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10:96702047 C / T


Filter Status
PASS
dbSNP
rs1799853
Allele Frequency
0.09144
Filtering AF
0.1246 (European (Non-Finnish))
Allele Count
11092 / 121310
UCSC
10-96702047-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 4 transcripts in 2 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) 8464 66730 546 0.1268
East Asian 3 8624 0 0.0003479
Other 86 908 3 0.09471
African 245 10406 3 0.02354
Latino 760 11516 20 0.066
South Asian 760 16512 25 0.04603
European (Finnish) 774 6614 54 0.117
Total 11092 121310 651 0.09144

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.