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Detailed information for vg1007457578:

Variant ID: vg1007457578 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 7457578
Reference Allele: CAlternative Allele: A
Primary Allele: CSecondary Allele: A

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.81, A: 0.17, others allele: 0.00, population size: 182. )

Flanking Sequence (100 bp) in Reference Genome:


CTGAAAATTTCATTTGAAGAATTTCCTCAAAATTCAAAGATCCTAAATGCAATTTTGAAATTCAAACATGTATTGATGCAAAAATTTCAATTGTGGAAAA[C/A]
AAATATGCAGATACATACCAATTTACCTGTTGGCGAAGGTTGCGTCATTTTAAGTCCGACGTGCAAGACCGTACCTCCTTCCAGTTTAGTTCGCGGATTT

Reverse complement sequence

AAATCCGCGAACTAAACTGGAAGGAGGTACGGTCTTGCACGTCGGACTTAAAATGACGCAACCTTCGCCAACAGGTAAATTGGTATGTATCTGCATATTT[G/T]
TTTTCCACAATTGAAATTTTTGCATCAATACATGTTTGAATTTCAAAATTGCATTTAGGATCTTTGAATTTTGAGGAAATTCTTCAAATGAAATTTTCAG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: