Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs221873399
- Species
- Mus musculus
- Symbol
- rs221873399
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Phactr3
- Location
- 2:177769563
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000068.8:g.177769563A>G
- HGVS.c name
- ENSEMBL:ENSMUST00000108916.1:c.103+8468A>G
- ENSEMBL:ENSMUST00000108917.1:c.103+8468A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:177760768...177980285 (219.52 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:ENSMUST00000108916 | protein_coding | Intron 1/12 |
| |||||
ENSEMBL:ENSMUST00000108917 | protein_coding | Intron 1/12 |
| |||||
RefSeq:NM_001177789.1 | protein_coding | Intron 1/12 |
| |||||
RefSeq:NM_001177790.1 | protein_coding | Intron 1/12 |
| |||||
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