Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323668533
- Species
- Rattus norvegicus
- Symbol
- rs3323668533
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Nox1
- Location
- X:97326878
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)X:97326878T>A
- HGVS.c name
- RefSeq:XM_039099398.2:c.-148+4986A>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:97279056...97332291 (53.24 kb)
- Assembly version
- Not Available
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