Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs226165698
- Species
- Mus musculus
- Symbol
- rs226165698
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Eif3f
- Location
- 7:108534416
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)7:108534416T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000033342.1:c.376+402T>C
- RefSeq:NM_025344.2:c.376+402T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:108533622...108541149 (7.53 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction