Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs746286312
- Species
- Homo sapiens
- Symbol
- rs746286312
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ARRDC3
- Location
- 5:91375113
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:91375113C>T
- HGVS.c name
- ENSEMBL:ENST00000265138.4:c.679G>A
- ENSEMBL:ENST00000505631.1:n.232G>A
- HGVS.p name
- ENSP00000265138:p.Ala227Thr
- 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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