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Detailed information for vg0621146125:

Variant ID: vg0621146125 (JBrowse)Variation Type: SNP
Chromosome: chr06Position: 21146125
Reference Allele: TAlternative Allele: C
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TTTACAAGGGTTACGCCGTTATCATAATCGGAATGTTCGATCGCGAGCCTTTTTAGTCGGCGACCTGGTTCTGAGGAGAATTCAAACTACACAGGATCGG[T/C]
ATAAGTTATCTCCCTTGTGGGAAGGACCGTTCATAATCGCTGAAGTTACTCGGCCAGGTTCTTACCGACTCAAGCGTGAAGATGGTACTCTTGTCAACAA

Reverse complement sequence

TTGTTGACAAGAGTACCATCTTCACGCTTGAGTCGGTAAGAACCTGGCCGAGTAACTTCAGCGATTATGAACGGTCCTTCCCACAAGGGAGATAACTTAT[A/G]
CCGATCCTGTGTAGTTTGAATTCTCCTCAGAACCAGGTCGCCGACTAAAAAGGCTCGCGATCGAACATTCCGATTATGATAACGGCGTAACCCTTGTAAA

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: