Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1202823800
- Species
- Homo sapiens
- Symbol
- rs1202823800
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RETREG1
- Location
- 5:16477755
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:16477755C>T
- HGVS.c name
- ENSEMBL:ENST00000306320.10:c.907G>A
- ENSEMBL:ENST00000399793.6:c.484G>A
- HGVS.p name
- ENSP00000304642:p.Val303Met
- ENSP00000382691:p.Val162Met
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:16473038...16617101 (144.06 kb)
- Assembly version
- Not Available
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