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:

25 variations found. LOC_Os02g38040 (leucine-rich repeat family protein; putative; expressed), ranging from 22,978,829 bp to 22,981,571 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
vg0222978874 (J) chr02 22978874 CCTCTCT CT CCT 85.40% 1.04% CCTCTCTCT -> CCTCTCTCTC T,CCTCTCT, CCT,CCTCTC TCTCTCTCT, C,CCTCTCTC TCTCT NA
LOC_Os02g38040.1 Alt: CCTCTCTCTCTCT| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: CCTCTCTCTCTCT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.1 Alt: CCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: CCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.2 Alt: CCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: CCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: CCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: CCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: CCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: CCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: CCTCTCTCTCT| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: CCTCTCTCTCT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.1 Alt: CCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: CCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.2 Alt: CCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: CCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: CCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: CCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: CCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: CCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: CCT| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: CCT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.1 Alt: CCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: CCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.2 Alt: CCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: CCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: CCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: CCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: CCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: CCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: C| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.2 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: CCTCTCTCTCTCTCT| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: CCTCTCTCTCTCTCT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.1 Alt: CCTCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: CCTCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.2 Alt: CCTCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: CCTCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: CCTCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: CCTCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: CCTCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: CCTCTCTCTCTCTCT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: CCTCTCT| 5_prime_UTR_variant MODIFIER(snpEff)
LOC_Os02g38029.1 Alt: CCTCTCT| upstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38020.1 Alt: CCTCTCT| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.1 Alt: CCTCTCT| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38020.2 Alt: CCTCTCT| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.4 Alt: CCTCTCT| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.3 Alt: CCTCTCT| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.5 Alt: CCTCTCT| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.6 Alt: CCTCTCT| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.2 Alt: CCTCTCT| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 92.404; most accessible tissue: Zhenshan97 flag leaf, score: 95.641
vg0222978950 (J) chr02 22978950 G T 99.00% 0.00% G -> T NA
LOC_Os02g38040.1 Alt: T| 5_prime_UTR_premature_start_codon_gain_variant LOW(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: T| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.2 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 92.976; most accessible tissue: Zhenshan97 flag leaf, score: 95.466
vg0222979271 (J) chr02 22979271 C T 99.00% 0.00% C -> T NA
LOC_Os02g38040.1 Alt: T| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 88.513; most accessible tissue: Zhenshan97 flag leaf, score: 94.128
vg0222979456 (J) chr02 22979456 G A 96.60% 0.00% G -> A NA
LOC_Os02g38040.1 Alt: A| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 85.137; most accessible tissue: Zhenshan97 flag leaf, score: 92.620
vg0222979619 (J) chr02 22979619 C T 96.60% 0.00% C -> T NA
LOC_Os02g38040.1 Alt: T| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 77.244; most accessible tissue: Zhenshan97 flag leaf, score: 88.918
vg0222979709 (J) chr02 22979709 AT A 99.60% 0.00% AT -> A NA
LOC_Os02g38029.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.2 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 72.310; most accessible tissue: Callus, score: 87.432
vg0222979755 (J) chr02 22979755 C G 95.50% 0.00% C -> G NA
LOC_Os02g38029.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.2 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 68.605; most accessible tissue: Callus, score: 87.432
vg0222979913 (J) chr02 22979913 G A 99.80% 0.00% G -> A NA
LOC_Os02g38029.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38020.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38020.2 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.4 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.3 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.5 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.6 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.2 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38040.1 Alt: A| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 56.315; most accessible tissue: Zhenshan97 flag leaf, score: 74.825
vg0222979993 (J) chr02 22979993 ATT AT 85.30% 0.53% ATT -> ATTT,AT,A, TTT NA
LOC_Os02g38029.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.2 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: ATTT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.1 Alt: ATTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: ATTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.2 Alt: ATTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: ATTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: ATTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: ATTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: ATTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: ATTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: ATTT| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: TTT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.1 Alt: TTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: TTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.2 Alt: TTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: TTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: TTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: TTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: TTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: TTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: TTT| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: AT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.1 Alt: AT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: AT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.2 Alt: AT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: AT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: AT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: AT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: AT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: AT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: AT| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 55.890; most accessible tissue: Callus, score: 82.461
vg0222980080 (J) chr02 22980080 G T 96.20% 0.00% G -> T NA
LOC_Os02g38029.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38020.2 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 47.489; most accessible tissue: Zhenshan97 flag leaf, score: 64.768
vg0222980308 (J) chr02 22980308 G C 98.30% 0.00% G -> C NA
LOC_Os02g38040.1 Alt: C| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/possibly damaging(PolyPhen-2)
The average chromatin accessibility score: 72.722; most accessible tissue: Callus, score: 81.261
vg0222980338 (J) chr02 22980338 G A 99.60% 0.00% G -> A NA
LOC_Os02g38040.1 Alt: A| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 71.943; most accessible tissue: Zhenshan97 flag leaf, score: 80.373
vg0222980378 (J) chr02 22980378 A G 96.60% 0.00% A -> G NA
LOC_Os02g38040.1 Alt: G| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 71.913; most accessible tissue: Zhenshan97 flag leaf, score: 81.605
vg0222980452 (J) chr02 22980452 G A 99.50% 0.00% G -> A NA
LOC_Os02g38029.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.4 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.3 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.5 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.6 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.2 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38040.1 Alt: A| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 79.798; most accessible tissue: Callus, score: 87.013
vg0222980472 (J) chr02 22980472 C T 96.70% 0.00% C -> T NA
LOC_Os02g38029.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 81.770; most accessible tissue: Callus, score: 87.013
vg0222980479 (J) chr02 22980479 A T 96.10% 0.00% A -> T NA
LOC_Os02g38029.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 81.827; most accessible tissue: Callus, score: 87.013
vg0222980482 (J) chr02 22980482 T G 99.80% 0.00% T -> G,A NA
LOC_Os02g38029.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.4 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.3 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.5 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.6 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.2 Alt: A| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38040.1 Alt: A| intron_variant MODIFIER(snpEff)
LOC_Os02g38029.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.4 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.3 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.5 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.6 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38050.2 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os02g38040.1 Alt: G| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 81.927; most accessible tissue: Callus, score: 87.013
vg0222981020 (J) chr02 22981020 G A 99.00% 0.00% G -> A NA
LOC_Os02g38040.1 Alt: A| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 92.214; most accessible tissue: Minghui63 root, score: 95.636
vg0222981032 (J) chr02 22981032 C T 95.40% 0.00% C -> T NA
LOC_Os02g38040.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 92.184; most accessible tissue: Minghui63 root, score: 95.647
vg0222981184 (J) chr02 22981184 A G 96.10% 0.00% A -> G NA
LOC_Os02g38040.1 Alt: G| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 91.321; most accessible tissue: Minghui63 root, score: 95.261
vg0222981332 (J) chr02 22981332 TTG T 99.00% 0.00% TTG -> T NA
LOC_Os02g38040.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 85.895; most accessible tissue: Minghui63 root, score: 93.779
vg0222981421 (J) chr02 22981421 C CAGG 96.70% 0.00% C -> CAGG NA
LOC_Os02g38040.1 Alt: CAGG| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: CAGG| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: CAGG| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: CAGG| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: CAGG| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: CAGG| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: CAGG| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: CAGG| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 83.155; most accessible tissue: Minghui63 root, score: 92.642
vg0222981442 (J) chr02 22981442 CTG C 96.70% 0.00% CTG -> C NA
LOC_Os02g38040.1 Alt: C| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 84.599; most accessible tissue: Callus, score: 95.364
vg0222981540 (J) chr02 22981540 G T 96.60% 0.00% G -> T NA
LOC_Os02g38040.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 82.699; most accessible tissue: Callus, score: 95.364
vg0222981570 (J) chr02 22981570 T A 96.60% 0.00% T -> A NA
LOC_Os02g38040.1 Alt: A| splice_region_variant LOW(snpEff)/silent_mutation(CooVar)
LOC_Os02g38040.1 Alt: A| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38029.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.4 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.3 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.5 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.6 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g38050.2 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 83.515; most accessible tissue: Callus, score: 95.364