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Search Results:

11 variations found. Os04g0581800/LOC_Os04g49260 (heavy metal-associated domain containing protein; expressed), ranging from 29,408,861 bp to 29,409,617 bp (including 0 kb upstream and 0 kb downstream of the gene).

Gene IDAnnotation
LOC_Os04g49260 heavy metal-associated domain containing protein, expressed; RAP ID: Os04g0581800; MSU ID: LOC_Os04g49260

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
vg0429408874 (J) chr04 29408874 C T 98.70% 0.00% C -> T NA
LOC_Os04g49260.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g49270.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 88.092; most accessible tissue: Zhenshan97 panicle, score: 93.752
vg0429408876 (J) chr04 29408876 C A 89.90% 0.00% C -> A NA
LOC_Os04g49260.1 Alt: A| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g49270.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 88.055; most accessible tissue: Zhenshan97 panicle, score: 93.752
vg0429409018 (J) chr04 29409018 C T 95.30% 0.00% C -> T
mr1745 (Jap_All); LR P-value: 1.16E-06;
mr1064_2 (Jap_All); LR P-value: 7.05E-06;
mr1113_2 (Jap_All); LR P-value: 8.41E-06;
mr1745_2 (Jap_All); LR P-value: 9.16E-10
LOC_Os04g49260.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g49270.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 90.121; most accessible tissue: Zhenshan97 panicle, score: 94.811
vg0429409042 (J) chr04 29409042 G A 99.60% 0.00% G -> A NA
LOC_Os04g49260.1 Alt: A| 3_prime_UTR_variant MODIFIER(snpEff)
LOC_Os04g49270.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 90.004; most accessible tissue: Zhenshan97 panicle, score: 95.081
vg0429409127 (J) chr04 29409127 C G 99.50% 0.00% C -> G NA
LOC_Os04g49260.1 Alt: G| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 87.665; most accessible tissue: Minghui63 panicle, score: 93.837
vg0429409176 (J) chr04 29409176 G T 92.50% 0.00% G -> T NA
LOC_Os04g49260.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 88.212; most accessible tissue: Minghui63 panicle, score: 93.294
vg0429409271 (J) chr04 29409271 G C 98.30% 0.00% G -> C NA
LOC_Os04g49260.1 Alt: C| stop_gained HIGH(snpEff)/stop_gained(CooVar)
The average chromatin accessibility score: 87.790; most accessible tissue: Minghui63 panicle, score: 94.033
vg0429409312 (J) chr04 29409312 A G 89.90% 0.00% A -> G NA
LOC_Os04g49270.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g49260.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 88.088; most accessible tissue: Minghui63 panicle, score: 94.218
vg0429409315 (J) chr04 29409315 G A 60.50% 0.08% A -> G
mr1082 (Ind_All); LR P-value: 1.45E-06;
mr1226 (Ind_All); LR P-value: 3.47E-07;
mr1342 (All); LR P-value: 3.45E-09;
mr1560 (Ind_All); LR P-value: 4.57E-06;
mr1689 (All); LR P-value: 2.53E-22;
mr1819 (All); LR P-value: 8.21E-11
N Alt: DEL/silent_mutation(CooVar)
LOC_Os04g49270.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g49260.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 88.123; most accessible tissue: Minghui63 panicle, score: 94.218
vg0429409436 (J) chr04 29409436 T C 53.90% 0.34% T -> C
mr1076 (All); LR P-value: 5.54E-27;
mr1131 (All); LR P-value: 4.43E-20;
mr1156 (All); LR P-value: 6.02E-15;
mr1169 (All); LR P-value: 2.28E-12;
mr1179 (All); LR P-value: 2.90E-18;
mr1199 (All); LR P-value: 7.39E-16;
mr1204 (All); LR P-value: 8.72E-30;
mr1237 (All); LR P-value: 2.11E-31;
mr1244 (All); LR P-value: 1.26E-21;
mr1404 (All); LR P-value: 9.75E-34;
mr1713 (All); LR P-value: 3.33E-11;
mr1938 (All); LR P-value: 3.02E-11;
mr1970 (All); LR P-value: 4.72E-64;
mr1973 (All); LR P-value: 7.27E-80;
mr1131_2 (All); LR P-value: 1.31E-18;
mr1147_2 (All); LR P-value: 6.27E-13;
mr1199_2 (All); LR P-value: 1.19E-17;
mr1244_2 (All); LR P-value: 4.74E-27;
mr1571_2 (All); LR P-value: 8.75E-32;
mr1970_2 (All); LR P-value: 1.59E-66;
mr1970_2 (Ind_All); LR P-value: 1.68E-06;
mr1973_2 (All); LR P-value: 1.07E-95;
mr1973_2 (Ind_All); LR P-value: 9.90E-07
LOC_Os04g49260.1 Alt: C| splice_region_variant&intron_variant LOW(snpEff)/silent_mutation(CooVar)
LOC_Os04g49270.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 87.912; most accessible tissue: Minghui63 panicle, score: 95.014
vg0429409611 (J) chr04 29409611 T G 95.60% 0.00% T -> G NA
LOC_Os04g49260.1 Alt: G| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g49270.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 89.006; most accessible tissue: Minghui63 panicle, score: 96.769