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:

16 variations found. LOC_Os02g07770 (Myb transcription factor; putative; expressed), ranging from 4,058,207 bp to 4,060,231 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
vg0204058310 (J) chr02 4058310 C T 68.40% 0.00% C -> T
mr1561 (All); LR P-value: 9.62E-07;
mr1826 (All); LR P-value: 2.72E-07;
mr1826 (Ind_All); LR P-value: 5.43E-06;
mr1929_2 (All); LR P-value: 6.34E-06
LOC_Os02g07770.1 Alt: T| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 60.529; most accessible tissue: Minghui63 panicle, score: 85.556
vg0204058436 (J) chr02 4058436 C T 96.00% 0.00% C -> T NA
LOC_Os02g07770.1 Alt: T| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 62.421; most accessible tissue: Minghui63 panicle, score: 87.238
vg0204058642 (J) chr02 4058642 G T 99.20% 0.00% G -> T NA
LOC_Os02g07770.1 Alt: T| missense_variant MODERATE(snpEff)
The average chromatin accessibility score: 65.472; most accessible tissue: Minghui63 panicle, score: 88.893
vg0204058900 (J) chr02 4058900 G T 99.90% 0.00% G -> T NA
LOC_Os02g07770.1 Alt: T| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 57.373; most accessible tissue: Zhenshan97 panicle, score: 77.482
vg0204058910 (J) chr02 4058910 C G 98.20% 0.00% C -> G NA
LOC_Os02g07770.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 56.488; most accessible tissue: Zhenshan97 panicle, score: 76.605
vg0204059008 (J) chr02 4059008 TGTAGTT ATGGTAA TAATTAA T 96.00% 0.00% TGTAGTTATG GTAATAATTA A -> T NA
LOC_Os02g07770.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 52.034; most accessible tissue: Callus, score: 74.473
vg0204059211 (J) chr02 4059211 T G 58.60% 0.00% T -> G NA
LOC_Os02g07770.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 42.632; most accessible tissue: Callus, score: 80.707
vg0204059219 (J) chr02 4059219 TTGGTGC AA ATGGTGC AA 58.00% 0.00% TTGGTGCAA -> ATGGTGCAA, T NA
LOC_Os02g07770.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g07770.1 Alt: ATGGTGCAA| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 42.858; most accessible tissue: Callus, score: 80.707
vg0204059351 (J) chr02 4059351 A G 98.20% 0.00% A -> G NA
LOC_Os02g07770.1 Alt: G| splice_region_variant&intron_variant LOW(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 39.750; most accessible tissue: Callus, score: 60.214
vg0204059356 (J) chr02 4059356 G T 58.70% 0.00% G -> T NA
LOC_Os02g07770.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 39.874; most accessible tissue: Callus, score: 60.214
vg0204059402 (J) chr02 4059402 C CA 49.90% 0.91% C -> CA,CAA,CAA A NA
N Alt: DEL/silent_mutation(CooVar)
LOC_Os02g07770.1 Alt: CA| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g07770.1 Alt: CAAA| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g07770.1 Alt: CAA| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 41.332; most accessible tissue: Callus, score: 60.214
vg0204059404 (J) chr02 4059404 A AC 98.10% 0.00% A -> AC NA
The average chromatin accessibility score: 41.274; most accessible tissue: Callus, score: 60.214
vg0204059521 (J) chr02 4059521 C G 98.30% 0.00% C -> G NA
LOC_Os02g07770.1 Alt: G| splice_region_variant&intron_variant LOW(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 41.447; most accessible tissue: Callus, score: 81.190
vg0204059647 (J) chr02 4059647 G T 98.30% 0.00% G -> T NA
LOC_Os02g07770.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 42.628; most accessible tissue: Callus, score: 57.499
vg0204059965 (J) chr02 4059965 G A 98.10% 0.00% G -> A NA
LOC_Os02g07770.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 61.112; most accessible tissue: Minghui63 panicle, score: 85.556
STR0204059646 (J) chr02 4059646 TG TT 98.20% 0.00% TG -> TT NA