Variant (rsID / SNP)

rs8177832

rs8177832 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOBEC3G. Location: chromosome 22, position 39,477,566. The table records no clinical significance for this variant.

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Reference-table entries

APOBEC3GNot classified

Variant type: missense_variant
Chromosome / position: 22:39477566
HGVS: NM_021822.4,c.557A>G,p.His186Arg
Allele change: Missense_H119R

Associated conditions / phenotypes

Acquired Immunodeficiency Syndrome|Liver Cirrhosis|Hepatocellular Carcinoma|Hepatitis B|Hepatitis

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.