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Search Results:

12 variations found. LOC_Os02g44080 (aquaporin protein; putative; expressed), ranging from 26,608,360 bp to 26,609,658 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
vg0226608386 (J) chr02 26608386 T C 52.60% 0.00% C -> T
mr1609 (All); LR P-value: 4.06E-11;
mr1713 (All); LR P-value: 1.81E-11;
mr1133_2 (All); LR P-value: 2.35E-14;
mr1148_2 (All); LR P-value: 1.43E-15;
mr1227_2 (All); LR P-value: 1.61E-07;
mr1272_2 (All); LR P-value: 1.05E-07;
mr1349_2 (Ind_All); LR P-value: 6.29E-06;
mr1479_2 (All); LR P-value: 1.43E-08;
mr1726_2 (All); LR P-value: 1.58E-14;
mr1835_2 (All); LR P-value: 1.18E-09;
mr1836_2 (All); LR P-value: 9.10E-16;
mr1871_2 (Ind_All); LR P-value: 2.93E-06;
mr1895_2 (Ind_All); LR P-value: 1.82E-06;
mr1904_2 (All); LR P-value: 3.64E-13
LOC_Os02g44080.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 43.419; most accessible tissue: Minghui63 root, score: 58.187
vg0226608559 (J) chr02 26608559 AAACGGA ATTGGAA GTTGTTC GGTCAAG TATAGGA AATT A 50.40% 0.00% A -> AAACGGAATT GGAAGTTGTT CGGTCAAGTA TAGGAAATT NA
The average chromatin accessibility score: 68.656; most accessible tissue: Minghui63 panicle, score: 81.412
vg0226608561 (J) chr02 26608561 A ACGGAAT TGGAAGT TGTTCGG 99.40% 0.00% A -> ACGGAAT,AC GGAATTGGAA GTTGTTCGG, ACGGAATTGG AAGTTGT,AC GGAATTGGAA GTTG,ACGGA ATTGGAAG,A CGGAATTGGA AGT NA
LOC_Os02g44080.1 Alt: ACGGAATTGGAAGTTG| 3_prime_UTR_variant MODIFIER(snpEff)
LOC_Os02g44080.1 Alt: ACGGAATTGGAAG| 3_prime_UTR_variant MODIFIER(snpEff)
LOC_Os02g44080.1 Alt: ACGGAAT| 3_prime_UTR_variant MODIFIER(snpEff)
LOC_Os02g44080.1 Alt: ACGGAATTGGAAGTTGTTCGG| 3_prime_UTR_variant MODIFIER(snpEff)
LOC_Os02g44080.1 Alt: ACGGAATTGGAAGTTGT| 3_prime_UTR_variant MODIFIER(snpEff)
LOC_Os02g44080.1 Alt: ACGGAATTGGAAGT| 3_prime_UTR_variant MODIFIER(snpEff)
The average chromatin accessibility score: 68.411; most accessible tissue: Minghui63 panicle, score: 80.641
vg0226608626 (J) chr02 26608626 T C 99.00% 0.00% T -> C NA
LOC_Os02g44080.1 Alt: C| stop_retained_variant LOW(snpEff)
The average chromatin accessibility score: 71.600; most accessible tissue: Minghui63 panicle, score: 84.005
vg0226608644 (J) chr02 26608644 G A 99.90% 0.00% G -> A NA
LOC_Os02g44080.1 Alt: A| synonymous_variant LOW(snpEff)
The average chromatin accessibility score: 72.979; most accessible tissue: Minghui63 panicle, score: 84.552
vg0226609014 (J) chr02 26609014 G A 92.70% 0.00% G -> A
mr1230 (All); LR P-value: 4.98E-06;
mr1278 (All); LR P-value: 4.84E-07;
mr1424 (All); LR P-value: 7.34E-07;
mr1438 (All); LR P-value: 7.83E-06;
mr1884 (All); LR P-value: 2.91E-06;
mr1871_2 (Ind_All); LR P-value: 5.59E-07;
mr1892_2 (All); LR P-value: 4.29E-06;
mr1895_2 (Ind_All); LR P-value: 4.58E-06;
mr1919_2 (All); LMM P-value: 7.88E-06; LR P-value: 7.85E-06
LOC_Os02g44080.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 76.876; most accessible tissue: Minghui63 panicle, score: 84.552
vg0226609031 (J) chr02 26609031 A G 60.40% 0.00% G -> A NA
LOC_Os02g44080.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 77.040; most accessible tissue: Minghui63 panicle, score: 84.552
vg0226609424 (J) chr02 26609424 G A 99.90% 0.00% G -> A NA
LOC_Os02g44080.1 Alt: A| intron_variant MODIFIER(snpEff)
The average chromatin accessibility score: 70.745; most accessible tissue: Zhenshan97 root, score: 86.891
vg0226609449 (J) chr02 26609449 G A 99.60% 0.00% G -> A NA
LOC_Os02g44080.1 Alt: A| missense_variant MODERATE(snpEff)
The average chromatin accessibility score: 70.649; most accessible tissue: Zhenshan97 root, score: 86.362
vg0226609469 (J) chr02 26609469 G A 60.40% 0.00% A -> G NA
LOC_Os02g44080.1 Alt: G| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 70.922; most accessible tissue: Zhenshan97 root, score: 86.891
vg0226609582 (J) chr02 26609582 ATT AT 60.10% 0.00% AT -> ATT,A,ATTT NA
LOC_Os02g44080.1 Alt: A| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g44080.1 Alt: ATTT| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os02g44080.1 Alt: ATT| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 63.730; most accessible tissue: Zhenshan97 root, score: 87.735
vg0226609631 (J) chr02 26609631 G A 60.40% 0.00% A -> G NA
LOC_Os02g44080.1 Alt: G| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 64.005; most accessible tissue: Zhenshan97 root, score: 88.318