Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198832992
- Species
- Rattus norvegicus
- Symbol
- rs198832992
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rxra
- Location
- 3:11053228
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)3:11053228T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000012892.5:c.295-1045T>C
- ENSEMBL:ENSRNOT00000099288.1:c.385-1045T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:10989832...11076366 (86.53 kb)
- Assembly version
- Not Available
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