Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs778381761
- Species
- Homo sapiens
- Symbol
- rs778381761
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FBXO9
- Location
- 6:53081065
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)6:53081065C>T
- HGVS.c name
- ENSEMBL:ENST00000244426.10:c.535C>T
- ENSEMBL:ENST00000323557.12:c.505C>T
- HGVS.p name
- ENSP00000244426:p.Pro179Ser
- ENSP00000326968:p.Pro169Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:53051991...53100873 (48.88 kb)
- Assembly version
- Not Available
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