Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs890279081
- Species
- Homo sapiens
- Symbol
- rs890279081
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CLUL1
- Location
- 18:625012
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)18:625012T>C
- HGVS.c name
- ENSEMBL:ENST00000338387.11:c.403T>C
- ENSEMBL:ENST00000400606.6:c.403T>C
- HGVS.p name
- ENSP00000341128:p.Trp135Arg
- ENSP00000383449:p.Trp135Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:596988...650334 (53.35 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction