Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs374743911
- Species
- Homo sapiens
- Symbol
- rs374743911
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DKK2
- Location
- 4:106924560
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:106924560T>A
- HGVS.c name
- ENSEMBL:ENST00000285311.8:c.514A>T
- ENSEMBL:ENST00000510463.1:c.376A>T
- HGVS.p name
- ENSP00000285311:p.Met172Leu
- ENSP00000421255:p.Met72Leu
- 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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