Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs579150721
- Species
- Mus musculus
- Symbol
- rs579150721
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Eya2
- Location
- 2:165437870
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000068.8:g.165437870C>G
- HGVS.c name
- ENSEMBL:ENSMUST00000088132.1:c.-11+686C>G
- RefSeq:NM_001271963.2:c.-11+686C>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:165436952...165613647 (176.70 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:ENSMUST00000088132 | protein_coding | Intron 1/15 |
| |||||
RefSeq:NM_001271963.2 | protein_coding | Intron 1/15 |
| |||||
RefSeq:XM_036158267.1 | protein_coding | Intron 1/14 |
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