Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs262940966
- Species
- Mus musculus
- Symbol
- rs262940966
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E2f7
- Location
- 10:110583358
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000076.7:g.110583358T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000073781.1:c.93+1073T>C
- ENSEMBL:ENSMUST00000173294.1:n.335-546T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:110581300...110623245 (41.95 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction