Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322482455
- Species
- Rattus norvegicus
- Symbol
- rs3322482455
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Fam20b
- Location
- 13:68817920
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051348.1:g.68817920A>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000006018.4:c.574+2111T>C
- ENSEMBL:ENSRNOT00000059524.4:c.3486-21544A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:68801663...68839979 (38.32 kb)
- Assembly version
- Not Available
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