Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs147788981
- Species
- Homo sapiens
- Symbol
- rs147788981
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ARRDC3
- Location
- 5:91378745
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000005.10:g.91378745G>A
- HGVS.c name
- ENSEMBL:ENST00000265138.4:c.311C>T
- ENSEMBL:ENST00000503192.5:n.301C>T
- HGVS.p name
- ENSP00000265138:p.Thr104Ile
- 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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