Variant (rsID / SNP)
rs1264581
rs1264581 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM39. Location: chromosome 6, position 30,297,505. The table records no clinical significance for this variant.
Reference-table entries
TRIM39Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:30297505
- HGVS
- NM_021253.4,c.411C>T,p.Ala137Ala
- Allele change
- Synonymous_A137A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.