Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3321333803
- Species
- Rattus norvegicus
- Symbol
- rs3321333803
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Nphp3
- Location
- 8:104639845
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_051343.1:g.104639845A>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000014636.7:c.1461A>G
- RefSeq:NM_001191882.1:c.1461A>G
- HGVS.p name
- ENSRNOP00000014636:p.Ile487Met
- NP_001178811:p.Ile487Met
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:104621864...104662383 (40.52 kb)
- Assembly version
- Not Available
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Data currently unavailable; sequence viewer under construction