Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs45950042
- Species
- Mus musculus
- Symbol
- rs45950042
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sox5
- Location
- 6:144637027
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)6:144637027C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000149451.1:n.107-65615G>A
- RefSeq:XM_011241577.3:c.-219-65615G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:143774151...144727703 (953.55 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction