Interested in working on the development of this resource? Apply here.

8:145740627 C / T


Warning! This variant is only covered in 23038 individuals (adjusted allele number = 46076).
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
rs117642173
Allele Frequency
0.0001302
Filtering AF
0.000104 (European (Non-Finnish))
Allele Count
6 / 46076
UCSC
8-145740627-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.

Population Frequencies
Population Allele Count Allele Number Number of Homozygotes Allele Frequency
European (Non-Finnish) 6 24964 0 0.0002403
East Asian 0 2540 0 0
Other 0 360 0 0
African 0 3986 0 0
Latino 0 2484 0 0
South Asian 0 9600 0 0
European (Finnish) 0 2142 0 0
Total 6 46076 0 0.0001302

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.