Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs255948311
- Species
- Mus musculus
- Symbol
- rs255948311
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Slc17a6
- Location
- 7:51279578
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000073.7:g.51279578G>C
- HGVS.c name
- ENSEMBL:ENSMUST00000032710.1:c.458+2868G>C
- ENSEMBL:ENSMUST00000207375.1:n.505+2868G>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:51271754...51320867 (49.11 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:ENSMUST00000032710 | protein_coding | Slc17a6 | Intron 3/11 |
| ||||
ENSEMBL:ENSMUST00000207375 | transcript | Slc17a6 | Intron 2/3 |
| ||||
ENSEMBL:ENSMUST00000207945 | protein_coding | Slc17a6 | Intron 3/8 |
| ||||
ENSEMBL:ENSMUST00000208597 | transcript | Slc17a6 | Intron 1/5 |
| ||||
RefSeq:NM_001355150.1 | protein_coding | Slc17a6 | Intron 3/11 |
| ||||
RefSeq:NM_080853.3 | protein_coding | Slc17a6 | Intron 3/11 |
| ||||
RefSeq:XM_006540601.5 | protein_coding | Slc17a6 | Intron 3/11 |
| ||||
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