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Detailed information for vg0620000170:

Variant ID: vg0620000170 (JBrowse)Variation Type: SNP
Chromosome: chr06Position: 20000170
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TCGGCGCATTCGTCGCCATCGTCGGCATCGTCGTCCTGGCCGTCATCTTCTACACCCGTTCGTCCGCCCGTCACGCCGCCCCCGGCGCGGCGCCCGACGC[G/A]
GTCACCGCGCTCCAGGGGCAGCAGCAGCAGCGCGGCCTCGGCCTCGGCCCCGACGACGTCTCCGTGCTCCCGACGTTCACGTACCACGCCGCCGCCACCG

Reverse complement sequence

CGGTGGCGGCGGCGTGGTACGTGAACGTCGGGAGCACGGAGACGTCGTCGGGGCCGAGGCCGAGGCCGCGCTGCTGCTGCTGCCCCTGGAGCGCGGTGAC[C/T]
GCGTCGGGCGCCGCGCCGGGGGCGGCGTGACGGGCGGACGAACGGGTGTAGAAGATGACGGCCAGGACGACGATGCCGACGATGGCGACGAATGCGCCGA

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 91.70% 0.90% 1.93% 5.44% NA
All Indica  2759 89.50% 0.00% 2.25% 8.26% NA
All Japonica  1512 93.80% 2.80% 1.65% 1.72% NA
Aus  269 100.00% 0.00% 0.00% 0.00% NA
Indica I  595 88.90% 0.00% 4.37% 6.72% NA
Indica II  465 81.90% 0.00% 4.09% 13.98% NA
Indica III  913 93.40% 0.00% 0.99% 5.59% NA
Indica Intermediate  786 89.80% 0.00% 1.02% 9.16% NA
Temperate Japonica  767 94.30% 0.70% 1.96% 3.13% NA
Tropical Japonica  504 93.30% 5.00% 1.59% 0.20% NA
Japonica Intermediate  241 93.80% 5.00% 0.83% 0.41% NA
VI/Aromatic  96 100.00% 0.00% 0.00% 0.00% NA
Intermediate  90 92.20% 0.00% 4.44% 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
vg0620000170 G -> A LOC_Os06g34360.1 synonymous_variant ; p.Ala48Ala; LOW synonymous_codon Average:85.261; most accessible tissue: Zhenshan97 flower, score: 95.508 N N N N
vg0620000170 G -> DEL LOC_Os06g34360.1 N frameshift_variant Average:85.261; most accessible tissue: Zhenshan97 flower, score: 95.508 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)
vg0620000170 G A -0.04 -0.03 -0.05 -0.01 -0.03 -0.05