Variant (rsID / SNP)
rs1135352
rs1135352 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTPN14. Location: chromosome 1, position 214,542,819. The table records no clinical significance for this variant.
Reference-table entries
PTPN14Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 1:214542819
- HGVS
- NM_005401.5,c.3252A>G,p.Glu1084Glu
- Allele change
- Synonymous_E1084E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.