Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs207464938
- Species
- Homo sapiens
- Symbol
- rs207464938
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DKK2
- Location
- 4:107046609
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)4:107046609A>G
- HGVS.c name
- ENSEMBL:ENST00000510463.1:c.84+81333T>C
- ENSEMBL:ENST00000513208.5:c.-78-120660T>C
- HGVS.p name
- Not Available
- 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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