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Detailed information for vg0420986488:

Variant ID: vg0420986488 (JBrowse)Variation Type: SNP
Chromosome: chr04Position: 20986488
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GTCAGCTGTAGCCTGGAAGTAAAGCAATCGTCAGTTTCTTTTGAGGTTGCTCTGTCTTCTGATTGTTTGCCTGGGTATGAATATTACCTTGTGATTTTCA[C/T]
GTTGCTACGTAGAAGATCTGAAAGGATTCGATCCATCTTTTTCCTTGTGTCTTACTAAAAGAAATTAGCATGCAGTATGCGAAATGTTAAGTTTGCTTAT

Reverse complement sequence

ATAAGCAAACTTAACATTTCGCATACTGCATGCTAATTTCTTTTAGTAAGACACAAGGAAAAAGATGGATCGAATCCTTTCAGATCTTCTACGTAGCAAC[G/A]
TGAAAATCACAAGGTAATATTCATACCCAGGCAAACAATCAGAAGACAGAGCAACCTCAAAAGAAACTGACGATTGCTTTACTTCCAGGCTACAGCTGAC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: