Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs775222060
- Species
- Homo sapiens
- Symbol
- rs775222060
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EFL1
- Location
- 15:82151520
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)15:82151520C>T
- HGVS.c name
- ENSEMBL:ENST00000268206.12:c.2934G>A
- ENSEMBL:ENST00000359445.8:c.2781G>A
- HGVS.p name
- :p.Gln349=
- ENSP00000268206:p.Gln978=
- 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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