Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198085565
- Species
- Rattus norvegicus
- Symbol
- rs198085565
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Wfikkn2
- Location
- 10:79190956
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)10:79190956C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000003784.8:c.195+250G>A
- RefSeq:NM_001398592.1:c.195+250G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:79185563...79191657 (6.09 kb)
- Assembly version
- Not Available
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