Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3320548757
- Species
- Rattus norvegicus
- Symbol
- rs3320548757
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Tmeff1
- Location
- 5:62978109
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)5:62978109C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000113773.1:c.674-5438C>T
- ENSEMBL:ENSRNOT00000119982.1:c.755-5438C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:62910740...62996494 (85.75 kb)
- Assembly version
- Not Available
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