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Detailed information for vg1125117714:

Variant ID: vg1125117714 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 25117714
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CCTCTATTTATTTTAAGGATTTGCAATGATTCATATTTGTCACCGTGGGTACCAGCACTATGTCCTGGGACTGGTACTGTGATCGCGGTTTCGTAGGAAG[C/T]
GGTTCACGCCGTTTTTCCTACGACACGCTCCTGTCAGGTGCCGTTGTACGAGCACAGCCGTCCCTGTCACGGAGGATATTACTAGGAGCCCGAGGGCTGG

Reverse complement sequence

CCAGCCCTCGGGCTCCTAGTAATATCCTCCGTGACAGGGACGGCTGTGCTCGTACAACGGCACCTGACAGGAGCGTGTCGTAGGAAAAACGGCGTGAACC[G/A]
CTTCCTACGAAACCGCGATCACAGTACCAGTCCCAGGACATAGTGCTGGTACCCACGGTGACAAATATGAATCATTGCAAATCCTTAAAATAAATAGAGG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: