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Detailed information for vg0335115022:

Variant ID: vg0335115022 (JBrowse)Variation Type: SNP
Chromosome: chr03Position: 35115022
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TTAAGCCTAATTAATCCGTCATAGCACATGTGGGTTACTGTAACACATATGGCTAATCATGGATTAATTAGGCTCAAAAGATTCGTATCGCGATTTTCAT[A/G]
CACACTGTGCAATTAGTTTTTTATTTTATTTATATTTAATATATACTTTATACATATGTCCAAAGATTCGATGTGATGTTTTTGGGATTTTTTTTCTTTT

Reverse complement sequence

AAAAGAAAAAAAATCCCAAAAACATCACATCGAATCTTTGGACATATGTATAAAGTATATATTAAATATAAATAAAATAAAAAACTAATTGCACAGTGTG[T/C]
ATGAAAATCGCGATACGAATCTTTTGAGCCTAATTAATCCATGATTAGCCATATGTGTTACAGTAACCCACATGTGCTATGACGGATTAATTAGGCTTAA

Allele Frequencies:

Populations Population SizeFrequency of G(primary allele) Frequency of A(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 81.70% 14.50% 3.81% 0.00% NA
All Indica  2759 94.20% 2.60% 3.15% 0.00% NA
All Japonica  1512 54.40% 39.80% 5.75% 0.00% NA
Aus  269 100.00% 0.00% 0.00% 0.00% NA
Indica I  595 83.90% 6.90% 9.24% 0.00% NA
Indica II  465 95.10% 2.60% 2.37% 0.00% NA
Indica III  913 99.80% 0.20% 0.00% 0.00% NA
Indica Intermediate  786 95.20% 2.20% 2.67% 0.00% NA
Temperate Japonica  767 28.00% 63.20% 8.74% 0.00% NA
Tropical Japonica  504 89.90% 8.10% 1.98% 0.00% NA
Japonica Intermediate  241 64.30% 31.50% 4.15% 0.00% NA
VI/Aromatic  96 96.90% 2.10% 1.04% 0.00% NA
Intermediate  90 83.30% 11.10% 5.56% 0.00% NA

Allele Effect:

Var ID Var Locus snpEff Annotation CooVar Annotation Chromatin Accessibility Score PolyPhen-2 Effect PolyPhen-2 Score SIFT Effect SIFT Score
vg0335115022 A -> G LOC_Os03g61930.1 upstream_gene_variant ; 2489.0bp to feature; MODIFIER silent_mutation Average:87.53; most accessible tissue: Callus, score: 93.932 N N N N
vg0335115022 A -> G LOC_Os03g61940.1 upstream_gene_variant ; 722.0bp to feature; MODIFIER silent_mutation Average:87.53; most accessible tissue: Callus, score: 93.932 N N N N
vg0335115022 A -> G LOC_Os03g61950.1 upstream_gene_variant ; 247.0bp to feature; MODIFIER silent_mutation Average:87.53; most accessible tissue: Callus, score: 93.932 N N N N
vg0335115022 A -> G LOC_Os03g61930.3 upstream_gene_variant ; 3615.0bp to feature; MODIFIER silent_mutation Average:87.53; most accessible tissue: Callus, score: 93.932 N N N N
vg0335115022 A -> G LOC_Os03g61930.2 upstream_gene_variant ; 2489.0bp to feature; MODIFIER silent_mutation Average:87.53; most accessible tissue: Callus, score: 93.932 N N N N
vg0335115022 A -> G LOC_Os03g61930.4 upstream_gene_variant ; 2489.0bp to feature; MODIFIER silent_mutation Average:87.53; most accessible tissue: Callus, score: 93.932 N N N N
vg0335115022 A -> G LOC_Os03g61950.2 upstream_gene_variant ; 247.0bp to feature; MODIFIER silent_mutation Average:87.53; most accessible tissue: Callus, score: 93.932 N N N N
vg0335115022 A -> G LOC_Os03g61940-LOC_Os03g61950 intergenic_region ; MODIFIER silent_mutation Average:87.53; most accessible tissue: Callus, score: 93.932 N N N N

Effects Predicted by Deep Convolutional Neural Networks

For each variant, we constructed two sequences that contain the variation site and the sequence around it, differing only in the variation site. We then used Basenji to predict the chromatin accessibility of each tissue for the two sequences, respectively, and scored the effect of the variant by comparing the changes in chromatin accessibility corresponding to the two genotypes in the 1 kb region around the variation site. The effect score was defined as the logarithmic ratio of the predicted chromatin accessibility of the alternative genotype to the value of the reference genotype.

Var ID Ref Alt Root (RT) Young Leaf (YL) Flag Leaf (FL) Young Panicle (YP) Lemma & Palea (LP) Stamen & Pistil (SP)
vg0335115022 A G -0.06 -0.05 -0.04 -0.03 -0.03 -0.03

Putative Genotype-Phenotype Associations:

Var ID LMM P-value LR P-value Trait Subpopulation Is leadSNP Publication
vg0335115022 NA 3.59E-08 mr1002 All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0335115022 NA 2.05E-07 mr1002 Jap_All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0335115022 7.58E-07 6.19E-15 mr1002_2 All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0335115022 NA 8.39E-12 mr1002_2 Jap_All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0335115022 NA 8.41E-06 mr1173_2 All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0335115022 NA 4.00E-13 mr1182_2 All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0335115022 NA 1.07E-06 mr1182_2 Jap_All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0335115022 NA 5.90E-10 mr1282_2 All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0335115022 1.30E-06 NA mr1691_2 All YES Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251