Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs767046988
- Species
- Homo sapiens
- Symbol
- rs767046988
- Category
- Variant
- Variant type
- SNP
- Overlaps
- WDR7
- Location
- 18:56779469
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)18:56779469C>T
- HGVS.c name
- ENSEMBL:ENST00000254442.8:c.2986C>T
- ENSEMBL:ENST00000357574.7:c.2887C>T
- HGVS.p name
- ENSP00000254442:p.Pro996Ser
- ENSP00000350187:p.Pro963Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:56651343...57036606 (385.26 kb)
- Assembly version
- Not Available
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