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11:121393684 G / A


Filter Status
PASS
dbSNP
rs2298813
Allele Frequency
0.07219
Filtering AF
0.1153 (East Asian)
Allele Count
8733 / 120972
UCSC
11-121393684-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 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) 3220 66478 84 0.04844
East Asian 1045 8608 61 0.1214
Other 46 906 1 0.05077
African 1008 10334 59 0.09754
Latino 1339 11536 79 0.1161
South Asian 1787 16500 116 0.1083
European (Finnish) 288 6610 12 0.04357
Total 8733 120972 412 0.07219

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.