Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs197856039
- Species
- Rattus norvegicus
- Symbol
- rs197856039
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rbbp9
- Location
- 3:131927017
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)3:131927017A>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000010678.5:c.314-87T>C
- RefSeq:NM_019219.3:c.335-87T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:131925095...131939042 (13.95 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction