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13:32914592 C / T


Filter Status
PASS
dbSNP
rs1799954
Allele Frequency
0.003246
Filtering AF
0.004473 (European (Non-Finnish))
Allele Count
392 / 120780
UCSC
13-32914592-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 1 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) 326 66364 0 0.004912
East Asian 0 8650 0 0
Other 1 900 0 0.001111
African 20 10186 0 0.001963
Latino 44 11564 0 0.003805
South Asian 0 16504 0 0
European (Finnish) 1 6612 0 0.0001512
Total 392 120780 0 0.003246

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.