Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323747972
- Species
- Rattus norvegicus
- Symbol
- rs3323747972
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sox9
- Location
- 10:97807979
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051345.1:g.97807979G>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000003511.7:c.432-71G>T
- RefSeq:NM_080403.2:c.432-71G>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:97806485...97811994 (5.51 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction