Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197998132
- Species
- Rattus norvegicus
- Symbol
- rs197998132
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Tmeff1
- Location
- 5:62928053
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051340.1:g.62928053A>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000113773.1:c.95-2580A>G
- ENSEMBL:ENSRNOT00000119982.1:c.176-2580A>G
- 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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