Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197652178
- Species
- Rattus norvegicus
- Symbol
- rs197652178
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sap30l
- Location
- 10:41980062
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- 5 prime UTR variant
- HGVS.g name
- (mRatBN7.2)10:41980062C>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000003473.7:c.-122C>A
- RefSeq:NM_001398798.1:c.-122C>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:41979687...41992307 (12.62 kb)
- Assembly version
- Not Available
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