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. Os02g0832150/LOC_Os02g58540 (RING-H2 finger protein; putative; expressed), ranging from 35,783,283 bp to 35,784,146 bp (including 0 kb upstream and 0 kb downstream of the gene).

Gene IDAnnotation
LOC_Os02g58540 RING-H2 finger protein, putative, expressed; RAP ID: Os02g0832150; MSU ID: LOC_Os02g58540

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
vg0235783402 (J) chr02 35783402 G A 98.80% 0.00% G -> A NA
LOC_Os02g58540.1 Alt: A| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g58530.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g58550.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g58550.2 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 79.868; most accessible tissue: Minghui63 flower, score: 85.758
vg0235783514 (J) chr02 35783514 G GGGCGGT GGCGGT 57.90% 0.00% GGGCGGTGGC GGT -> G NA
LOC_Os02g58540.1 Alt: G| inframe_deletion MODERATE(snpEff)/inframe_variant(CooVar)
The average chromatin accessibility score: 87.426; most accessible tissue: Callus, score: 93.514
vg0235783638 (J) chr02 35783638 GCAGGTG GCGTGGG TCCCCAG C G 99.90% 0.00% GCAGGTGGCG TGGGTCCCCA GC -> G NA
LOC_Os02g58540.1 Alt: G| disruptive_inframe_deletion MODERATE(snpEff)
LOC_Os02g58530.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g58550.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g58550.2 Alt: G| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 90.303; most accessible tissue: Zhenshan97 panicle, score: 93.133
vg0235783760 (J) chr02 35783760 C CCTG 88.30% 0.00% CCTG -> C NA
LOC_Os02g58540.1 Alt: C| inframe_deletion MODERATE(snpEff)/inframe_variant(CooVar)
The average chromatin accessibility score: 93.227; most accessible tissue: Zhenshan97 panicle, score: 95.654
vg0235783884 (J) chr02 35783884 A G 99.90% 0.00% A -> G NA
LOC_Os02g58540.1 Alt: G| synonymous_variant LOW(snpEff)
LOC_Os02g58530.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g58550.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g58550.2 Alt: G| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 91.961; most accessible tissue: Zhenshan97 panicle, score: 96.528
vg0235783924 (J) chr02 35783924 A G 59.30% 0.00% G -> A
mr1021 (All); LR P-value: 1.35E-19;
mr1029 (All); LR P-value: 2.57E-06;
mr1047 (All); LR P-value: 3.79E-10;
mr1189 (All); LR P-value: 1.85E-06;
mr1325 (All); LR P-value: 4.36E-11;
mr1326 (All); LR P-value: 2.70E-13;
mr1580 (All); LR P-value: 1.13E-19;
mr1625 (All); LR P-value: 5.25E-06;
mr1657 (All); LR P-value: 1.01E-11;
mr1744 (All); LR P-value: 1.55E-12;
mr1782 (All); LR P-value: 7.88E-06;
mr1796 (All); LR P-value: 1.19E-07;
mr1990 (All); LR P-value: 2.92E-06;
mr1064_2 (All); LR P-value: 3.51E-60;
mr1270_2 (All); LR P-value: 2.00E-27;
mr1316_2 (All); LR P-value: 6.52E-22;
mr1323_2 (All); LR P-value: 1.72E-27;
mr1326_2 (All); LR P-value: 2.04E-13;
mr1744_2 (All); LR P-value: 1.44E-16;
mr1745_2 (All); LR P-value: 1.01E-40;
mr1782_2 (All); LR P-value: 1.55E-10;
mr1932_2 (All); LR P-value: 4.57E-30;
mr1970_2 (All); LR P-value: 1.37E-62;
mr1973_2 (All); LR P-value: 8.78E-99
LOC_Os02g58540.1 Alt: A| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 91.799; most accessible tissue: Zhenshan97 panicle, score: 96.702
vg0235784118 (J) chr02 35784118 A G 98.80% 0.00% A -> G NA
LOC_Os02g58540.1 Alt: G| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g58530.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g58550.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g58550.2 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 95.171; most accessible tissue: Zhenshan97 panicle, score: 98.187
vg0235784137 (J) chr02 35784137 G T 99.90% 0.00% G -> T NA
LOC_Os02g58540.1 Alt: T| 5_prime_UTR_variant MODIFIER(snpEff)
LOC_Os02g58530.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g58550.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g58550.2 Alt: T| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 95.076; most accessible tissue: Zhenshan97 panicle, score: 98.145
STR0235783761 (J) chr02 35783761 CTGC CTGCTGC 85.30% 0.00% CTGCTGC -> CTGC NA