Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs50978657
- Species
- Mus musculus
- Symbol
- rs50978657
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Unc5cl
- Location
- 17:48769633
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)17:48769633T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000074574.1:c.949+167T>C
- ENSEMBL:ENSMUST00000161418.1:c.55+167T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:48761929...48846742 (84.81 kb)
- Assembly version
- Not Available
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