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Detailed information for vg0136191693:

Variant ID: vg0136191693 (JBrowse)Variation Type: SNP
Chromosome: chr01Position: 36191693
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CGTTGGATCCGTCACCACTAATCATCGTCTCCTAACCATAAGCTCTGGTTTGCCCCCGTCATCAAGGCCAACCCATCATCCTCCTCCATCTCCGTGGCTT[C/T]
GATGTGGCCGCCGATGCCTCACCTCCAACTCGTGTCTACCTCCCACTGTCGGGCCGTTGCCTCCGACATCTCTTTAAGCATGGCGATGTCCCTCTTCTTT

Reverse complement sequence

AAAGAAGAGGGACATCGCCATGCTTAAAGAGATGTCGGAGGCAACGGCCCGACAGTGGGAGGTAGACACGAGTTGGAGGTGAGGCATCGGCGGCCACATC[G/A]
AAGCCACGGAGATGGAGGAGGATGATGGGTTGGCCTTGATGACGGGGGCAAACCAGAGCTTATGGTTAGGAGACGATGATTAGTGGTGACGGATCCAACG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: