Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs104981455
- Species
- Rattus norvegicus
- Symbol
- rs104981455
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Nol8
- Location
- 17:15013616
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- 5 prime UTR variant
- HGVS.g name
- (mRatBN7.2)17:15013616C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000073035.2:c.-555G>A
- ENSEMBL:ENSRNOT00000093381.2:c.-555G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:14990394...15013848 (23.45 kb)
- Assembly version
- Not Available
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