Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1582371030
- Species
- Homo sapiens
- Symbol
- rs1582371030
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ARRDC3
- Location
- 5:91374955
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)5:91374955G>A
- HGVS.c name
- ENSEMBL:ENST00000265138.4:c.837C>T
- ENSEMBL:ENST00000505631.1:n.390C>T
- HGVS.p name
- ENSP00000265138:p.Asp279=
- NP_001316599:p.Asp59=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:91368631...91383317 (14.69 kb)
- Assembly version
- Not Available
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