Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198948772
- Species
- Rattus norvegicus
- Symbol
- rs198948772
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Trpv1
- Location
- 10:57857895
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051345.1:g.57857895C>G
- HGVS.c name
- RefSeq:NM_031982.1:c.1041+43C>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
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