Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs375521492
- Species
- Homo sapiens
- Symbol
- rs375521492
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MAP3K15
- Location
- X:19407271
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000023.11:g.19407271A>C
- HGVS.c name
- ENSEMBL:ENST00000338883.9:c.1761T>G
- ENSEMBL:ENST00000359173.7:n.1089T>G
- HGVS.p name
- ENSP00000345629:p.Phe587Leu
- XP_011543812:p.Phe145Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:19360056...19515508 (155.45 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction