Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3320952959
- Species
- Rattus norvegicus
- Symbol
- rs3320952959
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Btbd7
- Location
- 6:122006122
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051341.1:g.122006122A>T
- HGVS.c name
- RefSeq:XM_008764818.4:c.-107+3732T>A
- RefSeq:XM_008764819.4:c.-107+3186T>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:121920365...122010114 (89.75 kb)
- Assembly version
- Not Available
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