Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197743056
- Species
- Rattus norvegicus
- Symbol
- rs197743056
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Trpv1
- Location
- 10:57857898
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)10:57857898A>G
- HGVS.c name
- RefSeq:NM_031982.1:c.1041+46A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:57851428...57876513 (25.09 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction