Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197131274
- Species
- Rattus norvegicus
- Symbol
- rs197131274
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Kiaa1191
- Location
- 17:10055544
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)17:10055544T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000023125.8:c.337+943T>C
- ENSEMBL:ENSRNOT00000098242.1:c.337+943T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:10049142...10061819 (12.68 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction