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SNV:4-153243324-G-C (GRCh37)
Dataset
- gnomAD v2.1.1
- GRCh38
- gnomAD v4.1.0807,162 samples
- gnomAD v4.1.0 (non-UKB)314,392 samples
- gnomAD v3.1.276,156 samples
- gnomAD v3.1.2 (non-cancer)74,023 samples
- gnomAD v3.1.2 (non-neuro)67,442 samples
- gnomAD v3.1.2 (non-v2)57,344 samples
- gnomAD v3.1.2 (non-TOPMed)40,433 samples
- gnomAD v3.1.2 (controls/biobanks)16,465 samples
- GRCh37
- gnomAD v2.1.1141,456 samples
- gnomAD v2.1.1 (non-TOPMed)135,743 samples
- gnomAD v2.1.1 (non-cancer)134,187 samples
- gnomAD v2.1.1 (non-neuro)114,704 samples
- gnomAD v2.1.1 (controls)60,146 samples
- ExAC60,706 samples
| Exomes | Genomes | Total | |
|---|---|---|---|
| Filters | No variant | Pass | |
| Allele Count | 50 | 50 | |
| Allele Number | 31356 | 31356 | |
| Allele Frequency | 0.001595 | 0.001595 | |
| Grpmax Filtering AF (95% confidence) | 0.002074 European (non-Finnish) | ||
| Number of homozygotes | 0 | 0 | |
| Mean depth of coverage | – | 29.7 |
External Resources
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Report an issue with this variantGenetic Ancestry Group Frequencies
| 42 | 15398 | 0 | 0.002728 | ||
| 2 | 1082 | 0 | 0.001848 | ||
| 1 | 848 | 0 | 0.001179 | ||
| 5 | 8710 | 0 | 0.0005741 | ||
| 0 | 290 | 0 | 0.000 | ||
| 0 | 1560 | 0 | 0.000 | ||
| 0 | 3468 | 0 | 0.000 | ||
| 0 | 0 | 0 | - | ||
| XX | 19 | 13906 | 0 | 0.001366 | |
| XY | 31 | 17450 | 0 | 0.001777 | |
| Total | 50 | 31356 | 0 | 0.001595 | |
* Allele frequencies for some sub-continental populations were not computed for genome samples.
Include:
Related Variants
Liftover
This variant lifts over to the following GRCh38 variant:
- 4-152322172-G-C
View variant in gnomAD v4.1.0
Variant Co-occurrence
Check if this variant occurs on the same haplotype as another variant.
Nearby Variants
Variant Effect Predictor
This variant falls on 3 transcripts in 1 gene.
Note The gene symbols shown below are provided by VEP and may differ from the symbol shown on gene pages.
3' UTR
FBXW7
- ENST00000281708.4Ensembl canonical transcript for FBXW7
- HGVSc
- c.*709C>G
- ENST00000263981.5
- HGVSc
- c.*709C>G
- ENST00000296555.5
- HGVSc
- c.*709C>G
- ENST00000281708.4
Age Distribution
- Exome
- Genome
- Variant carriers
- All individuals
Genotype Quality Metrics
- Genotype quality
- Depth
- Allele balance for heterozygotes
- Exome
- Genome
- Variant carriers
- All individuals
Note: This plot may include low-quality genotypes that were excluded from allele counts in the tables above.
Site Quality Metrics
- Metric distribution
- All metric values
- Exome
- Genome
Value: 2.476e+4 (genome samples)
This is the site quality distribution for all genome variants with 0.001 <= AF < 0.002.
Note: These are site-level quality metrics, they may be unpredictable for multi-allelic sites.
Read Data
Always load read data