Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319399676
- Species
- Rattus norvegicus
- Symbol
- rs3319399676
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Brix1
- Location
- 2:59452341
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051337.1:g.59452341G>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000024285.7:c.901-95C>A
- RefSeq:NM_001029915.1:c.790-95C>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:59450608...59461495 (10.89 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction