Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs149168939
- Species
- Homo sapiens
- Symbol
- rs149168939
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CSF1R
- Location
- 5:150077284
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000005.10:g.150077284C>T
- HGVS.c name
- ENSEMBL:ENST00000286301.7:c.881G>A
- ENSEMBL:ENST00000502660.5:n.1008G>A
- HGVS.p name
- ENSP00000286301:p.Arg294Gln
- ENSP00000445282:p.Arg294Gln
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction