Search for Variation information by Variation ID:

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

Detailed information for vg1121157956:

Variant ID: vg1121157956 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 21157956
Reference Allele: TAlternative Allele: A
Primary Allele: TSecondary Allele: A

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 1.00, A: 0.01, others allele: 0.00, population size: 268. )

Flanking Sequence (100 bp) in Reference Genome:


TTTGAGTCATTGCTCACCAAACAAATTGCGGAAATTATATTTGTCCAACAACAATATTACGGGAACTCTACCAGCTCAGAGTATGGGCCAATTTACCAGC[T/A]
TAGCCAATATTGGTTTCTCTTTCAACCAGCTCACAGGGCACGTGCCTCCTGAGATTGGTAAACTAGCTAGTTTGACTCACCTTGACCTAAGTGAAAATAA

Reverse complement sequence

TTATTTTCACTTAGGTCAAGGTGAGTCAAACTAGCTAGTTTACCAATCTCAGGAGGCACGTGCCCTGTGAGCTGGTTGAAAGAGAAACCAATATTGGCTA[A/T]
GCTGGTAAATTGGCCCATACTCTGAGCTGGTAGAGTTCCCGTAATATTGTTGTTGGACAAATATAATTTCCGCAATTTGTTTGGTGAGCAATGACTCAAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: