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11:18291289 T / C


Filter Status
PASS
dbSNP
rs1059559
Allele Frequency
0.0004943
Filtering AF
0.003659 (African)
Allele Count
60 / 121390
UCSC
11-18291289-T-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 4 transcripts in 2 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) 4 66718 0 5.995e-05
East Asian 2 8654 0 0.0002311
Other 0 908 0 0
African 49 10406 0 0.004709
Latino 5 11578 0 0.0004319
South Asian 0 16512 0 0
European (Finnish) 0 6614 0 0
Total 60 121390 0 0.0004943

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.