Variant (rsID / SNP)

rs9934227

rs9934227 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TEPP. Location: chromosome 16, position 58,019,396. The table records no clinical significance for this variant.

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Reference-table entries

TEPPNot classified

Variant type: missense_variant
Chromosome / position: 16:58019396
HGVS: NM_199046.3,c.614G>A,p.Ser205Asn
Allele change: Missense_S260N

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.