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

16:81399037 G / C

Filter Status
PASS
dbSNP
rs119485088
Allele Frequency
8.236e-06
Filtering AF
0 (None)
Allele Count
1 / 121412
UCSC
16-81399037-G-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 2 transcripts in 1 genes:

missense
non coding transcript exon
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) 1 66740 0 1.498e-05
East Asian 0 8654 0 0
Other 0 908 0 0
African 0 10406 0 0
Latino 0 11578 0 0
South Asian 0 16512 0 0
European (Finnish) 0 6614 0 0
Total 1 121412 0 8.236e-06
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.