Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319570494
- Species
- Rattus norvegicus
- Symbol
- rs3319570494
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Med12l
- Location
- 2:143449698
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)2:143449698T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000014470.8:c.-1851-41696T>C
- ENSEMBL:ENSRNOT00000018573.8:c.-98-4246A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:143252139...143576507 (324.37 kb)
- Assembly version
- Not Available
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