Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs33234912
- Species
- Mus musculus
- Symbol
- rs33234912
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Srrm4
- Location
- 5:116728990
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)5:116728990T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000076124.1:c.131+403A>G
- RefSeq:NM_001403397.1:c.131+403A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:116577334...116729876 (152.54 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:ENSMUST00000076124 | protein_coding | Intron 1/12 |
| |||||
RefSeq:NM_001403397.1 | protein_coding | Intron 2/13 |
| |||||
RefSeq:NM_026886.4 | protein_coding | Intron 1/12 |
| |||||
Showing 1 - 3 of 3 rows
per page