The ExAC browser will be decommissioned in December. ExAC data is available in the gnomAD browser.

16:55731946 G / A


Filter Status
PASS
dbSNP
rs998424
Allele Frequency
0.3037
Filtering AF
0.4143 (Latino)
Allele Count
36870 / 121386
UCSC
16-55731946-G-A
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 9 transcripts in 1 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) 22379 66734 3791 0.3353
East Asian 2541 8644 373 0.294
Other 242 908 36 0.2665
African 1165 10406 70 0.112
Latino 4911 11576 1077 0.4242
South Asian 3302 16512 342 0.2
European (Finnish) 2330 6606 415 0.3527
Total 36870 121386 6104 0.3037

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.