Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs3319794497
- Species
- Rattus norvegicus
- Symbol
- rs3319794497
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Dnlz
- Location
- 3:9177562
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051338.1:g.9177562G>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000025386.7:c.-1387-58C>T
- ENSEMBL:ENSRNOT00000091484.2:c.323-58C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:9169793...9180551 (10.76 kb)
- Assembly version
- Not Available
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