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4:110638810 C / T


Filter Status
PASS
dbSNP
rs2285714
Allele Frequency
0.3725
Filtering AF
0.421 (European (Non-Finnish))
Allele Count
45212 / 121386
UCSC
4-110638810-C-T
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 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) 28372 66734 6097 0.4252
East Asian 1974 8642 235 0.2284
Other 324 908 59 0.3568
African 764 10406 28 0.07342
Latino 4541 11572 905 0.3924
South Asian 6695 16510 1379 0.4055
European (Finnish) 2542 6614 496 0.3843
Total 45212 121386 9199 0.3725

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.