Variant (rsID / SNP)

rs10431309

rs10431309 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOBEC1. Location: chromosome 12, position 7,803,646. The table records no clinical significance for this variant.

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Reference-table entries

APOBEC1Not classified

Variant type: synonymous_variant
Chromosome / position: 12:7803646
HGVS: NM_001304566.1,c.534C>T,p.Tyr178Tyr
Allele change: Synonymous_Y133Y

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.