Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323055550
- Species
- Rattus norvegicus
- Symbol
- rs3323055550
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Eif4ebp1
- Location
- 16:64791936
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051351.1:g.64791936C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000096679.1:c.*212-53G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:64790226...64805984 (15.76 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction