Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1348109062
- Species
- Homo sapiens
- Symbol
- rs1348109062
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RXRA
- Location
- 9:134417178
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000009.12:g.134417178C>T
- HGVS.c name
- ENSEMBL:ENST00000356384.4:n.1041C>T
- ENSEMBL:ENST00000481739.2:c.631C>T
- HGVS.p name
- ENSP00000419692:p.Arg211Cys
- ENSP00000500402:p.Arg184Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:134317098...134440585 (123.49 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction