Search for Variation information by Variation ID:

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

Detailed information for vg0133471333:

Variant ID: vg0133471333 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 33471333
Reference Allele: CAlternative Allele: G
Primary Allele: GSecondary Allele: C

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.65, C: 0.35, others allele: 0.00, population size: 218. )

Flanking Sequence (100 bp) in Reference Genome:


TATTTGGCGGAGTTCGTATATTCAAATTAAGCTGCTTTAGATTATAATCTGAAGCTGGGCCAAATATGGCCTTCCTCCTACTAACCTAGTTTATCGGTCG[C/G]
ATTGTTAAAACGGCTTTATATTTCATTCAACATCGGTGTCTGAAAATCATTTCGTACATGAGAAACTAAATTTGCACAATTTTCATTATCAACAGTTACT

Reverse complement sequence

AGTAACTGTTGATAATGAAAATTGTGCAAATTTAGTTTCTCATGTACGAAATGATTTTCAGACACCGATGTTGAATGAAATATAAAGCCGTTTTAACAAT[G/C]
CGACCGATAAACTAGGTTAGTAGGAGGAAGGCCATATTTGGCCCAGCTTCAGATTATAATCTAAAGCAGCTTAATTTGAATATACGAACTCCGCCAAATA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: