Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs228293222
- Species
- Mus musculus
- Symbol
- rs228293222
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Dcst1
- Location
- 3:89258066
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)3:89258066T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000070820.1:c.1948-245A>G
- RefSeq:NM_029974.2:c.1948-245A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:89257526...89272560 (15.03 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:ENSMUST00000070820 | protein_coding | Intron 15/15 |
| |||||
RefSeq:NM_029974.2 | protein_coding | Intron 15/15 |
| |||||
RefSeq:XM_017319855.1 | protein_coding | Intron 1/15 |
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