Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs217486105
- Species
- Mus musculus
- Symbol
- rs217486105
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Pcyt1a
- Location
- 16:32251001
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000082.7:g.32251001C>A
- HGVS.c name
- ENSEMBL:ENSMUST00000079791.1:c.-11+1152C>A
- ENSEMBL:ENSMUST00000104893.1:c.-11+889C>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:32249739...32293883 (44.14 kb)
- Assembly version
- Not Available
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