Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322361460
- Species
- Rattus norvegicus
- Symbol
- rs3322361460
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Lemd1
- Location
- 13:43697018
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051348.1:g.43697018G>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000076457.3:c.203-277G>C
- ENSEMBL:ENSRNOT00000080556.2:c.351-277G>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:43631705...43697948 (66.24 kb)
- Assembly version
- Not Available
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