Variant (rsID / SNP)
rs11866002
rs11866002 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNOT1. Location: chromosome 16, position 58,587,737. The table records no clinical significance for this variant.
Reference-table entries
CNOT1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 16:58587737
- HGVS
- NM_016284.5,c.2919G>A,p.Gln973Gln
- Allele change
- Synonymous_Q968Q
Associated conditions / phenotypes
Osteogenic Sarcoma|Leukemia, Chronic Lymphocytic
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.