Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323599338
- Species
- Rattus norvegicus
- Symbol
- rs3323599338
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Unc5b
- Location
- 20:28713056
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)20:28713056C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000038537.6:c.884-98G>A
- RefSeq:NM_022207.2:c.905-98G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:28697726...28764537 (66.81 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction