Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs557440944
- Species
- Homo sapiens
- Symbol
- rs557440944
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MTO1
- Location
- 6:73482132
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)6:73482132T>G
- HGVS.c name
- ENSEMBL:ENST00000370300.8:c.1428T>G
- ENSEMBL:ENST00000370305.5:c.1206T>G
- HGVS.p name
- ENSP00000359323:p.Ile476Met
- ENSP00000359328:p.Ile402Met
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:73461578...73509236 (47.66 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction