Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1135259832
- Species
- Mus musculus
- Symbol
- rs1135259832
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ifng
- Location
- 10:118280227
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)10:118280227G>A
- HGVS.c name
- ENSEMBL:ENSMUST00000068592.1:c.361-832G>A
- RefSeq:NM_008337.4:c.361-832G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:118276951...118281797 (4.85 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction