Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322632876
- Species
- Rattus norvegicus
- Symbol
- rs3322632876
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Nefh
- Location
- 14:79832858
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (mRatBN7.2)14:79832858A>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000011604.5:c.1295T>C
- ENSEMBL:ENSRNOT00000110325.1:c.1295T>C
- HGVS.p name
- ENSRNOP00000011604:p.Met432Thr
- ENSRNOP00000096290:p.Met432Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:79830362...79840351 (9.99 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction