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Detailed information for vg1015507336:

Variant ID: vg1015507336 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 15507336
Reference Allele: TAlternative Allele: C
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 1.00, others allele: 0.00, population size: 309. )

Flanking Sequence (100 bp) in Reference Genome:


GCACCACGGATGTCATAAAAATTGATAACATGGATGCACAAGTGTTTAAAGCTCTGCTTGTTTTTATCTACACGGACACTTGGCCAGAGATAGATCAAGA[T/C]
GAGACGACTATGGTTCAACTACTCGTTGCAGCCAATAAGTATAGCCTATCAAGACTGAAGATAATGTGCGAAGATAGGTTGTGCAGCTATATTGATACAA

Reverse complement sequence

TTGTATCAATATAGCTGCACAACCTATCTTCGCACATTATCTTCAGTCTTGATAGGCTATACTTATTGGCTGCAACGAGTAGTTGAACCATAGTCGTCTC[A/G]
TCTTGATCTATCTCTGGCCAAGTGTCCGTGTAGATAAAAACAAGCAGAGCTTTAAACACTTGTGCATCCATGTTATCAATTTTTATGACATCCGTGGTGC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: