Variant (rsID / SNP)

rs958912

rs958912 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP10B. Location: chromosome 5, position 160,097,496. The table records no clinical significance for this variant.

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Reference-table entries

ATP10BNot classified

Variant type: missense_variant
Chromosome / position: 5:160097496
HGVS: NM_001366652.1,c.649T>C,p.Cys217Arg
Allele change: Missense_C217R

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.