Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs766184517
- Species
- Homo sapiens
- Symbol
- rs766184517
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LOXHD1
- Location
- 18:46477888
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000018.10:g.46477888C>T
- HGVS.c name
- ENSEMBL:ENST00000300591.11:c.3073G>A
- ENSEMBL:ENST00000398686.8:c.1123G>A
- HGVS.p name
- ENSP00000300591:p.Glu1025Lys
- ENSP00000381676:p.Glu375Lys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:46476961...46657220 (180.26 kb)
- Assembly version
- Not Available
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