Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs50660690
- Species
- Mus musculus
- Symbol
- rs50660690
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Clcn7
- Location
- 17:25379084
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000083.7:g.25379084G>A
- HGVS.c name
- ENSEMBL:ENSMUST00000040729.1:c.2245-20G>A
- ENSEMBL:ENSMUST00000160961.1:c.2185-20G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:25352365...25381078 (28.71 kb)
- Assembly version
- Not Available
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