Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs106500891
- Species
- Rattus norvegicus
- Symbol
- rs106500891
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Actr8
- Location
- 16:5179635
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)16:5179635C>T
- HGVS.c name
- RefSeq:XM_039094615.2:c.*41-113C>T
- RefSeq:XM_039094616.2:c.*40+981C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:5164129...5186353 (22.22 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction