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Detailed information for vg1007456082:

Variant ID: vg1007456082 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 7456082
Reference Allele: TAlternative Allele: C
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 0.65, C: 0.34, others allele: 0.00, population size: 222. )

Flanking Sequence (100 bp) in Reference Genome:


CATTTTGCCATTTTGTACATTCCTTGCCATTATGTGTGTCTCCCTGTATGTTCCACATGCACAAGATTCTTCTATGGTTTGCAGGGGAATGGTTAGTTCA[T/C]
GATAGTTGTACAAATGATACCCCGCATTTGGCAACGGGATTTCATTTGTACAATCGGGGAAAAAGTATATCAAAGATCCATCTACTCCATGTTTAAGAAT

Reverse complement sequence

ATTCTTAAACATGGAGTAGATGGATCTTTGATATACTTTTTCCCCGATTGTACAAATGAAATCCCGTTGCCAAATGCGGGGTATCATTTGTACAACTATC[A/G]
TGAACTAACCATTCCCCTGCAAACCATAGAAGAATCTTGTGCATGTGGAACATACAGGGAGACACACATAATGGCAAGGAATGTACAAAATGGCAAAATG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: