Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322093677
- Species
- Rattus norvegicus
- Symbol
- rs3322093677
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Wdr53
- Location
- 11:68549440
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)11:68549440C>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000002392.5:c.-17+1210G>T
- ENSEMBL:ENSRNOT00000095477.1:c.50+1569G>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:68542647...68551148 (8.50 kb)
- Assembly version
- Not Available
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