Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198408263
- Species
- Rattus norvegicus
- Symbol
- rs198408263
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Hspb2
- Location
- 8:51087185
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051343.1:g.51087185T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000013960.3:c.538-4112A>G
- ENSEMBL:ENSRNOT00000080736.2:c.235+1000A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:51081342...51094533 (13.19 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction