Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322374291
- Species
- Rattus norvegicus
- Symbol
- rs3322374291
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Smg7
- Location
- 13:65023642
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051348.1:g.65023642C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000092336.2:c.105-1886G>A
- ENSEMBL:ENSRNOT00000092397.2:c.30-1886G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:64986145...65050698 (64.55 kb)
- Assembly version
- Not Available
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