Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3321675679
- Species
- Rattus norvegicus
- Symbol
- rs3321675679
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Plekhm3
- Location
- 9:66166280
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (mRatBN7.2)9:66166280T>C
- HGVS.c name
- RefSeq:XM_006245080.5:c.*5780A>G
- RefSeq:XM_017596816.3:c.*5780A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:66166233...66325332 (159.10 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction