Search for Variation information by Variation ID:

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

Detailed information for vg1121803238:

Variant ID: vg1121803238 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 21803238
Reference Allele: AAlternative Allele: G
Primary Allele: ASecondary Allele: G

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 1.00, others allele: 0.00, population size: 104. )

Flanking Sequence (100 bp) in Reference Genome:


TTATCAGGGTGCTAGCCGATAAGTTAATGCTAGTGTTTTATCGGGGTGCTAGCCGATAAGTTATCTGGACATTGCATCGGCTTACAAAGATTACATACAA[A/G]
TTGGATTTAGCCGATTGCAACAAAGGTTTCACTGTTTATCTAAATTGATTGGATTTTATGACATCGGAATTTTAGCCGATGTATGCTTTAACCATCGAAT

Reverse complement sequence

ATTCGATGGTTAAAGCATACATCGGCTAAAATTCCGATGTCATAAAATCCAATCAATTTAGATAAACAGTGAAACCTTTGTTGCAATCGGCTAAATCCAA[T/C]
TTGTATGTAATCTTTGTAAGCCGATGCAATGTCCAGATAACTTATCGGCTAGCACCCCGATAAAACACTAGCATTAACTTATCGGCTAGCACCCTGATAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: