Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs151230279
- Species
- Homo sapiens
- Symbol
- rs151230279
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DACH2
- Location
- X:86651051
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)X:86651051C>T
- HGVS.c name
- ENSEMBL:ENST00000373125.9:c.656C>T
- ENSEMBL:ENST00000373131.5:c.617C>T
- HGVS.p name
- ENSP00000362217:p.Ala219Val
- ENSP00000362223:p.Ala206Val
- 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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