Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs48960019
- Species
- Mus musculus
- Symbol
- rs48960019
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Snx29
- Location
- 16:11366774
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)16:11366774G>A
- HGVS.c name
- ENSEMBL:ENSMUST00000096273.1:c.659-22789G>A
- ENSEMBL:ENSMUST00000122168.1:c.614-22789G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:11140772...11573336 (432.56 kb)
- Assembly version
- Not Available
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