Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs582212084
- Species
- Mus musculus
- Symbol
- rs582212084
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Spmip3
- Location
- 1:177577695
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)1:177577695A>C
- HGVS.c name
- ENSEMBL:ENSMUST00000016106.1:c.326-2787A>C
- RefSeq:NM_027077.2:c.326-2787A>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:177557380...177580890 (23.51 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:ENSMUST00000016106 | protein_coding | Intron 4/5 |
| |||||
RefSeq:NM_027077.2 | protein_coding | Intron 4/5 |
| |||||
RefSeq:XM_006496976.5 | protein_coding | Intron 4/5 |
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RefSeq:XR_373615.4 | transcript | Intron 3/4 |
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