Interested in working on the development of this resource? Apply here.

11:18632984 T / C


Filter Status
PASS
dbSNP
rs10128711
Allele Frequency
0.6354
Filtering AF
0.7236 (European (Non-Finnish))
Allele Count
76600 / 120560
UCSC
11-18632984-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) 48338 66302 17600 0.7291
East Asian 4264 8528 1069 0.5
Other 573 898 187 0.6381
African 2057 10336 227 0.199
Latino 7175 11442 2246 0.6271
South Asian 10274 16486 3251 0.6232
European (Finnish) 3919 6568 1143 0.5967
Total 76600 120560 25723 0.6354

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.