Variant (rsID / SNP)
rs2227857
rs2227857 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRKCA. Location: chromosome 17, position 64,685,078. The table records no clinical significance for this variant.
Reference-table entries
PRKCANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:64685078
- HGVS
- NM_002737.3,c.831G>A,p.Leu277Leu
- Allele change
- Synonymous_L277L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.