Interested in working on the development of this resource? Apply here.

11:68201295 C / T


Filter Status
PASS
dbSNP
rs3736228
Allele Frequency
0.1392
Filtering AF
0.2109 (East Asian)
Allele Count
15218 / 109350
UCSC
11-68201295-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 3 transcripts in 1 genes:

missense
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) 8393 59644 564 0.1407
East Asian 1766 8048 179 0.2194
Other 91 776 7 0.1173
African 416 8806 8 0.04724
Latino 2135 10682 208 0.1999
South Asian 2126 15974 164 0.1331
European (Finnish) 291 5420 9 0.05369
Total 15218 109350 1139 0.1392

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.