Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2150031602
- Species
- Homo sapiens
- Symbol
- rs2150031602
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MTO1
- Location
- 6:73473647
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000006.12:g.73473647G>C
- HGVS.c name
- ENSEMBL:ENST00000370300.8:c.818G>C
- ENSEMBL:ENST00000370305.5:c.596G>C
- HGVS.p name
- ENSP00000359323:p.Trp273Ser
- ENSP00000359328:p.Trp199Ser
- 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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