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Detailed information for vg0607344108:

Variant ID: vg0607344108 (JBrowse)Variation Type: SNP
Chromosome: chr06Position: 7344108
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TCCCAAATTGTTTTGGTGCTTCGTAAAGATGTTTATCACCTCAGAGACAAAATGTAATGTATTCTGTCCTGAAGAGCAACCAAGGTCGGCAACAACCATG[A/G]
TATTAGCTAGAAGGGTTGCGTACAGTTCTCGGATTGCCTTATCAAGGACAAACTTAGCCTCAATCATAGCTTTCGCCTAGCACCATATATACATACATGT

Reverse complement sequence

ACATGTATGTATATATGGTGCTAGGCGAAAGCTATGATTGAGGCTAAGTTTGTCCTTGATAAGGCAATCCGAGAACTGTACGCAACCCTTCTAGCTAATA[T/C]
CATGGTTGTTGCCGACCTTGGTTGCTCTTCAGGACAGAATACATTACATTTTGTCTCTGAGGTGATAAACATCTTTACGAAGCACCAAAACAATTTGGGA

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 85.30% 5.10% 4.13% 5.48% NA
All Indica  2759 90.20% 0.00% 0.47% 9.31% NA
All Japonica  1512 72.80% 15.80% 11.31% 0.07% NA
Aus  269 97.40% 0.00% 2.60% 0.00% NA
Indica I  595 96.80% 0.00% 0.34% 2.86% NA
Indica II  465 98.50% 0.00% 0.43% 1.08% NA
Indica III  913 79.80% 0.00% 0.44% 19.72% NA
Indica Intermediate  786 92.40% 0.00% 0.64% 7.00% NA
Temperate Japonica  767 60.90% 21.90% 17.21% 0.00% NA
Tropical Japonica  504 90.70% 5.80% 3.37% 0.20% NA
Japonica Intermediate  241 73.40% 17.40% 9.13% 0.00% NA
VI/Aromatic  96 100.00% 0.00% 0.00% 0.00% NA
Intermediate  90 93.30% 1.10% 4.44% 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
vg0607344108 A -> G LOC_Os06g13350.1 missense_variant ; p.Ile53Thr; MODERATE nonsynonymous_codon ; I53T Average:51.444; most accessible tissue: Zhenshan97 flower, score: 89.684 benign -1.489 TOLERATED 1.00
vg0607344108 A -> DEL LOC_Os06g13350.1 N frameshift_variant Average:51.444; most accessible tissue: Zhenshan97 flower, score: 89.684 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)
vg0607344108 A G 0.03 0.03 0.03 0.05 0.05 0.06

Putative Genotype-Phenotype Associations:

Var ID LMM P-value LR P-value Trait Subpopulation Is leadSNP Publication
vg0607344108 1.92E-06 1.92E-06 mr1460_2 Jap_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