Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3321805252
- Species
- Rattus norvegicus
- Symbol
- rs3321805252
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Utp18
- Location
- 10:78833775
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)10:78833775C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000003582.8:c.573-287G>A
- ENSEMBL:ENSRNOT00000111110.1:c.573-287G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:78811879...78839627 (27.75 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction