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14:73664718 T / C


Warning! This variant is only covered in 46880 individuals (adjusted allele number = 93760).
This means that the site is covered in fewer than 80% of the individuals in ExAC, which may indicate a low-quality site.


Filter Status
PASS
dbSNP
rs3025786
Allele Frequency
0.04433
Filtering AF
0.06837 (European (Non-Finnish))
Allele Count
4156 / 93760
UCSC
14-73664718-T-C
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 10 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) 3434 48828 92 0.07033
East Asian 3 7042 0 0.000426
Other 29 738 1 0.0393
African 73 8300 0 0.008795
Latino 241 8850 3 0.02723
South Asian 194 14220 3 0.01364
European (Finnish) 182 5782 2 0.03148
Total 4156 93760 101 0.04433

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.