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Detailed information for vg0101299481:

Variant ID: vg0101299481 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 1299481
Reference Allele: CAlternative Allele: G
Primary Allele: CSecondary Allele: G

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CATCAAGATCTAAAACTTTTATTTTTGTTATTTCTTCATCCGATGAAATGTTAGTAATATTATTCACAAATTTTACATATATGTGTTATAATTTATAAAC[C/G]
AGATAAGATATATGTCAATTTTGTAAACAATGCTACTATCACTTTCTCGTATGAAGAAATGACCAAAATAAAAGTTTTAGATCTTGATGAGTTATTCAAC

Reverse complement sequence

GTTGAATAACTCATCAAGATCTAAAACTTTTATTTTGGTCATTTCTTCATACGAGAAAGTGATAGTAGCATTGTTTACAAAATTGACATATATCTTATCT[G/C]
GTTTATAAATTATAACACATATATGTAAAATTTGTGAATAATATTACTAACATTTCATCGGATGAAGAAATAACAAAAATAAAAGTTTTAGATCTTGATG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: