Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3323718332
- Species
- Rattus norvegicus
- Symbol
- rs3323718332
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Zfp326
- Location
- 14:3952122
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)14:3952122G>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000072818.3:c.931-1772C>G
- ENSEMBL:ENSRNOT00000076571.3:c.927-493C>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:3941210...3980419 (39.21 kb)
- Assembly version
- Not Available
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