Search for Variation information by Variation ID:

Please input a variation ID (e.g., vg0722097923 , STR0500036000 ).

Detailed information for vg1013082033:

Variant ID: vg1013082033 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 13082033
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 1.00, others allele: 0.00, population size: 241. )

Flanking Sequence (100 bp) in Reference Genome:


CATTACCTTGGAATAATAGTTAAATTTATCTACCCATCTAATCGAACGTGCATGTGGTTACTTCATTGCGTGCATGAATGCTGTTCCTGGTATATATTGC[G/A]
TTGACACTTAGATACACAGGTACACAGGTCTTAAAAAAAGAGCACATAGGAACCAACTAACCTGGTGCGTCTAGGCCGCCTCAACTAAATGTGTTCCATA

Reverse complement sequence

TATGGAACACATTTAGTTGAGGCGGCCTAGACGCACCAGGTTAGTTGGTTCCTATGTGCTCTTTTTTTAAGACCTGTGTACCTGTGTATCTAAGTGTCAA[C/T]
GCAATATATACCAGGAACAGCATTCATGCACGCAATGAAGTAACCACATGCACGTTCGATTAGATGGGTAGATAAATTTAACTATTATTCCAAGGTAATG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: