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14:34269721 C / T


Warning! This variant is only covered in 3014 individuals (adjusted allele number = 6028).
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
rs10141940
Allele Frequency
0.1281
Filtering AF
0.1484 (European (Non-Finnish))
Allele Count
772 / 6028
UCSC
14-34269721-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 6 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) 225 1354 17 0.1662
East Asian 1 84 0 0.0119
Other 12 74 1 0.1622
African 13 114 1 0.114
Latino 4 46 0 0.08696
South Asian 516 4352 29 0.1186
European (Finnish) 1 4 0 0.25
Total 772 6028 48 0.1281

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.