Search for Variation information by Variation ID:

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

Detailed information for vg1119375564:

Variant ID: vg1119375564 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 19375564
Reference Allele: TAlternative Allele: C
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.99, T: 0.01, others allele: 0.00, population size: 213. )

Flanking Sequence (100 bp) in Reference Genome:


ACACTGTTGGTTGTGACTTGTATGTTAATAATCCGTCATATTGCTATCTGTATGAAGTAGATGGTAACAAATCCGAGTCATCGGCACCTGCATGCGCCGC[T/C]
GCTGCCGCCTGCACGTAGAGACACCCTGACGCCACCGCATGACGTATTCCCCTTTGTCAATGGTTGCCGAATCAATCCAGACCTGTCCTTGTCGATCCGC

Reverse complement sequence

GCGGATCGACAAGGACAGGTCTGGATTGATTCGGCAACCATTGACAAAGGGGAATACGTCATGCGGTGGCGTCAGGGTGTCTCTACGTGCAGGCGGCAGC[A/G]
GCGGCGCATGCAGGTGCCGATGACTCGGATTTGTTACCATCTACTTCATACAGATAGCAATATGACGGATTATTAACATACAAGTCACAACCAACAGTGT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: