Variant (rsID / SNP)
rs17310144
rs17310144 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC14. Location: chromosome 3, position 123,665,902. The table records no clinical significance for this variant.
Reference-table entries
CCDC14Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:123665902
- HGVS
- NM_001366335.1,c.949A>C,p.Thr317Pro
- Allele change
- Missense_T324P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.