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Search Results:

3 variations found. LOC_Os10g17150 (retrotransposon protein; putative; unclassified), ranging from 8,611,043 bp to 8,612,297 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
vg1008612250 (J) chr10 8612250 G A 14.80% 80.13% G -> A NA
LOC_Os10g17150.1 Alt: A| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
LOC_Os10g17150.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 4.409; most accessible tissue: Minghui63 panicle, score: 7.125
vg1008612253 (J) chr10 8612253 A C 14.70% 80.47% A -> C NA
LOC_Os10g17150.1 Alt: C| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
LOC_Os10g17150.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 4.409; most accessible tissue: Minghui63 panicle, score: 7.125
vg1008612264 (J) chr10 8612264 C A 14.60% 80.28% C -> A NA
LOC_Os10g17150.1 Alt: A| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
LOC_Os10g17150.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 4.409; most accessible tissue: Minghui63 panicle, score: 7.125