Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs226678877
- Species
- Mus musculus
- Symbol
- rs226678877
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Cct8
- Location
- 16:87283651
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)16:87283651C>G
- HGVS.c name
- ENSEMBL:ENSMUST00000026704.1:c.942-102G>C
- ENSEMBL:ENSMUST00000175750.1:c.217-102G>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:87280213...87292757 (12.54 kb)
- Assembly version
- Not Available
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