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Detailed information for vg0918111800:

Variant ID: vg0918111800 (JBrowse)Variation Type: INDEL
Chromosome: chr09Position: 18111800
Reference Allele: CTTTTAlternative Allele: C,CT,CTTT,CTT,CTTTTT
Primary Allele: CTTTTSecondary Allele: CTTT

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TTCGCGATCTCCCTCTGTTACTATGCTCCTTGTTTTACTGCAATGCGTGCTCTGTGTTTGCGTAATTGCTTGTATGAACGCTGCCTCACTCACGGTTAGG[CTTTT/C,CT,CTTT,CTT,CTTTTT]
TTTTTTTTTTGCCGGTAATATTACACAGAGTACGAACTCTGTAAACGCGCTGATGTGTAGTCGCTATCTTTTATACTACTGTTGTGGGTGTGGCACAATG

Reverse complement sequence

CATTGTGCCACACCCACAACAGTAGTATAAAAGATAGCGACTACACATCAGCGCGTTTACAGAGTTCGTACTCTGTGTAATATTACCGGCAAAAAAAAAA[AAAAG/G,AG,AAAG,AAG,AAAAAG]
CCTAACCGTGAGTGAGGCAGCGTTCATACAAGCAATTACGCAAACACAGAGCACGCATTGCAGTAAAACAAGGAGCATAGTAACAGAGGGAGATCGCGAA

Allele Frequencies:

Populations Population SizeFrequency of CTTTT(primary allele) Frequency of CTTT(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 40.70% 36.70% 11.15% 0.00% CT: 10.07%; CTT: 1.21%; CTTTTT: 0.23%
All Indica  2759 14.60% 53.60% 14.06% 0.00% CT: 17.04%; CTT: 0.69%
All Japonica  1512 90.80% 4.60% 3.77% 0.00% CTTTTT: 0.73%; CTT: 0.07%
Aus  269 19.70% 45.70% 20.82% 0.00% CTT: 13.38%; CT: 0.37%
Indica I  595 14.10% 30.40% 10.08% 0.00% CT: 45.38%
Indica II  465 14.00% 57.00% 24.09% 0.00% CT: 4.73%; CTT: 0.22%
Indica III  913 15.30% 71.60% 10.62% 0.00% CTT: 1.20%; CT: 1.20%
Indica Intermediate  786 14.40% 48.30% 15.14% 0.00% CT: 21.25%; CTT: 0.89%
Temperate Japonica  767 87.00% 7.00% 5.61% 0.00% CTTTTT: 0.39%
Tropical Japonica  504 96.20% 2.60% 0.79% 0.00% CTTTTT: 0.40%
Japonica Intermediate  241 91.70% 1.20% 4.15% 0.00% CTTTTT: 2.49%; CTT: 0.41%
VI/Aromatic  96 40.60% 42.70% 15.62% 0.00% CTT: 1.04%
Intermediate  90 61.10% 21.10% 12.22% 0.00% CT: 5.56%

Allele Effect:

Var ID Var Locus snpEff Annotation CooVar Annotation Chromatin Accessibility Score PolyPhen-2 Effect PolyPhen-2 Score SIFT Effect SIFT Score
vg0918111800 CTTTT -> CTT LOC_Os09g29790.1 upstream_gene_variant ; 2490.0bp to feature; MODIFIER silent_mutation Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> CTT LOC_Os09g29810.1 upstream_gene_variant ; 3322.0bp to feature; MODIFIER silent_mutation Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> CTT LOC_Os09g29800.1 intron_variant ; MODIFIER silent_mutation Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> CTTT LOC_Os09g29790.1 upstream_gene_variant ; 2491.0bp to feature; MODIFIER silent_mutation Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> CTTT LOC_Os09g29810.1 upstream_gene_variant ; 3321.0bp to feature; MODIFIER silent_mutation Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> CTTT LOC_Os09g29800.1 intron_variant ; MODIFIER silent_mutation Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> CTTTTT LOC_Os09g29790.1 upstream_gene_variant ; 2492.0bp to feature; MODIFIER silent_mutation Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> CTTTTT LOC_Os09g29810.1 upstream_gene_variant ; 3320.0bp to feature; MODIFIER silent_mutation Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> CTTTTT LOC_Os09g29800.1 intron_variant ; MODIFIER silent_mutation Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> C LOC_Os09g29790.1 upstream_gene_variant ; 2488.0bp to feature; MODIFIER N Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> C LOC_Os09g29810.1 upstream_gene_variant ; 3324.0bp to feature; MODIFIER N Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> C LOC_Os09g29800.1 intron_variant ; MODIFIER N Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> CT LOC_Os09g29790.1 upstream_gene_variant ; 2489.0bp to feature; MODIFIER silent_mutation Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> CT LOC_Os09g29810.1 upstream_gene_variant ; 3323.0bp to feature; MODIFIER silent_mutation Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N
vg0918111800 CTTTT -> CT LOC_Os09g29800.1 intron_variant ; MODIFIER silent_mutation Average:80.205; most accessible tissue: Callus, score: 84.784 N N N N