Interested in working on the development of this resource? Apply here.

8:22886020 A / G


Filter Status
PASS
dbSNP
rs13265018
Allele Frequency
0.8899
Filtering AF
0.963 (East Asian)
Allele Count
108041 / 121406
UCSC
8-22886020-A-G
ClinVar
Click to search for variant in Clinvar
Note: Plot may include low-quality genotypes that were excluded from allele counts in the table above

Note: These are site-level quality metrics: they may be unpredictable for multi-allelic sites.

Annotations

This variant falls on 8 transcripts in 1 genes:

missense non coding transcript exon
Note: This list may not include additional transcripts in the same gene that the variant does not overlap.
Population Frequencies
Population Allele Count Allele Number Number of Homozygotes Allele Frequency
European (Non-Finnish) 60172 66738 27138 0.9016
East Asian 8485 8654 4158 0.9805
Other 823 908 372 0.9064
African 7817 10406 2955 0.7512
Latino 10288 11574 4591 0.8889
South Asian 14295 16512 6224 0.8657
European (Finnish) 6161 6614 2871 0.9315
Total 108041 121406 48309 0.8899

Read Data

This interactive IGV.js visualization shows reads that went into calling this variant.
Note: These are reassembled reads produced by GATK HaplotypeCaller --bamOutput so they accurately represent what HaplotypeCaller was seeing when it called this variant.