Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs376049108
- Species
- Homo sapiens
- Symbol
- rs376049108
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EFL1
- Location
- 15:82151519
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)15:82151519G>A
- HGVS.c name
- ENSEMBL:ENST00000268206.12:c.2935C>T
- ENSEMBL:ENST00000359445.8:c.2782C>T
- HGVS.p name
- :p.Arg350Cys
- ENSP00000268206:p.Arg979Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:82130206...82262773 (132.57 kb)
- Assembly version
- Not Available
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