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8:22880162 G / C


Filter Status
PASS
dbSNP
rs1047275
Allele Frequency
0.5331
Filtering AF
0.59 (European (Non-Finnish))
Allele Count
64364 / 120740
UCSC
8-22880162-G-C
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 10 transcripts in 3 genes:

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) 39538 66456 11811 0.595
East Asian 4046 8568 944 0.4722
Other 523 906 152 0.5773
African 2956 10326 436 0.2863
Latino 5996 11456 1542 0.5234
South Asian 6754 16448 1412 0.4106
European (Finnish) 4551 6580 1563 0.6916
Total 64364 120740 17860 0.5331

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.