Search for Variation information by Variation ID:

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

Detailed information for vg0133648958:

Variant ID: vg0133648958 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 33648958
Reference Allele: CAlternative Allele: A
Primary Allele: CSecondary Allele: A

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.55, A: 0.45, others allele: 0.00, population size: 80. )

Flanking Sequence (100 bp) in Reference Genome:


CTTTCCATCTCTTATAGTTTGAACCATCAAAAGCATGTGGTTTCAGTGCAGCAGCAAAGCCAACTACCGAAAATGACCTATCAGGTTTTTGGATTGTTGG[C/A]
AATATAGTCATTAATCGGCATATTTTAATCCAAGAAATTGAAACAATGATCATGGCATAAGCAGCGTAGGGTGATCTTAACATAACCAGTAGCATACTAT

Reverse complement sequence

ATAGTATGCTACTGGTTATGTTAAGATCACCCTACGCTGCTTATGCCATGATCATTGTTTCAATTTCTTGGATTAAAATATGCCGATTAATGACTATATT[G/T]
CCAACAATCCAAAAACCTGATAGGTCATTTTCGGTAGTTGGCTTTGCTGCTGCACTGAAACCACATGCTTTTGATGGTTCAAACTATAAGAGATGGAAAG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: