Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1031779475
- Species
- Homo sapiens
- Symbol
- rs1031779475
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NKRF
- Location
- X:119605889
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000023.11:g.119605889T>A
- HGVS.c name
- ENSEMBL:ENST00000304449.8:c.-175A>T
- ENSEMBL:ENST00000673710.1:n.555A>T
- HGVS.p name
- ENSP00000508667:p.Pro35=
- NP_001404819:p.Gln36Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:119588337...119606443 (18.11 kb)
- Assembly version
- Not Available
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