Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs773148640
- Species
- Homo sapiens
- Symbol
- rs773148640
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EFR3A
- Location
- 8:131986249
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000008.11:g.131986249G>A
- HGVS.c name
- ENSEMBL:ENST00000254624.10:c.1925G>A
- ENSEMBL:ENST00000519656.1:c.1817G>A
- HGVS.p name
- ENSP00000254624:p.Arg642Lys
- ENSP00000428086:p.Arg606Lys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:131904093...132013642 (109.55 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction