: 8.98E-06;
mr1659_2 (Ind_All); LR P-value: 2.40E-06;
mr1735_2 (Ind_All); LR P-value: 6.36E-06;
mr1835_2 (All); LR P-value: 3.35E-13;
mr1835_2 (Ind_All); LR P-value: 8.70E-10;
mr1838_2 (Ind_All); LR P-value: 4.00E-08;
mr1904_2 (All); LR P-value: 9.41E-16;
mr1904_2 (Ind_All); LR P-value: 5.25E-11
LOC_Os11g04690.1 Alt: T| initiator_codon_variant LOW(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 65.452; most accessible tissue: Zhenshan97 panicle, score: 80.486
vg1101998891 (J) chr11 1998891 G A 99.20% 0.00% G -> A NA
LOC_Os11g04690.1 Alt: A| stop_gained HIGH(snpEff)/stop_gained(CooVar)
The average chromatin accessibility score: 64.340; most accessible tissue: Zhenshan97 panicle, score: 79.799
vg1101998893 (J) chr11 1998893 C G 98.50% 0.00% C -> G
mr1156 (Jap_All); LR P-value: 1.89E-06;
mr1179 (Jap_All); LR P-value: 4.74E-06;
mr1951 (Jap_All); LR P-value: 3.40E-08
LOC_Os11g04690.1 Alt: G| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 63.529; most accessible tissue: Zhenshan97 panicle, score: 79.071
vg1101999007 (J) chr11 1999007 G A 56.50% 0.00% G -> A
mr1030 (All); LR P-value: 7.75E-06;
mr1272 (Ind_All); LR P-value: 1.77E-06;
mr1565 (All); LR P-value: 3.22E-09;
mr1663 (All); LR P-value: 3.07E-09;
mr1686 (Ind_All); LR P-value: 3.46E-07;
mr1835 (Ind_All); LR P-value: 1.12E-06;
mr1904 (Ind_All); LMM P-value: 4.29E-08; LR P-value: 4.86E-14;
mr1024_2 (Ind_All); LR P-value: 4.95E-10;
mr1078_2 (Ind_All); LR P-value: 1.00E-08;
mr1183_2 (All); LR P-value: 7.73E-20;
mr1265_2 (Ind_All); LR P-value: 3.25E-08;
mr1302_2 (All); LR P-value: 4.27E-07;
mr1486_2 (Ind_All); LR P-value: 2.23E-06;
mr1528_2 (Ind_All); LR P-value: 8.32E-08;
mr1558_2 (Ind_All); LR P-value: 6.81E-08;
mr1565_2 (All); LR P-value: 1.39E-11;
mr1565_2 (Ind_All); LR P-value: 2.05E-11;
mr1593_2 (Ind_All); LR P-value: 2.30E-08;
mr1598_2 (Ind_All); LR P-value: 4.80E-09;
mr1604_2 (All); LR P-value: 4.23E-07;
mr1641_2 (Ind_All); LR P-value: 7.40E-06;
mr1659_2 (All); LR P-value: 4.62E-10;
mr1659_2 (Ind_All); LR P-value: 7.43E-07;
mr1735_2 (Ind_All); LR P-value: 5.05E-07;
mr1824_2 (All); LR P-value: 4.38E-07;
mr1835_2 (Ind_All); LR P-value: 2.40E-09;
mr1838_2 (All); LR P-value: 3.15E-15;
mr1838_2 (Ind_All); LR P-value: 5.38E-08;
mr1904_2 (Ind_All); LR P-value: 2.05E-09
LOC_Os11g04690.1 Alt: A| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 66.756; most accessible tissue: Zhenshan97 panicle, score: 79.071
vg1101999096 (J) chr11 1999096 C T 56.50% 0.32% C -> T
mr1030 (All); LR P-value: 9.59E-06;
mr1663 (All); LR P-value: 2.14E-09;
mr1686 (Ind_All); LR P-value: 2.93E-07;
mr1835 (Ind_All); LR P-value: 1.14E-06;
mr1904 (Ind_All); LMM P-value: 3.78E-08; LR P-value: 4.55E-14;
mr1024_2 (Ind_All); LR P-value: 4.78E-10;
mr1078_2 (Ind_All); LR P-value: 1.04E-08;
mr1265_2 (Ind_All); LR P-value: 6.01E-08;
mr1302_2 (All); LR P-value: 7.11E-07;
mr1486_2 (Ind_All); LR P-value: 2.48E-06;
mr1528_2 (Ind_All); LR P-value: 1.31E-07;
mr1558_2 (Ind_All); LR P-value: 9.85E-08;
mr1565_2 (All); LR P-value: 4.51E-11;
mr1565_2 (Ind_All); LR P-value: 1.12E-10;
mr1593_2 (Ind_All); LR P-value: 7.38E-08;
mr1659_2 (All); LR P-value: 9.12E-10;
mr1659_2 (Ind_All); LR P-value: 1.91E-06;
mr1735_2 (Ind_All); LR P-value: 1.04E-06;
mr1824_2 (All); LR P-value: 8.28E-07;
mr1835_2 (Ind_All); LR P-value: 2.21E-09;
mr1838_2 (All); LR P-value: 1.12E-14;
mr1838_2 (Ind_All); LR P-value: 1.65E-07;
mr1904_2 (Ind_All); LR P-value: 1.69E-09
LOC_Os11g04690.1 Alt: T| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
LOC_Os11g04690.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 63.300; most accessible tissue: Minghui63 panicle, score: 78.920
vg1101999220 (J) chr11 1999220 G GC 99.80% 0.00% G -> GC NA
LOC_Os11g04690.1 Alt: GC| frameshift_variant HIGH(snpEff)/frameshift_variant(CooVar)
The average chromatin accessibility score: 68.466; most accessible tissue: Minghui63 panicle, score: 77.956
vg1101999320 (J) chr11 1999320 C T 64.50% 0.00% T -> C NA
LOC_Os11g04690.1 Alt: C| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 66.966; most accessible tissue: Minghui63 root, score: 76.119
vg1101999349 (J) chr11 1999349 G A 54.70% 0.32% G -> A
mr1565 (All); LR P-value: 2.54E-10;
mr1663 (All); LR P-value: 4.54E-10;
mr1686 (Ind_All); LR P-value: 4.14E-07;
mr1835 (Ind_All); LR P-value: 1.14E-06;
mr1904 (All); LMM P-value: 2.15E-06;
mr1904 (Ind_All); LMM P-value: 3.73E-08; LR P-value: 3.94E-14;
mr1024_2 (Ind_All); LR P-value: 4.39E-10;
mr1078_2 (Ind_All); LR P-value: 1.23E-08;
mr1265_2 (Ind_All); LR P-value: 2.93E-08;
mr1486_2 (Ind_All); LR P-value: 2.73E-06;
mr1528_2 (Ind_All); LR P-value: 5.96E-08;
mr1558_2 (Ind_All); LR P-value: 1.08E-07;
mr1565_2 (All); LR P-value: 1.25E-12;
mr1565_2 (Ind_All); LR P-value: 1.07E-10;
mr1593_2 (Ind_All); LR P-value: 7.43E-08;
mr1659_2 (All); LR P-value: 2.46E-10;
mr1659_2 (Ind_All); LR P-value: 2.00E-06;
mr1683_2 (All); LR P-value: 1.55E-07;
mr1715_2 (All); LR P-value: 1.22E-16;
mr1735_2 (Ind_All); LR P-value: 1.07E-06;
mr1824_2 (All); LR P-value: 2.72E-07;
mr1835_2 (Ind_All); LR P-value: 2.74E-09;
mr1838_2 (All); LR P-value: 1.48E-16;
mr1838_2 (Ind_All); LR P-value: 1.86E-07;
mr1904_2 (Ind_All); LR P-value: 3.48E-09
LOC_Os11g04690.1 Alt: A| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
LOC_Os11g04690.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 65.203; most accessible tissue: Minghui63 root, score: 76.721
vg1101999370 (J) chr11 1999370 C G 98.20% 0.00% C -> G NA
LOC_Os11g04690.1 Alt: G| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 65.124; most accessible tissue: Minghui63 root, score: 76.425