Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs770626857
- Species
- Homo sapiens
- Symbol
- rs770626857
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FBXO9
- Location
- 6:53078841
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)6:53078841T>C
- HGVS.c name
- ENSEMBL:ENST00000244426.10:c.380T>C
- ENSEMBL:ENST00000323557.12:c.350T>C
- HGVS.p name
- ENSP00000244426:p.Ile127Thr
- ENSP00000326968:p.Ile117Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:53051991...53100873 (48.88 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction