Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197042578
- Species
- Rattus norvegicus
- Symbol
- rs197042578
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sap30bp
- Location
- 10:101172223
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051345.1:g.101172223T>C
- HGVS.c name
- RefSeq:NM_001108305.1:c.264+2073T>C
- RefSeq:XM_039086430.2:c.216+4632T>C
- 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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