Variant (rsID / SNP)

rs2076101

rs2076101 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOBEC3F. Location: chromosome 22, position 39,445,554. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

APOBEC3FNot classified

Variant type: missense_variant
Chromosome / position: 22:39445554
HGVS: NM_145298.6,c.691G>A,p.Val231Ile
Allele change: Missense_V231I

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.