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Search Results:

8 variations found. Os04g0386900/LOC_Os04g31730 (expressed protein), ranging from 18,997,865 bp to 18,998,795 bp (including 0 kb upstream and 0 kb downstream of the gene).

Gene IDAnnotation
LOC_Os04g31730 expressed protein; RAP ID: Os04g0386900; MSU ID: LOC_Os04g31730

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
vg0418997870 (J) chr04 18997870 A AGT 97.40% 0.00% A -> AGT NA
LOC_Os04g31730.1 Alt: AGT| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31700.1 Alt: AGT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31740.1 Alt: AGT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31710.1 Alt: AGT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31720.1 Alt: AGT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 61.903; most accessible tissue: Callus, score: 74.819
vg0418997871 (J) chr04 18997871 A T 97.40% 0.00% A -> T NA
LOC_Os04g31730.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31700.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31740.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31710.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31720.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 61.903; most accessible tissue: Callus, score: 74.819
vg0418997883 (J) chr04 18997883 T A 97.40% 0.00% T -> A NA
LOC_Os04g31730.1 Alt: A| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31700.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31740.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31710.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31720.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 61.814; most accessible tissue: Callus, score: 74.819
vg0418998002 (J) chr04 18998002 G GGCA 98.00% 0.00% G -> GGCA NA
LOC_Os04g31730.1 Alt: GGCA| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31740.1 Alt: GGCA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31710.1 Alt: GGCA| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31720.1 Alt: GGCA| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 70.425; most accessible tissue: Callus, score: 85.546
vg0418998438 (J) chr04 18998438 A AT 69.80% 0.00% A -> AT,ATT,ATT T,ATTTT NA
LOC_Os04g31740.1 Alt: ATTTT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31710.1 Alt: ATTTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31720.1 Alt: ATTTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31730.1 Alt: ATTTT| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31740.1 Alt: ATTT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31710.1 Alt: ATTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31720.1 Alt: ATTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31730.1 Alt: ATTT| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31740.1 Alt: ATT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31710.1 Alt: ATT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31720.1 Alt: ATT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31730.1 Alt: ATT| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31740.1 Alt: AT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31710.1 Alt: AT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31720.1 Alt: AT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31730.1 Alt: AT| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 79.238; most accessible tissue: Minghui63 panicle, score: 92.526
vg0418998442 (J) chr04 18998442 A T 65.30% 0.00% A -> T
mr1062_2 (Jap_All); LR P-value: 3.03E-07;
mr1405_2 (All); LR P-value: 3.73E-06;
mr1462_2 (All); LR P-value: 3.45E-06
LOC_Os04g31740.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31710.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31720.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g31730.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 80.119; most accessible tissue: Minghui63 panicle, score: 92.666
vg0418998451 (J) chr04 18998451 TGG T 99.70% 0.00% TGG -> T NA
LOC_Os04g31730.1 Alt: T| splice_region_variant&intron_variant LOW(snpEff)
LOC_Os04g31740.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)
LOC_Os04g31710.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
LOC_Os04g31720.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 80.385; most accessible tissue: Minghui63 panicle, score: 92.928
STR0418998003 (J) chr04 18998003 GCAG GCAGCAG 93.30% 0.00% GCAG -> GCAGCAG NA