Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs74418158
- Species
- Homo sapiens
- Symbol
- rs74418158
- Category
- Variant
- Variant type
- SNP
- Overlaps
- IL1RAP
- Location
- 3:190656441
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.190656441A>G
- HGVS.c name
- ENSEMBL:ENST00000317757.8:c.1898A>G
- ENSEMBL:ENST00000443369.6:c.1898A>G
- HGVS.p name
- ENSP00000314807:p.Asn633Ser
- ENSP00000408893:p.Asn633Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:190514051...190659750 (145.70 kb)
- Assembly version
- Not Available
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