Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs222175326
- Species
- Mus musculus
- Symbol
- rs222175326
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Nr3c1
- Location
- 18:39630912
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)18:39630912C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000237944.1:c.-13-10614G>A
- RefSeq:NM_001361212.1:c.-13-10614G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:39543598...39652474 (108.88 kb)
- Assembly version
- Not Available
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