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Detailed information for vg0725372256:

Variant ID: vg0725372256 (JBrowse)Variation Type: INDEL
Chromosome: chr07Position: 25372256
Reference Allele: TAlternative Allele: TGG
Primary Allele: TGGSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CCTCGGGGTTCAAATCGAGCTTGAATTTGTGGTTTTTTTTGGGGAGGGTTTTTTTTTTCTTTTTGGTGTTGTTTTTGGATGCGAGTGTGGCTTGGCAGGG[T/TGG]
TGGTGGTGGTGATGCCATGATGCACATGCTGGTGGCCCCCGATGGAGGCGGCGGAGGGGAGATGCCGCCGCCGTACGGGGGAGCCGCGGCGGCGCCGCCG

Reverse complement sequence

CGGCGGCGCCGCCGCGGCTCCCCCGTACGGCGGCGGCATCTCCCCTCCGCCGCCTCCATCGGGGGCCACCAGCATGTGCATCATGGCATCACCACCACCA[A/CCA]
CCCTGCCAAGCCACACTCGCATCCAAAAACAACACCAAAAAGAAAAAAAAAACCCTCCCCAAAAAAAACCACAAATTCAAGCTCGATTTGAACCCCGAGG

Allele Frequencies:

Populations Population SizeFrequency of TGG(primary allele) Frequency of T(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 68.00% 30.90% 1.08% 0.00% NA
All Indica  2759 93.00% 6.00% 1.05% 0.00% NA
All Japonica  1512 23.70% 76.20% 0.13% 0.00% NA
Aus  269 87.40% 5.60% 7.06% 0.00% NA
Indica I  595 90.40% 8.60% 1.01% 0.00% NA
Indica II  465 91.20% 7.10% 1.72% 0.00% NA
Indica III  913 96.70% 2.60% 0.66% 0.00% NA
Indica Intermediate  786 91.60% 7.30% 1.15% 0.00% NA
Temperate Japonica  767 3.70% 96.30% 0.00% 0.00% NA
Tropical Japonica  504 57.30% 42.50% 0.20% 0.00% NA
Japonica Intermediate  241 17.00% 82.60% 0.41% 0.00% NA
VI/Aromatic  96 6.20% 93.80% 0.00% 0.00% NA
Intermediate  90 54.40% 44.40% 1.11% 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
vg0725372256 T -> TGG LOC_Os07g42400.1 frameshift_variant ; p.Gly9fs; HIGH frameshift_variant Average:97.998; most accessible tissue: Zhenshan97 flower, score: 98.588 N N N N
vg0725372256 T -> TGG LOC_Os07g42400.2 frameshift_variant ; p.Gly9fs; HIGH frameshift_variant Average:97.998; most accessible tissue: Zhenshan97 flower, score: 98.588 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)
vg0725372256 T TGG 0.02 -0.02 0.03 0.03 0.03 0.03