Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs774478741
- Species
- Homo sapiens
- Symbol
- rs774478741
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RNF175
- Location
- 4:153712533
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:153712533T>C
- HGVS.c name
- ENSEMBL:ENST00000347063.9:c.808A>G
- ENSEMBL:ENST00000513656.5:n.774A>G
- HGVS.p name
- ENSP00000340979:p.Lys270Glu
- NP_775933:p.Lys270Glu
- 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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