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Detailed information for vg0301337606:

Variant ID: vg0301337606 (JBrowse)	Variation Type: SNP
Chromosome: chr03	Position: 1337606
Reference Allele: C	Alternative Allele: A
Primary Allele: C	Secondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:

CATGATTTTGTTTTCGAAGAAAGCTTGATAAAAATCTGATTAGCTTCCACCCACCCCTCGATTTAGAATTAAATTGGGTTTGATCCCTCATGGGGATGTT[C/A]
TCTCATTATTTGCATATAATATATCACTCCACAAACATGCAAGTTCATATTCAACTTCTATATCTTGTAAAAAAACCAAATTTGATTATGAATATACGTT

Reverse complement sequence

AACGTATATTCATAATCAAATTTGGTTTTTTTACAAGATATAGAAGTTGAATATGAACTTGCATGTTTGTGGAGTGATATATTATATGCAAATAATGAGA[G/T]
AACATCCCCATGAGGGATCAAACCCAATTTAATTCTAAATCGAGGGGTGGGTGGAAGCTAATCAGATTTTTATCAAGCTTTCTTCGAAAACAAAATCATG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: