Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs201891647
- Species
- Homo sapiens
- Symbol
- rs201891647
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RNF175
- Location
- 4:153720219
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000004.12:g.153720219C>T
- HGVS.c name
- ENSEMBL:ENST00000347063.9:c.595G>A
- ENSEMBL:ENST00000503694.5:n.588G>A
- HGVS.p name
- ENSP00000340979:p.Glu199Lys
- ENSP00000427472:p.Glu139Lys
- 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