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8:145729727 C / A


Filter Status
PASS
dbSNP
rs1063739
Allele Frequency
0.4747
Filtering AF
0.5673 (Latino)
Allele Count
56541 / 119100
UCSC
8-145729727-C-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 18 transcripts in 5 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) 30664 65406 7096 0.4688
East Asian 4224 8548 1046 0.4942
Other 423 876 111 0.4829
African 2362 10130 287 0.2332
Latino 6607 11412 1913 0.579
South Asian 9187 16474 2621 0.5577
European (Finnish) 3074 6254 691 0.4915
Total 56541 119100 13765 0.4747

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.