Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs8171587
- Species
- Rattus norvegicus
- Symbol
- rs8171587
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Lrrc73
- Location
- 9:14726349
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (mRatBN7.2)9:14726349G>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000061185.3:c.*56C>T
- RefSeq:NM_001024360.2:c.*56C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:14726157...14730144 (3.99 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction