Search for Variation information by Variation ID:

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

Detailed information for vg0227603361:

Variant ID: vg0227603361 (JBrowse)	Variation Type: SNP
Chromosome: chr02	Position: 27603361
Reference Allele: G	Alternative Allele: A
Primary Allele: G	Secondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.99, A: 0.02, others allele: 0.00, population size: 117. )

Flanking Sequence (100 bp) in Reference Genome:

CATTTTAGTCAAAGTTGAATAAAATAATTCCAAATTCACAAAAAAAAATTCGGCCAAAATAATATCATTGGGGGGGGGGGTCCGATATGATCGAAATTTC[G/A]
TTCCGGAATTTTGAACCCTGGATATACCTGGATACAAATTAGACAACAATTCAATGCTTCAAACTTGTTTAGTTGTGCATGACGTGCAAATTCTGTTATA

Reverse complement sequence

TATAACAGAATTTGCACGTCATGCACAACTAAACAAGTTTGAAGCATTGAATTGTTGTCTAATTTGTATCCAGGTATATCCAGGGTTCAAAATTCCGGAA[C/T]
GAAATTTCGATCATATCGGACCCCCCCCCCCAATGATATTATTTTGGCCGAATTTTTTTTTGTGAATTTGGAATTATTTTATTCAACTTTGACTAAAATG

Allele Frequencies:

Allele Effect: