Search for Variation information by Variation ID:

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

Detailed information for vg0202629950:

Variant ID: vg0202629950 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 2629950
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.99, others allele: 0.00, population size: 236. )

Flanking Sequence (100 bp) in Reference Genome:


TTAAATCTGTAGTTTTGTGATGTATTGTGCAAAGTACCTGTAGTTTTGTGATAAACGTAGACACTAAATCTGTAGTTTTGTGAAATATATTCTTAAATAT[A/G]
TAGTTTTGTGATAGAATGTACAAAATATATGCAGTTTTATGAAATTTACTCGATTTCTGTATACATAAATCTCTCTCACTAGACGTAGGAGTAAAACTCT

Reverse complement sequence

AGAGTTTTACTCCTACGTCTAGTGAGAGAGATTTATGTATACAGAAATCGAGTAAATTTCATAAAACTGCATATATTTTGTACATTCTATCACAAAACTA[T/C]
ATATTTAAGAATATATTTCACAAAACTACAGATTTAGTGTCTACGTTTATCACAAAACTACAGGTACTTTGCACAATACATCACAAAACTACAGATTTAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: