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X:152990761 A / G


Warning! This variant is only covered in 1771 individuals (adjusted allele number = 3543).
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
Not found in dbSNP
Allele Frequency
0.0002822
Allele Count
1 / 3543
UCSC
X-152990761-A-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 11 transcripts in 2 genes:

missense
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 1383 0 0 0
East Asian 0 124 0 0 0
Other 0 38 0 0 0
African 0 371 0 0 0
Latino 0 54 0 0 0
South Asian 1 1571 0 1 0.0006365
European (Finnish) 0 2 0 0 0
Total 1 3543 0 1 0.0002822

Read Data

This interactive IGV.js visualization shows reads that went into calling this variant.