Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1647554050
- Species
- Homo sapiens
- Symbol
- rs1647554050
- Category
- Variant
- Variant type
- SNP
- Overlaps
- WARS2
- Location
- 1:119032978
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:119032978G>A
- HGVS.c name
- ENSEMBL:ENST00000235521.5:c.1016C>T
- ENSEMBL:ENST00000369426.9:c.*382C>T
- HGVS.p name
- ENSP00000235521:p.Ser339Leu
- XP_005270407:p.Ser321Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:119031216...119140672 (109.46 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction