Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs30392346
- Species
- Mus musculus
- Symbol
- rs30392346
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Frem2
- Location
- 3:53496368
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000069.7:g.53496368C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000091137.1:c.5377+768G>A
- RefSeq:NM_172862.3:c.5377+768G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:53421359...53564776 (143.42 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction