Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs572893491
- Species
- Homo sapiens
- Symbol
- rs572893491
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MTO1
- Location
- 6:73473355
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)6:73473355T>G
- HGVS.c name
- ENSEMBL:ENST00000370300.8:c.536-10T>G
- ENSEMBL:ENST00000370305.5:c.314-10T>G
- HGVS.p name
- Not Available
- 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
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