Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs579696054
- Species
- Mus musculus
- Symbol
- rs579696054
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Prm2
- Location
- 16:10610447
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)16:10610447C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000189593.1:c.-44-541G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:10609241...10609969 (0.73 kb)
- Assembly version
- Not Available
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