Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs107946741
- Species
- Mus musculus
- Symbol
- rs107946741
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rhot2
- Location
- 17:26058047
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)17:26058047C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000043897.1:c.*295G>A
- ENSEMBL:ENSMUST00000176751.1:c.*76+219G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:26057431...26063499 (6.07 kb)
- Assembly version
- Not Available
- Viewer Help
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