Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs778449680
- Species
- Homo sapiens
- Symbol
- rs778449680
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RMDN1
- Location
- 8:86507007
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000008.11:g.86507007C>T
- HGVS.c name
- ENSEMBL:ENST00000406452.8:c.235G>A
- ENSEMBL:ENST00000430676.6:c.235G>A
- HGVS.p name
- ENSP00000385927:p.Ala79Thr
- ENSP00000409661:p.Ala79Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:86468257...86514357 (46.10 kb)
- Assembly version
- Not Available
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