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Detailed information for vg1000973578:

Variant ID: vg1000973578 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 973578
Reference Allele: TAlternative Allele: C
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GAACGGGAAGAATCTGAGTTTATATCATCTTCCAGAGCATTGAAATCAGATTCAGTAATTTTGCTGCCAGGGATAAGGATTTTTTATATACCTGCCAACT[T/C]
CTTCAGCCTTTTAGCCGATTTTCCCCTTTGTTTGCCAATTCCCATTCGATGATCAAATTTGAGCTCTTGGTTGGCATTAAGAAGCCTAGAGCTCTACCTT

Reverse complement sequence

AAGGTAGAGCTCTAGGCTTCTTAATGCCAACCAAGAGCTCAAATTTGATCATCGAATGGGAATTGGCAAACAAAGGGGAAAATCGGCTAAAAGGCTGAAG[A/G]
AGTTGGCAGGTATATAAAAAATCCTTATCCCTGGCAGCAAAATTACTGAATCTGATTTCAATGCTCTGGAAGATGATATAAACTCAGATTCTTCCCGTTC

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: