Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs49169278
- Species
- Mus musculus
- Symbol
- rs49169278
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Camkmt
- Location
- 17:85496498
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)17:85496498G>A
- HGVS.c name
- ENSEMBL:ENSMUST00000095188.1:c.376+75223G>A
- ENSEMBL:ENSMUST00000234822.1:n.497-13707G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:85397989...85766017 (368.03 kb)
- Assembly version
- Not Available
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