Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs261858599
- Species
- Mus musculus
- Symbol
- rs261858599
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Cnot9
- Location
- 1:74545912
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)1:74545912C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000087215.1:c.24+292C>T
- ENSEMBL:ENSMUST00000137100.1:n.155+539C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:74545217...74570001 (24.78 kb)
- Assembly version
- Not Available
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