Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197221690
- Species
- Rattus norvegicus
- Symbol
- rs197221690
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sap30bp
- Location
- 10:101186547
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)10:101186547C>G
- HGVS.c name
- RefSeq:NM_001108305.1:c.307+2204C>G
- RefSeq:XM_039086430.2:c.259+2204C>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:101165777...101198503 (32.73 kb)
- Assembly version
- Not Available
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