Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs581771808
- Species
- Mus musculus
- Symbol
- rs581771808
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E2f6
- Location
- 12:16862012
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)12:16862012T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000020908.1:c.108+696T>C
- ENSEMBL:ENSMUST00000220794.1:c.109-278T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:16860932...16876753 (15.82 kb)
- Assembly version
- Not Available
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