Variant (rsID / SNP)
rs1062391
rs1062391 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EEF1D. Location: chromosome 8, position 144,662,353. The table records no clinical significance for this variant.
Reference-table entries
EEF1DNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 8:144662353
- HGVS
- NM_001130053.5,c.1734C>T,p.Ala578Ala
- Allele change
- Synonymous_A188A
Associated conditions / phenotypes
Synonymous_A212A|Synonymous_A188A|Synonymous_A578A|Synonymous_A188A|Synonymous_A212A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.