Search for Variation information by Variation ID:

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

Detailed information for vg0141857437:

Variant ID: vg0141857437 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 41857437
Reference Allele: AAlternative Allele: T
Primary Allele: ASecondary Allele: T

Inferred Ancestral Allele : A (evidence from allele frequency in Oryza rufipogon: A: 0.98, T: 0.03, others allele: 0.00, population size: 268. )

Flanking Sequence (100 bp) in Reference Genome:


AGTAGTAGTAGTAGTAGTACCGACTTGCATAATAGTTAACGAAGTTGATTGATAGTACAGTTAACGATTATTCCGGCCCTGTACGTGCCAACGAACAAAA[A/T]
GATGATCACCAATGAGATCAGTGCCATTGTCGTTCTTCCATATGGACAAATGCTACTACATTCTCAATGCTCAGGCACAAGAATTGAGCTTGCCCTGTGA

Reverse complement sequence

TCACAGGGCAAGCTCAATTCTTGTGCCTGAGCATTGAGAATGTAGTAGCATTTGTCCATATGGAAGAACGACAATGGCACTGATCTCATTGGTGATCATC[T/A]
TTTTGTTCGTTGGCACGTACAGGGCCGGAATAATCGTTAACTGTACTATCAATCAACTTCGTTAACTATTATGCAAGTCGGTACTACTACTACTACTACT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: