Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs3320718906
- Species
- Rattus norvegicus
- Symbol
- rs3320718906
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Cep85
- Location
- 5:146399009
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051340.1:g.146399009T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000065983.3:c.-17+4990A>G
- ENSEMBL:ENSRNOT00000078063.2:c.-17+4996A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:146356571...146404155 (47.58 kb)
- Assembly version
- Not Available
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