Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs572409353
- Species
- Homo sapiens
- Symbol
- rs572409353
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ZNF326
- Location
- 1:90022323
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:90022323C>T
- HGVS.c name
- ENSEMBL:ENST00000340281.9:c.1379C>T
- ENSEMBL:ENST00000370447.3:c.1112C>T
- HGVS.p name
- ENSP00000340796:p.Ala460Val
- ENSP00000359476:p.Ala371Val
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction