Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs948807667
- Species
- Homo sapiens
- Symbol
- rs948807667
- Category
- Variant
- Variant type
- SNP
- Overlaps
- WDR33
- Location
- 2:127719932
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000002.12:g.127719932C>T
- HGVS.c name
- ENSEMBL:ENST00000322313.9:c.2093G>A
- HGVS.p name
- ENSP00000325377:p.Ser698Asn
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:127701027...127811187 (110.16 kb)
- Assembly version
- Not Available
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