Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs228625798
- Species
- Mus musculus
- Symbol
- rs228625798
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Mllt10
- Location
- 2:18206069
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)2:18206069C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000028076.1:c.2070-2343C>T
- ENSEMBL:ENSMUST00000114669.1:c.441-2343C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:18060048...18217199 (157.15 kb)
- Assembly version
- Not Available
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