Genomes | |
---|---|
Filters | Pass |
Allele Count | 34 |
Allele Number | 152010 |
Allele Frequency | 0.0002237 |
Grpmax Filtering AF (95% confidence) | 0.001414 Admixed American |
Number of homozygotes | 0 |
Mean depth of coverage | 31.8 |
Note Local ancestry data is available for this variant by selecting the tab below. See our blog post on local ancestry inference for Admixed American samples in gnomAD for more information.
30 | 15270 | 0 | 0.001965 | ||
1 | 5186 | 0 | 0.0001928 | ||
3 | 41354 | 0 | 0.00007254 | ||
0 | 68008 | 0 | 0.000 | ||
0 | 10590 | 0 | 0.000 | ||
0 | 912 | 0 | 0.000 | ||
0 | 316 | 0 | 0.000 | ||
0 | 4818 | 0 | 0.000 | ||
0 | 3468 | 0 | 0.000 | ||
0 | 2088 | 0 | 0.000 | ||
XX | 12 | 77780 | 0 | 0.0001543 | |
XY | 22 | 74230 | 0 | 0.0002964 | |
Total | 34 | 152010 | 0 | 0.0002237 |
This variant falls on 11 transcripts in 1 gene.
Note The gene symbols shown below are provided by VEP and may differ from the symbol shown on gene pages.
Transcript-specific predictors SIFT and Polyphen are listed with Variant Effect Predictor annotations.
Note This variant has multiple REVEL scores
Genomic constraint values displayed are for the region: 3-134545000-134546000
Read more about this constraint.
Expected | Observed | Constraint |
---|---|---|
190.5 | 191 | Z = -0.03 o/e = 1 |
View the genomic constraint values for the 40kb region surrounding this variant: 3-134525602-134565602
or find more information on the ClinVar website. Data displayed here is from ClinVar's February 1, 2025 release.
Value: 2.393e+4 (genome samples)
Site quality approximation for all variants with 0.0002 <= AF < 0.0005.