Variant (rsID / SNP)
rs2465647
rs2465647 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USP28. Location: chromosome 11, position 113,679,119. The table records no clinical significance for this variant.
Reference-table entries
USP28Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:113679119
- HGVS
- NM_001400785.1,c.2208G>A,p.Ser736Ser
- Allele change
- Synonymous_S709S
Associated conditions / phenotypes
Synonymous_S448S|Synonymous_S735S|Synonymous_S611S|Synonymous_S610S|Synonymous_S610S|Synonymous_S736S|Synonymous_S735S|Synonymous_S732S|Synonymous_S383S|Synonymous_S709S|Synonymous_S383S|Synonymous_S402S|Synonymous_S402S|Synonymous_S383S|Synonymous_S383S|Synonymous_S610S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.