Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs749351702
- Species
- Homo sapiens
- Symbol
- rs749351702
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MTO1
- Location
- 6:73479746
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000006.12:g.73479746G>A
- HGVS.c name
- ENSEMBL:ENST00000370300.8:c.840G>A
- ENSEMBL:ENST00000370305.5:c.618G>A
- HGVS.p name
- ENSP00000359323:p.Leu280=
- ENSP00000359328:p.Leu206=
- 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