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Search Results:

2 variations found. LOC_Os08g36880 (transposon protein; putative; CACTA; En%2FSpm sub-class), ranging from 23,301,886 bp to 23,303,467 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
vg0823302212 (J) chr08 23302212 GTATATA TATATA GTATA 22.90% 54.25% GTATATATAT ATA -> GTATATATA, GTATATA,GT ATA,GTA,G NA
LOC_Os08g36870.1 Alt: GTATATATA| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g36880.1 Alt: GTATATATA| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
LOC_Os08g36870.1 Alt: GTATATA| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g36880.1 Alt: GTATATA| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g36870.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g36880.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g36870.1 Alt: GTA| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g36880.1 Alt: GTA| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g36870.1 Alt: GTATA| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g36880.1 Alt: GTATA| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.386; most accessible tissue: Minghui63 panicle, score: 7.125
vg0823303282 (J) chr08 23303282 C T 29.50% 55.40% C -> T NA
LOC_Os08g36880.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
LOC_Os08g36880.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 4.371; most accessible tissue: Minghui63 panicle, score: 7.125