Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1474211875
- Species
- Homo sapiens
- Symbol
- rs1474211875
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RETREG1
- Location
- 5:16474801
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)5:16474801T>C
- HGVS.c name
- ENSEMBL:ENST00000306320.10:c.1434A>G
- ENSEMBL:ENST00000399793.6:c.1011A>G
- HGVS.p name
- ENSP00000304642:p.Ala478=
- ENSP00000382691:p.Ala337=
- 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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