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11:67925546 T / C


Filter Status
PASS
dbSNP
rs144458991
Allele Frequency
0.002809
Filtering AF
0.003948 (European (Non-Finnish))
Allele Count
341 / 121410
UCSC
11-67925546-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 3 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) 291 66740 0 0.00436
East Asian 0 8654 0 0
Other 0 908 0 0
African 10 10404 0 0.0009612
Latino 20 11578 0 0.001727
South Asian 17 16512 1 0.00103
European (Finnish) 3 6614 0 0.0004536
Total 341 121410 1 0.002809

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.