Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs690016558
- Species
- Homo sapiens
- Symbol
- rs690016558
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CSF1R
- Location
- 5:150056053
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:150056053T>A
- HGVS.c name
- ENSEMBL:ENST00000286301.7:c.2527A>T
- ENSEMBL:ENST00000504875.5:n.2527A>T
- HGVS.p name
- ENSP00000286301:p.Ile843Phe
- ENSP00000501699:p.Ile843Phe
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:150053291...150113372 (60.08 kb)
- Assembly version
- Not Available
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