Search for Variation information by Variation ID:

Please input a variation ID (e.g., vg0722097923 , STR0500036000 ).

Detailed information for vg0504952991:

Variant ID: vg0504952991 (JBrowse)Variation Type: SNP
Chromosome: chr05Position: 4952991
Reference Allele: AAlternative Allele: T
Primary Allele: ASecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GAAGCCAGAAGCTGGGTTTCAGAGCTTTTCCAGATTCTCAGAAGCTGGCTACCAAACAGCTGCTTTTCAGAATCTAAAGCTCCCCCAAACAGACCTAAAA[A/T]
CTACCTACAGCCGATAGATGACTATGGTCATGTTTCTTCCTTCTCTTTTACTTTTTGATTCACGTGATCCTACTTCTAGATTTTGGTTTTGTGAAGCTAA

Reverse complement sequence

TTAGCTTCACAAAACCAAAATCTAGAAGTAGGATCACGTGAATCAAAAAGTAAAAGAGAAGGAAGAAACATGACCATAGTCATCTATCGGCTGTAGGTAG[T/A]
TTTTAGGTCTGTTTGGGGGAGCTTTAGATTCTGAAAAGCAGCTGTTTGGTAGCCAGCTTCTGAGAATCTGGAAAAGCTCTGAAACCCAGCTTCTGGCTTC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: