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Detailed information for vg0725884656:

Variant ID: vg0725884656 (JBrowse)Variation Type: INDEL
Chromosome: chr07Position: 25884656
Reference Allele: CCGGCGGCGGAlternative Allele: C
Primary Allele: CSecondary Allele: CCGGCGGCGG

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GGCAGGAGGACGATCCACCTCAAGAGCAAGGATGGCAAGCAGCATGATGTGACGGAGGCGTCGGCGAGGCTGTCCAAGACCATCGCCGGGATGATTCTCG[CCGGCGGCGG/C]
CGGCGGCGGCGCCGACCAGTGCATCCCGACCCCCGACATCGACCACGATACCCTCCGCGTGGTGATGCAGTACTGCGACAAGCACGCCGCCGACGACGCC

Reverse complement sequence

GGCGTCGTCGGCGGCGTGCTTGTCGCAGTACTGCATCACCACGCGGAGGGTATCGTGGTCGATGTCGGGGGTCGGGATGCACTGGTCGGCGCCGCCGCCG[CCGCCGCCGG/G]
CGAGAATCATCCCGGCGATGGTCTTGGACAGCCTCGCCGACGCCTCCGTCACATCATGCTGCTTGCCATCCTTGCTCTTGAGGTGGATCGTCCTCCTGCC

Allele Frequencies:

Populations Population SizeFrequency of C(primary allele) Frequency of CCGGCGGCGG(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 59.60% 40.30% 0.11% 0.00% NA
All Indica  2759 95.40% 4.50% 0.14% 0.00% NA
All Japonica  1512 0.80% 99.20% 0.00% 0.00% NA
Aus  269 52.80% 46.80% 0.37% 0.00% NA
Indica I  595 96.10% 3.50% 0.34% 0.00% NA
Indica II  465 91.20% 8.80% 0.00% 0.00% NA
Indica III  913 98.80% 1.20% 0.00% 0.00% NA
Indica Intermediate  786 93.30% 6.50% 0.25% 0.00% NA
Temperate Japonica  767 0.10% 99.90% 0.00% 0.00% NA
Tropical Japonica  504 1.80% 98.20% 0.00% 0.00% NA
Japonica Intermediate  241 0.80% 99.20% 0.00% 0.00% NA
VI/Aromatic  96 3.10% 96.90% 0.00% 0.00% NA
Intermediate  90 33.30% 66.70% 0.00% 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
vg0725884656 CCGGCGGCGG -> C LOC_Os07g43180.1 disruptive_inframe_deletion ; p.Gly84_Gly86del; MODERATE inframe_variant Average:87.351; most accessible tissue: Zhenshan97 young leaf, score: 91.967 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)
vg0725884656 CCGGC* C -0.03 0.0 -0.01 -0.1 -0.02 -0.01