Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322992221
- Species
- Rattus norvegicus
- Symbol
- rs3322992221
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Eif4ebp1
- Location
- 16:64790938
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- NC_051351.1:g.64790938A>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000096679.1:c.*1157T>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
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