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16:11374994 C / A


Filter Status
PASS
dbSNP
rs35576928
Allele Frequency
0.01009
Filtering AF
0.01315 (European (Non-Finnish))
Allele Count
1225 / 121400
UCSC
16-11374994-C-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 5 transcripts in 3 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) 927 66730 6 0.01389
East Asian 1 8654 0 0.0001156
Other 11 908 1 0.01211
African 21 10406 0 0.002018
Latino 16 11576 0 0.001382
South Asian 1 16512 0 6.056e-05
European (Finnish) 248 6614 5 0.0375
Total 1225 121400 12 0.01009

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.