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7:99367392 C / G


Filter Status
PASS
dbSNP
rs4986908
Allele Frequency
0.001723
Filtering AF
0.002123 (European (Non-Finnish))
Allele Count
209 / 121320
UCSC
7-99367392-C-G
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 2 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) 162 66704 1 0.002429
East Asian 1 8640 0 0.0001157
Other 1 908 0 0.001101
African 18 10406 0 0.00173
Latino 4 11540 0 0.0003466
South Asian 19 16512 0 0.001151
European (Finnish) 4 6610 0 0.0006051
Total 209 121320 1 0.001723

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.