Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197347841
- Species
- Rattus norvegicus
- Symbol
- rs197347841
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Pgap4
- Location
- 5:63949732
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051340.1:g.63949732C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000104584.1:c.-2028+1320G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:63930682...63951716 (21.03 kb)
- Assembly version
- Not Available
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