Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs2063867246
- Species
- Homo sapiens
- Symbol
- rs2063867246
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DDX3X
- Location
- X:41342667
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)X:41342667G>A
- HGVS.c name
- ENSEMBL:ENST00000399959.7:c.440+14G>A
- ENSEMBL:ENST00000441189.4:c.443+14G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:41333308...41364472 (31.16 kb)
- Assembly version
- Not Available
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