Variant: 22-42127852-C-T(GRCh38)

Allele Count: 2
Allele Number: 5976
Allele Frequency: 3.3467e-4
Number of Homozygotes: 0

Reference:

dbSNP: rs79292917

gnomAD: 22-42127852-C-T

Browser:

Genotype Quality Metrics

Site Quality Metrics

External data population frequency
DatasetPopulationPopulation abbrAllele Frequency
1KGP3East AsianEAS0.0
South AsianSAS0.0
AfricanAFR0.0
AmericasAMR1.4000e-3
European ancestryEUR2.0000e-3
total5.9904e-4
gnomAD v3 GenomesEast AsianEAS0.0
South AsianSAS0.0
AficanAFR9.6353e-4
LatinoAMR1.0309e-3
AmishAMI0.0134
European(Finnish)FIN3.2523e-3
European(non-Finnish)NFE4.1063e-3
Ashkenazi JewishASJ1.2034e-3
otherOTH1.8657e-3
total2.6133e-3

Region annotation
RegionGene IDGene DetailExonic functionConsequence
EnsemblexonicCYP2D6-synonymous SNVCYP2D6:ENST00000359033.4:exon5:c.G822A:p.P274P,CYP2D6:ENST00000389970.7:exon6:c.G909A:p.P303P
RefSeqexonicCYP2D6;CYP2D7-synonymous SNVCYP2D6:NM_001025161:exon5:c.G822A:p.P274P,CYP2D6:NM_000106:exon6:c.G975A:p.P325P

Nonsynonymous impact
MethodScoreRank Scorepredicted consequence
SIFT---
PolyPhen2_HDIV---
PolyPhen2_HVAR---
FATHMM---
CADD---

Clinical annotation
ClinVar SignificanceClinVar Disease NameClinVar Allele IDTag-value
----

Loss of function predict

Loss of Function (LoF) variants are indentified by package LOFTEE developed recently by gnomAD group to assess stop-gained, splice site disrupting and frameshift variants as “low-confidence” (LC) or “high-confidence” (HC) LoF variants.

LoFLoF_filterLoF_flagsLoF_info
----

Pharmacogenomics
Belong to HaplotypeDrugGuideineURLCPIC_LevelPharmGKB_Level_of_EvidencePGx_on_
FDA_Label
CPIC_Publications
_PMID
CYP2D6*59atomoxetineCYP2D6 and Atomoxetinehttps://cpicpgx.org/cpic-guideline-for-atomoxetine-based-on-cyp2d6-genotype/A1AActionable PGx30801677
CYP2D6*59codeineCYP2D6 and Codeinehttps://cpicpgx.org/guidelines/guideline-for-codeine-and-cyp2d6/A1AActionable PGx22205192;24458010
CYP2D6*59ondansetronCYP2D6 and Ondansetron and Tropisetronhttps://cpicpgx.org/guidelines/guideline-for-ondansetron-and-tropisetron-and-cyp2d6-genotype/A1AInformative PGx28002639
CYP2D6*59tamoxifenCYP2D6 and Tamoxifenhttps://cpicpgx.org/guidelines/cpic-guideline-for-tamoxifen-based-on-cyp2d6-genotype/A1AActionable PGx29385237
CYP2D6*59fluvoxamineCYP2D6, CYP2C19 and Selective Serotonin Reuptake Inhibitorshttps://cpicpgx.org/guidelines/guideline-for-selective-serotonin-reuptake-inhibitors-and-cyp2d6-and-cyp2c19/A1AActionable PGx25974703
CYP2D6*59clomipramineCYP2D6, CYP2C19 and Tricyclic Antidepressantshttps://cpicpgx.org/guidelines/guideline-for-tricyclic-antidepressants-and-cyp2d6-and-cyp2c19/B1AActionable PGx23486447;27997040