Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322271908
- Species
- Rattus norvegicus
- Symbol
- rs3322271908
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Tor3a
- Location
- 13:68786832
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051348.1:g.68786832C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000005726.5:c.812+3142G>A
- ENSEMBL:ENSRNOT00000059524.4:c.3485+23106C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:68769605...68798738 (29.13 kb)
- Assembly version
- Not Available
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