Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322211148
- Species
- Rattus norvegicus
- Symbol
- rs3322211148
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Lemd1
- Location
- 13:43677907
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)13:43677907C>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000076457.3:c.202+9583C>G
- ENSEMBL:ENSRNOT00000080556.2:c.273+5130C>G
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction