Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs541386879
- Species
- Homo sapiens
- Symbol
- rs541386879
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DKK2
- Location
- 4:106925861
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000004.12:g.106925861C>T
- HGVS.c name
- ENSEMBL:ENST00000285311.8:c.311G>A
- ENSEMBL:ENST00000510463.1:c.173G>A
- HGVS.p name
- ENSP00000285311:p.Arg104Gln
- ENSP00000421255:p.Arg4Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:106921802...107283806 (362.00 kb)
- Assembly version
- Not Available
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