Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197167971
- Species
- Rattus norvegicus
- Symbol
- rs197167971
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Utp18
- Location
- 10:78814803
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051345.1:g.78814803T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000003582.8:c.1525-156A>G
- ENSEMBL:ENSRNOT00000111110.1:c.1471-156A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:78811879...78839627 (27.75 kb)
- Assembly version
- Not Available
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