Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs27484852
- Species
- Mus musculus
- Symbol
- rs27484852
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Skint7
- Location
- 4:111830914
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)4:111830914T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000055014.1:c.-3+601T>C
- ENSEMBL:ENSMUST00000106568.1:c.-3+601T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:111830120...111845420 (15.30 kb)
- Assembly version
- Not Available
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