Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs763354083
- Species
- Homo sapiens
- Symbol
- rs763354083
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ARRDC3
- Location
- 5:91371456
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant&splice region variant
- HGVS.g name
- NC_000005.10:g.91371456T>C
- HGVS.c name
- ENSEMBL:ENST00000265138.4:c.1189A>G
- ENSEMBL:ENST00000511391.1:n.163A>G
- HGVS.p name
- ENSP00000265138:p.Ile397Val
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction