Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319281902
- Species
- Rattus norvegicus
- Symbol
- rs3319281902
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Kiaa0825
- Location
- 2:7227366
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051337.1:g.7227366G>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000071535.2:c.3704+102029G>T
- RefSeq:NM_001419450.1:c.3704+102029G>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:6874474...7437032 (562.56 kb)
- Assembly version
- Not Available
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