Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs779682569
- Species
- Homo sapiens
- Symbol
- rs779682569
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SCD5
- Location
- 4:82798444
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000004.12:g.82798444C>T
- HGVS.c name
- ENSEMBL:ENST00000273908.4:c.94G>A
- ENSEMBL:ENST00000319540.9:c.94G>A
- HGVS.p name
- ENSP00000273908:p.Gly32Ser
- ENSP00000316329:p.Gly32Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:82629539...82798796 (169.26 kb)
- Assembly version
- Not Available
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