Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs753934786
- Species
- Homo sapiens
- Symbol
- rs753934786
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DACH2
- Location
- X:86816034
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant&splice region variant
- HGVS.g name
- NC_000023.11:g.86816034A>T
- HGVS.c name
- ENSEMBL:ENST00000373125.9:c.1685A>T
- ENSEMBL:ENST00000373131.5:c.1646A>T
- HGVS.p name
- ENSP00000362217:p.Asp562Val
- ENSP00000362223:p.Asp549Val
- 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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