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5:131705800 C / T


Filter Status
PASS
dbSNP
rs202088921
Allele Frequency
0.0005515
Filtering AF
0.000727 (European (Non-Finnish))
Allele Count
55 / 99736
UCSC
5-131705800-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 7 transcripts in 3 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) 51 54742 0 0.0009316
East Asian 0 7222 0 0
Other 0 710 0 0
African 0 7900 0 0
Latino 1 9520 0 0.000105
South Asian 1 15278 0 6.545e-05
European (Finnish) 2 4364 0 0.0004583
Total 55 99736 0 0.0005515

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.