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

22:20230301 G / A


Filter Status
PASS
dbSNP
rs74315508
Allele Frequency
0.0003422
Filtering AF
0.00102 (Latino)
Allele Count
40 / 116898
UCSC
22-20230301-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 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) 13 63926 0 0.0002034
East Asian 0 8520 0 0
Other 1 844 0 0.001185
African 8 9690 0 0.0008256
Latino 18 11402 0 0.001579
South Asian 0 16470 0 0
European (Finnish) 0 6046 0 0
Total 40 116898 0 0.0003422

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.