Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs946383299
- Species
- Homo sapiens
- Symbol
- rs946383299
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SOWAHD
- Location
- X:119759559
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000023.11:g.119759559G>T
- HGVS.c name
- ENSEMBL:ENST00000343905.5:c.892G>T
- RefSeq:NM_001105576.3:c.892G>T
- HGVS.p name
- ENSP00000340975:p.Val298Leu
- NP_001099046:p.Val298Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:119758588...119760202 (1.61 kb)
- Assembly version
- Not Available
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