Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198091029
- Species
- Rattus norvegicus
- Symbol
- rs198091029
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ube2m
- Location
- 1:73662851
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- 5 prime UTR variant
- HGVS.g name
- NC_051336.1:g.73662851A>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000031007.7:c.*563T>G
- RefSeq:NM_001108471.1:c.*563T>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:73662576...73666113 (3.54 kb)
- Assembly version
- Not Available
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