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8:6735399 C / T


Filter Status
PASS
dbSNP
rs11362
Allele Frequency
0.4254
Filtering AF
0.4377 (South Asian)
Allele Count
51515 / 121108
UCSC
8-6735399-C-T
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 2 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) 29017 66584 6381 0.4358
East Asian 3254 8626 601 0.3772
Other 402 908 90 0.4427
African 3189 10376 502 0.3073
Latino 4545 11514 889 0.3947
South Asian 7360 16494 1678 0.4462
European (Finnish) 3748 6606 1073 0.5674
Total 51515 121108 11214 0.4254

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.