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10:73550117 C / G


Filter Status
PASS
dbSNP
rs11592462
Allele Frequency
0.4291
Filtering AF
0.5124 (South Asian)
Allele Count
51084 / 119038
UCSC
10-73550117-C-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 1 transcripts in 1 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 Allele Frequency
European (Non-Finnish) 31976 65854 7665 0.4856
East Asian 1400 8536 101 0.164
Other 411 886 100 0.4639
African 2766 9556 379 0.2895
Latino 3183 11396 456 0.2793
South Asian 8572 16432 2272 0.5217
European (Finnish) 2776 6378 575 0.4352
Total 51084 119038 11548 0.4291

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.