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Detailed information for vg1218136630:

Variant ID: vg1218136630 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 18136630
Reference Allele: TAlternative Allele: C
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.83, T: 0.16, others allele: 0.00, population size: 159. )

Flanking Sequence (100 bp) in Reference Genome:


AGTTGAAAGAAAAGGGGTACATACGTCCGAGTACTTCCCCATGGGGTGCTCCTGTGATTTTTGTAGAGAAGAAAGACAAGACGAAGAGGATGTGCGTCGA[T/C]
TACAGAGCTCTCAATGAAGTCACCATCAAAAACAAGTACCCTCTTCCCCGGATCGATGATCTATTCGATCAGCTTAAAGGTGCCACTGTATTCTCCAAGA

Reverse complement sequence

TCTTGGAGAATACAGTGGCACCTTTAAGCTGATCGAATAGATCATCGATCCGGGGAAGAGGGTACTTGTTTTTGATGGTGACTTCATTGAGAGCTCTGTA[A/G]
TCGACGCACATCCTCTTCGTCTTGTCTTTCTTCTCTACAAAAATCACAGGAGCACCCCATGGGGAAGTACTCGGACGTATGTACCCCTTTTCTTTCAACT

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: