Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs141761454
- Species
- Homo sapiens
- Symbol
- rs141761454
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DYNLT3
- Location
- X:37841079
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000023.11:g.37841079C>T
- HGVS.c name
- ENSEMBL:ENST00000378578.9:c.223G>A
- ENSEMBL:ENST00000378581.7:c.223G>A
- HGVS.p name
- ENSP00000367841:p.Ala75Thr
- ENSP00000367844:p.Ala75Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:37836757...37847571 (10.81 kb)
- Assembly version
- Not Available
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