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Detailed information for vg1011049314:

Variant ID: vg1011049314 (JBrowse)Variation Type: SNP
Chromosome: chr10Position: 11049314
Reference Allele: TAlternative Allele: C
Primary Allele: TSecondary Allele: C

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CAAATCATCATCTGGGAGACCTTTTCTAAGAAGGGTAATTTGAAACCATGCCATTATAATTTTGCAAAGTTTGAGATATGCCATCGGTATCTCAATGACA[T/C]
GTAGGACCCACATGAGTCAATAACAGCATATATCAAATTTTGTAAAATTATAATGGCATGGTTTCAATTTTCCCTTTTAAGAAAGGGTGGTTATAAAGTA

Reverse complement sequence

TACTTTATAACCACCCTTTCTTAAAAGGGAAAATTGAAACCATGCCATTATAATTTTACAAAATTTGATATATGCTGTTATTGACTCATGTGGGTCCTAC[A/G]
TGTCATTGAGATACCGATGGCATATCTCAAACTTTGCAAAATTATAATGGCATGGTTTCAAATTACCCTTCTTAGAAAAGGTCTCCCAGATGATGATTTG

Allele Frequencies:

Allele Effect:

Putative Genotype-Phenotype Associations: