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Detailed information for vg0823069329:

Variant ID: vg0823069329 (JBrowse)Variation Type: INDEL
Chromosome: chr08Position: 23069329
Reference Allele: AAlternative Allele: AT
Primary Allele: ASecondary Allele: AT

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


ACGGACGGCAGGTCCGGAGCCACTGGTGCTCGCTGTAGATAAGAAACGGTTCCCACCGATGGGATAATAGTTTTGAATGATAAAAAGTTGCTTCAATAAT[A/AT]
TTTTGCTCAGCGACCAGGGACACTCGCTGACCGTCGGCATCGTGCAGCCGCGCAAGCTCATCGTGGACACCGGCAGCGACCTCATCTGGACGCAGTGCAA

Reverse complement sequence

TTGCACTGCGTCCAGATGAGGTCGCTGCCGGTGTCCACGATGAGCTTGCGCGGCTGCACGATGCCGACGGTCAGCGAGTGTCCCTGGTCGCTGAGCAAAA[T/AT]
ATTATTGAAGCAACTTTTTATCATTCAAAACTATTATCCCATCGGTGGGAACCGTTTCTTATCTACAGCGAGCACCAGTGGCTCCGGACCTGCCGTCCGT

Allele Frequencies:

Populations Population SizeFrequency of A(primary allele) Frequency of AT(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 81.70% 1.20% 9.88% 7.26% NA
All Indica  2759 69.50% 1.80% 16.60% 12.07% NA
All Japonica  1512 99.70% 0.10% 0.20% 0.07% NA
Aus  269 97.40% 0.70% 0.37% 1.49% NA
Indica I  595 58.30% 0.70% 32.77% 8.24% NA
Indica II  465 65.40% 2.40% 16.99% 15.27% NA
Indica III  913 80.10% 3.20% 4.27% 12.49% NA
Indica Intermediate  786 68.20% 0.80% 18.45% 12.60% NA
Temperate Japonica  767 99.50% 0.00% 0.39% 0.13% NA
Tropical Japonica  504 100.00% 0.00% 0.00% 0.00% NA
Japonica Intermediate  241 99.60% 0.40% 0.00% 0.00% NA
VI/Aromatic  96 96.90% 1.00% 0.00% 2.08% NA
Intermediate  90 90.00% 1.10% 5.56% 3.33% NA

Allele Effect:

Var ID Var Locus snpEff Annotation CooVar Annotation Chromatin Accessibility Score PolyPhen-2 Effect PolyPhen-2 Score SIFT Effect SIFT Score
vg0823069329 A -> AT LOC_Os08g36540.1 frameshift_variant ; p.Leu10fs; HIGH frameshift_variant Average:81.674; most accessible tissue: Minghui63 root, score: 93.106 N N N N
vg0823069329 A -> DEL LOC_Os08g36540.1 N frameshift_variant Average:81.674; most accessible tissue: Minghui63 root, score: 93.106 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)
vg0823069329 A AT 0.06 0.12 0.11 0.01 0.03 0.06