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X:153001998 C / T

Warning! This variant is only covered in 29590 individuals (adjusted allele number = 59181).
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
rs73633774
Allele Frequency
0.008178
Filtering AF
0.0668 (African)
Allele Count
484 / 59181
UCSC
X-153001998-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 3 transcripts in 2 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 Number of Hemizygotes Allele Frequency
European (Non-Finnish) 4 31866 0 2 0.0001255
East Asian 0 4507 0 0 0
Other 0 377 0 0 0
African 455 6295 7 104 0.07228
Latino 24 6454 0 3 0.003719
South Asian 1 7565 0 1 0.0001322
European (Finnish) 0 2117 0 0 0
Total 484 59181 7 110 0.008178
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.