Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs215570737
- Species
- Mus musculus
- Symbol
- rs215570737
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Plxdc2
- Location
- 2:16711038
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000068.8:g.16711038A>C
- HGVS.c name
- ENSEMBL:ENSMUST00000028081.1:c.1128+2844A>C
- ENSEMBL:ENSMUST00000114702.1:c.1122+2850A>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:16361115...16760650 (399.54 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:ENSMUST00000028081 | protein_coding | Plxdc2 | Intron 10/13 |
| ||||
ENSEMBL:ENSMUST00000114702 | protein_coding | Plxdc2 | Intron 10/13 |
| ||||
ENSEMBL:ENSMUST00000114703 | protein_coding | Plxdc2 | Intron 9/12 |
| ||||
ENSEMBL:ENSMUST00000126173 | transcript | Plxdc2 | Intron 5/8 |
| ||||
RefSeq:NM_026162.6 | protein_coding | Plxdc2 | Intron 10/13 |
| ||||
RefSeq:XM_006497531.4 | protein_coding | Plxdc2 | Intron 10/13 |
| ||||
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