Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198953799
- Species
- Rattus norvegicus
- Symbol
- rs198953799
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Akr1c3
- Location
- 17:66122459
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051352.1:g.66122459A>G
- HGVS.c name
- RefSeq:NM_138510.2:c.571-1554A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:66110963...66127873 (16.91 kb)
- Assembly version
- Not Available
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