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Detailed information for vg0826172820:

Variant ID: vg0826172820 (JBrowse)Variation Type: SNP
Chromosome: chr08Position: 26172820
Reference Allele: CAlternative Allele: T
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TATTGTAGGACTGAGGGAGTAGTAGGTTTTTTCGGTACGTTGATCGAGCTAAACTAAGTTTGTGTTTAGTTAATTCTAAAGTTGAAAGTTTGGGTTAAAA[C/T]
TGATATGATGTGACTAAAAAGTTACGTGTATGATAGGTTGATGTGATGAAAAAGTTGGAAGTTTGGATCTAAACATAGCCTTAGTTCCAAAGTTTTTCTT

Reverse complement sequence

AAGAAAAACTTTGGAACTAAGGCTATGTTTAGATCCAAACTTCCAACTTTTTCATCACATCAACCTATCATACACGTAACTTTTTAGTCACATCATATCA[G/A]
TTTTAACCCAAACTTTCAACTTTAGAATTAACTAAACACAAACTTAGTTTAGCTCGATCAACGTACCGAAAAAACCTACTACTCCCTCAGTCCTACAATA

Allele Frequencies:

Populations Population SizeFrequency of T(primary allele) Frequency of C(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 90.40% 6.70% 2.88% 0.00% NA
All Indica  2759 99.70% 0.00% 0.25% 0.00% NA
All Japonica  1512 71.80% 20.20% 8.07% 0.00% NA
Aus  269 98.90% 0.40% 0.74% 0.00% NA
Indica I  595 99.80% 0.20% 0.00% 0.00% NA
Indica II  465 99.80% 0.00% 0.22% 0.00% NA
Indica III  913 100.00% 0.00% 0.00% 0.00% NA
Indica Intermediate  786 99.20% 0.00% 0.76% 0.00% NA
Temperate Japonica  767 48.10% 37.80% 14.08% 0.00% NA
Tropical Japonica  504 98.80% 0.80% 0.40% 0.00% NA
Japonica Intermediate  241 90.50% 4.60% 4.98% 0.00% NA
VI/Aromatic  96 99.00% 1.00% 0.00% 0.00% NA
Intermediate  90 85.60% 8.90% 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
vg0826172820 C -> T LOC_Os08g41460.1 upstream_gene_variant ; 4497.0bp to feature; MODIFIER silent_mutation Average:68.388; most accessible tissue: Zhenshan97 panicle, score: 91.206 N N N N
vg0826172820 C -> T LOC_Os08g41460.8 upstream_gene_variant ; 1194.0bp to feature; MODIFIER silent_mutation Average:68.388; most accessible tissue: Zhenshan97 panicle, score: 91.206 N N N N
vg0826172820 C -> T LOC_Os08g41460.4 upstream_gene_variant ; 3514.0bp to feature; MODIFIER silent_mutation Average:68.388; most accessible tissue: Zhenshan97 panicle, score: 91.206 N N N N
vg0826172820 C -> T LOC_Os08g41460.9 upstream_gene_variant ; 3514.0bp to feature; MODIFIER silent_mutation Average:68.388; most accessible tissue: Zhenshan97 panicle, score: 91.206 N N N N
vg0826172820 C -> T LOC_Os08g41460.2 upstream_gene_variant ; 4497.0bp to feature; MODIFIER silent_mutation Average:68.388; most accessible tissue: Zhenshan97 panicle, score: 91.206 N N N N
vg0826172820 C -> T LOC_Os08g41460.3 upstream_gene_variant ; 4497.0bp to feature; MODIFIER silent_mutation Average:68.388; most accessible tissue: Zhenshan97 panicle, score: 91.206 N N N N
vg0826172820 C -> T LOC_Os08g41460.10 upstream_gene_variant ; 4497.0bp to feature; MODIFIER silent_mutation Average:68.388; most accessible tissue: Zhenshan97 panicle, score: 91.206 N N N N
vg0826172820 C -> T LOC_Os08g41460.6 upstream_gene_variant ; 4501.0bp to feature; MODIFIER silent_mutation Average:68.388; most accessible tissue: Zhenshan97 panicle, score: 91.206 N N N N
vg0826172820 C -> T LOC_Os08g41440-LOC_Os08g41460 intergenic_region ; MODIFIER silent_mutation Average:68.388; most accessible tissue: Zhenshan97 panicle, score: 91.206 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)
vg0826172820 C T -0.07 -0.05 -0.05 -0.04 -0.06 -0.04

Putative Genotype-Phenotype Associations:

Var ID LMM P-value LR P-value Trait Subpopulation Is leadSNP Publication
vg0826172820 NA 3.12E-11 mr1712 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
vg0826172820 NA 2.11E-06 mr1748 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
vg0826172820 7.97E-07 7.76E-09 mr1872 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
vg0826172820 NA 5.77E-06 mr1910 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
vg0826172820 NA 8.34E-10 mr1977 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
vg0826172820 NA 6.53E-07 mr1977 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