Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs766883578
- Species
- Homo sapiens
- Symbol
- rs766883578
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RNF175
- Location
- 4:153720281
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:153720281T>C
- HGVS.c name
- ENSEMBL:ENST00000347063.9:c.533A>G
- ENSEMBL:ENST00000503694.5:n.526A>G
- HGVS.p name
- ENSP00000340979:p.Asp178Gly
- ENSP00000427472:p.Asp118Gly
- 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
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