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Gene ID/Symbol/Name (e.g., LOC_Os01g08570 or hwh1 or Os01g0180900 or gly%ltransferase, note: wildcard character '%' is also acceptable.):
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Search Results:

21 variations found. Os11g0136600/LOC_Os11g04170 (CAMK_CAMK_like.42 - CAMK includes calcium%2Fcalmodulin depedent protein kinases; expressed), ranging from 1,691,860 bp to 1,694,301 bp (including 0 kb upstream and 0 kb downstream of the gene).

Gene IDAnnotation
LOC_Os11g04170 CAMK_CAMK_like.42 - CAMK includes calcium/calmodulin depedent protein kinases, expressed; RAP ID: Os11g0136600; MSU ID: LOC_Os11g04170
MSU IDRAP IDSymbolNameExplanationRecommended Gene SymbolRecommended Gene Name
LOC_Os11g04170Os11g0136600OsCDPK25, OsCPK25calcium-dependent protein kinaseAC123528.CDPK25CALCIUM-DEPENDENT PROTEIN KINASE 25

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
vg1101691860 (J) chr11 1691860 T C 99.40% 0.00% T -> C NA
LOC_Os11g04150.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04170.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04160.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04174.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04180.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04160-LOC_Os11g04170 Alt: C| intergenic_region MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 68.171; most accessible tissue: Zhenshan97 root, score: 82.361
vg1101692021 (J) chr11 1692021 G T 99.20% 0.00% G -> T NA
LOC_Os11g04170.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 62.114; most accessible tissue: Minghui63 panicle, score: 74.563
vg1101692044 (J) chr11 1692044 AGGCGGC GGCGACG GAAGCGG C AGGC 98.40% 0.00% AGGCGGCGGC GACGGAAGCG GC -> A,AGGC NA
LOC_Os11g04170.1 Alt: A| inframe_deletion MODERATE(snpEff)/inframe_variant(CooVar)
LOC_Os11g04170.1 Alt: AGGC| inframe_deletion MODERATE(snpEff)/inframe_variant(CooVar)
The average chromatin accessibility score: 62.212; most accessible tissue: Zhenshan97 root, score: 74.877
vg1101692318 (J) chr11 1692318 C T 99.00% 0.00% C -> T NA
LOC_Os11g04170.1 Alt: T| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 62.809; most accessible tissue: Zhenshan97 panicle, score: 77.482
vg1101692327 (J) chr11 1692327 A C 99.00% 0.00% A -> C,G NA
LOC_Os11g04170.1 Alt: G| synonymous_variant LOW(snpEff)
LOC_Os11g04150.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04160.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04174.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04180.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04170.1 Alt: C| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 63.181; most accessible tissue: Zhenshan97 panicle, score: 78.302
vg1101692470 (J) chr11 1692470 C T 99.80% 0.00% C -> T NA
LOC_Os11g04170.1 Alt: T| missense_variant MODERATE(snpEff)
LOC_Os11g04150.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04160.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04174.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04180.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 64.902; most accessible tissue: Zhenshan97 panicle, score: 84.824
vg1101692555 (J) chr11 1692555 G A 67.20% 26.07% G -> A NA
LOC_Os11g04170.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
LOC_Os11g04170.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 66.420; most accessible tissue: Zhenshan97 panicle, score: 85.254
vg1101692762 (J) chr11 1692762 G A 55.70% 33.24% G -> A,C NA
LOC_Os11g04170.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
LOC_Os11g04170.1 Alt: DEL/frameshift_variant(CooVar)
LOC_Os11g04170.1 Alt: C| synonymous_variant LOW(snpEff)
LOC_Os11g04150.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04160.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04174.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04180.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 68.980; most accessible tissue: Zhenshan97 panicle, score: 87.451
vg1101692786 (J) chr11 1692786 C Unkown 99.70% 0.00% C -> T NA
LOC_Os11g04170.1 Alt: T| synonymous_variant LOW(snpEff)
LOC_Os11g04150.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04160.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04174.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04180.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 69.695; most accessible tissue: Zhenshan97 panicle, score: 87.451
vg1101692944 (J) chr11 1692944 T C 99.00% 0.00% T -> C NA
LOC_Os11g04150.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04160.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04174.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04180.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04170.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 68.091; most accessible tissue: Zhenshan97 panicle, score: 86.432
vg1101692951 (J) chr11 1692951 CT C 84.40% 7.00% CT -> C,CTT NA
LOC_Os11g04150.1 Alt: CTT| upstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04160.1 Alt: CTT| downstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04174.1 Alt: CTT| downstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04180.1 Alt: CTT| downstream_gene_variant MODIFIER(snpEff)
LOC_Os11g04170.1 Alt: CTT| intron_variant MODIFIER(snpEff)
N Alt: DEL/silent_mutation(CooVar)
LOC_Os11g04150.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04160.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04174.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04180.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04170.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 68.140; most accessible tissue: Zhenshan97 panicle, score: 86.788
vg1101692965 (J) chr11 1692965 T A 98.60% 0.28% T -> A NA
LOC_Os11g04150.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04160.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04174.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04180.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04170.1 Alt: A| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 67.131; most accessible tissue: Zhenshan97 panicle, score: 85.665
vg1101693216 (J) chr11 1693216 T C 98.80% 0.00% T -> C NA
LOC_Os11g04160.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04174.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04180.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04170.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 47.465; most accessible tissue: Zhenshan97 panicle, score: 69.946
vg1101693413 (J) chr11 1693413 A G 99.00% 0.00% A -> G NA
LOC_Os11g04160.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04174.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04180.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04170.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 36.999; most accessible tissue: Zhenshan97 panicle, score: 59.590
vg1101693429 (J) chr11 1693429 CTTAG C 56.10% 28.61% CTTAG -> C NA
N Alt: DEL/silent_mutation(CooVar)
LOC_Os11g04160.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04174.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04180.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04170.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 39.108; most accessible tissue: Zhenshan97 panicle, score: 61.671
vg1101693431 (J) chr11 1693431 T TC 62.40% 24.04% T -> TC NA
LOC_Os11g04160.1 Alt: TC| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04174.1 Alt: TC| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04180.1 Alt: TC| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04170.1 Alt: TC| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 40.693; most accessible tissue: Zhenshan97 panicle, score: 65.386
vg1101693521 (J) chr11 1693521 C T 55.20% 33.96% C -> T NA
LOC_Os11g04170.1 Alt: T| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
LOC_Os11g04170.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 37.008; most accessible tissue: Zhenshan97 root, score: 60.612
vg1101693689 (J) chr11 1693689 G T 34.00% 57.43% G -> T,C NA
LOC_Os11g04160.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04174.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04180.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04170.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
LOC_Os11g04160.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04174.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04180.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04170.1 Alt: C| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 30.447; most accessible tissue: Zhenshan97 panicle, score: 52.263
vg1101693903 (J) chr11 1693903 T G 67.00% 27.40% T -> G NA
N Alt: DEL/silent_mutation(CooVar)
LOC_Os11g04160.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04174.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04180.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04170.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 28.150; most accessible tissue: Zhenshan97 root, score: 39.742
vg1101694274 (J) chr11 1694274 A G 54.70% 0.23% A -> G
mr1565 (All); LR P-value: 1.48E-10;
mr1904 (Ind_All); LR P-value: 2.64E-10;
mr1170_2 (All); LR P-value: 1.06E-07;
mr1184_2 (All); LR P-value: 1.89E-07;
mr1278_2 (All); LR P-value: 6.23E-07;
mr1329_2 (All); LR P-value: 3.83E-06;
mr1418_2 (All); LR P-value: 1.75E-06;
mr1420_2 (All); LR P-value: 8.84E-06;
mr1488_2 (All); LR P-value: 1.42E-06;
mr1508_2 (All); LR P-value: 2.04E-06;
mr1524_2 (All); LR P-value: 4.10E-06;
mr1556_2 (All); LR P-value: 6.72E-06;
mr1683_2 (All); LR P-value: 2.81E-09;
mr1779_2 (All); LR P-value: 3.77E-06;
mr1838_2 (All); LR P-value: 6.43E-14;
mr1992_2 (All); LR P-value: 3.28E-06
N Alt: DEL/silent_mutation(CooVar)
LOC_Os11g04170.1 Alt: G| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04160.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04174.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os11g04180.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 25.671; most accessible tissue: Zhenshan97 root, score: 38.035
STR1101692017 (J) chr11 1692017 AGCAG AGCAT 85.80% 0.00% AGCAG -> AGCAT NA