Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198246357
- Species
- Rattus norvegicus
- Symbol
- rs198246357
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Slc6a6
- Location
- 4:124254367
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)4:124254367C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000012875.7:c.1097-398C>T
- ENSEMBL:ENSRNOT00000086982.2:c.1133-398C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:124195186...124268880 (73.69 kb)
- Assembly version
- Not Available
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