Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319616714
- Species
- Rattus norvegicus
- Symbol
- rs3319616714
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Wars2
- Location
- 2:186502672
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051337.1:g.186502672C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000104876.1:c.91-5006C>T
- ENSEMBL:ENSRNOT00000106687.1:c.91-26414C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:186459444...186543581 (84.14 kb)
- Assembly version
- Not Available
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