Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3321216681
- Species
- Rattus norvegicus
- Symbol
- rs3321216681
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Efr3a
- Location
- 7:97607540
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)7:97607540G>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000045357.4:c.992-788G>C
- ENSEMBL:ENSRNOT00000102392.1:c.1073-788G>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:97552677...97633369 (80.69 kb)
- Assembly version
- Not Available
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