Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs768079972
- Species
- Homo sapiens
- Symbol
- rs768079972
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DKK2
- Location
- 4:106924040
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:106924040C>T
- HGVS.c name
- ENSEMBL:ENST00000285311.8:c.694G>A
- ENSEMBL:ENST00000510463.1:c.556G>A
- HGVS.p name
- ENSP00000285311:p.Asp232Asn
- ENSP00000421255:p.Asp132Asn
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction