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Detailed information for vg1101692951:

Variant ID: vg1101692951 (JBrowse)Variation Type: INDEL
Chromosome: chr11Position: 1692951
Reference Allele: CTAlternative Allele: C,CTT
Primary Allele: CTSecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TCGTCAGGAAGATGCTCAACATCAACCCCAAGGAGAGGCTTACAGCATTCCAAGTGCTCAGTAAGTTTATTTGTTACAGATTAATTACTCAAATCTGCTC[CT/C,CTT]
TTTTTTTTCATATAGAGGTACAGTTTGGATTAATTTTCCCTTTATTGGTGTCAGAATTAAATTTGGATTCATTTGGATCAATTTGGATTTGCAGATCACC

Reverse complement sequence

GGTGATCTGCAAATCCAAATTGATCCAAATGAATCCAAATTTAATTCTGACACCAATAAAGGGAAAATTAATCCAAACTGTACCTCTATATGAAAAAAAA[AG/G,AAG]
GAGCAGATTTGAGTAATTAATCTGTAACAAATAAACTTACTGAGCACTTGGAATGCTGTAAGCCTCTCCTTGGGGTTGATGTTGAGCATCTTCCTGACGA

Allele Frequencies:

Populations Population SizeFrequency of CT(primary allele) Frequency of C(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 84.40% 1.20% 7.38% 7.00% NA
All Indica  2759 78.50% 0.90% 9.75% 10.87% NA
All Japonica  1512 98.80% 1.00% 0.13% 0.07% NA
Aus  269 60.60% 0.70% 27.88% 10.78% NA
Indica I  595 35.50% 1.80% 30.59% 32.10% NA
Indica II  465 90.80% 0.20% 3.23% 5.81% NA
Indica III  913 98.60% 0.20% 0.88% 0.33% NA
Indica Intermediate  786 80.40% 1.40% 8.14% 10.05% NA
Temperate Japonica  767 99.10% 0.50% 0.26% 0.13% NA
Tropical Japonica  504 99.20% 0.80% 0.00% 0.00% NA
Japonica Intermediate  241 97.10% 2.90% 0.00% 0.00% NA
VI/Aromatic  96 90.60% 8.30% 1.04% 0.00% NA
Intermediate  90 86.70% 10.00% 2.22% 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
vg1101692951 CT -> CTT LOC_Os11g04150.1 upstream_gene_variant ; 4854.0bp to feature; MODIFIER N Average:68.14; most accessible tissue: Zhenshan97 panicle, score: 86.788 N N N N
vg1101692951 CT -> CTT LOC_Os11g04160.1 downstream_gene_variant ; 1613.0bp to feature; MODIFIER N Average:68.14; most accessible tissue: Zhenshan97 panicle, score: 86.788 N N N N
vg1101692951 CT -> CTT LOC_Os11g04174.1 downstream_gene_variant ; 1519.0bp to feature; MODIFIER N Average:68.14; most accessible tissue: Zhenshan97 panicle, score: 86.788 N N N N
vg1101692951 CT -> CTT LOC_Os11g04180.1 downstream_gene_variant ; 3474.0bp to feature; MODIFIER N Average:68.14; most accessible tissue: Zhenshan97 panicle, score: 86.788 N N N N
vg1101692951 CT -> CTT LOC_Os11g04170.1 intron_variant ; MODIFIER N Average:68.14; most accessible tissue: Zhenshan97 panicle, score: 86.788 N N N N
vg1101692951 CT -> DEL N N silent_mutation Average:68.14; most accessible tissue: Zhenshan97 panicle, score: 86.788 N N N N
vg1101692951 CT -> C LOC_Os11g04150.1 upstream_gene_variant ; 4853.0bp to feature; MODIFIER silent_mutation Average:68.14; most accessible tissue: Zhenshan97 panicle, score: 86.788 N N N N
vg1101692951 CT -> C LOC_Os11g04160.1 downstream_gene_variant ; 1612.0bp to feature; MODIFIER silent_mutation Average:68.14; most accessible tissue: Zhenshan97 panicle, score: 86.788 N N N N
vg1101692951 CT -> C LOC_Os11g04174.1 downstream_gene_variant ; 1520.0bp to feature; MODIFIER silent_mutation Average:68.14; most accessible tissue: Zhenshan97 panicle, score: 86.788 N N N N
vg1101692951 CT -> C LOC_Os11g04180.1 downstream_gene_variant ; 3475.0bp to feature; MODIFIER silent_mutation Average:68.14; most accessible tissue: Zhenshan97 panicle, score: 86.788 N N N N
vg1101692951 CT -> C LOC_Os11g04170.1 intron_variant ; MODIFIER silent_mutation Average:68.14; most accessible tissue: Zhenshan97 panicle, score: 86.788 N N N N