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Detailed information for vg1003193153:

Variant ID: vg1003193153 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 3193153
Reference Allele: TAlternative Allele: A,G
Primary Allele: ASecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CCGTTGGGTTATTTCTGGTCGTGACAAGTTGGTATCAGAGCCCCCTTGACCCTAGGACGAGCTTTAGATCCCAAGCCTTAGCAATATTTTCGAAATAAAA[T/A,G]
TCCTTTCTTATTTGTGAAAATCCTCTAGTCTCTCTCTGTCCCGCTGCTTCATTTATCGTCAAAATCTGATCTTTAAAATGTTGCTATTCTCTTTTGTTTT

Reverse complement sequence

AAAACAAAAGAGAATAGCAACATTTTAAAGATCAGATTTTGACGATAAATGAAGCAGCGGGACAGAGAGAGACTAGAGGATTTTCACAAATAAGAAAGGA[A/T,C]
TTTTATTTCGAAAATATTGCTAAGGCTTGGGATCTAAAGCTCGTCCTAGGGTCAAGGGGGCTCTGATACCAACTTGTCACGACCAGAAATAACCCAACGG

Allele Frequencies:

Populations Population SizeFrequency of A(primary allele) Frequency of T(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 49.70% 37.30% 12.78% 0.21% G: 0.02%
All Indica  2759 82.70% 8.30% 8.70% 0.29% G: 0.04%
All Japonica  1512 1.10% 96.00% 2.98% 0.00% NA
Aus  269 6.30% 5.90% 87.73% 0.00% NA
Indica I  595 86.70% 9.70% 2.52% 1.01% NA
Indica II  465 79.40% 3.40% 17.20% 0.00% NA
Indica III  913 82.00% 10.70% 7.12% 0.11% NA
Indica Intermediate  786 82.40% 7.10% 10.18% 0.13% G: 0.13%
Temperate Japonica  767 0.50% 99.20% 0.26% 0.00% NA
Tropical Japonica  504 2.20% 89.90% 7.94% 0.00% NA
Japonica Intermediate  241 0.40% 98.30% 1.24% 0.00% NA
VI/Aromatic  96 7.30% 32.30% 59.38% 1.04% NA
Intermediate  90 28.90% 41.10% 28.89% 1.11% NA

Allele Effect:

Var ID Var Locus snpEff Annotation CooVar Annotation Chromatin Accessibility Score PolyPhen-2 Effect PolyPhen-2 Score SIFT Effect SIFT Score
vg1003193153 T -> G LOC_Os10g06210.1 upstream_gene_variant ; 3411.0bp to feature; MODIFIER silent_mutation Average:12.368; most accessible tissue: Callus, score: 27.457 N N N N
vg1003193153 T -> G LOC_Os10g06230.1 upstream_gene_variant ; 1168.0bp to feature; MODIFIER silent_mutation Average:12.368; most accessible tissue: Callus, score: 27.457 N N N N
vg1003193153 T -> G LOC_Os10g06220.1 intron_variant ; MODIFIER silent_mutation Average:12.368; most accessible tissue: Callus, score: 27.457 N N N N
vg1003193153 T -> A LOC_Os10g06210.1 upstream_gene_variant ; 3411.0bp to feature; MODIFIER silent_mutation Average:12.368; most accessible tissue: Callus, score: 27.457 N N N N
vg1003193153 T -> A LOC_Os10g06230.1 upstream_gene_variant ; 1168.0bp to feature; MODIFIER silent_mutation Average:12.368; most accessible tissue: Callus, score: 27.457 N N N N
vg1003193153 T -> A LOC_Os10g06220.1 intron_variant ; MODIFIER silent_mutation Average:12.368; most accessible tissue: Callus, score: 27.457 N N N N
vg1003193153 T -> DEL N N silent_mutation Average:12.368; most accessible tissue: Callus, score: 27.457 N N N N

Putative Genotype-Phenotype Associations:

Var ID LMM P-value LR P-value Trait Subpopulation Is leadSNP Publication
vg1003193153 NA 1.75E-12 mr1326 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
vg1003193153 NA 2.29E-06 mr1761 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
vg1003193153 5.34E-07 4.03E-07 mr1768 Ind_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
vg1003193153 NA 1.11E-08 mr1322_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
vg1003193153 NA 2.74E-12 mr1325_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
vg1003193153 NA 2.38E-16 mr1342_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