Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs3318817166
- Species
- Rattus norvegicus
- Symbol
- rs3318817166
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Stxbp5
- Location
- 1:4236725
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051336.1:g.4236725A>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000040559.6:c.1405+1746T>A
- ENSEMBL:ENSRNOT00000044778.5:c.1405+1746T>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:4182489...4335290 (152.80 kb)
- Assembly version
- Not Available
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