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Detailed information for vg0234905499:

Variant ID: vg0234905499 (JBrowse)Variation Type: INDEL
Chromosome: chr02Position: 34905499
Reference Allele: TGATTCAAlternative Allele: T
Primary Allele: TGATTCASecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


ATACTTTAGGATAAACCATCCTTAAAGAACTTGGATTACCCTTGTATAATGACTGTGTTGGCGGCAAGGAAGAATCACATCCAGAGGTATCAATAGCATA[TGATTCA/T]
GAAGAAAGCTTGCCGTTAGGTGATTCACTTTTGTTGATATAAAGATCTGATGTAAAGTTGGAAGCTAACATACACATTGGAGTAGAAGCATCAAATGAGT

Reverse complement sequence

ACTCATTTGATGCTTCTACTCCAATGTGTATGTTAGCTTCCAACTTTACATCAGATCTTTATATCAACAAAAGTGAATCACCTAACGGCAAGCTTTCTTC[TGAATCA/A]
TATGCTATTGATACCTCTGGATGTGATTCTTCCTTGCCGCCAACACAGTCATTATACAAGGGTAATCCAAGTTCTTTAAGGATGGTTTATCCTAAAGTAT

Allele Frequencies:

Allele Effect: