Variant (rsID / SNP)
rs205498
rs205498 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM25. Location: chromosome 17, position 54,978,794. The table records no clinical significance for this variant.
Reference-table entries
TRIM25Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:54978794
- HGVS
- NM_005082.5,c.1073C>T,p.Pro358Leu
- Allele change
- Missense_P358L
Associated conditions / phenotypes
Measles
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.