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14:34269775 C / G


Warning! This variant is only covered in 589 individuals (adjusted allele number = 1178).
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
rs10142034
Allele Frequency
0.1188
Filtering AF
0.1333 (European (Non-Finnish))
Allele Count
140 / 1178
UCSC
14-34269775-C-G
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) 30 162 1 0.1852
East Asian 0 22 0 0
Other 2 12 1 0.1667
African 5 22 1 0.2273
Latino 1 8 0 0.125
South Asian 102 952 4 0.1071
European (Finnish) 0 0 0 NA
Total 140 1178 7 0.1188

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.