Variant (rsID / SNP)

rs1088680

rs1088680 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRKCH. Location: chromosome 14, position 61,997,226. The table records no clinical significance for this variant.

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Reference-table entries

PRKCHNot classified

Variant type: synonymous_variant
Chromosome / position: 14:61997226
HGVS: NM_006255.5,c.1674C>T,p.Asn558Asn
Allele change: Synonymous_N558N

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.