Variant (rsID / SNP)
rs28936673
rs28936673 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CPT2. Location: chromosome 1, position 53,679,173. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
CPT2Pathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:53679173
- Cytoband
- 1p32.3
- HGVS
- NM_000098.3(CPT2):c.1883A>C (p.Tyr628Ser)
- Allele change
- Missense_Y628S
Associated conditions / phenotypes
Carnitine palmitoyl transferase II deficiency, severe infantile form|Carnitine palmitoyltransferase II deficiency|Carnitine palmitoyl transferase II deficiency, myopathic form
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.