Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2049569572
- Species
- Homo sapiens
- Symbol
- rs2049569572
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SOD1
- Location
- 21:31663814
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)21:31663814T>C
- HGVS.c name
- ENSEMBL:ENST00000270142.11:c.97T>C
- ENSEMBL:ENST00000389995.4:c.40T>C
- HGVS.p name
- ENSP00000270142:p.Trp33Arg
- ENSP00000374645:p.Trp14Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr21:31659666...31668931 (9.27 kb)
- Assembly version
- Not Available
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