Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs239082615
- Species
- Mus musculus
- Symbol
- rs239082615
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Gpx4
- Location
- 10:79889566
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)10:79889566T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000105372.1:c.84+17T>C
- ENSEMBL:ENSMUST00000144698.1:n.294-782T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:79883000...79892273 (9.27 kb)
- Assembly version
- Not Available
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