Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs587062660
- Species
- Mus musculus
- Symbol
- rs587062660
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Scyl2
- Location
- 10:89484097
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000076.7:g.89484097T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000092227.1:c.1762-1376A>G
- ENSEMBL:ENSMUST00000105294.1:n.627-1376A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:89474583...89522147 (47.56 kb)
- Assembly version
- Not Available
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