Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs587262050
- Species
- Mus musculus
- Symbol
- rs587262050
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Snx9
- Location
- 17:5898646
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)17:5898646C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000002436.1:c.12+6825C>T
- ENSEMBL:ENSMUST00000231803.1:n.195+6825C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:5891604...5982229 (90.63 kb)
- Assembly version
- Not Available
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