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Detailed information for vg1101470344:

Variant ID: vg1101470344 (JBrowse)Variation Type: INDEL
Chromosome: chr11Position: 1470344
Reference Allele: CAlternative Allele: CGCTCCCCTCTCCTCTCTCTCCAT,T
Primary Allele: CGCTCCCCTCTCCTCTCTCT CCATSecondary Allele: C

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 1.00, T: 0.03, others allele: 0.00, population size: 36. )

Flanking Sequence (100 bp) in Reference Genome:


CCGCCCTGTCGTCCTCGCCACCCTGTCCTCCTCCCCCTGTCGTCCCCGCGGTCCGTCGCCGCCACCGCCACCGCCGCCTGGCGAGTCATCCTGTGCTACA[C/CGCTCCCCTCTCCTCTCTCTCCAT,T]
GGACATTTTGGGCATAAAAGTCTCCAAAGTGGCATTTCATCCGGTAAACAATGTATTGAGTGGCATTTTATCTGGTGCATTATATTGAGTGGCATTTTAT

Reverse complement sequence

ATAAAATGCCACTCAATATAATGCACCAGATAAAATGCCACTCAATACATTGTTTACCGGATGAAATGCCACTTTGGAGACTTTTATGCCCAAAATGTCC[G/ATGGAGAGAGAGGAGAGGGGAGCG,A]
TGTAGCACAGGATGACTCGCCAGGCGGCGGTGGCGGTGGCGGCGACGGACCGCGGGGACGACAGGGGGAGGAGGACAGGGTGGCGAGGACGACAGGGCGG

Allele Frequencies:

Populations Population SizeFrequency of CGCTCCCCTCTCCTCTCTCT CCAT(primary allele) Frequency of C(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 71.00% 23.20% 5.50% 0.00% T: 0.25%
All Indica  2759 92.80% 0.90% 6.02% 0.00% T: 0.29%
All Japonica  1512 29.00% 66.90% 4.03% 0.00% T: 0.07%
Aus  269 88.80% 0.70% 9.67% 0.00% T: 0.74%
Indica I  595 93.80% 0.20% 5.88% 0.00% T: 0.17%
Indica II  465 89.70% 1.30% 8.60% 0.00% T: 0.43%
Indica III  913 94.10% 0.40% 5.26% 0.00% T: 0.22%
Indica Intermediate  786 92.40% 1.80% 5.47% 0.00% T: 0.38%
Temperate Japonica  767 11.50% 87.40% 1.17% 0.00% NA
Tropical Japonica  504 55.80% 34.10% 9.92% 0.00% T: 0.20%
Japonica Intermediate  241 28.60% 70.50% 0.83% 0.00% NA
VI/Aromatic  96 64.60% 32.30% 2.08% 0.00% T: 1.04%
Intermediate  90 64.40% 30.00% 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
vg1101470344 C -> T LOC_Os11g03740.1 upstream_gene_variant ; 823.0bp to feature; MODIFIER silent_mutation Average:83.86; most accessible tissue: Zhenshan97 panicle, score: 94.949 N N N N
vg1101470344 C -> T LOC_Os11g03734.1 downstream_gene_variant ; 2702.0bp to feature; MODIFIER silent_mutation Average:83.86; most accessible tissue: Zhenshan97 panicle, score: 94.949 N N N N
vg1101470344 C -> T LOC_Os11g03750.1 downstream_gene_variant ; 1475.0bp to feature; MODIFIER silent_mutation Average:83.86; most accessible tissue: Zhenshan97 panicle, score: 94.949 N N N N
vg1101470344 C -> T LOC_Os11g03760.1 downstream_gene_variant ; 2487.0bp to feature; MODIFIER silent_mutation Average:83.86; most accessible tissue: Zhenshan97 panicle, score: 94.949 N N N N
vg1101470344 C -> T LOC_Os11g03740-LOC_Os11g03750 intergenic_region ; MODIFIER silent_mutation Average:83.86; most accessible tissue: Zhenshan97 panicle, score: 94.949 N N N N
vg1101470344 C -> CGCTCCCCTCTCCTCTCTCTCCAT LOC_Os11g03740.1 upstream_gene_variant ; 824.0bp to feature; MODIFIER silent_mutation Average:83.86; most accessible tissue: Zhenshan97 panicle, score: 94.949 N N N N
vg1101470344 C -> CGCTCCCCTCTCCTCTCTCTCCAT LOC_Os11g03734.1 downstream_gene_variant ; 2703.0bp to feature; MODIFIER silent_mutation Average:83.86; most accessible tissue: Zhenshan97 panicle, score: 94.949 N N N N
vg1101470344 C -> CGCTCCCCTCTCCTCTCTCTCCAT LOC_Os11g03750.1 downstream_gene_variant ; 1474.0bp to feature; MODIFIER silent_mutation Average:83.86; most accessible tissue: Zhenshan97 panicle, score: 94.949 N N N N
vg1101470344 C -> CGCTCCCCTCTCCTCTCTCTCCAT LOC_Os11g03760.1 downstream_gene_variant ; 2486.0bp to feature; MODIFIER silent_mutation Average:83.86; most accessible tissue: Zhenshan97 panicle, score: 94.949 N N N N
vg1101470344 C -> CGCTCCCCTCTCCTCTCTCTCCAT LOC_Os11g03740-LOC_Os11g03750 intergenic_region ; MODIFIER silent_mutation Average:83.86; most accessible tissue: Zhenshan97 panicle, score: 94.949 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)
vg1101470344 C CGCTC* 0.44 0.27 0.23 0.32 0.41 0.42
vg1101470344 C T -0.01 -0.01 -0.01 -0.01 -0.01 -0.01

Putative Genotype-Phenotype Associations:

Var ID LMM P-value LR P-value Trait Subpopulation Is leadSNP Publication
vg1101470344 1.27E-06 NA mr1623 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
vg1101470344 NA 6.04E-06 mr1623 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
vg1101470344 NA 2.38E-10 mr1630 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