Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs106772429
- Species
- Rattus norvegicus
- Symbol
- rs106772429
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Tspan18
- Location
- 3:79194104
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051338.1:g.79194104G>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000011650.6:c.-92-12567C>G
- RefSeq:NM_001107750.2:c.-92-12567C>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:79160060...79299907 (139.85 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction