Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs207478531
- Species
- Homo sapiens
- Symbol
- rs207478531
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DACH2
- Location
- X:86607403
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)X:86607403A>G
- HGVS.c name
- ENSEMBL:ENST00000373125.9:c.641-43633A>G
- ENSEMBL:ENST00000373131.5:c.602-43633A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:86148451...86832604 (684.15 kb)
- Assembly version
- Not Available
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