Variant: 22-42130761-C-T(GRCh38)

Allele Count: 8
Allele Number: 5978
Allele Frequency: 1.3382e-3
Number of Homozygotes: 0

Reference:

dbSNP: rs769258

gnomAD: 22-42130761-C-T

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Genotype Quality Metrics

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External data population frequency
DatasetPopulationPopulation abbrAllele Frequency
1KGP3East AsianEAS3.0000e-3
South AsianSAS6.1000e-3
AfricanAFR2.3000e-3
AmericasAMR0.0274
European ancestryEUR0.0527
total0.0168
gnomAD v3 GenomesEast AsianEAS3.5302e-3
South AsianSAS7.9681e-3
AficanAFR9.6233e-3
LatinoAMR0.0215
AmishAMI4.4543e-3
European(Finnish)FIN0.0700
European(non-Finnish)NFE0.0613
Ashkenazi JewishASJ0.0343
otherOTH0.0337
total0.0393

Region annotation
RegionGene IDGene DetailExonic functionConsequence
EnsemblexonicCYP2D6-nonsynonymous SNVCYP2D6:ENST00000359033.4:exon1:c.G31A:p.V11M
RefSeqexonicCYP2D6;CYP2D7-nonsynonymous SNVCYP2D6:NM_000106:exon1:c.G31A:p.V11M,CYP2D6:NM_001025161:exon1:c.G31A:p.V11M

Nonsynonymous impact
MethodScoreRank Scorepredicted consequence
SIFT0.110.291T
PolyPhen2_HDIV0.6430.386P
PolyPhen2_HVAR0.0240.190B
FATHMM2.690.123T
CADD0.2490.1185.192

Clinical annotation
ClinVar SignificanceClinVar Disease NameClinVar Allele IDTag-value
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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
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Pharmacogenomics
Belong to HaplotypeDrugGuideineURLCPIC_LevelPharmGKB_Level_of_EvidencePGx_on_
FDA_Label
CPIC_Publications
_PMID
CYP2D6*35atomoxetineCYP2D6 and Atomoxetinehttps://cpicpgx.org/cpic-guideline-for-atomoxetine-based-on-cyp2d6-genotype/A1AActionable PGx30801677
CYP2D6*35codeineCYP2D6 and Codeinehttps://cpicpgx.org/guidelines/guideline-for-codeine-and-cyp2d6/A1AActionable PGx22205192;24458010
CYP2D6*35ondansetronCYP2D6 and Ondansetron and Tropisetronhttps://cpicpgx.org/guidelines/guideline-for-ondansetron-and-tropisetron-and-cyp2d6-genotype/A1AInformative PGx28002639
CYP2D6*35tamoxifenCYP2D6 and Tamoxifenhttps://cpicpgx.org/guidelines/cpic-guideline-for-tamoxifen-based-on-cyp2d6-genotype/A1AActionable PGx29385237
CYP2D6*35fluvoxamineCYP2D6, CYP2C19 and Selective Serotonin Reuptake Inhibitorshttps://cpicpgx.org/guidelines/guideline-for-selective-serotonin-reuptake-inhibitors-and-cyp2d6-and-cyp2c19/A1AActionable PGx25974703
CYP2D6*35clomipramineCYP2D6, CYP2C19 and Tricyclic Antidepressantshttps://cpicpgx.org/guidelines/guideline-for-tricyclic-antidepressants-and-cyp2d6-and-cyp2c19/B1AActionable PGx23486447;27997040