Variant (rsID / SNP)

rs149397148

rs149397148 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP10B. Location: chromosome 5, position 160,061,565. The table records no clinical significance for this variant.

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Reference-table entries

ATP10BNot classified

Variant type: missense_variant
Chromosome / position: 5:160061565
HGVS: NM_001366652.1,c.1177G>T,p.Gly393Trp
Allele change: Missense_G393W

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.