Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs236548228
- Species
- Mus musculus
- Symbol
- rs236548228
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Grid2
- Location
- 6:64440858
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)6:64440858A>G
- HGVS.c name
- ENSEMBL:ENSMUST00000095852.1:c.2193+34024A>G
- RefSeq:NM_001370966.1:c.2193+34024A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:63232860...64681307 (1,448.45 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:ENSMUST00000095852 | protein_coding | Grid2 | Intron 13/15 |
| ||||
RefSeq:NM_001370966.1 | protein_coding | Grid2 | Intron 13/15 |
| ||||
RefSeq:NM_008167.3 | protein_coding | Grid2 | Intron 13/15 |
| ||||
RefSeq:XM_036165857.1 | protein_coding | Grid2 | Intron 13/16 |
| ||||
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