Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs386352279
- Species
- Homo sapiens
- Symbol
- rs386352279
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ARRDC3
- Location
- 5:91374125
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:91374125T>C
- HGVS.c name
- ENSEMBL:ENST00000265138.4:c.1022A>G
- RefSeq:NR_138071.2:n.1392A>G
- HGVS.p name
- ENSP00000265138:p.Glu341Gly
- 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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