Search for Variation by Gene:

Gene ID/Symbol/Name (e.g., LOC_Os01g08570 or hwh1 or Os01g0180900 or gly%ltransferase, note: wildcard character '%' is also acceptable.):
Upstream (kb, optional, must <= 10 kb) : Downstream (kb, optional, must <= 10 kb) :
Variations Type:

Optional: (The selected data will be displayed in the result page.)

 Show Gene Expression Atlas  Show Chromatin Accessibility Map
 Show Non-coding variation Scores

Search Results:

10 variations found. Os01g0866000/LOC_Os01g64620 (zinc finger; C3HC4 type domain containing protein; expressed), ranging from 37,505,154 bp to 37,506,089 bp (including 0 kb upstream and 0 kb downstream of the gene).

Gene IDAnnotation
LOC_Os01g64620 zinc finger, C3HC4 type domain containing protein, expressed; RAP ID: Os01g0866000; MSU ID: LOC_Os01g64620

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
vg0137505314 (J) chr01 37505314 TCGGCGG CGGCGGC CGCCGGC GCGTCGC CTGGTCC GGCTGGG CGCGTGT TGGAAGG CGGCG T 97.50% 0.00% TCGGCGGCGG CGGCCGCCGG CGCGTCGCCT GGTCCGGCTG GGCGCGTGTT GGAAGGCGGC G -> T NA
LOC_Os01g64620.1 Alt: T| disruptive_inframe_deletion MODERATE(snpEff)/inframe_variant(CooVar)
The average chromatin accessibility score: 90.584; most accessible tissue: Minghui63 root, score: 95.301
vg0137505385 (J) chr01 37505385 G A 91.10% 3.87% G -> A NA
LOC_Os01g64620.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
LOC_Os01g64620.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 87.554; most accessible tissue: Minghui63 panicle, score: 95.218
vg0137505628 (J) chr01 37505628 G C 49.90% 4.95% G -> C,A NA
LOC_Os01g64620.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
LOC_Os01g64620.1 Alt: DEL/frameshift_variant(CooVar)
LOC_Os01g64620.1 Alt: C| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 87.333; most accessible tissue: Minghui63 panicle, score: 95.282
vg0137505701 (J) chr01 37505701 G T 56.50% 3.22% T -> G NA
LOC_Os01g64620.1 Alt: G| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
LOC_Os01g64620.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 90.680; most accessible tissue: Zhenshan97 panicle, score: 94.949
vg0137505782 (J) chr01 37505782 C T 99.70% 0.00% C -> T NA
LOC_Os01g64620.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/probably damaging(PolyPhen-2)
The average chromatin accessibility score: 89.991; most accessible tissue: Zhenshan97 panicle, score: 93.845
vg0137505826 (J) chr01 37505826 C T 81.40% 3.91% T -> C NA
LOC_Os01g64620.1 Alt: DEL/frameshift_variant(CooVar)
LOC_Os01g64620.1 Alt: C| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 88.710; most accessible tissue: Zhenshan97 panicle, score: 92.660
vg0137505927 (J) chr01 37505927 T TCA 64.20% 0.00% TCA -> T NA
LOC_Os01g64620.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.2 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.4 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 85.438; most accessible tissue: Callus, score: 91.795
vg0137505966 (J) chr01 37505966 T C 55.10% 0.04% T -> C
mr1213 (All); LR P-value: 4.80E-32;
mr1583 (All); LR P-value: 4.96E-15;
mr1592 (All); LR P-value: 1.55E-13;
mr1717 (All); LR P-value: 9.19E-07;
mr1770 (All); LR P-value: 7.50E-10;
mr1215_2 (All); LR P-value: 1.75E-07;
mr1218_2 (All); LR P-value: 2.18E-20;
mr1352_2 (All); LR P-value: 3.32E-16;
mr1538_2 (All); LMM P-value: 1.21E-06;
mr1850_2 (All); LR P-value: 5.03E-13;
mr1870_2 (Ind_All); LR P-value: 1.49E-06;
mr1885_2 (All); LR P-value: 2.68E-07
N Alt: DEL/silent_mutation(CooVar)
LOC_Os01g64620.1 Alt: C| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.2 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.4 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 84.190; most accessible tissue: Callus, score: 91.795
vg0137506002 (J) chr01 37506002 GT GTT 64.30% 0.00% GTT -> GT,GTTT,G NA
LOC_Os01g64620.1 Alt: G| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.2 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.4 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64620.1 Alt: GT| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.1 Alt: GT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.2 Alt: GT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.4 Alt: GT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64620.1 Alt: GTTT| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.1 Alt: GTTT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.2 Alt: GTTT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.4 Alt: GTTT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 81.135; most accessible tissue: Callus, score: 91.795
vg0137506082 (J) chr01 37506082 C T 64.50% 0.00% T -> C NA
LOC_Os01g64620.1 Alt: C| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.2 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os01g64630.4 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 76.789; most accessible tissue: Minghui63 root, score: 86.064