Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs199220190
- Species
- Rattus norvegicus
- Symbol
- rs199220190
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ube2h
- Location
- 4:58912122
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051339.1:g.58912122C>T
- HGVS.c name
- RefSeq:NM_001172127.1:c.53+17939G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:58834674...58930156 (95.48 kb)
- Assembly version
- Not Available
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