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10:96741053 A / C


Filter Status
PASS
dbSNP
rs1057910
Allele Frequency
0.06371
Filtering AF
0.1089 (South Asian)
Allele Count
7725 / 121260
UCSC
10-96741053-A-C
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) 4591 66710 171 0.06882
East Asian 292 8642 6 0.03379
Other 60 908 3 0.06608
African 131 10404 2 0.01259
Latino 411 11480 10 0.0358
South Asian 1868 16512 128 0.1131
European (Finnish) 372 6604 16 0.05633
Total 7725 121260 336 0.06371

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.