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Detailed information for vg1109241491:

Variant ID: vg1109241491 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 9241491
Reference Allele: AAlternative Allele: C
Primary Allele: CSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CACAATCATTTCCTATTTAATTTTACCTATTTTTTTAATAACCGTGTCCAACTCTAAAAATGCTTATATTCTAGTACTGAGGGAGTACATAATCCTATGG[A/C]
TGTCACTAAAATATTTCGACAGCTTTCCAAAATTCTCATATGTATCCAATTCAATTGTTGCACACTTAGTAGGCAGCTGTAAGCCCCCGGCATGGTGTTG

Reverse complement sequence

CAACACCATGCCGGGGGCTTACAGCTGCCTACTAAGTGTGCAACAATTGAATTGGATACATATGAGAATTTTGGAAAGCTGTCGAAATATTTTAGTGACA[T/G]
CCATAGGATTATGTACTCCCTCAGTACTAGAATATAAGCATTTTTAGAGTTGGACACGGTTATTAAAAAAATAGGTAAAATTAAATAGGAAATGATTGTG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: