Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs29477122
- Species
- Mus musculus
- Symbol
- rs29477122
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sap30l
- Location
- 11:57693696
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)11:57693696C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000020826.1:c.198+581C>T
- RefSeq:NM_001081168.2:c.198+581C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:57692463...57701043 (8.58 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction