Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs106389185
- Species
- Rattus norvegicus
- Symbol
- rs106389185
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ccdc63
- Location
- 12:34432782
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)12:34432782A>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000046604.6:c.-67-139A>G
- ENSEMBL:ENSRNOT00000119110.1:c.55-206A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:34424344...34453085 (28.74 kb)
- Assembly version
- Not Available
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