Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3318817658
- Species
- Rattus norvegicus
- Symbol
- rs3318817658
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Stxbp5
- Location
- 1:4187207
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)1:4187207G>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000115103.1:c.3501+293C>T
- RefSeq:NM_178346.2:c.3417+293C>T
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction