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

10:96708974 A / G


Filter Status
PASS
dbSNP
rs2256871
Allele Frequency
0.006715
Filtering AF
0.07097 (African)
Allele Count
810 / 120634
UCSC
10-96708974-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 2 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) 11 66486 0 0.0001654
East Asian 1 8538 0 0.0001171
Other 2 904 0 0.002212
African 772 10242 21 0.07538
Latino 22 11382 0 0.001933
South Asian 2 16498 0 0.0001212
European (Finnish) 0 6584 0 0
Total 810 120634 21 0.006715

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.