Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1325653538
- Species
- Homo sapiens
- Symbol
- rs1325653538
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DACH2
- Location
- X:86149074
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000023.11:g.86149074T>C
- HGVS.c name
- ENSEMBL:ENST00000373125.9:c.454T>C
- ENSEMBL:ENST00000373131.5:c.454T>C
- HGVS.p name
- ENSP00000362217:p.Phe152Leu
- ENSP00000362223:p.Phe152Leu
- 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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