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SNV:9-21350078-A-T (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 | 5768 | 5768 | |
| Allele Number | 31368 | 31368 | |
| Allele Frequency | 0.1839 | 0.1839 | |
| Grpmax Filtering AF (95% confidence) | 0.2758 East Asian | ||
| Number of homozygotes | 556 | 556 | |
| Mean depth of coverage | – | 32.6 |
External Resources
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Report an issue with this variantGenetic Ancestry Group Frequencies
| 464 | 1556 | 69 | 0.2982 | ||
| 203 | 844 | 26 | 0.2405 | ||
| 61 | 290 | 5 | 0.2103 | ||
| 203 | 1084 | 20 | 0.1873 | ||
| 641 | 3470 | 72 | 0.1847 | ||
| 2734 | 15410 | 242 | 0.1774 | ||
| 1462 | 8714 | 122 | 0.1678 | ||
| 0 | 0 | 0 | - | ||
| XX | 2603 | 13912 | 254 | 0.1871 | |
| XY | 3165 | 17456 | 302 | 0.1813 | |
| Total | 5768 | 31368 | 556 | 0.1839 | |
* 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:
- 9-21350079-A-T
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 1 transcript 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
IFNA6
- ENST00000380210.1Ensembl canonical transcript for IFNA6
- HGVSc
- c.*239T>A
- ENST00000380210.1
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: 3.155e+6 (genome samples)
This is the site quality distribution for all genome variants with 0.1 <= AF < 0.2.
Note: These are site-level quality metrics, they may be unpredictable for multi-allelic sites.
Read Data
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