Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198005806
- Species
- Rattus norvegicus
- Symbol
- rs198005806
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ube2m
- Location
- 1:73663678
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_051336.1:g.73663678T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000031007.7:c.330A>G
- ENSEMBL:ENSRNOT00000108453.1:c.375A>G
- HGVS.p name
- ENSRNOP00000034271:p.Ile110Met
- ENSRNOP00000083234:p.Ile125Met
- 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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