Variant (rsID / SNP)

rs1219725

rs1219725 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CPXM2. Location: chromosome 10, position 125,528,048. The table records no clinical significance for this variant.

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Reference-table entries

CPXM2Not classified

Variant type: synonymous_variant
Chromosome / position: 10:125528048
HGVS: NM_198148.3,c.1293C>T,p.Tyr431Tyr
Allele change: Synonymous_Y431Y

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.