Search for Variation information by Variation ID:

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

Detailed information for vg1005270327:

Variant ID: vg1005270327 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 5270327
Reference Allele: AAlternative Allele: G
Primary Allele: ASecondary Allele: G

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.77, G: 0.23, others allele: 0.00, population size: 43. )

Flanking Sequence (100 bp) in Reference Genome:


ATTTTCTTTGCTCCCTATTAGTAACAGCAACCGGTACCAACCGGGACAAAAAGATTGATTATTTCAACCGAGACTAGTCCTGGATTGCTACTCCCGGTTG[A/G]
AAAACCGAGACTAAAAGGGGTTAACAACCGGGAGTAAAAATAGTTTCTCCACCAGTGGATGGACCTGTATATCCCCCGACGTGAAGGCCACGGAATGGAG

Reverse complement sequence

CTCCATTCCGTGGCCTTCACGTCGGGGGATATACAGGTCCATCCACTGGTGGAGAAACTATTTTTACTCCCGGTTGTTAACCCCTTTTAGTCTCGGTTTT[T/C]
CAACCGGGAGTAGCAATCCAGGACTAGTCTCGGTTGAAATAATCAATCTTTTTGTCCCGGTTGGTACCGGTTGCTGTTACTAATAGGGAGCAAAGAAAAT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: