Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs554858143
- Species
- Homo sapiens
- Symbol
- rs554858143
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RNF175
- Location
- 4:153751442
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:153751442A>G
- HGVS.c name
- ENSEMBL:ENST00000347063.9:c.100T>C
- ENSEMBL:ENST00000503694.5:n.248T>C
- HGVS.p name
- ENSP00000340979:p.Trp34Arg
- XP_011530184:p.Trp34Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:153710160...153760024 (49.86 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction