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Search Results:

32 variations found. Os10g0542800/LOC_Os10g39670 (protein kinase family protein; putative; expressed), ranging from 21,199,762 bp to 21,204,782 bp (including 0 kb upstream and 0 kb downstream of the gene).

Gene IDAnnotation
LOC_Os10g39670 protein kinase family protein, putative, expressed; RAP ID: Os10g0542800; MSU ID: LOC_Os10g39670

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
vg1021199771 (J) chr10 21199771 T C 58.30% 0.00% C -> T NA
LOC_Os10g39670.1 Alt: T| 5_prime_UTR_premature_start_codon_gain_variant LOW(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: T| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021199972 (J) chr10 21199972 C T 99.60% 0.00% C -> T NA
LOC_Os10g39670.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021200026 (J) chr10 21200026 C T 93.70% 0.00% C -> T NA
LOC_Os10g39670.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021200822 (J) chr10 21200822 G GA 99.40% 0.00% G -> GA,GAGCACA CGCAATGGTA AAGTAA,GAG CACAC,GAGC ACACGCAATG GTAAAGTAAG GT NA
LOC_Os10g39680.1 Alt: GAGCACACGCAATGGTAAAGTAA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: GAGCACACGCAATGGTAAAGTAA| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39680.1 Alt: GA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: GA| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39680.1 Alt: GAGCACAC| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: GAGCACAC| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39680.1 Alt: GAGCACACGCAATGGTAAAGTAAGGT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: GAGCACACGCAATGGTAAAGTAAGGT| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021200823 (J) chr10 21200823 GCCATTC C G 99.70% 0.00% GCCATTCC -> G,TCCATTCC NA
LOC_Os10g39680.1 Alt: TCCATTCC| upstream_gene_variant MODIFIER(snpEff)
LOC_Os10g39670.1 Alt: TCCATTCC| intron_variant MODIFIER(snpEff)
LOC_Os10g39680.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os10g39670.1 Alt: G| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021200832 (J) chr10 21200832 A AC 99.70% 0.00% A -> AC NA
LOC_Os10g39680.1 Alt: AC| upstream_gene_variant MODIFIER(snpEff)
LOC_Os10g39670.1 Alt: AC| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021200835 (J) chr10 21200835 C G 99.70% 0.00% C -> G NA
LOC_Os10g39680.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os10g39670.1 Alt: G| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021200842 (J) chr10 21200842 C T 64.80% 0.19% T -> C NA
LOC_Os10g39680.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021200882 (J) chr10 21200882 G A 64.30% 0.32% A -> G NA
LOC_Os10g39680.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021200901 (J) chr10 21200901 A G 99.80% 0.00% A -> G,T NA
LOC_Os10g39680.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os10g39670.1 Alt: G| intron_variant MODIFIER(snpEff)
LOC_Os10g39680.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)
LOC_Os10g39670.1 Alt: T| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021201007 (J) chr10 21201007 A G 58.40% 0.11% G -> A NA
LOC_Os10g39680.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021201023 (J) chr10 21201023 A T 98.90% 0.00% A -> T NA
LOC_Os10g39680.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021201027 (J) chr10 21201027 G A 93.60% 0.00% G -> A NA
LOC_Os10g39680.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021201034 (J) chr10 21201034 A G 58.50% 0.04% G -> A NA
LOC_Os10g39680.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021201072 (J) chr10 21201072 G Unkown 96.70% 1.27% G -> A NA
LOC_Os10g39680.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os10g39670.1 Alt: A| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021201077 (J) chr10 21201077 C T 65.10% 0.00% T -> C NA
LOC_Os10g39680.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021201164 (J) chr10 21201164 G T 93.60% 0.00% G -> T NA
LOC_Os10g39680.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021201487 (J) chr10 21201487 G A 93.70% 0.00% G -> A NA
LOC_Os10g39680.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021201778 (J) chr10 21201778 T C 65.10% 0.00% C -> T NA
LOC_Os10g39680.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021201875 (J) chr10 21201875 C G 99.70% 0.00% C -> G NA
LOC_Os10g39680.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os10g39670.1 Alt: G| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021202066 (J) chr10 21202066 C T 93.70% 0.00% C -> T NA
LOC_Os10g39680.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021202569 (J) chr10 21202569 T C 93.70% 0.00% T -> C NA
LOC_Os10g39680.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021202776 (J) chr10 21202776 G A 99.90% 0.00% G -> A NA
LOC_Os10g39680.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os10g39670.1 Alt: A| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021203352 (J) chr10 21203352 C T 93.70% 0.00% C -> T NA
LOC_Os10g39680.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021203353 (J) chr10 21203353 A T 65.10% 0.00% T -> A NA
LOC_Os10g39680.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39670.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021203566 (J) chr10 21203566 G C 99.70% 0.00% G -> C NA
LOC_Os10g39670.1 Alt: C| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021203586 (J) chr10 21203586 C T 93.70% 0.00% C -> T NA
LOC_Os10g39670.1 Alt: T| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021203857 (J) chr10 21203857 C T 58.60% 0.00% T -> C NA
LOC_Os10g39670.1 Alt: C| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021204375 (J) chr10 21204375 G A 64.90% 0.08% A -> G NA
LOC_Os10g39670.1 Alt: G| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39680.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39690.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021204435 (J) chr10 21204435 ATTAAAA AGGAAAA CCCAT A 93.70% 0.00% ATTAAAAAGG AAAACCCAT -> A NA
LOC_Os10g39670.1 Alt: A| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39680.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39690.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021204565 (J) chr10 21204565 G A 99.90% 0.00% G -> A NA
LOC_Os10g39670.1 Alt: A| 3_prime_UTR_variant MODIFIER(snpEff)
LOC_Os10g39680.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os10g39690.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021204648 (J) chr10 21204648 A G 93.70% 0.00% A -> G NA
LOC_Os10g39670.1 Alt: G| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39680.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g39690.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125