Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319174443
- Species
- Rattus norvegicus
- Symbol
- rs3319174443
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Atg2a
- Location
- 1:203561539
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- NC_051336.1:g.203561539C>T
- HGVS.c name
- RefSeq:NM_001109545.1:c.5515-8C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:203542559...203562242 (19.68 kb)
- Assembly version
- Not Available
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Data currently unavailable; sequence viewer under construction