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7:141673345 C / G


Filter Status
PASS
dbSNP
rs713598
Allele Frequency
0.4459
Filtering AF
0.669 (Latino)
Allele Count
54099 / 121330
UCSC
7-141673345-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 2 transcripts in 2 genes:

missense
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) 27101 66700 5496 0.4063
East Asian 5783 8634 1969 0.6698
Other 382 908 79 0.4207
African 4908 10398 1121 0.472
Latino 7884 11568 2735 0.6815
South Asian 5763 16508 1039 0.3491
European (Finnish) 2278 6614 403 0.3444
Total 54099 121330 12842 0.4459

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.