Variant (rsID / SNP)
rs2302212
rs2302212 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NCAPG. Location: chromosome 4, position 17,818,885. The table records no clinical significance for this variant.
Reference-table entries
NCAPGNot classified
- Variant type
- splice_region_variant&synonymous_variant
- Chromosome / position
- 4:17818885
- HGVS
- NM_022346.5,c.777T>C,p.Asp259Asp
- Allele change
- Synonymous_D259D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.