Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs779341057
- Species
- Homo sapiens
- Symbol
- rs779341057
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DDX3X
- Location
- X:41347426
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000023.11:g.41347426C>T
- HGVS.c name
- ENSEMBL:ENST00000441189.4:c.1785C>T
- ENSEMBL:ENST00000457138.7:c.1836C>T
- HGVS.p name
- ENSP00000392494:p.His612=
- ENSP00000414281:p.His595=
- 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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