Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322796906
- Species
- Rattus norvegicus
- Symbol
- rs3322796906
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Tdrd3
- Location
- 15:63412007
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)15:63412007C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000110490.1:c.792+69C>T
- ENSEMBL:ENSRNOT00000119103.1:c.858+69C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:63340531...63497208 (156.68 kb)
- Assembly version
- Not Available
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