Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs778504217
- Species
- Homo sapiens
- Symbol
- rs778504217
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ZNF326
- Location
- 1:90027670
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.90027670A>T
- HGVS.c name
- ENSEMBL:ENST00000340281.9:c.1718A>T
- ENSEMBL:ENST00000370447.3:c.1451A>T
- HGVS.p name
- ENSP00000340796:p.Asp573Val
- ENSP00000359476:p.Asp484Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:89995110...90035533 (40.42 kb)
- Assembly version
- Not Available
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