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

X:153006177 G / A


Warning! This variant is only covered in 43016 individuals (adjusted allele number = 86033).
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
rs193922095
Allele Frequency
0.0003022
Allele Count
26 / 86033
UCSC
X-153006177-G-A
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) 0 46863 0 0 0
East Asian 0 6597 0 0 0
Other 0 618 0 0 0
African 6 8235 0 0 0.0007286
Latino 0 9271 0 0 0
South Asian 20 10070 0 14 0.001986
European (Finnish) 0 4379 0 0 0
Total 26 86033 0 14 0.0003022

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.