12:21636438 G / T

dbSNP
Not found in dbSNP
Allele Frequency
0.000416
Allele Count
1 / 2404
UCSC
12-21636438-G-T
ClinVar
Click to search for variant in Clinvar
gnomAD Browser
Click to search for variant in gnomAD Browser
Site Quality
220.46
Filter Status
PASS
 Note: These are site-level quality metrics: they may be unpredictable for multi-allelic sites.
Population Frequencies
Population Allele Count Allele Number Number of Homozygotes Number of Heterozygotes Homozygous Genotype Freq. Heterozygous Genotype Freq. Allele Frequency
Arab 0 204 0 0 0.0 0.0 0
Azeri 0 200 0 0 0.0 0.0 0
Baloch 0 202 0 0 0.0 0.0 0
Gilaki 0 198 0 0 0.0 0.0 0
Kurd 0 200 0 0 0.0 0.0 0
Lur 1 200 0 1 0.0 0.01 0.005
Mazani 0 200 0 0 0.0 0.0 0
Persian 0 200 0 0 0.0 0.0 0
Persian Gulf Islander 0 200 0 0 0.0 0.0 0
Sistani 0 200 0 0 0.0 0.0 0
Turkmen 0 200 0 0 0.0 0.0 0
Zartoshti 0 200 0 0 0.0 0.0 0
Total 1 2404 0 1 0.0 0.0008319467554076539 0.000416
Annotations

This variant falls on 4 transcripts in 1 genes:

Note: This list may not include additional transcripts in the same gene that the variant does not overlap.

Additional Annotations
Metric Prediction
SIFT Pred (C) Damaging
Polyphen2 HVAR Pred (C) Probably damaging
MutationTaster Pred (C) Damaging
MutationAssessor Pred (C) Predicted functional (high)
FATHMM Pred (C) Tolerated
FATHMM MKL Coding Pred (C) Damaging
N of 6 Predicted Damaging 5 of 6 Predicted as Damaging
N of 6 Predicted Tolerated 1 of 6 Predicted as Tolerated
MetaSVM Pred Damaging
MetaLR Pred Tolerated
GERP++ RS 4.67
CADD Score (Phred Scale) 29
Ada Score ?
RF Score ?
PDIVAS Score ?
ConSplice Score ?
REVEL Score 0.614

Quality Metrics

Note: Plot may include low-quality genotypes that were excluded from allele counts in the table above