Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs238750407
- Species
- Mus musculus
- Symbol
- rs238750407
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Fgd6
- Location
- 10:93872637
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)10:93872637G>C
- HGVS.c name
- ENSEMBL:ENSMUST00000020208.1:c.16+465G>C
- RefSeq:NM_053072.3:c.16+465G>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:93871863...93981201 (109.34 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction