Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs583572577
- Species
- Mus musculus
- Symbol
- rs583572577
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Cpap
- Location
- 14:56793001
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)14:56793001A>C
- HGVS.c name
- ENSEMBL:ENSMUST00000065302.1:c.827-343T>G
- ENSEMBL:ENSMUST00000225951.1:c.827-343T>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:56764218...56812882 (48.66 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:ENSMUST00000065302 | protein_coding | Cpap | Intron 4/16 |
| ||||
ENSEMBL:ENSMUST00000225951 | protein_coding | Cpap | Intron 5/17 |
| ||||
RefSeq:NM_001014996.3 | protein_coding | Cpap | Intron 4/16 |
| ||||
RefSeq:NM_001403533.1 | protein_coding | Cpap | Intron 5/17 |
| ||||
RefSeq:NM_001403534.1 | protein_coding | Cpap | Intron 4/16 |
| ||||
RefSeq:XM_006518849.4 | protein_coding | Cpap | Intron 5/17 |
| ||||
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