Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs245159050
- Species
- Mus musculus
- Symbol
- rs245159050
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ccl22
- Location
- 8:95475021
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)8:95475021T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000034231.1:c.197+1368T>C
- ENSEMBL:ENSMUST00000156137.1:n.340+1368T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:95472312...95478016 (5.70 kb)
- Assembly version
- Not Available
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