Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3321081045
- Species
- Rattus norvegicus
- Symbol
- rs3321081045
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Scyl2
- Location
- 7:24103641
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)7:24103641C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000119175.1:c.177+2448G>A
- RefSeq:NM_001191780.1:c.177+2448G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:24064404...24117338 (52.93 kb)
- Assembly version
- Not Available
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