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11:108124761 T / C


Filter Status
PASS
dbSNP
rs4986761
Allele Frequency
0.007927
Filtering AF
0.01039 (European (Non-Finnish))
Allele Count
947 / 119470
UCSC
11-108124761-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 5 transcripts in 1 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) 727 65788 6 0.01105
East Asian 2 8534 0 0.0002344
Other 10 896 0 0.01116
African 20 9844 0 0.002032
Latino 65 11416 0 0.005694
South Asian 91 16404 1 0.005547
European (Finnish) 32 6588 0 0.004857
Total 947 119470 7 0.007927

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.