Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs237131748
- Species
- Mus musculus
- Symbol
- rs237131748
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rab39
- Location
- 9:53616609
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)9:53616609T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000068449.1:c.227+580A>G
- RefSeq:NM_175562.3:c.227+580A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:53595410...53617532 (22.12 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction