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Search Results:

9 variations found. Os02g0785000/LOC_Os02g54370 (hypro1; putative; expressed), ranging from 33,324,527 bp to 33,325,924 bp (including 0 kb upstream and 0 kb downstream of the gene).

Gene IDAnnotation
LOC_Os02g54370 hypro1, putative, expressed; RAP ID: Os02g0785000; MSU ID: LOC_Os02g54370

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
vg0233324638 (J) chr02 33324638 A G 99.70% 0.00% A -> G NA
LOC_Os02g54370.1 Alt: G| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g54350.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g54360.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 55.260; most accessible tissue: Zhenshan97 root, score: 68.908
vg0233324652 (J) chr02 33324652 T A 56.10% 0.00% A -> T,AT
mr1047 (All); LR P-value: 1.11E-08;
mr1164 (All); LR P-value: 2.63E-15;
mr1379 (All); LR P-value: 6.35E-10;
mr1559 (All); LR P-value: 5.15E-08;
mr1580 (All); LR P-value: 1.14E-20;
mr1825 (All); LR P-value: 3.85E-17;
mr1084_2 (All); LR P-value: 2.68E-08;
mr1133_2 (All); LR P-value: 6.35E-15;
mr1148_2 (All); LR P-value: 2.39E-15;
mr1198_2 (All); LR P-value: 3.96E-10;
mr1205_2 (All); LR P-value: 1.85E-07;
mr1227_2 (All); LR P-value: 2.12E-06;
mr1228_2 (All); LR P-value: 2.30E-11;
mr1548_2 (All); LR P-value: 1.01E-06;
mr1558_2 (All); LR P-value: 1.73E-57;
mr1571_2 (All); LR P-value: 5.36E-33;
mr1575_2 (All); LR P-value: 7.64E-14;
mr1579_2 (All); LR P-value: 2.27E-14;
mr1580_2 (All); LR P-value: 9.03E-34;
mr1646_2 (All); LR P-value: 9.60E-10;
mr1677_2 (All); LR P-value: 7.37E-06;
mr1680_2 (All); LR P-value: 2.07E-10;
mr1686_2 (All); LR P-value: 4.42E-15;
mr1698_2 (All); LR P-value: 1.18E-22;
mr1825_2 (All); LR P-value: 2.51E-33;
mr1922_2 (All); LR P-value: 7.50E-22;
mr1924_2 (All); LR P-value: 2.08E-22;
mr1940_2 (All); LR P-value: 1.43E-09;
mr1950_2 (All); LR P-value: 5.77E-15
LOC_Os02g54370.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g54350.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g54360.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g54370.1 Alt: AT| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g54350.1 Alt: AT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g54360.1 Alt: AT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 57.107; most accessible tissue: Zhenshan97 root, score: 71.691
vg0233324706 (J) chr02 33324706 G T 51.80% 0.00% G -> T
mr1026 (All); LR P-value: 8.41E-33;
mr1047 (All); LR P-value: 7.95E-09;
mr1063 (All); LR P-value: 1.94E-51;
mr1065 (All); LR P-value: 3.33E-54;
mr1078 (All); LR P-value: 6.09E-50;
mr1091 (All); LR P-value: 1.77E-38;
mr1108 (All); LR P-value: 8.33E-46;
mr1110 (All); LR P-value: 2.87E-35;
mr1112 (All); LR P-value: 4.23E-45;
mr1144 (All); LR P-value: 1.35E-42;
mr1161 (All); LR P-value: 3.31E-33;
mr1200 (All); LR P-value: 4.20E-46;
mr1208 (All); LR P-value: 3.69E-29;
mr1234 (All); LR P-value: 4.52E-46;
mr1237 (All); LR P-value: 3.06E-33;
mr1260 (All); LR P-value: 3.03E-08;
mr1261 (All); LR P-value: 1.15E-14;
mr1352 (All); LR P-value: 1.49E-09;
mr1580 (All); LR P-value: 1.24E-19;
mr1657 (All); LR P-value: 5.10E-12;
mr1870 (All); LR P-value: 4.28E-16;
mr1063_2 (All); LR P-value: 8.14E-55;
mr1065_2 (All); LR P-value: 3.44E-63;
mr1078_2 (All); LR P-value: 4.15E-63;
mr1091_2 (All); LR P-value: 1.48E-48;
mr1108_2 (All); LR P-value: 1.95E-56;
mr1110_2 (All); LR P-value: 2.06E-38;
mr1112_2 (All); LR P-value: 3.26E-61;
mr1144_2 (All); LR P-value: 2.37E-51;
mr1161_2 (All); LR P-value: 1.93E-33;
mr1164_2 (All); LR P-value: 5.07E-21;
mr1189_2 (All); LR P-value: 3.77E-12;
mr1228_2 (All); LR P-value: 6.27E-10;
mr1234_2 (All); LR P-value: 5.36E-59;
mr1260_2 (All); LR P-value: 1.27E-19;
mr1323_2 (All); LR P-value: 8.39E-26;
mr1531_2 (All); LR P-value: 2.86E-19;
mr1580_2 (All); LR P-value: 7.00E-33;
mr1728_2 (All); LR P-value: 4.30E-11;
mr1734_2 (All); LR P-value: 1.70E-11;
mr1825_2 (All); LR P-value: 1.43E-32;
mr1870_2 (All); LR P-value: 8.69E-19
LOC_Os02g54370.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g54350.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g54360.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 67.826; most accessible tissue: Zhenshan97 root, score: 75.275
vg0233325181 (J) chr02 33325181 G A 94.00% 0.00% G -> A
mr1260_2 (All); LR P-value: 1.43E-16;
mr1911_2 (All); LR P-value: 1.78E-14
LOC_Os02g54370.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 77.960; most accessible tissue: Zhenshan97 young leaf, score: 84.814
vg0233325660 (J) chr02 33325660 G A 98.10% 0.00% G -> A NA
LOC_Os02g54370.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 61.786; most accessible tissue: Zhenshan97 root, score: 74.466
vg0233325754 (J) chr02 33325754 GTCGTCG TCGTCT G 99.90% 0.00% GTCGTCGTCG TCT -> G NA
LOC_Os02g54370.1 Alt: G| disruptive_inframe_deletion MODERATE(snpEff)
LOC_Os02g54360.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os02g54390.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 64.002; most accessible tissue: Callus, score: 81.364
vg0233325810 (J) chr02 33325810 C G 94.00% 0.00% C -> G NA
LOC_Os02g54370.1 Alt: G| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 67.467; most accessible tissue: Zhenshan97 root, score: 82.361
STR0233324651 (J) chr02 33324651 AT AA 55.20% 0.00% AA -> AT NA
STR0233325178 (J) chr02 33325178 GTCGT GTCAT 96.00% 0.00% GTCGT -> GTCAT NA