Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs31386120
- Species
- Mus musculus
- Symbol
- rs31386120
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Styxl2
- Location
- 1:165951585
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)1:165951585G>A
- HGVS.c name
- ENSEMBL:ENSMUST00000085992.1:c.110+3054C>T
- ENSEMBL:ENSMUST00000192369.1:c.110+3054C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:165925717...165955467 (29.75 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction
Variant Molecular Consequences
Sequence feature | Sequence feature type | Associated gene | Location | Molecular consequence | Codon and amino acid change | |||
|---|---|---|---|---|---|---|---|---|
ENSEMBL:ENSMUST00000085992 | protein_coding | Styxl2 | Intron 2/5 |
| ||||
ENSEMBL:ENSMUST00000192369 | protein_coding | Styxl2 | Intron 2/5 |
| ||||
RefSeq:NM_001033344.3 | protein_coding | Styxl2 | Intron 2/5 |
| ||||
RefSeq:NM_001160049.1 | protein_coding | Styxl2 | Intron 2/5 |
| ||||
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