Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs105687894
- Species
- Rattus norvegicus
- Symbol
- rs105687894
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ubap1
- Location
- 5:56531563
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)5:56531563C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000096821.1:c.-7-7928C>T
- RefSeq:NM_001012190.1:c.-7-7928C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:56520722...56561153 (40.43 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction