Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs775838916
- Species
- Homo sapiens
- Symbol
- rs775838916
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRAT
- Location
- 4:154744531
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:154744531C>T
- HGVS.c name
- ENSEMBL:ENST00000336356.4:c.205C>T
- ENSEMBL:ENST00000499392.1:n.472-3658C>T
- HGVS.p name
- ENSP00000337224:p.Arg69Cys
- ENSP00000422324:p.Arg69Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:154626945...154753120 (126.18 kb)
- Assembly version
- Not Available
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