Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs29376927
- Species
- Mus musculus
- Symbol
- rs29376927
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Scyl2
- Location
- 10:89478915
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)10:89478915G>T
- HGVS.c name
- ENSEMBL:ENSMUST00000092227.1:c.2023-943C>A
- ENSEMBL:ENSMUST00000105294.1:n.888-943C>A
- 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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