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Detailed information for vg1127529196:

Variant ID: vg1127529196 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 27529196
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GCAAGTACTTATCTTCTGTCAATGTCTTGAGCGAGTGAAACACTGGTGGAGAAACCATCTTTTGTCGATCGGCCGAATTCCACAATAGTCCCGGTTGCAA[C/T]
AAAAACCGGGACTAAAGATGATCTTTAGTCCCGGTTAAAAAGGGTAACGGGCATATTTGATCTTTAGTCCTGGTTGGTAACACCAACCTCTTTAGTCCCG

Reverse complement sequence

CGGGACTAAAGAGGTTGGTGTTACCAACCAGGACTAAAGATCAAATATGCCCGTTACCCTTTTTAACCGGGACTAAAGATCATCTTTAGTCCCGGTTTTT[G/A]
TTGCAACCGGGACTATTGTGGAATTCGGCCGATCGACAAAAGATGGTTTCTCCACCAGTGTTTCACTCGCTCAAGACATTGACAGAAGATAAGTACTTGC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: