Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs142224306
- Species
- Homo sapiens
- Symbol
- rs142224306
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RNF175
- Location
- 4:153715537
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:153715537A>C
- HGVS.c name
- ENSEMBL:ENST00000347063.9:c.756T>G
- ENSEMBL:ENST00000503694.5:n.749T>G
- HGVS.p name
- ENSP00000340979:p.Cys252Trp
- NP_775933:p.Cys252Trp
- 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