Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319570606
- Species
- Rattus norvegicus
- Symbol
- rs3319570606
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Serpini2
- Location
- 2:160031774
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051337.1:g.160031774T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000013452.6:c.867-1726A>G
- RefSeq:NM_001134409.2:c.867-1726A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:160014721...160044280 (29.56 kb)
- Assembly version
- Not Available
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