Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs955408829
- Species
- Homo sapiens
- Symbol
- rs955408829
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LOXHD1
- Location
- 18:46477644
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)18:46477644C>T
- HGVS.c name
- ENSEMBL:ENST00000300591.11:c.3307+10G>A
- ENSEMBL:ENST00000398686.8:c.1367G>A
- HGVS.p name
- ENSP00000381676:p.Arg456His
- ENSP00000381692:p.Arg456His
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction