Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs586243276
- Species
- Mus musculus
- Symbol
- rs586243276
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Pfdn2
- Location
- 1:171181529
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)1:171181529T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000006579.1:c.58-2569T>C
- ENSEMBL:ENSMUST00000135941.1:c.76-2569T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:171173238...171186822 (13.58 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction